Papers citing Map Manager software

sorted by first author
January, 2004

A-C | D-F | G-J | K-M | N-Q | R-U | V-Z

A-C

Abbott C, and Chambers D (1994). Analysis of CAG Trinucleotide Repeats From Mouse cDNA Sequences. Annals of Human Genetics 58: 87-94.
Abbott CM, Blank R, Eppig JT, Friedman JM, Huppi KE, Jackson I, Mock BA, Stoye J, and Wiseman R (1992). Mouse Chromosome-4. Mammalian Genome 3: S55-S64.
Abe H, Nakano M, Nakatsuka A, Nakayama M, Koshioka M, and Yamagishi M (2002). Genetic analysis of floral anthocyanin pigmentation traits in Asiatic hybrid lily using molecular linkage maps. Theoretical and Applied Genetics 105: 1175-1182.
Adarichev VA, Bardos T, Christodoulou S, Phillips MT, Mikecz K, and Glant TT (2002). Major histocompatibility complex controls susceptibility and dominant inheritance, but not the severity of the disease in mouse models of rheumatoid arthritis. Immunogenetics 54: 184-192.
Adarichev VA, Nesterovitch AB, Bardos T, Biesczat D, Chandrasekaran R, Vermes C, Mikecz K, Finnegan A, and Glant TT (2003). Sex effect on clinical and immunologic quantitative trait loci in a murine model of rheumatoid arthritis. Arthritis and Rheumatism 48: 1708-1720.
Adarichev VA, Valdez JC, Bardos T, Finnegan A, Mikecz K, and Glant TT (2003). Combined autoimmune models of arthritis reveal shared and independent qualitative (Binary) and quantitative trait loci. Journal of Immunology 170: 2283-2292.
Adiletta DC, Elliott RW, and Woodworth ME (1993). Characterization of Murine Middle Repetitive DNA. Dna and Cell Biology 12: 319-327.
Airey DC, Lu L, and Williams RW (2001). Genetic control of the mouse cerebellum: Identification of quantitative trait loci modulating size and architecture. Journal of Neuroscience 21: 5099-5109.
Akiyoshi S, Kanda H, Okazaki Y, Akama T, Nomura K, Hayashizaki Y, and Kitagawa T (2000). A genetic linkage map of the MSM Japanese wild mouse strain with restriction landmark genomic scanning (RLGS). Mammalian Genome 11: 356-359.
Alagramam KN, Kwon HY, Cacheiro NLA, Stubbs L, Wright CG, Erway LC, and Woychik RP (1999). A new mouse insertional mutation that causes sensorineural deafness and vestibular defects. Genetics 152: 1691-1699.
Alexander RC, Wright R, and Freed W (1996). Quantitative trait loci contributing to phencyclidine-induced and amphetamine-induced locomotor behavior in inbred mice. Neuropsychopharmacology 15: 484-490.
Aljanabi SM, Honeycutt RJ, and Sobral BWS (1994). Chromosome Assortment in Saccharum. Theoretical and Applied Genetics 89: 959-963.
Allen J, Colleaux L, Davidson D, Graham E, Lee M, Hill R, Abbott C, and Gordon C (1997). Expression and mapping of the mouse S7/Pmsc2 gene, homolog of an essential mitotic gene in yeast. Mammalian Genome 8: 352-354.
Allen RD, Dobkins JA, Harper JM, and Slayback DL (1999). Genetics of graft-versus-host disease, I. A locus on Chromosome 1 influences development of acute graft-versus-host disease in a major histocompatibility complex mismatched murine model. Immunology 96: 254-261.
Allen RM, and Seyfried TN (1994). Genetic-Analysis of Nucleotide Triphosphatase-Activity in the Mouse-Brain. Genetics 137: 257-265.
Alli C, and Consalez GG (1998). Linkage mapping of Csrp to proximal mouse Chromosome 3. Mammalian Genome 9: 172-173.
Almind K, Kulkarni RN, Lannon SM, and Kahn CR (2003). Identification of interactive loci linked to insulin and leptin in mice with genetic insulin resistance. Diabetes 52: 1535-1543.
Amanna IJ, Clise-Dwyer K, Nashold FE, Hoag KA, and Hayes CE (2001). Cutting edge: A/WySnJ transitional B cells overexpress the chromosome 15 proapoptotic Blk gene and succumb to premature apoptosis. Journal of Immunology 167: 6069-6072.
Anderson JA, Sorrells ME, and Tanksley SD (1993). Rflp Analysis of Genomic Regions Associated With Resistance to Preharvest Sprouting in Wheat. Crop Science 33: 453-459.
Andrews KL, Mudd JL, Li C, and Miner JH (2002). Quantitative trait loci influence renal disease progression in a mouse model of Alport syndrome. American Journal of Pathology 160: 721-730.
Anna CH, and Devereux TR (1997). Sequence and chromosomal mapping of the mouse homolog (Madh4) of the human DPC4/MADH4 gene. Mammalian Genome 8: 443-444.
Anunciado RVP, Nishimura M, Mori M, Ishikawa A, Tanaka S, Hori F, Ohno T, and Namikawa T (2001). Quantitative trait loci for body weight in the intercross between SM/J and A/J mice. Experimental Animals 50: 319-324.
Anunciado RVP, Nishimura M, Mori M, Ishikawa A, Tanaka S, Horio F, Ohno T, and Namikawa T (2003). Quantitative trait locus analysis of serum insulin, triglyceride, total cholesterol and phospholipid levels in the (SM/J x A/J)F-2 mice. Experimental Animals 52: 37-42.
Anunciado RVP, Ohno T, Mori M, Ishikawa A, Tanaka S, Horio F, Nishimura M, and Namikawa T (2000). Distribution of body weight, blood insulin and lipid levels in the SMXA recombinant inbred strains and the QTL analysis. Experimental Animals 49: 217-224.
Apte SS, Fukai N, Beier DR, and Olsen BR (1997). The matrix metalloproteinase-14 (MMP-14) gene is structurally distinct from other MMP genes and is co-expressed with the TIMP-2 gene during mouse embryogenesis. Journal of Biological Chemistry 272: 25511-25517.
Aruga J, Nagai T, Tokuyama T, Hayashizaki Y, Okazaki Y, Chapman VM, and Mikoshiba K (1996). The mouse Zic gene family - Homologues of the Drosophila pair- rule gene odd-paired. Journal of Biological Chemistry 271: 1043-1047.
Assaf S, Hazard D, Pitel F, Morisson M, Alizadeh M, Gondret F, Diot C, Vignal A, Douaire M, and Lagarrigue S (2003). Cloning of cDNA encoding the nuclear form of chicken sterol response element binding protein-2 (SREBP-2), chromosomal localization, and tissue expression of chicken SREBP-1 and-2 genes. Poultry Science 82: 54-61.
Aszodi A, Beier DR, Hiripi L, Bosze Z, and Fassler R (1998). Sequence, structure and chromosomal localization of Crtm gene encoding mouse cartilage matrix protein and its exclusion as a candidate for murine achondroplasia. Matrix Biology 16: 563-573.
Aubagnac S, Brahic M, and Bureau JF (1999). Viral load and a locus on chromosome 11 affect the late clinical disease caused by Theiler's virus. Journal of Virology 73: 7965-7971.
Azuara V, and Pereira P (2000). Genetic mapping of two murine loci that influence the development of IL-4-producing Thy-1(dull) gamma delta thymocytes. Journal of Immunology 165: 42-48.
Azuma N, Seo HC, Lie O, Fu Q, Gould RM, Hiraiwa M, Burt DW, Paton IR, Morrice DR, O'Brien JS, and Kishimoto Y (1998). Cloning, expression and map assignment of chicken prosaposin. Biochemical Journal 330: 321-327.
Bariana HS, Hayden MJ, Ahmed NU, Bell JA, Sharp PJ, and McIntosh RA (2001). Mapping of durable adult plant and seedling resistances to stripe rust and stem rust diseases in wheat. Australian Journal of Agricultural Research 52: 1247-1255.
Baron B, Poirier C, Simonchazottes D, Barnier C, and Guenet JL (1992). A New Strategy Useful For Rapid Identification of Microsatellites From DNA Libraries With Large Size Inserts. Nucleic Acids Research 20: 3665-3669.
Barr AR, Chalmers KJ, Karakousis A, Kretschmer JM, Manning S, Lance RCM, Lewis J, Jeffries SP, and Langridge P (1998). RFLP mapping of a new cereal cyst nematode resistance locus in barley. Plant Breeding 117: 185-187.
Barr AR, Jefferies SP, Broughton S, Chalmers KJ, Kretschmer JM, Boyd WJR, Collins HM, Roumeliotis S, Logue SJ, Coventry SJ, Moody DB, Read BJ, Poulsen D, Lance RCM, Platz GJ, Park RF, Panozzo JF, Karakousis A, Lim P, Verbyla AP, and Eckermann PJ (2003). Mapping and QTL analysis of the barley population Alexis x Sloop. Australian Journal of Agricultural Research 54: 1117-1123.
Batey IL, Hayden MJ, Cai S, Sharp PJ, Cornish GB, Morell MK, and Appels R (2001). Genetic mapping of commercially significant starch characteristics in wheat crosses. Australian Journal of Agricultural Research 52: 1287-1296.
Batey IL, Hayden MJ, Cai S, Sharp PJ, Cornish GB, Morell MK, and Appels R (2002). Genetic mapping of commercially significant starch characteristics in wheat crosses (vol 52, pg 1287, 2001). Australian Journal of Agricultural Research 53: 1083-U22.
Battersby BJ, Loredo-Osti JC, and Shoubridge EA (2003). Nuclear genetic control of mitochondrial DNA segregation. Nature Genetics 33: 183-186.
Bauer E, Weyen J, Schiemann A, Graner A, and Ordon F (1997). Molecular mapping of novel resistance genes against Barley Mild Mosaic Virus (BaMMV). Theoretical and Applied Genetics 95: 1263-1269.
Beaumont C, Protais J, Pitel F, Leveque G, Malo D, Lantier F, Plisson-Petit F, Colin P, Protais M, Le Roy P, Elsen JM, Milan D, Lantier I, Neau A, Salvat G, and Vignal A (2003). Effect of two candidate genes on the Salmonella carrier state in fowl. Poultry Science 82: 721-726.
Beccari T, Appolloni MG, Stirling JL, and Orlacchio A (1996). Assignment of lysosomal alpha-D-mannosidase to mouse Chromosome 8. Mammalian Genome 7: 707-708.
Beckers J, Schlautmann N, and Gossler A (2000). The mouse rib-vertebrae mutation disrupts anterior-posterior somite patterning and genetically interacts with a Delta1 null allele. Mechanisms of Development 95: 35-46.
Beier DR (1993). Single-Strand Conformation Polymorphism (Sscp) Analysis As a Tool For Genetic-Mapping. Mammalian Genome 4: 627-631.
Beier DR, Dushkin H, and Sussman DJ (1992). Mapping Genes in the Mouse Using Single-Strand Conformation Polymorphism Analysis of Recombinant Inbred Strains and Interspecific Crosses. Proceedings of the National Academy of Sciences of the United States of America 89: 9102-9106.
Beier DR, Dushkin H, and Telle T (1995). Haplotype Analysis of Intra-Specific Backcross Curly-Tail Mice Confirms the Localization of Ct to Chromosome-4. Mammalian Genome 6: 269-272.
Bekes F, Gras PW, Anderssen RS, and Appels R (2001). Quality traits of wheat determined by small-scale dough testing methods. Australian Journal of Agricultural Research 52: 1325-1338.
Belknap JK (1998). Effect of within-strain sample size on QTL detection and mapping using recombinant inbred mouse strains. Behavior Genetics 28: 29-38.
Belknap JK, Hitzemann R, Crabbe JC, Phillips TJ, Buck KJ, and Williams RW (2001). QTL analysis and genomewide mutagenesis in mice: Complementary genetic approaches to the dissection of complex traits - Commentary. Behavior Genetics 31: 5-15.
Belknap JK, Mitchell SR, Otoole LA, Helms ML, and Crabbe JC (1996). Type I and Type II error rates for quantitative trait loci (QTL) mapping studies using recombinant inbred mouse strains. Behavior Genetics 26: 149-160.
Belknap JK, Mogil JS, Helms ML, Richards SP, Otoole LA, Bergeson SE, and Buck KJ (1995). Localization to Chromosome-10 of a Locus Influencing Morphine Analgesia in Crosses Derived from C57bl/6 and Dba/2 Strains. Life Sciences 57: PL117-PL124.
Belknap JK, Richards SP, Otoole LA, and Helms ML (1997). Short-term selective breeding as a tool for QTL mapping: Ethanol preference drinking in mice. Behavior Genetics 27: 55-66.
Bell CJ, and Ecker JR (1994). Assignment of 30 Microsatellite Loci to the Linkage Map of Arabidopsis. Genomics 19: 137-144.
Ben-Dor A, Chor B, and Pelleg D (2000). RHO - Radiation hybrid ordering. Genome Research 10: 365-378.
Bennett LM, Haugenstrano A, Cochran C, Brownlee HA, Fiedorek FT, and Wiseman RW (1995). Isolation of the Mouse Homolog of Brca1 and Genetic-Mapping to Mouse Chromosome-11. Genomics 29: 576-581.
Bergeson SE, Helms ML, O'Toole LA, Jarvis MW, Hain HS, Mogil JS, and Belknap JK (2001). Quantitative trait loci influencing morphine antinociception in four mapping populations. Mammalian Genome 12: 546-553.
Bergeson SE, Warren RK, Crabbe JC, Metten P, Erwin VG, and Belknap JK (2003). Chromosomal loci influencing chronic alcohol withdrawal severity. Mammalian Genome 14: 454-463.
Bermingham JR, Arden KC, Naumova AK, Sapienza C, Viars CS, Fu XD, Khotz J, Manley JL, and Rosenfeld MG (1995). Chromosomal Localization of Mouse and Human Genes Encoding the Splicing Factors Asf/Sf2 (Sfrs1) and Sc-35 (Sfrs2). Genomics 29: 70-79.
Berrios EF, Sarrafi A, Fabre F, Alibert G, and Gentzbittel L (2000). Genotypic variation and chromosomal location of QTLs for somatic embryogenesis revealed by epidermal layers culture of recombinant inbred lines in the sunflower (Helianthus annuus L.). Theoretical and Applied Genetics 101: 1307-1312.
Besse S, Allamand V, Vilquin JT, Li ZL, Poirier C, Vignier N, Hori H, Guenet JL, and Guicheney P (2003). Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin alpha 2 chain gene. Neuromuscular Disorders 13: 216-222.
Bielavska E, Kren V, Musilova A, Zidek V, and Pravenec M (2002). Genome scanning of the HXB/BXH sets of recombinant inbred strains of the rat for quantitative trait loci associated with conditioned taste aversion. Behavior Genetics 32: 51-56.
Biggs WH, Cavenee WK, and Arden KC (2001). Identification and characterization of members of the FKHR (FOX O) subclass of winged-helix transcription factors in the mouse. Mammalian Genome 12: 416-425.
Blake JA, Richardson JE, Davisson MT, Eppig JT, Battles J, Begley D, Blackburn R, Bradt D, Colby G, Corbani L, Davis G, Doolittle D, Drake T, Frazer K, Gilbert J, Grant P, LennonPierce M, Maltais L, May M, McIntire M, Merriam J, Ormsby J, Palazola R, Ringwald M, Rockwood S, Sharpe S, Shaw D, Reed D, StanleyWalls M, and Taylor L (1997). The Mouse Genome Database (MGD), a comprehensive public resource of genetic, phenotypic and genomic data. Nucleic Acids Research 25: 85-91.
Blanc I, Bach A, Lallemand Y, Perrin-Schmitt F, Guenet JL, and Robert B (2003). A new mouse limb mutation identifies a Twist allele that requires interacting loci on Chromosome 4 for its phenotypic expression. Mammalian Genome 14: 797-804.
Blizard DA (1992). Recombinant-Inbred Strains - General Methodological Considerations Relevant to the Study of Complex Characters. Behavior Genetics 22: 621-633.
Bois P, Stead JDH, Bakshi S, Williamson J, Neumann R, Moghadaszadeh B, and Jeffreys AJ (1998). Isolation and characterization of mouse minisatellites. Genomics 50: 317-330.
Bois P, Williamson J, Brown J, Dubrova YE, and Jeffreys AJ (1998). A novel unstable mouse VNTR family expanded from SINE B1 elements. Genomics 49: 122-128.
Bonne ACM, den Bieman MG, Gillissen GF, Kren V, Krenova D, Bila V, Zidek V, Kostka V, Musilova A, Pravenec M, van Zutphen BFM, and van Lith HA (2003). Genetic map of AFLP markers in the rat (Rattus norvegicus) derived from the H x B/Ipcv and B x H/Cub sets of recombinant inbred strains. Biochemical Genetics 41: 77-89.
Borowsky R, and Wilkens H (2002). Mapping a cave fish genome: Polygenic systems and regressive evolution. Journal of Heredity 93: 19-21.
Borsani G, DeGrandi A, Ballabio A, Bulfone A, Bernard L, Banfi S, Gattuso C, Mariani M, Dixon M, Donnai D, Metcalfe K, Winter R, Robertson M, Axton R, Brown A, van Heyningen V, and Hanson I (1999). EYA4, a novel vertebrate gene related to Drosophila eyes absent. Human Molecular Genetics 8: 11-23.
Bottger A, Lankhorst E, van Lith HA, van Zutphen LFM, Zidek V, Musilova A, Simakova M, Poledne R, Bila VT, Koen V, and Pravenec M (1998). A genetic and correlation analysis of liver cholesterol concentration in rat recombinant inbred strains fed a high cholesterol diet. Biochemical and Biophysical Research Communications 246: 272-275.
Bottger A, vanLith HA, Kren V, Krenova D, Bila V, Vorlicek J, Zidek V, Musilova A, Zdobinska M, Wang JM, vanZutphen BFM, Kurtz TW, and Pravenec M (1996). Quantitative trait loci influencing cholesterol and phospholipid phenotypes map to chromosomes that contain genes regulating blood pressure in the spontaneously hypertensive rat. Journal of Clinical Investigation 98: 856-862.
Bouchard G, Nelson HM, Lammert F, Rowe LB, Carey MC, and Paigen B (1999). High-resolution maps of the murine Chromosome 2 region containing the cholesterol gallstone locus, Lith1. Mammalian Genome 10: 1070-1074.
Boyd WJR, Li CD, Grime CR, Cakir M, Potipibool S, Kaveeta L, Men S, Kamali MRJ, Barr AR, Moody DB, Lance RCM, Logue SJ, Raman H, and Readj BJ (2003). Conventional and molecular genetic analysis of factors contributing to variation in the timing of heading among spring barley (Hordeum vulgare L.) genotypes grown over a mild winter growing season. Australian Journal of Agricultural Research 54: 1277-1301.
Boyle AEL, and Gill K (2001). Sensitivity of AXB/BXA recombinant inbred lines of mice to the locomotor activating effects of cocaine: a quantitative trait loci analysis. Pharmacogenetics 11: 255-264.
Brady KP, Dushkin H, Fornzler D, Koike T, Magner F, Her H, Gullans S, Segre GV, Green RM, and Beier DR (1999). A novel putative transporter maps to the osteosclerosis (oc) mutation and is not expressed in the oc mutant mouse. Genomics 56: 254-261.
Brady KP, Rowe LB, Her H, Stevens TJ, Eppig J, Sussman DJ, Sikela J, and Beier DR (1997). Genetic mapping of 262 loci derived from expressed sequences in a murine interspecific cross using single-strand conformational polymorphism analysis. Genome Research 7: 1085-1093.
Branford WW, Zhao GQ, Valerius MT, Weinstein M, Birkenmeier EH, Rowe LB, and Potter SS (1997). Spx1, a novel X-linked homeobox gene expressed during spermatogenesis. Mechanisms of Development 65: 87-98.
Broman KW, Wu H, Sen S, and Churchill GA (2003). R/qtl: QTL mapping in experimental crosses. Bioinformatics 19: 889-890.
Bronson RT, Donahue LR, Johnson KR, Tanner A, Lane PW, and Faust JR (1998). Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to Chromosome 9. American Journal of Medical Genetics 77: 289-297.
Browning VL, Chaudhry SS, Planchart A, Dixon MJ, and Schimenti JC (2001). Mutations of the mouse Twist and sy (Fibrillin 2) genes induced by chemical mutagenesis of ES cells. Genomics 73: 291-298.
Bucan M, Gatalica B, Nolan P, Chung A, Leroux A, Grossman MH, Nadeau JH, Emanuel BS, and Budarf M (1993). Comparative Mapping of 9 Human Chromosome-22q Loci in the Laboratory Mouse. Human Molecular Genetics 2: 1245-1252.
Buck K, Metten P, Belknap J, and Crabbe J (1999). Quantitative trait loci affecting risk for pentobarbital withdrawal map near alcohol withdrawal loci on mouse Chromosomes 1, 4, and 11. Mammalian Genome 10: 431-437.
Bulfone A, Menguzzato E, Broccoli V, Marchitiello A, Gattuso C, Mariani M, Consalez GG, Martinez S, Ballabio A, and Banfi S (2000). Barhl1, a gene belonging to a new subfamily of mammalian homeobox genes, is expressed in migrating neurons of the CNS. Human Molecular Genetics 9: 1443-1452.
Bureau JF, Drescher KM, Pease LR, Vikoren T, Delcroix M, Zoecklein L, Brahic M, and Rodriguez M (1998). Chromosome 14 contains determinants that regulate susceptibility to Theiler's virus-induced demyelination in the mouse. Genetics 148: 1941-1949.
Bureau JF, Le Goff S, Thomas D, Parlow AF, de la Torre JC, Homann D, Brahic M, and Oldstone MBA (2001). Disruption of differentiated functions during viral infection in vivo - V. Mapping of a locus involved in susceptibility of mice to growth hormone deficiency due to persistent lymphocytic choriomeningitis virus infection. Virology 281: 61-66.
Burt DW, Dey BR, Paton IR, Morrice DR, and Law AS (1995). The Chicken Transforming Growth Factor-Beta-3 Gene - Genomic Structure, Transcriptional Analysis, and Chromosomal Location. Dna and Cell Biology 14: 111-123.
Busfield SJ, Comrack CA, Yu G, Chickering TW, Smutko JS, Zhou H, Leiby KR, Holmgren LM, Gearing DP, and Pan Y (2000). Identification and gene organization of three novel members of the IL-1 family on human chromosome 2. Genomics 66: 213-216.
Bush AL, and Wise RP (1996). Crown rust resistance loci on linkage groups 4 and 13 in cultivated oat. Journal of Heredity 87: 427-432.
Butcher PA, Williams ER, Whitaker D, Ling S, Speed TP, and Moran GF (2002). Improving linkage analysis in outcrossed forest trees - an example from Acacia mangium. Theoretical and Applied Genetics 104: 1185-1191.
Byrne M, Murrell JC, Allen B, and Moran GF (1995). An Integrated Genetic-Linkage Map for Eucalypts Using Rflp, Rapd and Isozyme Markers. Theoretical and Applied Genetics 91: 869-875.
Cai HW, and Morishima H (2000). Genomic regions affecting seed shattering and seed dormancy in rice. Theoretical and Applied Genetics 100: 840-846.
Cai HW, and Morishima H (2002). QTL clusters reflect character associations in wild and cultivated rice. Theoretical and Applied Genetics 104: 1217-1228.
Cakir M, Gupta S, Platz GJ, Ablett GA, Loughman R, Emebiri LC, Poulsen D, Li CD, Lance RCM, Galwey NW, Jones MGK, and Appelsb R (2003). Mapping and validation of the genes for resistance to Pyrenophora teres f. teres in barley (Hordeum vulgare L.). Australian Journal of Agricultural Research 54: 1369-1377.
Cakir M, Poulsen D, Galwey NW, Ablett GA, Chalmers KJ, Platz GJ, Park RF, Lance RCM, Panozzo JF, Read BJ, Moody DB, Barr AR, Johnston P, Li CD, Boyd WJR, Grime CR, Appels R, Jones MGK, and Langridge P (2003). Mapping and QTL analysis of the barley population Tallon x Kaputar. Australian Journal of Agricultural Research 54: 1155-1162.
Cakir M, Spackman M, Wellings CR, Galwey NW, Moody DB, Poulsen D, Ogbonnaya FC, and Vivar H (2003). Molecular mapping as a tool for pre-emptive breeding for resistance to the exotic barley pathogen, Puccinia striiformis f. sp hordei. Australian Journal of Agricultural Research 54: 1351-1357.
Campbell KG, Finney PL, Bergman CJ, Gualberto DG, Anderson JA, Giroux MJ, Siritunga D, Zhu JQ, Gendre F, Roue C, Verel A, and Sorrells ME (2001). Quantitative trait loci associated with milling and baking quality in a soft x hard wheat cross. Crop Science 41: 1275-1285.
Caron J, Loredo-Osti JC, Laroche L, Skamene E, Morgan K, and Malo D (2002). Identification of genetic loci controlling bacterial clearance in experimental Salmonella enteritidis infection: an unexpected role of Nramp1 (Slc11a1) in the persistence of in infection in mice. Genes and Immunity 3: 196-204.
Carter M, Ulrich S, Oofuji Y, Williams DA, and Ross ME (1999). Crooked tail (Cd) models human folate-responsive neural tube defects. Human Molecular Genetics 8: 2199-2204.
Carver EA, Hamann J, Olsen AS, and Stubbs L (1999). Physical mapping of EMR1 and CD97 in human Chromosome 19 and assignment of Cd97 to mouse Chromosome 8 suggest an ancient genomic duplication. Mammalian Genome 10: 1039-1040.
Carver EA, Issel-Tarver L, Rine J, Olsen AS, and Stubbs L (1998). Location of mouse and human genes corresponding to conserved canine olfactory receptor gene subfamilies. Mammalian Genome 9: 349-354.
Cases S, Novak S, Zheng YW, Myers HM, Lear SR, Sande E, Welch CB, Lusis AJ, Spencer TA, Krause BR, Erickson SK, and Farese RV (1998). ACAT-2, a second mammalian acyl-CoA : cholesterol acyltransferase - Its cloning, expression, and characterization. Journal of Biological Chemistry 273: 26755-26764.
Cases S, Smith SJ, Zheng YW, Myers HM, Lear SR, Sande E, Novak S, Collins C, Welch CB, Lusis AJ, Erickson SK, and Farese RV (1998). Identification of a gene encoding an acyl CoA : diacylglycerol acyltransferase, a key enzyme in triacylglycerol synthesis. Proceedings of the National Academy of Sciences of the United States of America 95: 13018-13023.
Causse MA, Fulton TM, Cho YG, Ahn SN, Chunwongse J, Wu KS, Xiao JH, Yu ZH, Ronald PC, Harrington SE, Second G, McCouch SR, and Tanksley SD (1994). Saturated Molecular Map of the Rice Genome Based on an Interspecific Backcross Population. Genetics 138: 1251-1274.
Chakravarti S, and Magnuson T (1995). Localization of Mouse Lumican (Keratan Sulfate Proteoglycan) to Distal Chromosome 1o. Mammalian Genome 6: 367-368.
Chakravarti S, Phillips SL, and Hassell JR (1991). Assignment of the Perlecan (Heparan-Sulfate Proteoglycan) Gene to Mouse Chromosome-4. Mammalian Genome 1: 270-272.
Chambers DM, and Abbott CM (1996). Isolation and mapping of novel mouse brain cDNA clones containing trinucleotide repeats, and demonstration of novel alleles in recombinant inbred strains. Genome Research 6: 715-723.
Chambers DM, Kipling D, and Abbott CM (1998). Isolation of a microsatellite that reveals paralogy between the subtelomeric regions of mouse chromosomes 17 and 19: Further evidence for telomere-telomere exchange in the mouse. Genomics 53: 113-114.
Champoux MC, Wang G, Sarkarung S, Mackill DJ, Otoole JC, Huang N, and McCouch SR (1995). Locating Genes Associated With Root Morphology and Drought Avoidance in Rice Via Linkage to Molecular Markers. Theoretical and Applied Genetics 90: 969-981.
Chattopadhyay S, Kaul R, Charest A, Housman D, and Chen JZ (2000). SMAR1, a novel, alternatively spliced gene product, binds the scaffold/matrix-associated region at the T cell receptor beta locus. Genomics 68: 93-96.
Cheah YC, Nadeau JH, Pugh S, and Paigen B (1994). New Murine Polymorphisms Detected By Random Amplified Polymorphic DNA (Rapd) Pcr and Mapped By Use of Recombinant Inbred Strains. Mammalian Genome 5: 762-767.
Cheah YC, and Paigen B (1994). Strain Distribution Patterns For 50 Sslp Markers in the Murine Akxl Recombinant Inbred Set. Mammalian Genome 5: 189-190.
Cheah YC, and Paigen B (1996). Mapping new murine polymorphisms detected by random amplified polymorphic DNA (RAPD) PCR. Mammalian Genome 7: 549-550.
Chen H, Thalmann I, Adams JC, Avraham KB, Copeland NG, Jenkins NA, Beier DR, Corey DP, Thalmann R, and Duyk GM (1995). Cdna Cloning, Tissue Distribution, and Chromosomal Localization of Ocp2 a Gene Encoding a Putative Transcription-Associated Factor Predominantly Expressed in the Auditory Organs. Genomics 27: 389-398.
Chen JC, and Harrison DE (2002). Quantitative trait loci regulating relative lymphocyte proportions in mouse peripheral blood. Blood 99: 561-566.
Chi HB, Tiller GE, Dasouki MJ, Romano PR, Wang J, O'Keefe RJ, Puzas JE, Rosier RN, and Reynolds PR (1999). Multiple inositol polyphosphate phosphatase: Evolution as a distinct group within the histidine phosphatase family and chromosomal localization of the human and mouse genes to chromosomes 10q23 and 19. Genomics 56: 324-336.
Chiang PW, Zhang RB, Stubbs L, Zhang L, Zhu L, and Kurnit DM (1998). Comparison of murine Supt4h and a nearly identical expressed, processed gene: evidence of sequence conservation through gene conversion extending into the untranslated regions. Nucleic Acids Research 26: 4960-4964.
Cho BC, Shaughnessy JD, Largaespada DA, Bedigian HG, Buchberg AM, Jenkins NA, and Copeland NG (1995). Frequent Disruption of the Nf1 Gene By a Novel Murine Aids Virus-Related Provirus in Bxh-2 Murine Myeloid Lymphomas. Journal of Virology 69: 7138-7146.
Cho HY, Jedlicka AE, Reddy SPM, Zhang LY, Kensler TW, and Kleeberger SR (2002). Linkage analysis of susceptibility to hyperoxia - Nrf2 is a candidate gene. American Journal of Respiratory Cell and Molecular Biology 26: 42-51.
Cho YG, McCouch SR, Kuiper M, Kang MR, Pot J, Groenen JTM, and Eun MY (1998). Integrated map of AFLP, SSLP and RFLP markers using a recombinant inbred population of rice (Oryza sativa L.). Theoretical and Applied Genetics 97: 370-380.
Chou SR, Brownell A, Ko MSH, and Kaplan J (2000). Interferon-gamma receptor polymorphisms determine strain differences in accessibility of activated lymphocyte NK- triggering antigene to recognition by self-reactive NK cells. Cellular Immunology 200: 88-97.
Chu FF, Esworthy RS, and Burmeister M (1996). The mouse glutathione peroxidase Gpx2 gene maps to chromosome 12; Its pseudogene Gpx2-ps maps to chromosome 7. Genomics 33: 516-518.
Cicila GT, Garrett MR, Lee SJ, Liu J, Dene H, and Rapp JP (2001). High-resolution mapping of the blood pressure QTL on chromosome 7 using Dahl rat congenic strains. Genomics 72: 51-60.
Cisar CR, Balog JM, Okimoto R, Anthony NB, and Donoghue AM (2003). The chicken bone morphogenetic protein receptor type II(BMPR2) gene maps to chromosome 7. Animal Genetics 34: 475-476.
Clise-Dwyer K, Amanna IJ, Duzeski JL, Nashold FE, and Hayes CE (2001). Genetic studies of B-lymphocyte deficiency and mastocytosis in strain A/WySnJ mice. Immunogenetics 53: 729-735.
Cohen DE, Green RM, Wu MK, and Beier DR (1999). Cloning, tissue-specific expression, gene structure and chromosomal localization of human phosphatidylcholine transfer protein. Biochimica Et Biophysica Acta-Gene Structure and Expression 1447: 265-270.
Coimbra MRM, Kobayashi K, Koretsugu S, Hasegawa O, Ohara E, Ozaki A, Sakamoto T, Naruse K, and Okamoto N (2003). A genetic linkage map of the Japanese flounder, Paralichthys olivaceus. Aquaculture 220: 203-218.
Coleman RD, Gill GS, and Rebetzke GJ (2001). Identification of quantitative trait loci for traits conferring weed competitiveness in wheat (Triticum aestivum L.). Australian Journal of Agricultural Research 52: 1235-1246.
Colinayo VV, Qiao JH, Demant P, Krass K, Lusis AJ, and Drake TA (2002). Genetic characterization of the Dyscalc locus. Mammalian Genome 13: 283-288.
Colinayo VV, Qiao JH, Wang XP, Krass KL, Schadt E, Lusis AJ, and Drake TA (2003). Genetic loci for diet-induced atherosclerotic lesions and plasma lipids in mice. Mammalian Genome 14: 464-471.
Cook S, Johnson K, and Davisson M (1997). The mouse urate oxidase gene, Uox, maps to distal Chromosome 3. Mammalian Genome 8: 623-624.
Cook SA, Akeson EC, Calvano C, Johnson KR, Mandell J, Hawes NL, Bronson RT, Roderick TH, and Davisson MT (2001). Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene. Cytogenetics and Cell Genetics 93: 77-82.
Cook SA, Bronson RT, Donahue LR, BenArie N, and Davisson MT (1997). Cerebellar deficient folia (cdf): A new mutation on mouse Chromosome 6. Mammalian Genome 8: 108-112.
Cook SA, Johnson KR, Bronson RT, and Davisson MT (1995). Neuromuscular Degeneration (Nmd) - a Mutation On Mouse Chromosome-19 That Causes Motor-Neuron Degeneration. Mammalian Genome 6: 187-191.
Corradi A, Croci L, Stayton CL, Gulisano M, Boncinelli E, and Consalez GG (1996). cDNA sequence, map, and expression of the murine homolog of GTBP, a DNA mismatch repair gene. Genomics 36: 288-295.
Corva PM, and Medrano JF (2001). Quantitative trait loci (QTLs) mapping for growth traits in the mouse: A review. Genetics Selection Evolution 33: 105-132.
Coulter AA, Bearden CM, Liu XT, Koza RA, and Kozak LP (2003). Dietary fat interacts with QTLs controlling induction of Pgc-1 alpha and Ucp1 during conversion of white to brown fat. Physiological Genomics 14: 139-147.
Cox KB, Johnson KR, and Wood PA (1998). Chromosomal locations of the mouse fatty acid oxidation genes Cpt1a, Cpt1b, Cpt2, Acadvl, and metabolically related Crat gene. Mammalian Genome 9: 608-610.
Cox RD, Shedlovsky A, Hamvas R, Goldsworthy M, Whittington J, Connelly CS, Dove WF, and Lehrach H (1994). A 1.2-Mb Yac Contig Spans the Quaking Region. Genomics 21: 77-84.
Crosier PS, Lewis PM, Hall LR, Vitas MR, Morris CM, Beier DR, Wood CR, and Crosier KE (1994). Isolation of a Receptor Tyrosine Kinase (Dtk) From Embryonic Stem-Cells - Structure, Genetic-Mapping and Analysis of Expression. Growth Factors 11: 125-136.
Cui ZH, Nemoto K, Kawakami K, Gonda T, Nabika T, and Masuda J (2002). Fine linkage mapping of the blood pressure quantitative trait locus region on rat chromosome 1. Hypertension Research 25: 605-608.

D-F

Da Y, VanRaden PM, and Schook LB (2000). Detection and parameter estimation for quantitative trait loci using regression models and multiple markers. Genetics Selection Evolution 32: 357-381.
Dal Zotto L, Quaderi NA, Elliott R, Lingerfelter PA, Carrel L, Valsecchi V, Montini E, Yen CH, Chapman V, Kalcheva I, Arrigo G, Zuffardi O, Thomas S, Willard HF, Ballabio A, Disteche CM, and Rugarli EI (1998). The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. Human Molecular Genetics 7: 489-499.
Dalton TP, Miller ML, Wu XM, Menon A, Cianciolo E, McKinnon RA, Smith PW, Robinson LJ, and Nebert DW (2000). Refining the mouse chromosomal location of Cdm, the major gene associated with susceptibility to cadmium-induced testicular necrosis. Pharmacogenetics 10: 141-151.
Danciger JS, Danciger M, Nusinowitz S, Rickabaugh T, and Farber DB (1999). Genetic and physical maps of the mouse rd3 locus; exclusion of the ortholog of USH2A. Mammalian Genome 10: 657-661.
Danciger M, Lyon J, Worrill D, LaVail MM, and Yang HD (2003). A strong and highly significant QTL on chromosome 6 that protects the mouse from age-related retinal degeneration. Investigative Ophthalmology & Visual Science 44: 2442-2449.
Danciger M, Matthes MT, Yasamura D, Akhmedov NB, Rickabaugh T, Gentleman S, Redmond TM, La Vail MM, and Farber DB (2000). A QTL on distal Chromosome 3 that influences the severity of light-induced damage to mouse photoreceptors. Mammalian Genome 11: 422-427.
Danielson PE, Watson JB, Gerendasy DD, Erlander MG, Lovenberg TW, Delecea L, Sutcliffe JG, and Frankel WN (1994). Chromosomal Mapping of Mouse Genes Expressed Selectively Within the Central-Nervous-System. Genomics 19: 454-461.
Daval S, Pitel F, Le Nigen C, Douaire M, Vignal A, and Lagarrigue S (2000). Cloning and mapping of the ACLY gene to a chicken microchromosome. Animal Genetics 31: 412-413.
Davies PO, Melanitou E, Asano M, Avner PR, and Montagutelli X (1995). An Anchored Molecular Map of Mouse Chromosome-6 With an Analysis of Interference. Mammalian Genome 6: 738-740.
Davisson MT, Cook SA, Johnson KR, and Eicher EM (1994). Balding - a New Mutation On Mouse Chromosome-18 Causing Hair Loss and Immunological Defects. Journal of Heredity 85: 134-136.
Davisson MT, Johnson KR, Bronson RT, Ward-Bailey PF, Cook SA, Harris BS, and Donahue LR (2000). Grey intense: a new mouse mutation affecting pigmentation. Mammalian Genome 11: 1139-1141.
Dawson D, McConnell S, Wardle A, Gibbs M, and Burke T (1998). Characterization and mapping of 15 novel chicken microsatellite loci. Animal Genetics 29: 159-160.
de Conciliis L, Marchitiello A, Wapenaar MC, Borsani G, Giglio S, Mariani M, Consalez GG, Zuffardi O, Franco B, Ballabio A, and Banfi S (1998). Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil alpha- helical domains. Genomics 51: 243-250.
de Haan G, Ausema A, Wilkens M, Molineux G, and Dontje B (2000). Efficient mobilization of haematopoietic progenitors after a single injection of pegylated recombinant human granulocyte colony-stimulating factor in mouse strains with distinct marrow-cell pool sizes. British Journal of Haematology 110: 638-646.
de Haan G, Bystrykh LV, Weersing E, Dontje B, Geiger H, Ivanova N, Lemischka IR, Vellenga E, and Van Zant G (2002). A genetic and genomic analysis identifies a cluster of genes associated with hematopoietic cell turnover. Blood 100: 2056-2062.
de Haan G, Gelman R, Watson A, Yunis E, and Van Zant G (1998). A putative gene causes variability in lifespan among genotypically identical mice. Nature Genetics 19: 114-116.
de Haan G, and Van Zant G (1997). Intrinsic and extrinsic control of hemopoietic stem cell numbers: Mapping of a stem cell gene. Journal of Experimental Medicine 186: 529-536.
de Haan G, and Van Zant G (1999). Dynamic changes in mouse hematopoietic stem cell numbers during aging. Blood 93: 3294-3301.
de Haan G, and Van Zant G (1999). Genetic analysis of hemopoietic cell cycling in mice suggests its involvement in organismal life span. Faseb Journal 13: 707-713.
de Wolf ID, Fielmich-Bouman XM, van Oost BA, Beynen AC, Kren V, Pravenec M, van Zutphen LFM, and van Lith HA (2001). Genetic and correlation analysis of hepatic copper content in the rat. Biochemical and Biophysical Research Communications 289: 1247-1251.
Deak F, Mates L, Krysan K, Liu Z, Szabo PE, Mann JR, Beier DR, and Kiss I (1999). Characterization and chromosome location of the mouse link protein gene (Crtl1). Cytogenetics and Cell Genetics 87: 75-79.
Degg NL, Weil MM, Edwards A, Haines J, Coster M, Moody J, Ellender M, Cox R, and Silver A (2003). Adenoma multiplicity in irradiated Apc(Min) mice is modified by chromosome 16 segments from BALB/c. Cancer Research 63: 2361-2363.
deHaan G, and VanZant G (1997). Intrinsic and extrinsic control of hemopoietic stem cell numbers: Mapping of a stem cell gene. Journal of Experimental Medicine 186: 529-536.
deLecea L, RuizLozano P, Danielson PE, PeelleKirley J, Foye PE, Frankel WN, and Sutcliffe JG (1997). Cloning, mRNA expression, and chromosomal mapping of mouse and human preprocortistatin. Genomics 42: 499-506.
Delpire E, Rauchman MI, Beier DR, Hebert SC, and Gullans SR (1994). Molecular-Cloning and Chromosome Localization of a Putative Basolateral Na+-K+-2cl(-) Cotransporter From Mouse Inner Medullary Collecting Duct (Mimcd-3) Cells. Journal of Biological Chemistry 269: 25677-25683.
Demant P (2003). Cancer susceptibility in the mouse: Genetics, biology and implications for human cancer. Nature Reviews Genetics 4: 721-734.
Demeke T, Morris CF, Campbell KG, King GE, Anderson JA, and Chang HG (2001). Wheat polyphenol oxidase: Distribution and genetic mapping in three inbred line populations. Crop Science 41: 1750-1757.
Depatie C, Muise E, Lepage P, Gros P, and Vidal SM (1997). High-resolution linkage map in the proximity of the host resistance locus Cmv1. Genomics 39: 154-163.
Deussing J, Roth W, Rommerskirch W, Wiederanders B, vonFigura K, and Peters C (1997). The genes of the lysosomal cysteine proteinases cathepsin B, H, L, and S map to different mouse Chromosomes. Mammalian Genome 8: 241-245.
Devereux TR, Wiseman RW, Kaplan N, Garren S, Foley JF, White CM, Anna C, Watson MA, Patel A, Jarchow S, Maronpot RR, and Anderson MW (1994). Assignment of a Locus For Mouse Lung-Tumor Susceptibility to Proximal Chromosome-19. Mammalian Genome 5: 749-755.
Devey ME, Bell JC, Smith DN, Neale DB, and Moran GF (1996). A genetic linkage map for Pinus radiata based on RFLP, RAPD, and microsatellite markers. Theoretical and Applied Genetics 92: 673-679.
Devey ME, Sewell MM, Uren TL, and Neale DB (1999). Comparative mapping in loblolly and radiata pine using RFLP and microsatellite markers. Theoretical and Applied Genetics 99: 656-662.
deVillena FPM, and Sapienza C (1996). Genetic mapping of DXYMov15-associated sequences in the pseudoautosomal region of the C57BL/6J strain. Mammalian Genome 7: 237-239.
Diehl SR, and Erickson RP (1997). Genome scan for teratogen-induced clefting susceptibility loci in the mouse: Evidence of both allelic and locus heterogeneity distinguishing cleft lip and cleft palate. Proceedings of the National Academy of Sciences of the United States of America 94: 5231-5236.
Dietrich W, Katz H, Lincoln SE, Shin HS, Friedman J, Dracopoli NC, and Lander ES (1992). A Genetic-Map of the Mouse Suitable For Typing Intraspecific Crosses. Genetics 131: 423-447.
Dietrich WF, Damron DM, Isberg RR, Lander ES, and Swanson MS (1995). Lgn1, a Gene That Determines Susceptibility to Legionella- Pneumophila, Maps to Mouse Chromosome-13. Genomics 26: 443-450.
Dohmoto A, Shimizu K, Asada Y, and Maeda T (2002). Quantitative trait loci on chromosomes 10 and 11 influencing mandible size of SMXA RI mouse strains. Journal of Dental Research 81: 501-504.
Donahue LR, Chang B, Mohan S, Miyakoshi N, Wergedal JE, Baylink DJ, Hawes NL, Rosen CJ, Ward-Bailey P, Zheng QY, Bronson RT, Johnson KR, and Davisson MT (2003). Missense mutation in the mouse Col2al gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis. Journal of Bone and Mineral Research 18: 1612-1621.
Donahue LR, Cook SA, Johnson KR, Bronson RT, and Davisson MT (1996). Megencephaly: A new mouse mutation on chromosome 6 that causes hypertrophy of the brain. Mammalian Genome 7: 871-876.
Donaldson DD, Whitters MJ, Fitz LJ, Neben TY, Finnerty H, Henderson SL, O'Hara RM, Beier DR, Turner KJ, Wood CR, and Collins M (1998). The murine IL-13 receptor alpha 2: Molecular cloning, characterization, and comparison with marine IL-13 receptor. Journal of Immunology 161: 2317-2324.
Dong CM, Whitford R, and Langridge P (2002). A DNA mismatch repair gene links to the Ph2 locus in wheat. Genome 45: 116-124.
Dower NA, Seldin MF, Pugh S, and Stone JC (1992). Organization and Chromosomal Locations of Rap1a/Krev Sequences in the Mouse. Mammalian Genome 3: 162-167.
Downing C, Rodd-Henricks KK, Flaherty L, and Dudek BC (2003). Genetic analysis of the psychomotor stimulant effect of ethanol. Genes Brain and Behavior 2: 140-151.
Downing C, Shen EH, Simpson VJ, and Johnson TE (2003). Mapping quantitative trait loci mediating sensitivity to etomidate. Mammalian Genome 14: 367-375.
Doyle J, Hellevuo K, and Stubbs L (1996). The gene encoding adenylyl cyclase VII is located in central mouse Chromosome 8. Mammalian Genome 7: 320-321.
Doyle J, Hoffman S, Ucla C, Reith W, Mach B, and Stubbs L (1996). Locations of human and mouse genes encoding the RFX1 and RFX2 transcription factor proteins. Genomics 35: 227-230.
Doyle J, Ren XJ, Lennon G, and Stubbs L (1997). Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice. Mammalian Genome 8: 113-120.
Drake TA, Hannani K, Kabo JM, Villa V, Krass K, and Lusis AJ (2001). Genetic loci influencing natural variations in femoral bone morphometry in mice. Journal of Orthopaedic Research 19: 511-517.
Dumas P, Kren V, Krenova D, Pravenec M, Hamet P, and Tremblay J (2002). Identification and chromosomal localization of ecogenetic components of electrolyte excretion. Journal of Hypertension 20: 209-217.
Dumas P, Pausova Z, Kren V, Krenova D, Pravenec M, Dumont M, Ely D, Turner M, Sun YL, Tremblay J, and Hamet P (2000). Contribution of autosomal loci and the Y chromosome to the stress response in rats. Hypertension 35: 568-573.
Dumas P, Sun YL, Corbeil G, Tremblay S, Pausova Z, Kren V, Krenova D, Pravenec M, Hamet P, and Tremblay J (2000). Mapping of quantitative trait loci (QTL) of differential stress gene expression in rat recombinant inbred strains. Journal of Hypertension 18: 545-551.
Duner T, Conlon JM, Kukkonen JP, Akerman KEO, Yan YL, Postlethwait JH, and Larhammar D (2002). Cloning, structural characterization and functional expression of a zebrafish bradykinin B2-related receptor. Biochemical Journal 364: 817-824.
Dunlevy JR, Chakravarti S, Gyalzen P, Vergnes JP, and Hassell JR (1998). Cloning and chromosomal localization of mouse keratocan, a corneal keratan sulfate proteoglycan. Mammalian Genome 9: 316-319.
Dunn IC, Boswell T, Friedman-Einat M, Eshdat Y, Burt DW, and Paton IR (2000). Mapping of the leptin receptor gene (LEPR) to chicken chromosome 8. Animal Genetics 31: 290-290.
Eglinton JK, Langridge P, and Evans DE (1998). Thermostability variation in alleles of barley beta-amylase. Journal of Cereal Science 28: 301-309.
Eilertsen KJ, Tran T, Sundberg JP, Stenn KS, and Parimoo S (2000). High resolution genetic and physical mapping of the mouse asebia locus: A key gene locus for sebaceous gland differentiation. Journal of Experimental Animal Science 40: 165-170.
Elango R, Riba L, Housman D, and Hunter K (1996). Generation and mapping of Mus spretus strain-specific markers for rapid genomic scanning. Mammalian Genome 7: 340-343.
Elliott RW, Manly KF, and Hohman C (1999). A radiation hybrid map of mouse chromosome 13. Genomics 57: 365-370.
Elliott RW, and Pazik J (1995). An Interstitial Telomere Array Near Hba On Mouse Chr-11 Is a Candidate For the Homolog of the Telomere At Human 16p. Genomics 27: 217-218.
Elliott RW, and Yen CH (1991). DNA Variants with Telomere Probe Enable Genetic-Mapping of Ends of Mouse Chromosomes. Mammalian Genome 1: 118-122.
Emebiri LC, Devey ME, Matheson AC, and Slee MU (1998). Age-related changes in the expression of QTLs for growth in radiata pine seedlings. Theoretical and Applied Genetics 97: 1053-1061.
Encinas JA, Kikuchi K, Chedotal A, de Castro F, Goodman CS, and Kimura T (1999). Cloning, expression, and genetic mapping of Sema W, a member of the semaphorin family. Proceedings of the National Academy of Sciences of the United States of America 96: 2491-2496.
Eppig JT, Blake JA, Davisson MT, and Richardson JE (1998). Informatics for mouse genetics and genome mapping. Methods-a Companion to Methods in Enzymology 14: 179-190.
Ewing EE, Simko I, Smart CD, Bonierbale MW, Mizubuti ESG, May GD, and Fry WE (2000). Genetic mapping from field tests of qualitative and quantitative resistance to Phytophthora infestans in a population derived from Solanum tuberosum and Solanum berthaultii. Molecular Breeding 6: 25-36.
Fabritius AL, and Judelson HS (1997). Mating type loci segregate aberrantly in Phytophthora infestans but normally in Phytophthora parasitica: implications for models of mating-type determination. Current Genetics 32: 60-65.
Fabritius AL, Shattock RC, and Judelson HS (1997). Genetic analysis of metalaxyl insensitivity loci in Phytophthora infestans using linked DNA markers. Phytopathology 87: 1034-1040.
Favor J, Grimes P, NeuhauserKlaus A, Pretsch W, and Stambolian D (1997). The mouse Cat4 locus maps to Chromosome 8 and mutants express lens-corneal adhesion. Mammalian Genome 8: 403-406.
Favor J, and Neuhauser-Klaus A (2000). Saturation mutagenesis for dominant eye morphological defects in the mouse Mus musculus. Mammalian Genome 11: 520-525.
Favor J, Peters H, Hermann T, Schmahl W, Chatterjee B, Neuhauser-Klaus A, and Sandulache R (2001). Molecular characterization of Pax6(2Neu) through Pax6(10Neu): An extension of the Pax6 allelic series and the identification of two possible hypomorph alleles in the mouse Mus musculus. Genetics 159: 1689-1700.
Fiedorek FT, and Kay ES (1994). Mapping of Pcr-Based Markers for Mouse Chromosome-4 on a Backcross Penetrant for the Misty (M) Mutation. Mammalian Genome 5: 479-485.
Fiedorek FT, and Kay ES (1995). Mapping of the Insulin Promoter Factor-1 Gene (Ipf1) to Distal Mouse Chromosome-5. Genomics 28: 581-584.
Fiedorek FT, and Kay ES (1995). Mapping of the Focal Adhesion Kinase (Fadk) Gene to Mouse Chromosome-15 and Human-Chromosome-8. Mammalian Genome 6: 123-126.
Fierer J, Walls L, Wright F, and Kirkland TN (1999). Genes influencing resistance to Coccidioides immitis and the interleukin-10 response map to chromosomes 4 and 6 in mice. Infection and Immunity 67: 2916-2919.
Fleming MD, Romano MA, Su MA, Garrick LM, Garrick MD, and Andrews NC (1998). Nramp2 is mutated in the anemic Belgrade (b) rat: Evidence of a role for Nramp2 in endosomal iron transport. Proceedings of the National Academy of Sciences of the United States of America 95: 1148-1153.
Fleming MD, Trenor CC, Su MA, Foernzler D, Beier DR, Dietrich WF, and Andrews NC (1997). Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene. Nature Genetics 16: 383-386.
Foernzler D, and Beier DR (1999). Gene mapping in zebrafish using single-strand conformation polymorphism analysis. Methods in Cell Biology, Vol 60 60: 185-193.
Foernzler D, and Beier DR (1999). Gene mapping in zebrafish using single-strand conformation polymorphism analysis. In "Methods in Cell Biology, Vol 60", pp. 185-193.
Foulongne M, Pascal T, Arus P, and Kervella J (2003). The potential of Prunus davidiana for introgression into peach Prunus persica (L.) Batsch assessed by comparative mapping. Theoretical and Applied Genetics 107: 227-238.
Foulongne M, Pascal T, Pfeiffer F, and Kervella J (2003). QTLs for powdery mildew resistance in peach x Prunus davidiana crosses: consistency across generations and environments. Molecular Breeding 12: 33-50.
Fowler KJ, Kalitsis P, and Choo KHA (1999). Mouse mitotic spindle checkpoint Bub3 gene maps to the distal region of Chromosome 7 by interspecific backcross analysis. Cytogenetics and Cell Genetics 87: 91-92.
Fowler KJ, Saffery R, Irvine DV, Trowell HE, and Choo KHA (1998). Mouse centromere protein F (Cenpf) gene maps to the distal region of Chromosome 1 by interspecific backcross analysis. Cytogenetics and Cell Genetics 82: 180-181.
Fowler KJ, Saffery R, Kile BT, Irvine DV, Hudson DF, Trowell HE, and Choo KHA (1998). Genetic mapping of mouse centromere protein (Incenp and Cenpe) genes. Cytogenetics and Cell Genetics 82: 67-70.
Frankel WN, Sweet HO, and Davisson MT (1994). The Stumbler Mutation Maps to Proximal Mouse Chromosome-2. Mammalian Genome 5: 659-662.
Fridolfsson AK, Cheng H, Copeland NG, Jenkins NA, Liu HC, Raudsepp T, Woodage T, Chowdhary B, Halverson J, and Ellegren H (1998). Evolution of the avian sex chromosomes from an ancestral pair of autosomes. Proceedings of the National Academy of Sciences of the United States of America 95: 8147-8152.
Frohlich L, Liu Z, Beier DR, and Lanske B (2002). Genomic structure and refined chromosomal localization of the mouse Ptch2 gene. Cytogenetic and Genome Research 97: 106-110.
Fuchs P, Zorer M, Rezniczek GA, Spazierer D, Oehler S, Castanon MJ, Hauptmann R, and Wiche G (1999). Unusual 5 ' transcript complexity of plectin isoforms: novel tissue-specific exons modulate actin binding activity. Human Molecular Genetics 8: 2461-2472.
Fukiya S, Kodama M, Kito H, Sone T, and Tomita F (2001). Establishment of a new cross of the rice blast fungus derived from Japanese differential strain Ina168 and hermaphroditic rice pathogen Guy11. Bioscience Biotechnology and Biochemistry 65: 1464-1473.
Furuse T, Miura Y, Yagasaki K, Shiroishi T, and Koide T (2003). Identification of QTLs for differential capsaicin sensitivity between mouse strains KJR and C57BL/6. Pain 105: 169-175.
Furuse T, Takano-Shimizu T, Moriwaki K, Shiroishi T, and Koide T (2002). QTL analyses of spontaneous activity by using mouse strains from Mishima battery. Mammalian Genome 13: 411-415.

G-J

Gafvels ME, Paavola LG, Boyd CO, Nolan PM, Wittmaack F, Chawla A, Lazar MA, Bucan M, Angelin B, and Strauss JF (1994). Cloning of a Complementary Deoxyribonucleic-Acid Encoding the Murine Homolog of the Very-Low-Density Lipoprotein Apolipoprotein-E Receptor - Expression Pattern and Assignment of the Gene to Mouse Chromosome-19. Endocrinology 135: 387-394.
Garey CE, Schwarzman AL, Rise ML, and Seyfried TN (1994). Ceruloplasmin Gene Defect Associated With Epilepsy in El Mice. Nature Genetics 6: 426-431.
Garretson JD, and Neumann PE (1993). Further Evidence That a Mouse Chromosome-4 Locus Influences Cerebellar Folial Pattern. Brain Research 630: 221-225.
Garrett KM, Haque D, Berry D, Niekrasz I, Gan JP, Rotter A, and Seale TW (1997). The GABA(A) receptor alpha(6) subunit gene (Gabra6) is tightly linked to the alpha(1)-gamma(2) subunit cluster on mouse chromosome 11. Molecular Brain Research 45: 133-137.
Garrett MR, Dene H, and Rapp JP (2003). Time-course genetic analysis of albuminuria in Dahl salt-sensitive rats on low-salt diet. Journal of the American Society of Nephrology 14: 1175-1187.
Garvey SM, Rajan C, Lerner AP, Frankel WN, and Cox GA (2002). The muscular dystrophy with myositis (mdm) mouse mutation disrupts a skeletal muscle-specific domain of titin. Genomics 79: 146-149.
Gates MA, Kim L, Egan ES, Cardozo T, Sirotkin HI, Dougan ST, Lashkari D, Abagyan R, Schier AF, and Talbot WS (1999). A genetic linkage map for zebrafish: Comparative analysis and localization of genes and expressed sequences. Genome Research 9: 334-347.
Ge SF, Romanov MN, Sharp PJ, Burt DW, Paton IR, and Dunn IC (2001). Mapping of the luteinizing hormone/choriogonadotropin receptor gene (LHCGR) to chicken chromosome 3. Animal Genetics 32: 50-50.
Geldermann H, Muller E, Moser G, Reiner G, Bartenschlager H, Cepica S, Stratil A, Kuryl J, Moran C, Davoli R, and Brunsch C (2003). Genome-wide linkage and QTL mapping in porcine F-2 families generated from Pietrain, Meishan and Wild Boar crosses. Journal of Animal Breeding and Genetics 120: 363-393.
Genger RK, Williams KJ, Raman H, Read BJ, Wallwork H, Burdon JJ, and Brown AHD (2003). Leaf scald resistance genes in Hordeum vulgare and Hordeum vulgare ssp spontaneum: parallels between cultivated and wild barley. Australian Journal of Agricultural Research 54: 1335-1342.
Gerling IC, Karlsen AE, Chapman HD, Andersen HU, Boel E, Cunningham JM, Nerup J, and Leiter EH (1994). The Inducible Nitric-Oxide Synthase Gene, Nos2, Maps to Mouse Chromosome-11. Mammalian Genome 5: 318-320.
Gershenfeld HK, Neumann PE, Li XH, St Jean PL, and Paul SM (1999). Mapping quantitative trait loci for seizure response to a GABA(A) receptor inverse agonist in mice. Journal of Neuroscience 19: 3731-3738.
Gershenfeld HK, and Paul SM (1997). Mapping quantitative trait loci for fear-like behaviors in mice. Genomics 46: 1-8.
Gibbs M, Dawson D, McCamley C, and Burke T (1995). Ten novel chicken dinucleotide repeat polymorphisms. Animal Genetics 26: 443-444.
Gibbs M, Dawson DA, McCamley C, Wardle AF, Armour JAL, and Burke T (1997). Chicken microsatellite markers isolated from libraries enriched for simple tandem repeats. Animal Genetics 28: 401-417.
Gill K, Boyle A, Lake K, and Desaulniers N (2000). Alcohol-induced locomotor activation in C57BL/6J, A/J, and AXB/BXA recombinant inbred mice: strain distribution patterns and quantitative trait loci analysis. Psychopharmacology 150: 412-421.
Gill K, Desaulniers N, Desjardins P, and Lake K (1998). Alcohol preference in AXB/BXA recombinant inbred mice: gender differences and gender-specific quantitative trait loci. Mammalian Genome 9: 929-935.
Gill KJ, and Boyle AE (2003). Confirmation of quantitative trait loci for cocaine-induced activation in the AcB/BcA series of recombinant congenic strains. Pharmacogenetics 13: 329-338.
GirardSantosuosso O, Bumstead N, Lantier I, Protais J, Colin P, Guillot JF, Beaumont C, Malo D, and Lantier F (1997). Partial conservation of the mammalian NRAMP1 syntenic group on chicken Chromosome 7. Mammalian Genome 8: 614-616.
Gohda T, Makita Y, Shike T, Tanimoto M, Funabiki K, Horikoshi S, and Tomino Y (2003). Identification of epistatic interaction involved in obesity using the KK/Ta mouse as a type 2 diabetes model - Is Zn-alpha(2) glycoprotein-1 a candidate gene for obesity? Diabetes 52: 2175-2181.
Gokce AF, McCallum J, Sato Y, and Havey MJ (2002). Molecular tagging of the Ms locus in onion. Journal of the American Society for Horticultural Science 127: 576-582.
Grandillo S, and Tanksley SD (1996). QTL analysis of horticultural traits differentiating the cultivated tomato from the closely related species Lycopersicon pimpinellifolium. Theoretical and Applied Genetics 92: 935-951.
Grandillo S, and Tanksley SD (1996). Genetic analysis of RFLPs, GATA microsatellites and RAPDs in a cross between L-esculentum and L-pimpinellifolium. Theoretical and Applied Genetics 92: 957-965.
Graner A, Streng S, Kellermann A, Schiemann A, Bauer E, Waugh R, Pellio B, and Ordon F (1999). Molecular mapping and genetic fine-structure of the rym5 locus encoding resistance to different strains of the Barley Yellow Mosaic Virus Complex. Theoretical and Applied Genetics 98: 285-290.
Grant DF, Spearow JL, Storms DH, Edelhoff S, Adler DA, Disteche CM, Taylor BA, and Hammock BD (1994). Chromosomal Mapping and Expression Levels of a Mouse Soluble Epoxide Hydrolase Gene. Pharmacogenetics 4: 64-72.
Green RM, Ananthanarayanan M, Suchy FJ, and Beier DR (1998). Genetic mapping of the Na+-taurocholate cotransporting polypeptide to mouse chromosome 12. Mammalian Genome 9: 598-598.
Grewal PK, Bolland DJ, Todd LC, and Hewitt JE (1998). High-resolution mapping of mouse Chromosome 8 identifies an evolutionary chromosomal breakpoint. Mammalian Genome 9: 603-607.
Grewal PK, and Hewitt JE (1997). Fath, the murine homolog of the Drosophila fat tumor suppressor gene, maps to Chromosome 8. Mammalian Genome 8: 383-384.
Grewal PK, vanDeutekom JCT, Mills KA, Lemmers R, Mathews KD, Frants RR, and Hewitt JE (1997). The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on Chromosome 8. Mammalian Genome 8: 394-398.
Griff IC, and Reed RR (1995). The Genetic-Basis For Specific Anosmia to Isovaleric Acid in the Mouse. Cell 83: 407-414.
Groenen MAM, Crooijmans R, Dijkhof RJM, Acar R, and van der Poel JJ (1999). Extending the chicken-human comparative map by placing 15 genes on the chicken linkage map. Animal Genetics 30: 418-422.
Gu LJ, Johnson MW, and Lusis AJ (1999). Quantitative trait focus analysis of plasma lipoprotein levels in an autoimmune mouse model - Interactions between lipoprotein metabolism, autoimmune disease, and atherogenesis. Arteriosclerosis Thrombosis and Vascular Biology 19: 442-453.
Gu LJ, Weinreb A, Wang XP, Zack DJ, Qiao JH, Weisbart R, and Lusis AJ (1998). Genetic determinants of autoimmune disease and coronary vasculitis in the MRL-lpr/lpr mouse model of systemic lupus erythematosus. Journal of Immunology 161: 6999-7006.
Gualtieri G, Kulikova O, Limpens E, Kim DJ, Cook DR, Bisseling T, and Geurts R (2002). Microsynteny between pea and Medicago truncatula in the SYM2 region. Plant Molecular Biology 50: 225-235.
Guay-Woodford LM, Green WJ, Lindsey JR, and Beier DR (2000). Germline and somatic loss of function of the mouse cpk gene causes biliary ductal pathology that is genetically modulated. Human Molecular Genetics 9: 769-778.
Guay-Woodford LM, Wright CJ, Walz G, and Churchill GA (2000). Quantitative trait loci modulate renal cystic disease severity in the mouse bpk model. Journal of the American Society of Nephrology 11: 1253-1260.
Gunther T, Sporle R, and Schughart K (1997). The open brain (opb) mutation maps to mouse Chromosome 1. Mammalian Genome 8: 583-585.
Guo ZJ, Mori M, Fu XY, Yao JJ, Xing YM, Korenaga T, Li GX, Matsushita T, Hosokawa M, and Higuchi K (2003). Amyloidosis modifier genes in the less amyloidogenic A/J mouse strain. Laboratory Investigation 83: 1605-1613.
Guttinger M, Sutti F, Panigada M, Porcellini S, Merati B, Mariani M, Teesalu T, Consalez GG, and Grassi F (1998). Epithelial V-like antigen (EVA), a novel member of the immunoglobulin superfamily, expressed in embryonic epithelia with a potential role as homotypic adhesion molecule in thymus histogenesis. Journal of Cell Biology 141: 1061-1071.
Haddad R, Morrow AD, Plass C, and Held WA (2000). Restriction Landmark Genomic Scanning of mouse liver tumors for gene amplification: Overexpression of cyclin A2. Biochemical and Biophysical Research Communications 274: 188-196.
Hadjantonakis AK, Sheward WJ, Harmar AJ, deGalan L, Hoovers JMN, and Little PFR (1997). Celsr1, a neural-specific gene encoding an unusual seven-pass transmembrane receptor, maps to mouse chromosome 15 and human chromosome 22qter. Genomics 45: 97-104.
Hain HS, Crabbe JC, Bergeson SE, and Belknap JK (2000). Cocaine-induced seizure thresholds: Quantitative trait loci detection and mapping in two populations derived from the C59BL/6 and DBA/2 mouse strains. Journal of Pharmacology and Experimental Therapeutics 293: 180-187.
Hanotte O, Pugh A, Maucher C, Dawson D, and Burke T (1997). Nine novel chicken microsatellite loci and their utility in other Galliformes. Animal Genetics 28: 311-313.
Hardy CL, Lu L, Nguyen P, Woodland DL, Williams RW, and Blackman MA (2001). Identification of quantitative trait loci controlling activation of TRBV4 CD8(+) T cells during murine gamma- herpesvirus-induced infectious mononucleosis. Immunogenetics 53: 395-400.
Harper JM, Slayback DL, Dobkins JA, and Allen RD (1999). A locus on chromosome 2 influences the development of acute graft-versus-host disease in a murine model. Bone Marrow Transplantation 23: 1183-1190.
Harris BS, Franz T, Ullrich S, Cook S, Bronson RT, and Davisson MT (1997). Forebrain overgrowth (fog): A new mutation in the mouse affecting neural tube development. Teratology 55: 231-240.
Hartsfield JK, and Everett ET (2000). The Ephx1(d) allele encoding an Arg338Cys substitution is associated with heat lability. Mammalian Genome 11: 915-918.
Hashimoto Y, Shindo-Okada N, Tani M, Nagamachi Y, Takeuchi K, Shiroishi T, Toma H, and Yokota J (1998). Expression of the Elm1 gene, a novel gene of the CCN (connective tissue growth factor, Cyr61/Cef10, and neuroblastoma overexpressed gene) family, suppresses in vivo tumor growth and metastasis of K-1735 murine melanoma cells. Journal of Experimental Medicine 187: 289-296.
Haston CK, Corey M, and Tsui LC (2002). Mapping of genetic factors influencing the weight of cystic fibrosis knockout mice. Mammalian Genome 13: 614-618.
Haston CK, McKerlie C, Newbigging S, Corey M, Rozmahel R, and Tsui LC (2002). Detection of modifier loci influencing the lung phenotype of cystic fibrosis knockout mice. Mammalian Genome 13: 605-613.
Haston CK, Wang M, Dejournett RE, Zhou XH, Ni D, Gu XJ, King TM, Weil MM, Newman RA, Amos CI, and Travis EL (2002). Bleomycin hydrolase and a genetic locus within the MHC affect risk for pulmonary fibrosis in mice. Human Molecular Genetics 11: 1855-1863.
Haston CK, Zhou XH, Gumbiner-Russo L, Irani R, Dejournett R, Gu XJ, Weil M, Amos CI, and Travis EL (2002). Universal and radiation-specific loci influence murine susceptibility to radiation-induced pulmonary fibrosis. Cancer Research 62: 3782-3788.
Hayakawa J, Nikaido H, Ohkawa T, and Kitoh J (1998). Cream fur: A new mouse mutation that may cause unusual lipid metabolism. Journal of Heredity 89: 342-346.
Hayashizaki Y, Hirotsune S, Okazaki Y, Shibata H, Akasako A, Muramatsu M, Kawai J, Hirasawa T, Watanabe S, Shiroishi T, Moriwaki K, Taylor BA, Matsuda Y, Elliott RW, Manly KF, and Chapman VM (1994). A Genetic-Linkage Map of the Mouse Using Restriction Landmark Genomic Scanning (Rlgs). Genetics 138: 1207-1238.
Hayashizaki Y, Shibata H, Hirotsune S, Sugino H, Okazaki Y, Sasaki N, Hirose K, Imoto H, Okuizumi H, Muramatsu M, Komatsubara H, Shiroishi T, Moriwaki K, Katsuki M, Hatano N, Sasaki H, Ueda T, Mise N, Takagi N, Plass C, and Chapman VM (1994). Identification of an Imprinted U2af Binding-Protein Related Sequence on Mouse Chromosome-11 Using the Rlgs Method. Nature Genetics 6: 33-40.
Hayden MJ, Khatkar S, and Sharp PJ (2001). Targetting microsatellites (SSRs) in genetic linkage maps of bread wheat. Australian Journal of Agricultural Research 52: 1143-1152.
Heber-Katz E (1999). The regenerating mouse ear. Seminars in Cell & Developmental Biology 10: 415-419.
Heine D, Khambata S, and Passmore HC (1998). High-resolution mapping and recombination interval analysis of mouse Chromosome 17. Mammalian Genome 9: 511-516.
Heine D, Passmore HC, Patel V, Shultz LD, WardBailey P, Cook SA, and Davisson MT (1996). Effect of the mouse scid mutation on meiotic recombination. Mammalian Genome 7: 497-500.
Hellewell KB, Rasmusson DC, and Gallo-Meagher M (2000). Enhancing yield of semidwarf barley. Crop Science 40: 352-358.
Henckaerts E, Geiger H, Langer JC, Rebollo P, Van Zant G, and Snoeck HW (2002). Genetically determined variation in the number of phenotypically defined hematopoietic progenitor and stem cells and in their response to early-acting cytokines. Blood 99: 3947-3954.
Hendrich B, Abbott C, McQueen H, Chambers D, Cross S, and Bird A (1999). Genomic structure and chromosomal mapping of the murine and human Mbd1, Mbd2, Mbd3, and Mbd4 genes. Mammalian Genome 10: 906-912.
Herranz M, Santos J, Salido E, Fernandez-Piqueras J, and Serrano M (1999). Mouse p73 gene maps to the distal part of chromosome 4 and might be involved in the progression of gamma-radiation-induced T-cell lymphomas. Cancer Research 59: 2068-2071.
Himmelbauer H, Wedemeyer N, Haaf T, Wanker EE, Schalkwyk LC, and Lehrach H (1998). IRS-PCR-based genetic mapping of the huntingtin interacting protein gene (HIP1) on mouse Chromosome 5. Mammalian Genome 9: 26-31.
Hinsdale ME, Farmer SC, Johnson KR, Davisson MT, Hamm DA, Tolwani RJ, and Wood PA (1995). RNA Expression and Chromosomal Location of the Mouse Long-Chain Acyl-Coa Dehydrogenase Gene. Genomics 28: 163-170.
Hirotsune S, Shibata H, Okazaki Y, Sugino H, Imoto H, Sasaki N, Hirose K, Okuizumi H, Muramatsu M, Plass C, Chapman VM, Tamatsukuri S, Miyamoto C, Furuichi Y, and Hayashizaki Y (1993). Molecular-Cloning of Polymorphic Markers On Rlgs Gel Using the Spot Target Cloning Method. Biochemical and Biophysical Research Communications 194: 1406-1412.
Ho JC, McCouch SR, and Smith ME (2002). Improvement of hybrid yield by advanced backcross QTL analysis in elite maize. Theoretical and Applied Genetics 105: 440-448.
Hodges SA, Whittall JB, Fulton M, and Yang JY (2002). Genetics of floral traits influencing reproductive isolation between Aquilegia formosa and Aquilegia pubescens. American Naturalist 159: S51-S60.
Hofstetter JR, Mayeda AR, Possidente B, and Nurnberger JI (1995). Quantitative Trait Loci (QTL) For Circadian-Rhythms of Locomotor-Activity in Mice. Behavior Genetics 25: 545-556.
Hood HM, Belknap JK, Crabbe JC, and Buck KJ (2001). Genomewide search for epistasis in a complex trait: Pentobarbital withdrawal convulsions in mice. Behavior Genetics 31: 93-100.
Hoopes RR, Reid R, Sen S, Szpirer C, Dixon P, Pannett AAJ, Thakker RV, Bushinsky DA, and Scheinman SJ (2003). Quantitative trait loci for hypercalciuria in a rat model of kidney stone disease. Journal of the American Society of Nephrology 14: 1844-1850.
Hopitzan A, Himmelbauer H, Spevak W, and Castanon MJ (2000). The mouse Psma1 gene coding for the alpha-type C2 proteasome subunit: Structural and functional analysis. mapping, and colocalization with Pde3b on mouse chromosome 7. Genomics 66: 313-323.
Hovland DN, Cantor RM, Lee GS, Machado AF, and Collins MD (2000). Identification of a murine locus conveying susceptibility to cadmium-induced forelimb malformations. Genomics 63: 193-201.
Howard BA, and Gusterson BA (2000). Mammary gland patterning in the AXB/BXA recombinant inbred strains of mouse. Mechanisms of Development 91: 305-309.
Hsu HC, Zhang HG, Li L, Yi N, Yang PA, Wu Q, Zhou J, Sun S, Xu X, Yang X, Lu L, Van Zant G, Williams RW, Allison DB, and Mountz JD (2003). Age-related thymic involution in C57BL/6J x DBA/2J recombinant-inbred mice maps to mouse chromosomes 9 and 10. Genes and Immunity 4: 402-410.
Hu J, Bumstead N, Burke D, Deleon FAP, Skamene E, Gros P, and Malo D (1995). Genetic and Physical Mapping of the Natural Resistance- Associated Macrophage Protein-1 (Nramp1) in Chicken. Mammalian Genome 6: 809-815.
Huang HM, Pravenec M, Wang JM, Kren V, StLezin E, Szpirer C, Szpirer J, and Kurtz TW (1995). Mapping and sequence analysis of the gene encoding the beta subunit of the epithelial sodium channel in experimental models of hypertension. Journal of Hypertension 13: 1247-1251.
Hughes S, Haynes A, O'Regan M, and Bumstead N (2001). Identification, mapping, and phylogenetic analysis of three novel chicken CC chemokines. Immunogenetics 53: 674-683.
Humphry ME, Konduri V, Lambrides CJ, Magner T, McIntyre CL, Aitken EAB, and Liu CJ (2002). Development of a mungbean (Vigna radiata) RFLP linkage map and its comparison with lablab (Lablab purpureus) revelas a high level of colinearity between the two genomes. Theoretical and Applied Genetics 105: 160-166.
Humphry ME, Magner T, McIntyre CL, Aitken EAB, and Liu CJ (2003). Identification of a major locus conferring resistance to powdery mildew (Erysiphe polygoni DC) in mungbean (Vigna radiata L. Wilczek) by QTL analysis. Genome 46: 738-744.
Hunter KW, Riba L, Schalkwyk L, Clark M, Resenchuk S, Beeghly A, Su J, Tinkov F, Lee P, Ramu E, Lehrach H, and Housman D (1996). Toward the construction of integrated physical and genetic maps of the mouse genome using interspersed repetitive sequence PCR (IRS-PCR) genomics. Genome Research 6: 290-299.
Hurlin PJ, Steingrimsson E, Copeland NG, Jenkins NA, and Eisenman RN (1999). Mga, a dual-specificity transcription factor that interacts with Max and contains a T-domain DNA-binding motif. Embo Journal 18: 7019-7028.
Hwang SY, Benjamin LE, Oh B, Rothstein JL, Ackerman SL, Beddington RSP, Solter D, and Knowles BB (1996). Genetic mapping and embryonic expression of a novel, maternally transcribed gene Mem3. Mammalian Genome 7: 586-590.
Hwang SY, Oh B, Fuchtbauer A, Fuchtbauer EM, Johnson KR, Solter D, and Knowles BB (1997). Maid: A maternally transcribed novel gene encoding a potential negative regulator of bHLH proteins in the mouse egg and zygote. Developmental Dynamics 209: 217-226.
Hwang SY, Oh B, Zhang Z, Miller W, Solter D, and Knowles BB (1999). The mouse cornichon gene family. Development Genes and Evolution 209: 120-125.
Hyman RW, Frank S, Warden CH, Daluiski A, Heller R, and Lusis AJ (1994). Quantitative Trait Locus Analysis of Susceptibility to Diet- Induced Atherosclerosis in Recombinant Inbred Mice. Biochemical Genetics 32: 397-407.
Iakoubova OA, Dushkin H, and Beier DR (1995). Localization of a Murine Recessive Polycystic Kidney-Disease Mutation and Modifying Loci That Affect Disease Severity. Genomics 26: 107-114.
Iakoubova OA, Dushkin H, and Beier DR (1997). Genetic analysis of a quantitative trait in a mouse model of polycystic kidney disease. American Journal of Respiratory and Critical Care Medicine 156: S72-S77.
Iakoubova OA, Pacella LA, Her H, and Beier DR (1997). LTW4 protein on mouse chromosome 1 is a member of a family of antioxidant proteins. Genomics 42: 474-478.
Ichitani K, Fukuta Y, Taura S, and Sato M (2001). Chromosomal location of Hwc2, one of the complementary hybrid weakness genes, in rice. Plant Breeding 120: 523-525.
Ida A, Hirose S, Hamano Y, Kodera S, Jiang Y, Abe M, Zhang DQ, Nishimura H, and Shirai T (1998). Multigenic control of lupus-associated antiphospholipid syndrome in a model of (NZW x BXSB) F1 mice. European Journal of Immunology 28: 2694-2703.
Idnurm A, and Howlett BJ (2001). Characterization of an opsin gene from the ascomycete Leptosphaeria maculans. Genome 44: 167-171.
Idnurm A, Warnecke DC, Heinz E, and Howlett BJ (2003). Characterisation of neutral trehalase and UDP-glucose : sterol glucosyltransferase genes from the plant pathogenic fungus Leptosphaeria maculans. Physiological and Molecular Plant Pathology 62: 305-313.
Ihrig M, Schrenzel MD, and Fox JG (1999). Differential susceptibility to hepatic inflammation and proliferation in AXB recombinant inbred mice chronically infected with Helicobacter hepaticus. American Journal of Pathology 155: 571-582.
Ikeda K, Naka S, Egashira M, Matsumoto M, Niikawa N, Iwata N, and Yoshimura A (2000). Construction of rice chromosome specific DNA libraries using chromosome microdissection technique and its application for mapping. Journal of the Faculty of Agriculture Kyushu University 45: 73-82.
Innes BA, and Dorin JR (2001). Submucosal gland distribution in the mouse has a genetic determination localized on Chromosome 9. Mammalian Genome 12: 124-128.
Ivandic V, Walther U, and Graner A (1998). Molecular mapping of a new gene in wild barley conferring complete resistance to leaf rust (Puccinia hordei Otth). Theoretical and Applied Genetics 97: 1235-1239.
Jackson AU, Galecki AT, Burke DT, and Miller RA (2003). Genetic polymorphisms in mouse genes regulating age-sensitive and age-stable T cell subsets. Genes and Immunity 4: 30-39.
Jacob JP, Milne S, Beck S, and Kaufman J (2000). The major and a minor class II beta-chain (B-LB) gene flank the Tapasin gene in the B-F/B-L region of the chicken major histocompatibility complex. Immunogenetics 51: 138-147.
Jacoby RF, Hohman C, Marshall DJ, Frick TJ, Schlack S, Broda M, Smutko J, and Elliott RW (1994). Genetic-Analysis of Colon-Cancer Susceptibility in Mice. Genomics 22: 381-387.
Jaradat SA, Ko MSH, and Grossman LI (1998). Tissue-specific expression and mapping of the Cox7ah gene in mouse. Genomics 49: 363-370.
Jaworski RL, Jirout M, Closson S, Breen L, Flodman PL, Spence MA, Kren V, Krenova D, Pravenec M, and Printz MP (2002). Heart rate and blood pressure quantitative trait loci for the airpuff startle reaction. Hypertension 39: 348-352.
Jefferies SP, Pallotta MA, Paull JG, Karakousis A, Kretschmer JM, Manning S, Islam A, Langridge P, and Chalmers KJ (2000). Mapping and validation of chromosome regions conferring boron toxicity tolerance in wheat (Triticum aestivum). Theoretical and Applied Genetics 101: 767-777.
Jenuth JP, Fung E, and Snyder FF (1994). Assignment of a Gene That Determines Erythrocytic Guanosine-5'- Triphosphate Concentration (Gtpc) to Mouse Chromosome-9. Genome 37: 399-404.
Ji H, Gauguier D, Ohmura K, Gonzalez A, Duchatelle V, Danoy P, Garchon HJ, Degott C, Lathrop M, Benoist C, and Mathis D (2001). Genetic influences on the end-stage effector phase of arthritis. Journal of Experimental Medicine 194: 321-330.
Jiang Y, Ohtsuji M, Abe M, Li N, Xiu Y, Wen XS, Shirai T, and Hirose S (2001). Polymorphism and chromosomal mapping of the mouse gene for B- cell activating factor belonging to the tumor necrosis factor family (Baff) and association with the autoimmune phenotype. Immunogenetics 53: 810-813.
Jiang ZM, Shih DM, Xia YR, Lusis AJ, de Beer FC, de Villiers WJS, van der Westhuyzen DR, and de Beer MC (1998). Structure, organization, and chromosomal mapping of the gene encoding macrosialin, a macrophage-restricted protein. Genomics 50: 199-205.
Jilek A, Engel E, Beier D, and Lepperdinger G (2000). Murine Bv8 gene maps near a synteny breakpoint of mouse chromosome 6 and human 3p21. Gene 256: 189-195.
Jirout M, Krenova D, Kren V, Breen L, Pravenec M, Schork NJ, and Printz MP (2003). New framework marker-based linkage map and SDPs for the Rat HXB/BXH strain set. Mammalian Genome 14: 537-546.
Johnson J, Suzuki Y, Mack D, Mui E, Estes R, David C, Skamene E, Forman J, and McLeod R (2002). Genetic analysis of influences on survival following Toxoplasma gondii infection. International Journal for Parasitology 32: 179-185.
Johnson KR, Cook SA, and Davisson MT (1994). Identification and Genetic-Mapping of 151 Dispersed Members of 16 Ribosomal-Protein Multigene Families in the Mouse. Mammalian Genome 5: 670-687.
Johnson KR, Cook SA, Erway LC, Matthews AN, Sanford LP, Paradies NE, and Friedman RA (1999). Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome. Human Molecular Genetics 8: 645-653.
Johnson KR, Cook SA, and Zheng QY (1998). The original shaker-with-syndactylism mutation (sy) is a contiguous gene deletion syndrome. Mammalian Genome 9: 889-892.
Johnson KR, Erway LC, Cook SA, Willott JF, and Zheng QY (1997). A major gene affecting age-related hearing loss in C57BL/6J mice. Hearing Research 114: 83-92.
Johnson KR, Gagnon LH, Webb LS, Peters LL, Hawes NL, Chang B, and Zheng QY (2003). Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene. Human Molecular Genetics 12: 3075-3086.
Johnson KR, Lane PW, Cook SA, Harris BS, Ward-Bailey PF, Bronson RT, Lyons BL, Shultz LD, and Davisson MT (2003). Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5. Genomics 81: 6-14.
Johnson KR, Lane PW, Wardbailey P, and Davisson MT (1995). Mapping the Mouse Dactylaplasia Mutation, Dac, and a Gene That Controls Its Expression, Mdac. Genomics 29: 457-464.
Johnson KR, Smith L, Johnson DK, Rhodes J, Rinchik EM, Thayer M, and Lewis EJ (1996). Mapping of the ARIX homeodomain gene to mouse chromosome 7 and human chromosome 11q13. Genomics 33: 527-531.
Johnson KR, Sweet HO, Donahue LR, Ward-Bailey P, Bronson RT, and Davisson MT (1998). A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly. Human Molecular Genetics 7: 1033-1038.
Johnson KR, and Zheng QY (2002). Ahl2, a second locus affecting age-related hearing loss in mice. Genomics 80: 461-464.
Johnson KR, Zheng QY, and Erway LC (2000). A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice. Genomics 70: 171-180.
Johnson M, Yang HS, Johanning GL, and Patel MS (1997). Characterization of the mouse dihydrolipoamide dehydrogenase (Dld) gene: Genomic structure, promoter sequence, and chromosomal localization. Genomics 41: 320-326.
Johnstone CN, White SJ, Tebbutt NC, Clay FJ, Ernst M, Biggs WH, Viars CS, Czekay S, Arden KC, and Heath JK (2002). Analysis of the regulation of the A33 antigen gene reveals intestine-specific mechanisms of gene expression. Journal of Biological Chemistry 277: 34531-34539.
Jonassen T, Marbois BN, Kim L, Chin A, Xia YR, Lusis AJ, and Clarke CF (1996). Isolation and sequencing of the rat Coq7 gene and the mapping of mouse Coq7 to chromosome 7. Archives of Biochemistry and Biophysics 330: 285-289.
Jones CT, Morrice DR, Paton IR, and Burt DW (1997). Gene homologs on human Chromosome 15q21-q26 and a chicken microchromosome identify a new conserved segment. Mammalian Genome 8: 436-440.
Jones JM, Bentley E, Meisler MH, and Darling SM (1998). Genetic mapping of the voltage-gated shaker potassium channel beta subunit Kcnab1 to mouse Chromosome 3. Mammalian Genome 9: 260-260.
Jordan MA, Silveira PA, Shepherd DP, Chu C, Kinder SJ, Chen JH, Palmisano LJ, Poulton LD, and Baxter AG (2000). Linkage analysis of systemic lupus erythematosus induced in diabetes-prone nonobese diabetic mice by Mycobacterium bovis. Journal of Immunology 165: 1673-1684.
Judelson HS, and Roberts S (1999). Multiple loci determining insensitivity to phenylamide fungicides in Phytophthora infestans. Phytopathology 89: 754-760.
Judelson HS, Spielman LJ, and Shattock RC (1995). Genetic-Mapping and Non-Mendelian Segregation of Mating-Type Loci in the Oomycete, Phytophthora-Infestans. Genetics 141: 503-512.
Jurgenson JE, Bowden RL, Zeller KA, Leslie JF, Alexander NJ, and Plattner RD (2002). A genetic map of Gibberella zeae (Fusarium graminearum). Genetics 160: 1451-1460.
Jurgenson JE, Zeller KA, and Leslie JF (2002). Expanded genetic map of Gibberella moniliformis (Fusarium verticillioides). Applied and Environmental Microbiology 68: 1972-1979.
Juriloff DM, Harris MJ, Banks KG, and Mah DG (2000). Gaping lids, gp, a mutation on centromeric Chromosome 11 that causes defective eyelid development in mice. Mammalian Genome 11: 440-447.

K-M

Kammholz SJ, Campbell AW, Sutherland MW, Hollamby GJ, Martin PJ, Eastwood RF, Barclay I, Wilson RE, Brennan PS, and Sheppard JA (2001). Establishment and characterisation of wheat genetic mapping populations. Australian Journal of Agricultural Research 52: 1079-1088.
Karakousis A, Barr AR, Chalmers KJ, Ablett GA, Holton TA, Henry RJ, Lim P, and Langridge P (2003). Potential of SSR markers for plant breeding and variety identification in Australian barley germplasm. Australian Journal of Agricultural Research 54: 1197-1210.
Karakousis A, Gustafson JP, Chalmers KJ, Barr AR, and Langridge P (2003). A consensus map of barley integrating SSR, RFLP, and AFLP markers. Australian Journal of Agricultural Research 54: 1173-1185.
Karlsson M, Reue K, Xia YR, Lusis AJ, Langin D, Tornqvist H, and Holm C (2001). Exon-intron organization and chromosomal localization of the mouse monoglyceride lipase gene. Gene 272: 11-18.
Kasuga T, Salimath SS, Shi JR, Gijzen M, Buzzell RI, and Bhattacharyya MK (1997). High resolution genetic and physical mapping of molecular markers linked to the Phytophthora resistance gene Rps1-k in soybean. Molecular Plant-Microbe Interactions 10: 1035-1044.
Kathir P, LaVoie M, Brazelton WJ, Haas NA, Lefebvre PA, and Silflow CD (2003). Molecular map of the Chlamydomonas reinhardtii nuclear genome. Eukaryotic Cell 2: 362-379.
Kato N, Tamada T, Nabika T, Ueno K, Gotoda T, Matsumoto C, Mashimo T, Sawamura M, Ikeda K, Nara Y, and Yamori Y (2000). Identification of quantitative trait loci for serum cholesterol levels in stroke-prone spontaneously hypertensive rats. Arteriosclerosis Thrombosis and Vascular Biology 20: 223-229.
Katz ML, Liu PC, Grob-Nunn SE, Shibuya H, and Johnson GS (1999). Characterization and chromosomal mapping of a mouse ortholog of the late-infantile ceroid-lipofuscinosis gene CLN2. Mammalian Genome 10: 1050-1053.
Kaushik N, and Stoye JP (1994). Intracisternal a-Type Particle Elements As Genetic-Markers - Detection By Repeat Element Viral Element Amplified Locus-Pcr. Mammalian Genome 5: 688-695.
Kawai F, Suzuki H, Hara A, Hirose K, and Watanabe S (1998). Human and mouse chromosomal mapping of Stac, a neuron-specific protein with an SH3 domain. Genomics 47: 140-142.
Kayo T, Fujita H, Nozaki J, E XF, and Koizumi A (2000). Identification of two chromosomal loci determining glucose intolerance in a C57BL/6 mouse strain. Comparative Medicine 50: 296-302.
Keddie JS, Carroll B, Jones JDG, and Gruissem W (1996). The DCL gene of tomato is required for chloroplast development and palisade cell morphogenesis in leaves. Embo Journal 15: 4208-4217.
Kell DB (2002). Genotype-phenotype mapping: genes as computer programs. Trends in Genetics 18: 555-559.
Kelly MA, Low MJ, Phillips TJ, Wakeland EK, and Yanagisawa M (2003). The mapping of quantitative trait loci underlying strain differences in locomotor activity between 129S6 and C57BU6J mice. Mammalian Genome 14: 692-702.
Kelly PD, Chu F, Woods IG, Ngo-Hazelett P, Cardozo T, Huang H, Kimm F, Liao LY, Yan YL, Zhou YY, Johnson SL, Abagyan R, Schier AF, Postlethwait JH, and Talbot WS (2000). Genetic linkage mapping of zebrafish genes and ESTs. Genome Research 10: 558-567.
Kemlink D, Jerabkova V, Janku M, Krenova D, and Kren V (2003). PXO set of recombinant inbred strains of the rat: A new strain distribution pattern containing 448 markers. Folia Biologica 49: 165-176.
Kern MJ, Argao EA, Birkenmeier EH, Rowe LB, and Potter SS (1994). Genomic Organization and Chromosome Localization of the Murine Homeobox Gene Pmx. Genomics 19: 334-340.
Khabaz-Saberi K, Graham RD, Pallotta MA, Rathjen AJ, and Williams KJ (2002). Genetic markers for manganese efficiency in durum wheat. Plant Breeding 121: 224-227.
Khoo G, Lim MH, Suresh H, Gan DKY, Lim KF, Chen F, Chan WK, Lim TM, and Phang VPE (2003). Genetic linkage maps of the guppy (Poecilia reticulata): Assignment of RAPD markers to multipoint linkage groups. Marine Biotechnology 5: 279-293.
Kikkawa Y, Oyama A, Ishii R, Miura I, Amano T, Ishii Y, Yoshikawa Y, Masuya H, Wakana S, Shiroishi T, Taya C, and Yonekawa H (2003). A small deletion hotspot in the type II keratin gene mK6irs1/Krt2-6g on mouse chromosome 15, a candidate for causing the wavy hair of the caracul (Ca) mutation. Genetics 165: 721-733.
Kim BC, Soh MS, Kang BJ, Furuya M, and Nam HG (1996). Two dominant photomorphogenic mutations of Arabidopsis thaliana identified as suppressor mutations of hy2. Plant Journal 9: 441-456.
Kim J, Ashworth L, Branscomb E, and Stubbs L (1997). The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger gene-rich region of human chromosome 19q13.4. Genome Research 7: 532-540.
Kim J, Park YS, Chung JH, and Stubbs L (1997). The gene encoding sepiapterin reductase is located in central mouse Chromosome 6. Mammalian Genome 8: 942-942.
Kim SH, Parrinello S, Kim J, and Campisi J (2003). Mus musculus and Mus spretus homologues of the human telomere-associated protein TIN2. Genomics 81: 422-432.
King DP, Vitaterna MH, Chang AM, Dove WF, Pinto LH, Turek FW, and Takahashi JS (1997). The mouse Clock mutation behaves as an antimorph and maps within the W-19H deletion, distal of Kit. Genetics 146: 1049-1060.
Kleeberger SR, Levitt RC, Zhang LY, Longphre M, Harkema L, Jedlicka A, Eleff SM, DiSilvestre D, and Holroyd KJ (1997). Linkage analysis of susceptibility to ozone-induced lung inflammation in inbred mice. Nature Genetics 17: 475-478.
Kleeberger SR, Reddy S, Zhang LY, and Jedlicka AE (2000). Genetic susceptibility to ozone-induced lung hyperpermeability - Role of toll-like receptor 4. American Journal of Respiratory Cell and Molecular Biology 22: 620-627.
Klein RF, Carlos AS, Vartanian KA, Chambers VK, Turner RJ, Phillips TJ, Belknap JK, and Orwoll ES (2001). Confirmation and fine mapping of chromosomal regions influencing peak bone mass in mice. Journal of Bone and Mineral Research 16: 1953-1961.
Klein RF, Mitchell SR, Phillips TJ, Belknap JK, and Orwoll ES (1998). Quantitative trait loci affecting peak bone mineral density in mice. Journal of Bone and Mineral Research 13: 1648-1656.
Klein RF, Turner RJ, Skinner LD, Vartanian KA, Serang M, Carlos AS, Shea M, Belknap JK, and Orwoll ES (2002). Mapping quantitative trait loci that influence femoral cross- sectional area in mice. Journal of Bone and Mineral Research 17: 1752-1760.
Klein S, Morrice DR, Sang H, Crittenden LB, and Burt DW (1996). Genetic and physical mapping of the chicken IGF1 gene to chromosome 1 and conservation of synteny with other vertebrate genomes. Journal of Heredity 87: 10-14.
Klingensmith J, Yang Y, Axelrod JD, Beier DR, Perrimon N, and Sussman DJ (1996). Conservation of dishevelled structure and function between flies and mice: Isolation and characterization of Dvl2. Mechanisms of Development 58: 15-26.
Klingenspor M, Bodnar J, Welch C, Xia XR, Lusis AJ, and Reue K (1997). Localization of ubiquitin gene family members to mouse Chromosomes 5, 11, and 18. Mammalian Genome 8: 789-790.
Klingenspor M, Bodnar J, Xia YR, Welch C, Lusis AJ, and Reue K (1997). Localization of profilin-1 (Pfn1) and a related sequence (Pfn1- rs) to mouse Chromosomes 11 and 15 respectively. Mammalian Genome 8: 539-540.
Klingenspor M, Xu P, Cohen RD, Welch C, and Reue K (1999). Altered gene expression pattern in the fatty liver dystrophy mouse reveals impaired insulin-mediated cytoskeleton dynamics. Journal of Biological Chemistry 274: 23078-23084.
Ko C, Lee TL, Lau PW, Li J, Davis BT, Voyiaziakis E, Allison DB, Chua SC, and Huang LS (2001). Two novel quantitative trait loci on mouse chromosomes 6 and 4 independently and synergistically regulate plasma apoB levels. Journal of Lipid Research 42: 844-855.
Ko MSH, Kitchen JR, Wang XH, Threat TA, Wang XQ, Hasegawa A, Sun T, Grahovac MJ, Kargul GJ, Lim MK, Cui YS, Sano Y, Tanaka T, Liang YL, Mason S, Paonessa PD, Sauls AD, DePalma GE, Sharara R, Rowe LB, Eppig J, Morrell C, and Doi H (2000). Large-scale cDNA analysis reveals phased gene expression patterns during preimplantation mouse development. Development 127: 1737-1749.
Ko MSH, Threat TA, Wang XQ, Horton JH, Cui YS, Wang XH, Pryor E, Paris J, Wells-Smith J, Kitchen JR, Rowe LB, Eppig J, Satoh T, Brant L, Fujiwara H, Yotsumoto S, and Nakashima H (1998). Genome-wide mapping of unselected transcripts from extraembryonic tissue of 7.5-day mouse embryos reveals enrichment in the t-complex and under-representation on the X chromosome. Human Molecular Genetics 7: 1967-1978.
Ko MSH, Wang X, Horton JH, Hagen MD, Takahashi N, Maezaki Y, and Nadeau JH (1994). Genetic-Mapping of 40 Cdna Clones on the Mouse Genome by Pcr. Mammalian Genome 5: 349-355.
Kobayashi M, Ohno T, Tsuji A, Nishimura M, and Horio F (2003). Combinations of nondiabetic parental genomes elicit impaired glucose tolerance in mouse SMXA recombinant inbred strains. Diabetes 52: 180-186.
Kohn MH, and Pelz HJ (2000). A gene-anchored map position of the rat warfarin-resistance locus, Rw, and its orthologs in mice and humans. Blood 96: 1996-1998.
Kohn MH, and Pelz JH (1999). Genomic assignment of the warfarin resistance locus, Rw, in the rat. Mammalian Genome 10: 696-698.
Komatsu S, Kiyosawa H, Yoshiki A, Okazaki Y, Yoshino M, Tomaru Y, Watanabe S, Muramatsu M, Kusakabe M, and Hayashizaki Y (2002). Identification of seven loci for static glucokinesis and dynamic glucokinesis in mice. Mammalian Genome 13: 293-298.
Kondo Y, Mori M, Kuramoto T, Yamada J, Beckmann JS, Simonchazottes D, Montagutelli X, Guenet JL, and Serikawa T (1993). DNA Segments Mapped By Reciprocal Use of Microsatellite Primers Between Mouse and Rat. Mammalian Genome 4: 571-576.
Koza RA, Hohmann SM, Guerra C, Rossmeisl M, and Kozak LP (2000). Synergistic gene interactions control the induction of the mitochondrial uncoupling protein (Ucp1) gene in white fat tissue. Journal of Biological Chemistry 275: 34486-34492.
Kozaiwa K, Sugawara K, Smith MF, Carl V, Yamschikov V, Belyea B, McEwen SB, Moskaluk CA, Pizarro TT, Cominelli F, and McDuffie M (2003). Identification of a quantitative trait locus for ileitis in a spontaneous mouse model of Crohn's disease: SAMP1/YitFc. Gastroenterology 125: 477-490.
Kraja AT, and Dudley JW (2000). QTL analysis of two maize inbred line crosses. Maydica 45: 1-12.
Krass KL, Colinayo V, Ghazalpour A, Vinters HV, Lusis AJ, and Drake TA (2003). Genetic loci contributing to age-related hippocampal lesions in mice. Neurobiology of Disease 13: 102-108.
Krebs O, Schreiner CM, Scott WJ, Bell SM, Robbins DJ, Goetz JA, Alt H, Hawes N, Wolf E, and Favor J (2003). Replicated anterior zeugopod (raz): a polydactylous mouse mutant with lowered Shh signaling in the limb bud. Development 130: 6037-6047.
Krenova D, Jirsova Z, Housa D, Liska F, Soltysova L, Kasparek R, Bila V, Pravenec M, and Kren V (1999). Genetic analysis of the rat hypodactylous mutation. Folia Biologica 45: 81-86.
Kuhl JC, Hanneman RE, and Havey MJ (2001). Characterization and mapping of Rpi1, a late-blight resistance locus from diploid (1EBN) Mexican Solanum pinnatisectum. Molecular Genetics and Genomics 265: 977-985.
Kuhl JC, Havey MJ, and Hanneman RE (2002). A genetic study of unilateral incompatibility between diploid (1EBN) Mexican species Solanum pinnatisectum and S- cardiophyllum subsp cardiophyllum. Sexual Plant Reproduction 14: 305-313.
Kuida S, and Beier DR (2000). Genetic localization of interacting modifiers affecting severity in a murine model of polycystic kidney disease. Genome Research 10: 49-54.
Kunieda T, Ide H, Nakagiri M, Yoneda K, Konfortov B, and Ogawa H (2000). Localization of the locus responsible for Chediak-Higashi syndrome in cattle to bovine chromosome 28. Animal Genetics 31: 87-90.
Kunieda T, Kobayashi E, Tachibana M, and Ikadai H (1999). A genetic linkage map of rat chromosome 9 with a new locus for variant activity of liver aldehyde oxidase. Experimental Animals 48: 43-45.
Kvist AP, Latvanlehto A, Sund M, Horelli-Kuitunen N, Rehn M, Palotie A, Beier D, and Pihlajaniemi T (1999). Complete exon-intron organization and chromosomal location of the gene for mouse type XIII collagen (col13a1) and comparison with its human homologue. Matrix Biology 18: 261-274.
Lakkis MM, Venta PJ, and Tashian RE (1997). Localization of the mitochondrial carbonic anhydrase V gene, Car5, on mouse Chromosome 8. Mammalian Genome 8: 225-226.
Lalouette A, Christians E, Guenet JL, and Vriz S (1997). Construction of a high-resolution genetic map encompassing the hotfoot locus. Mammalian Genome 8: 903-906.
Lammert F, Cohen DE, Paigen B, Carey MC, and Beier DR (1998). The gene encoding the multispecific organic anion transporter (Cmoat) of the hepatocyte canalicular membrane maps to mouse Chromosome 19. Mammalian Genome 9: 87-88.
Lammert F, Paigen B, and Carey MC (1998). Localization of the ileal sodium-bile salt cotransporter gene (Slc10a2) to mouse Chromosome 8. Mammalian Genome 9: 173-174.
Lammert F, Wang DQH, Wittenburg H, Bouchard G, Hillebrandt S, Taenzler B, Carey MC, and Paigen B (2002). Lith genes control mucin accumulation, cholesterol crystallization, and gallstone formation in A/J and AKR/J inbred mice. Hepatology 36: 1145-1154.
Lan Y, Jiang RL, Shawber C, Weinmaster G, and Gridley T (1997). The Jagged2 gene maps to Chromosome 12 and is a candidate for the lgl and sm mutations. Mammalian Genome 8: 875-876.
Landgren C, Beier DR, Fassler R, Heinegard D, and Sommarin Y (1998). The mouse chondroadherin gene: Characterization and chromosomal localization. Genomics 47: 84-91.
Lange R, Christoph A, Thiesen HJ, Vopper G, Johnson KR, Lemaire L, Plomann M, Cremer H, Barthels D, and Heinlein UAO (1995). Developmentally-Regulated Mouse Gene Nk10 Encodes a Zinc-Finger Repressor Protein With Differential DNA-Binding Domains. Dna and Cell Biology 14: 971-981.
Langridge P, Lagudah ES, Holton TA, Appels R, Sharp PJ, and Chalmers KJ (2001). Trends in genetic and genome analyses in wheat: a review. Australian Journal of Agricultural Research 52: 1043-1077.
Lassalle JM, Halley H, Milhaud JM, and Roullet P (1999). Genetic architecture of the hippocampal mossy fiber subfields in the BXD RI mouse strain series: A preliminary QTL analysis. Behavior Genetics 29: 273-282.
Lavenu A, Roland J, Poirier C, Cazenave PA, Babinet C, and Morello D (1996). Genomic structure and precise mapping of a thymic regulatory region on mouse chromosome 17 revealed by a c-myc transgene insertion. Genomics 34: 381-388.
Le Corvoisier P, Park HY, Carlson KM, Marchuk DA, and Rockman HA (2003). Multiple quantitative trait loci modify the heart failure phenotype in murine cardiomyopathy. Human Molecular Genetics 12: 3097-3107.
Le Voyer T, Lu ZC, Babb J, Lifsted T, Williams M, and Hunter K (2000). An epistatic interaction controls the latency of a transgene- induced mammary tumor. Mammalian Genome 11: 883-889.
Le Voyer T, Rouse J, Lu ZC, Lifsted T, Williams M, and Hunter KW (2001). Three loci modify growth of a transgene-induced mammary tumor: Suppression of proliferation associated with decreased microvessel density. Genomics 74: 253-261.
LeBoeuf RC, Caldwell M, Tu AY, and Albers JJ (1996). Phospholipid transfer protein maps to distal mouse chromosome 2. Genomics 34: 259-260.
Leder A, Wiener E, Lee MJ, Wickramasinghe SN, and Leder P (1999). A normal beta-globin allele as a modifier gene ameliorating the severity of alpha-thalassemia in mice. Proceedings of the National Academy of Sciences of the United States of America 96: 6291-6295.
Lee JM, Bush AL, Specht JE, and Shoemaker RC (1999). Mapping of duplicate genes in soybean. Genome 42: 829-836.
Lee JY, Greenbaum L, Haber BA, Nagle D, Lee V, Miles V, Mohn KL, Bucan M, and Taub R (1994). Structure and Localization of the Igfbp-1 Gene and Its Expression During Liver-Regeneration. Hepatology 19: 656-665.
Lee MJ, Stephenson DA, Groves MJ, Sweeney MG, Davis MB, An SF, Houlden H, Salih MAM, Timmerman V, de Jonghe P, Auer-Grumbach M, Di Maria E, Scaravilli F, Wood NW, and Reilly MM (2003). Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene. Human Molecular Genetics 12: 1917-1925.
Lee RL, Johnson KR, and Lerner TJ (1996). Isolation and chromosomal mapping of a mouse homolog of the Batten disease gene CLN3. Genomics 35: 617-619.
Leikauf GD, McDowell SA, Bachurski CJ, Aronow BJ, Gammon K, Wesselkamper SC, Hardie W, Wiest JS, Leikauf JE, Korfhagen TR, and Prows DR (2001). Functional genomics of oxidant-induced lung injury. In "Biological Reactive Intermediates Vi", pp. 479-487.
Leikauf GD, McDowell SA, Gammon K, Wesselkamper SC, Bachurski CJ, Puga A, Wiest JS, Leikauf JE, and Prows DR (2000). Functional genomics of particle-induced lung injury. Inhalation Toxicology 12: 59-73.
Leikauf GD, McDowell SA, Wesselkamper SC, Hardie WD, Leikauf JE, Korfhagen TR, and Prows DR (2002). Acute lung injury - Functional genomics and genetic susceptibility. Chest 121: 70S-75S.
Leiter EH, Reifsnyder PC, Flurkey K, Partke HJ, Junger E, and Herberg L (1998). NIDDM genes in mice - Deleterious synergism by both parental genomes contributes to diabetogenic thresholds. Diabetes 47: 1287-1295.
Lemaire L, Johnson KR, Bammer S, Petry P, Ruddle FH, and Heinlein UAO (1994). Chromosomal Assignment of 3 Novel Mouse Genes Expressed in Testicular Cells. Genomics 21: 409-414.
Lener M, Fernandes M, Poirier C, Bazzali-Hernandez C, Tosi M, and Meo T (1998). The C1 inhibitor encoding gene (C1nh) maps to mouse Chromosome 2. Mammalian Genome 9: 94-94.
Leveque G, Forgetta V, Morroll S, Smith AL, Bumstead N, Barrow P, Loredo-Osti JC, Morgan K, and Malo D (2003). Allelic variation in TLR4 is linked to susceptibility to Salmonella enterica serovar typhimurium infection in chickens. Infection and Immunity 71: 1116-1124.
Lexer C, Lai Z, and Rieseberg LH (2004). Candidate gene polymorphisms associated with salt tolerance in wild sunflower hybrids: implications for the origin of Helianthus paradoxus, a diploid hybrid species. New Phytologist 161: 225-233.
Lexer C, Welch ME, Durphy JL, and Rieseberg LH (2003). Natural selection for salt tolerance quantitative trait loci (QTLs) in wild sunflower hybrids: Implications for the origin of Helianthus paradoxus, a diploid hybrid species. Molecular Ecology 12: 1225-1235.
Li CD, Lance RCM, Collins HM, Tarr A, Roumeliotis S, Harasymow S, Cakir M, Fox GP, Grime CR, Broughton S, Young KJ, Raman H, Barr AR, Moody DB, and Readf BJ (2003). Quantitative trait loci controlling kernel discoloration in barley (Hordeum vulgare L.). Australian Journal of Agricultural Research 54: 1251-1259.
Li CD, Tarr A, Lance RCM, Harasymow S, Uhlmann J, Westcot S, Young KJ, Grime CR, Cakir M, Broughton S, and Appelsa R (2003). A major QTL controlling seed dormancy and pre-harvest sprouting/grain alpha-amylase in two-rowed barley (Hordeum vulgare L.). Australian Journal of Agricultural Research 54: 1303-1313.
Li DJ, Sun CQ, Fu YC, Li C, Zhu ZF, Chen L, Cai HW, and Wang XK (2002). Identification and mapping of genes for improving yield from Chinese common wild rice (O. Rufipogon Griff.) using advanced backcross QTL analysis. Chinese Science Bulletin 47: 1533-1537.
Li HZ, Wu DK, and Sullivan SL (1999). Characterization and expression of sema4g, a novel member of the semaphorin gene family. Mechanisms of Development 87: 169-173.
Li W, Elliott RW, Novak EK, and Swank RT (1999). cDNA sequence and mapping of the mouse Copb gene encoding the beta subunit of the COPI coatomer complex. Somatic Cell and Molecular Genetics 25: 177-183.
Libert C, Wielockx B, Hammond GL, Brouckaert P, Fiers W, and Elliott RW (1999). Identification of a locus on distal mouse chromosome 12 that controls resistance to tumor necrosis factor-induced lethal shock. Genomics 55: 284-289.
Lilley JM, Ludlow MM, McCouch SR, and Otoole JC (1996). Locating QTL for osmotic adjustment and dehydration tolerance in rice. Journal of Experimental Botany 47: 1427-1436.
Lin HH, Stubbs LJ, and Mucenski ML (1997). Identification and characterization of a seven transmembrane hormone receptor using differential display. Genomics 41: 301-308.
Lin L, Festing MFW, Devereux TR, Crist KA, Christiansen SC, Wang Y, Yang A, Svenson K, Paigen B, Malkinson AM, and You M (1998). Additional evidence that the K-ras protooncogene is a candidate for the major mouse pulmonary adenoma susceptibility (Pas-1) gene. Experimental Lung Research 24: 481-497.
Link RE, Kobilka BK, and Barsh GS (1993). Linkage Mapping of Alpha-2-Adrenergic Receptor Genes to Mouse Chromosome-2 and Chromosome-5. Mammalian Genome 4: 650-655.
Lionikas A, Blizard DA, Vandenbergh DJ, Glover MG, Stout JT, Vogler GP, McClearn GE, and Larsson L (2003). Genetic architecture of fast- and slow-twitch skeletal muscle weight in 200-day-old mice of the C57BL/6J and DBA/2J lineage. Physiological Genomics 16: 141-152.
Liu FX, Sun CQ, Tan LB, Fu YC, Li DJ, and Wang XK (2003). Identification and mapping of quantitative trait loci controlling cold-tolerance of Chinese common wild rice (O-rufipogon Griff.) at booting to flowering stages. Chinese Science Bulletin 48: 2068-2071.
Liu HC, and Cheng HH (2003). Genetic mapping of the chicken stem cell antigen 2 (SCA2) gene to chromosome 2 via PCR primer mutagenesis(1). Animal Genetics 34: 158-160.
Liu HC, Cheng HH, Tirunagaru V, Sofer L, and Burnside J (2001). A strategy to identify positional candidate genes conferring Marek's disease resistance by integrating DNA microarrays and genetic mapping. Animal Genetics 32: 351-359.
Liu HC, Kung HJ, Fulton JE, Morgan RW, and Cheng HH (2001). Growth hormone interacts with the Marek's disease virus SORF2 protein and is associated with disease resistance in chicken. Proceedings of the National Academy of Sciences of the United States of America 98: 9203-9208.
Lo AWI, Longmuir DFS, Fowler KJ, Kalitsis P, and Choo KHA (2000). Assignment of the Centromere Protein H (Cenph) gene to mouse chromosome band 13D1 by in situ hybridization and interspecific backcross analyses. Cytogenetics and Cell Genetics 90: 56-57.
Lowrey PL, Shimomura K, Antoch MP, Yamazaki S, Zemenides PD, Ralph MR, Menaker M, and Takahashi JS (2000). Positional syntenic cloning and functional characterization of the mammalian circadian mutation tau. Science 288: 483-491.
Lu L, Airey DC, and Williams RW (2001). Complex trait analysis of the hippocampus: Mapping and biometric analysis of two novel gene loci with specific effects on hippocampal structure in mice. Journal of Neuroscience 21: 3503-3514.
Lu LM, Shisa H, Tanuma J, and Hiai H (1999). Propylnitrosourea-induced T-lymphomas in LEXF RI strains of rats: genetic analysis. British Journal of Cancer 80: 855-861.
Lueders KK (1995). Multilocus Genomic Mapping With Intracisternal a-Particle Proviral Oligonucleotide Probes Hybridized to Mouse DNA in Dried Agarose Gels. Electrophoresis 16: 179-185.
Lueders KK, Elliott RW, Marenholz I, Mischke D, DuPree M, and Hamer D (1999). Genomic organization and mapping of the human and mouse neuronal beta 2-nicotinic acetylcholine receptor genes. Mammalian Genome 10: 900-905.
Lueders KK, and Frankel WN (1994). Mapping of Mouse Intracisternal a-Particle Proviral Markers in an Interspecific Backcross. Mammalian Genome 5: 473-478.
Lueders KK, Frankel WN, Mietz JA, and Kuff EL (1993). Genomic Mapping of Intracisternal a-Particle Proviral Elements. Mammalian Genome 4: 69-77.
Luo H, Chaudhuri A, Johnson KR, Neote K, Zbrzezna V, He Y, and Pogo AO (1997). Cloning, characterization, and mapping of a murine promiscuous chemokine receptor gene: Homolog of the human duffy gene. Genome Research 7: 932-941.
Luo ZW, Wu CI, and Kearsey MJ (2002). Precision and high-resolution mapping of quantitative trait loci by use of recurrent selection, backcross or intercross schemes. Genetics 161: 915-929.
Machleder D, Ivandic B, Welch C, Castellani L, Reue K, and Lusis AJ (1997). Complex genetic control of HDL levels in mice in response to an atherogenic diet - Coordinate regulation of HDL levels and bile acid metabolism. Journal of Clinical Investigation 99: 1406-1419.
Macias MP, Welch KC, Denzler KL, Larson KA, Lee NA, and Lee JJ (2000). Identification of a new murine eosinophil major basic protein (mMBP) gene: cloning and characterization of mMBP-2. Journal of Leukocyte Biology 67: 567-576.
MacTaggart TE, Ito M, Smithies O, and John SWM (1997). Mouse angiotensin receptor genes Agtr1a and Agtr1b map to chromosomes 13 and 3. Mammalian Genome 8: 294-295.
Magenis RE, Smith L, Nadeau JH, Johnson KR, Mountjoy KG, and Cone RD (1994). Mapping of the Acth, Msh, and Neural (Mc3 and Mc4) Melanocortin Receptors in the Mouse and Human. Mammalian Genome 5: 503-508.
Malek TR, Vincek V, Gatalica B, and Bucan M (1993). The Il-2 Receptor Beta-Chain Gene (Il-2rb) Is Closely Linked to the Pdgfb Locus On Mouse Chromosome-15. Immunogenetics 38: 154-156.
Malgaretti N, Pozzoli O, Bosetti A, Corradi A, Ciarmatori S, Panigada M, Bianchi ME, Martinez S, and Consalez GG (1997). Mmot1, a new helix-loop-helix transcription factor gene displaying a sharp expression boundary in the embryonic mouse brain. Journal of Biological Chemistry 272: 17632-17639.
Maliepaard C, Sillanpaa MJ, van Ooijen JW, Jansen RC, and Arjas E (2001). Bayesian versus frequentist analysis of multiple quantitative trait loci with an application to an outbred apple cross. Theoretical and Applied Genetics 103: 1243-1253.
Malkinson AM, Radcliffe RA, and Bauer AK (2002). Quantitative trait locus mapping of susceptibilities to butylated hydroxytoluene-induced lung tumor promotion and pulmonary inflammation in CXB mice. Carcinogenesis 23: 411-417.
Mangan ME, and Olmsted JB (1996). The gene for microtubule-associated protein 4 (Mtap4) maps to the distal region of mouse chromosome 9. Mammalian Genome 7: 918-919.
Manly KF (1993). A Macintosh Program For Storage and Analysis of Experimental Genetic-Mapping Data. Mammalian Genome 4: 303-313.
Manly KF (2000). Mathematica packages for simulation of experimental genetics. Bioinformatics 16: 408-409.
Manly KF, Cudmore RH, and Meer JM (2001). Map manager QTX, cross-platform software for genetic mapping. Mammalian Genome 12: 930-932.
Manly KF, and Olson JM (1999). Overview of QTL mapping software and introduction to map manager QT. Mammalian Genome 10: 327-334.
Mao NC, Steingrimsson E, DuHadaway J, Wasserman W, Ruiz JC, Copeland NG, Jenkins NA, and Prendergast GC (1999). The murine Bin1 gene functions early in myogenesis and defines a new region of synteny between mouse chromosome 18 and human chromosome 2. Genomics 56: 51-58.
Mariani M, Baldessari D, Francisconi S, Viggiano L, Rocchi M, Zappavigna V, Malgaretti N, and Consalez GG (1999). Two murine and human homologs of mab-21, a cell fate determination gene involved in Caenorhabditis elegans neural development. Human Molecular Genetics 8: 2397-2406.
Mariani P, Barrow PA, Cheng HH, Groenen MAM, Negrini R, and Bumstead N (2001). Localization to chicken Chromosome 5 of a novel locus determining salmonellosis resistance. Immunogenetics 53: 786-791.
Markel PD, Bennett B, Beeson MA, Gordon L, Simpson VJ, and Johnson TE (1996). Strain distribution patterns for genetic markers in the LSXSS recombinant-inbred series. Mammalian Genome 7: 408-412.
Markel PD, and Johnson TE (1994). Initial Characterization of Sts Markers in the Lsxss Series of Recombinant Inbred Strains. Mammalian Genome 5: 199-202.
Marshall JD, Mu JL, Cheah YC, Nesbitt MN, Frankel WN, and Paigen B (1992). The Axb and BXA Set of Recombinant Inbred Mouse Strains. Mammalian Genome 3: 669-680.
Mashimo T, Glaser P, Lucas M, Simon-Chazottes D, Ceccaldi PE, Montagutelli X, Despres P, and Guenet JL (2003). Structural and functional genomics and evolutionary relationships in the cluster of genes encoding murine 2 ',5 '-oligoadenylate synthetases. Genomics 82: 537-552.
Masuyama T, Fuse M, Yokoi N, Shinohara M, Tsujii H, Kanazawa M, Kanazawa Y, Komeda K, and Taniguchi K (2003). Genetic analysis for diabetes in a new rat model of nonobese type 2 diabetes, Spontaneously Diabetic Torii rat. Biochemical and Biophysical Research Communications 304: 196-206.
Masuyama T, Ishibiki J, Awata T, Noda M, Kanazawa Y, Sugawara M, and Komeda K (2000). An improved genetic linkage map of rat chromosome 20. Comparative Medicine 50: 369-373.
Mates L, Korpos E, Deak F, Liu ZQ, Beier DR, Aszodi A, and Kiss I (2002). Comparative analysis of the mouse and human genes (Matn2 and MATN2) for matrilin-2, a filament-forming protein widely distributed in extracellular matrices. Matrix Biology 21: 163-174.
Matesic LE, De Maio A, and Reeves RH (1999). Mapping lipopolysaccharide response loci in mice using recombinant inbred and congenic strains. Genomics 62: 34-41.
Matesic LE, Niemitz EL, De Maio A, and Reeves RH (2000). Quantitative trait loci modulate neutrophil infiltration in the liver during LPS-induced inflammation. Faseb Journal 14: 2247-2254.
Mathis C, Neumann PE, Gershenfeld H, Paul SM, and Crawley JN (1995). Genetic-Analysis of Anxiety-Related Behaviors and Responses to Benzodiazepine-Related Drugs in Axb and BXA Recombinant Inbred Mouse Strains. Behavior Genetics 25: 557-568.
Matin A, Collin GB, Asada Y, Varnum D, and Nadeau JH (1999). Susceptibility to testicular germ-cell tumours in a 129.MOLF- Chr 19 chromosome substitution strain. Nature Genetics 23: 237-240.
Matsuda Y, Takahara T, Kusakabe M, and Hayashizaki Y (1996). Comparative mapping of the reeler gene on human chromosome 7q22, rat chromosome 4q11.2, and mouse chromosome 5 A3-B1. Mammalian Genome 7: 468-469.
Mayeda AR, Hofstetter JR, Belknap JK, and Nurnberger JI (1996). Hypothetical quantitative trait loci (QTL) for circadian period of locomotor activity in CXB recombinant inbred strains of mice. Behavior Genetics 26: 505-511.
McBrearty BA, Clark LD, Zhang XM, Blankenhorn EP, and Heber-Katze E (1998). Genetic analysis of a mammalian wound-healing trait. Proceedings of the National Academy of Sciences of the United States of America 95: 11792-11797.
McCarthy L, Hunter K, Schalkwyk L, Riba L, Anson S, Mott R, Newell W, Bruley C, Bar I, Ramu E, Housman D, Cox R, and Lehrach H (1995). Efficient High-Resolution Genetic-Mapping of Mouse Interspersed Repetitive Sequence Pcr Products, Toward Integrated Genetic and Physical Mapping of the Mouse Genome. Proceedings of the National Academy of Sciences of the United States of America 92: 5302-5306.
McConnell SKJ, Dawson DA, Wardle A, and Burke T (1999). The isolation and mapping of 19 tetranucleotide microsatellite markers in the chicken. Animal Genetics 30: 183-189.
McGinnis JF, Lerious V, Pazik J, and Elliott RW (1993). Chromosomal Assignment of the Recoverin Gene and Cancer- Associated Retinopathy. Mammalian Genome 4: 43-45.
McKee-Johnson JW, Street VA, Erford SK, Robinson LC, and Tempel BL (1998). Physical and genetic maps of the deafwaddler region on distal mouse Chr 6. Genomics 49: 371-377.
Mehrabian M, Castellani LW, Wen PZ, Wong J, Rithaporn T, Hama SY, Hough GP, Johnson D, Albers JJ, Mottino GA, Frank JS, Navab M, Fogelman AM, and Lusis AJ (2000). Genetic control of HDL levels and composition in an interspecific mouse cross (CAST/Ei x C57BL/6J). Journal of Lipid Research 41: 1936-1946.
Mehrabian M, Wen PZ, Fisler J, Davis RC, and Lusis AJ (1998). Genetic loci controlling body fat, lipoprotein metabolism, and insulin levels in a multifactorial mouse model. Journal of Clinical Investigation 101: 2485-2496.
Meiner VL, Welch CL, Cases S, Myers HM, Lusis HAJ, and Farese RV (1998). Adrenocortical lipid depletion gene (ald) in AKR mice is associated with an acyl-CoA : cholesterol acyltransferase (ACAT) mutation. Journal of Biological Chemistry 273: 1064-1069.
Men AE, Borisov AY, Rozov SM, Ushakov KV, Tsyganov VE, Tikhonovich IA, and Gresshoff PM (1999). Identification of DNA amplification fingerprinting (DAF) markers close to the symbiosis-ineffective sym31 mutation of pea (Pisum sativum L.). Theoretical and Applied Genetics 98: 929-936.
Miao YW, Burt DW, Paton IR, Sharp PJ, and Dunn IC (1999). Mapping of the prolactin gene to chicken chromosome 2. Animal Genetics 30: 473-473.
Mielnicki LM, Elliott RW, and Pruitt SC (1993). Localization of the Murine Activating Transcription Factor-Iv Gene to Mouse Chromosome-15. Genomics 15: 197-199.
Miller RD, Hogg J, Ozaki JH, Gell D, Jackson SP, and Riblet R (1995). Gene For the Catalytic Subunit of Mouse DNA-Dependent Protein- Kinase Maps to the Scid Locus. Proceedings of the National Academy of Sciences of the United States of America 92: 10792-10795.
Miller RD, Ozaki JH, and Riblet R (1993). The Mouse Severe Combined Immune-Deficiency (Scid) Mutation Is Closely Linked to the B-Cell-Specific Developmental Genes Vpreb and Lambda-5. Genomics 16: 740-744.
Mills KA, Ellison JW, and Mathews KD (1996). The Ant1 gene maps near Klk3 on proximal mouse Chromosome 8. Mammalian Genome 7: 707-707.
Mills KA, Mathews KD, ScherpbierHeddema T, Buetow KH, Baldini A, Ballabio A, and Borsani G (1996). Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8. Genomics 36: 374-376.
Mills KA, Mathews KD, Scherpbierheddema T, Schelper RL, Schmalzel R, Bailey HL, Nadeau JH, Buetow KH, and Murray JC (1995). Genetic-Mapping Near the Myd Locus On Mouse Chromosome-8. Mammalian Genome 6: 278-280.
Mills KA, Sunada Y, Campbell KP, and Mathews KD (1995). A Syntrophin Gene Maps to Mouse Chromosome-8 and Is Not the Myodystrophy Gene. Mammalian Genome 6: 664-665.
Min-Oo G, Fortin A, Tam MF, Nantel A, Stevenson MM, and Gros P (2003). Pyruvate kinase deficiency in mice protects against malaria. Nature Genetics 35: 357-362.
Misener VL, Wielowieyski A, Brennan LA, Beebakhee G, and Jongstra J (1998). The mouse Lsp1 and Tnnt3 genes are 4.3 kb apart on distal mouse Chromosome 7. Mammalian Genome 9: 846-848.
Mitchem KL, Hibbard E, Beyer LA, Bosom K, Dootz GA, Dolan DF, Johnson KR, Raphael Y, and Kohrman DC (2002). Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6. Human Molecular Genetics 11: 1887-1898.
Miyoshi H, Kon Y, Seo KW, Jin HK, Hasegawa A, and Watanabe T (1999). Jumbled spine and ribs (Jsr): a new mutation on mouse Chromosome 5. Mammalian Genome 10: 213-217.
Mogil JS, Richards SP, Otoole LA, Helms ML, Mitchell SR, and Belknap JK (1997). Genetic sensitivity to hot-plate nociception in DBA/2J and C57BL/6J inbred mouse strains: Possible sex-specific mediation by delta(2)-opioid receptors. Pain 70: 267-277.
Mogil JS, Richards SP, Otoole LA, Helms ML, Mitchell SR, Kest B, and Belknap JK (1997). Identification of a sex-specific quantitative trait locus mediating nonopioid stress-induced analgesia in female mice. Journal of Neuroscience 17: 7995-8002.
Moisan MP, Llamas B, Cook MN, and Mormede P (2003). Further dissection of a genomic locus associated with behavioral activity in the Wistar-Kyoto hyperactive rat, an animal model of hyperkinesis. Molecular Psychiatry 8: 348-352.
Montini E, Andolfi G, Caruso A, Buchner G, Walpole SM, Mariani M, Consalez GG, Trump D, Ballabio A, and Franco B (1998). Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region. Genomics 51: 427-433.
Montini E, Rugarli EI, VandeVosse E, Andolfi G, Mariani M, Puca AA, Consalez GG, denDunnen JT, Ballabio A, and Franco B (1997). A novel human serine-threonine phosphatase related to the Drosophila retinal degeneration C (rdgC) gene is selectively expressed in sensory neurons of neural crest origin. Human Molecular Genetics 6: 1137-1145.
Moore KJ, and Nagle DL (2000). Complex trait analysis in the mouse: The strengths, the limitations and the promise yet to come. Annual Review of Genetics 34: 653-686.
Mori M, Akiyoshi S, Mizuno Y, Okuizumi H, Okazaki Y, Hayashizaki Y, and Nishimura M (1998). Genetic profile of the SMXA recombinant inbred mouse strains revealed with restriction landmark genomic scanning. Mammalian Genome 9: 695-709.
Morisson M, Pitel F, Fillon V, Pouzadoux A, Berge R, Vit JP, Zoorob R, Auffray C, Gellin J, and Vignal A (1998). Integration of chicken cytogenetic and genetic maps: 18 new polymorphic markers isolated from BAC and PAC clones. Animal Genetics 29: 348-355.
Morisson M, Plisson-Petit F, Dawson D, Pitel F, Fillon V, Gellin J, Burke T, and Vignal A (1999). Characterisation of 33 chicken microsatellite loci: 20 new locations on reference maps. Animal Genetics 30: 391-393.
Mount DB, Baekgaard A, Hall AE, Plata C, Xu J, Beier DR, Gamba G, and Hebert SC (1999). Isoforms of the Na-K-2Cl cotransporter in murine TAL I. Molecular char