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Muriel Davisson

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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TOP 3
Costa Alberto C S; Stasko Melissa R; Schmidt Cecilia; Davisson Muriel T
Behavioral validation of the Ts65Dn mouse model for Down syndrome of a genetic background free of the retinal degeneration mutation Pde6b(rd1).
Han Fengchan; Yu Heping; Zhang Jiangping; Tian Cong; Schmidt Cecilia; Nava Casey; Davisson Muriel T; Zheng Qing Y
Otitis media in a mouse model for Down syndrome.
Cook Susan A; Collin Gayle B; Bronson Roderick T; Naggert Jürgen K; Liu Dong P; Akeson Ellen C; Davisson Muriel T
A mouse model for Meckel syndrome type 3.

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All Publications

2010: Costa Alberto C S; Stasko Melissa R; Schmidt Cecilia; Davisson Muriel T
Behavioral validation of the Ts65Dn mouse model for Down syndrome of a genetic background free of the retinal degeneration mutation Pde6b(rd1).
Behavioural brain research 2010;206(1):52-62.
2009: Han Fengchan; Yu Heping; Zhang Jiangping; Tian Cong; Schmidt Cecilia; Nava Casey; Davisson Muriel T; Zheng Qing Y
Otitis media in a mouse model for Down syndrome.
International journal of experimental pathology 2009;90(5):480-8.
2009: Cook Susan A; Collin Gayle B; Bronson Roderick T; Naggert Jürgen K; Liu Dong P; Akeson Ellen C; Davisson Muriel T
A mouse model for Meckel syndrome type 3.
Journal of the American Society of Nephrology : JASN 2009;20(4):753-64.
2008: Voronov Sergey V; Frere Samuel G; Giovedi Silvia; Pollina Elizabeth A; Borel Christelle; Zhang Hong; Schmidt Cecilia; Akeson Ellen C; Wenk Markus R; Cimasoni Laurent; Arancio Ottavio; Davisson Muriel T; Antonarakis Stylianos E; Gardiner Katheleen; De Camilli Pietro; Di Paolo Gilbert
Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndrome.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(27):9415-20.
2007: Du Yunzhi; Stasko Melissa; Costa Alberto C; Davisson Muriel T; Gardiner Katheleen J
Editing of the serotonin 2C receptor pre-mRNA: Effects of the Morris Water Maze.
Gene 2007;391(1-2):186-97.
2007: Chang B; Hawes N L; Pardue M T; German A M; Hurd R E; Davisson M T; Nusinowitz S; Rengarajan K; Boyd A P; Sidney S S; Phillips M J; Stewart R E; Chaudhury R; Nickerson J M; Heckenlively J R; Boatright J H
Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.
Vision research 2007;47(5):624-33.
2007: Davisson M; Akeson E; Schmidt C; Harris B; Farley J; Handel M A
Impact of trisomy on fertility and meiosis in male mice.
Human reproduction (Oxford, England) 2007;22(2):468-76.
2006: Taft Robert A; Davisson Muriel; Wiles Michael V
Know thy mouse.
Trends in genetics : TIG 2006;22(12):649-53.
2006: Du Yunzhi; Davisson Muriel T; Kafadar Karen; Gardiner Katheleen
A-to-I pre-mRNA editing of the serotonin 2C receptor: comparisons among inbred mouse strains.
Gene 2006;382():39-46.
2006: Lee Jeong Woong; Beebe Kirk; Nangle Leslie A; Jang Jaeseon; Longo-Guess Chantal M; Cook Susan A; Davisson Muriel T; Sundberg John P; Schimmel Paul; Ackerman Susan L
Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration.
Nature 2006;443(7107):50-5.
2006: Davisson Muriel
FIMRe: Federation of International Mouse Resources: global networking of resource centers.
Mammalian genome : official journal of the International Mammalian Genome Society 2006;17(5):363-4.
2006: Davisson Muriel T; Taft Robert A
Strategies for managing an ever increasing mutant mouse repository.
Brain research 2006;1091(1):255-7.
2006: Simon-Chazottes Dominique; Tutois Sylvie; Kuehn Michael; Evans Martin; Bourgade Franck; Cook Sue; Davisson Muriel T; Guénet Jean-Louis
Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouse.
Genomics 2006;87(5):673-7.
2006: Gilbert Sandra L; Zhang Li; Forster Michele L; Anderson Jeffrey R; Iwase Tamaki; Soliven Betty; Donahue Leah Rae; Sweet Hope O; Bronson Roderick T; Davisson Muriel T; Wollmann Robert L; Lahn Bruce T
Trak1 mutation disrupts GABA(A) receptor homeostasis in hypertonic mice.
Nature genetics 2006;38(2):245-50.
2006: Akeson Ellen C; Donahue Leah Rae; Beamer Wesley G; Shultz Kathy L; Ackert-Bicknell Cheryl; Rosen Clifford J; Corrigan Jennifer; Davisson Muriel T
Chromosomal inversion discovered in C3H/HeJ mice.
Genomics 2006;87(2):311-3.
2006: Chang Bo; Heckenlively John R; Bayley Philippa R; Brecha Nicholas C; Davisson Muriel T; Hawes Norm L; Hirano Arlene A; Hurd Ronald E; Ikeda Akihiro; Johnson Britt A; McCall Maureen A; Morgans Catherine W; Nusinowitz Steve; Peachey Neal S; Rice Dennis S; Vessey Kirstan A; Gregg Ronald G
The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses.
Visual neuroscience 2006;23(1):11-24.
2005: Chang B; Hawes N L; Hurd R E; Wang J; Howell D; Davisson M T; Roderick T H; Nusinowitz S; Heckenlively J R
Mouse models of ocular diseases.
Visual neuroscience 2005;22(5):587-93.
2005: Martínez-Cué Carmen; Rueda Noemí; García Eva; Davisson Muriel T; Schmidt Cecilia; Flórez Jesús
Behavioral, cognitive and biochemical responses to different environmental conditions in male Ts65Dn mice, a model of Down syndrome.
Behavioural brain research 2005;163(2):174-85.
2005: Pang Ji-Jing; Chang Bo; Hawes Norman L; Hurd Ronald E; Davisson Muriel T; Li Jie; Noorwez Syed M; Malhotra Ritu; McDowell J Hugh; Kaushal Shalesh; Hauswirth William W; Nusinowitz Steven; Thompson Debra A; Heckenlively John R
Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).
Molecular vision 2005;11():152-62.
2005: Davisson Muriel T
Discovery genetics: serendipity in basic research.
ILAR journal / National Research Council, Institute of Laboratory Animal Resources 2005;46(4):338-45.
2005: Gardiner K; Davisson M T; Pritchard M; Patterson D; Groner Y; Crnic L S; Antonarakis S; Mobley W
Report on the 'Expert Workshop on the Biology of Chromosome 21: towards gene-phenotype correlations in Down syndrome', held June 11-14, 2004, Washington D.C.
Cytogenetic and genome research 2005;108(4):269-77.
2004: Gardiner Katheleen; Davisson Muriel T; Crnic Linda S
Building protein interaction maps for Down's syndrome.
Briefings in functional genomics & proteomics 2004;3(2):142-56.
2004: Lorenz-Depiereux Bettina; Guido Victoria E; Johnson Kenneth R; Zheng Qing Yin; Gagnon Leona H; Bauschatz Joiel D; Davisson Muriel T; Washburn Linda L; Donahue Leah Rae; Strom Tim M; Eicher Eva M
New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2004;15(3):151-61.
2004: Wenger Galen R; Schmidt Cecilia; Davisson Muriel T
Operant conditioning in the Ts65Dn mouse: learning.
Behavior genetics 2004;34(1):105-19.
2003: Liu Dong P; Schmidt Cecilia; Billings Timothy; Davisson Muriel T
Quantitative PCR genotyping assay for the Ts65Dn mouse model of Down syndrome.
BioTechniques 2003;35(6):1170-4, 1176, 1178 passim.
2003: Gardiner Katheleen; Fortna Andrew; Bechtel Lawrence; Davisson Muriel T
Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions.
Gene 2003;318():137-47.
2003: Donahue Leah Rae; Chang Bo; Mohan Subburaman; Miyakoshi Nao; Wergedal Jon E; Baylink David J; Hawes Norman L; Rosen Clifford J; Ward-Bailey Patricia; Zheng Qing Y; Bronson Roderick T; Johnson Kenneth R; Davisson Muriel T
A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2003;18(9):1612-21.
2003: Heckenlively John R; Hawes Norman L; Friedlander Martin; Nusinowitz Steven; Hurd Ronald; Davisson Muriel; Chang Bo
Mouse model of subretinal neovascularization with choroidal anastomosis.
Retina (Philadelphia, Pa.) 2003;23(4):518-22.
2003: Johnson Kenneth R; Lane Priscilla W; Cook Susan A; Harris Belinda S; Ward-Bailey Patricia F; Bronson Roderick T; Lyons Bonnie L; Shultz Leonard D; Davisson Muriel T
Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5.
Genomics 2003;81(1):6-14.
2003: Bauschatz Joiel D; Curtain Michelle M; Davisson Muriel T; Lane Priscilla W; Donahue Leah Rae
In collaboration: the Jackson Laboratory Craniofacial Resource.
Critical reviews in eukaryotic gene expression 2003;13(2-4):107-8.
2002: Moran Timothy H; Capone George T; Knipp Susan; Davisson Muriel T; Reeves Roger H; Gearhart John D
The effects of piracetam on cognitive performance in a mouse model of Down's syndrome.
Physiology & behavior 2002;77(2-3):403-9.
2002: Martínez-Cué Carmen; Baamonde Carmela; Lumbreras Marian; Paz Jesús; Davisson Muriel T; Schmidt Cecilia; Dierssen Mara; Flórez Jesús
Differential effects of environmental enrichment on behavior and learning of male and female Ts65Dn mice, a model for Down syndrome.
Behavioural brain research 2002;134(1-2):185-200.
2002: Gardiner Katheleen; Slavov Dobromir; Bechtel Lawrence; Davisson Muriel
Annotation of human chromosome 21 for relevance to Down syndrome: gene structure and expression analysis.
Genomics 2002;79(6):833-43.
2002: Chae Teresa H; Allen Kristina M; Davisson Muriel T; Sweet Hope O; Walsh Christopher A
Mapping of the mouse hyh gene to a YAC/BAC contig on proximal Chromosome 7.
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(5):239-44.
2002: Chang Bo; Wang Xin; Hawes Norman L; Ojakian Ryan; Davisson Muriel T; Lo Woo-Kuen; Gong Xiaohua
A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice.
Human molecular genetics 2002;11(5):507-13.
2002: Chang B; Hawes N L; Hurd R E; Davisson M T; Nusinowitz S; Heckenlively J R
Retinal degeneration mutants in the mouse.
Vision research 2002;42(4):517-25.
2001: Davisson M T; Bechtel L J; Akeson E C; Fortna A; Slavov D; Gardiner K
Evolutionary breakpoints on human chromosome 21.
Genomics 2001;78(1-2):99-106.
2001: Anagnostopoulos A V; Sharp J J; Mobraaten L E; Eppig J T; Davisson M T
Availability and characterization of transgenic and knockout mice with behavioral manifestations: where to look and what to search for.
Behavioural brain research 2001;125(1-2):33-7.
2001: Newton J M; Cohen-Barak O; Hagiwara N; Gardner J M; Davisson M T; King R A; Brilliant M H
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4.
American journal of human genetics 2001;69(5):981-8.
2001: Anagnostopoulos A V; Mobraaten L E; Sharp J J; Davisson M T
Transgenic and knockout databases: behavioral profiles of mouse mutants.
Physiology & behavior 2001;73(5):675-89.
2001: Akeson E C; Davisson M T
Mitotic chromosome preparations from mouse cells for karyotyping.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2001;Chapter 4():Unit4.10.
2001: Akeson E C; Lambert J P; Narayanswami S; Gardiner K; Bechtel L J; Davisson M T
Ts65Dn -- localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome.
Cytogenetics and cell genetics 2001;93(3-4):270-6.
2001: Cook S A; Akeson E C; Calvano C; Johnson K R; Mandell J; Hawes N L; Bronson R T; Roderick T H; Davisson M T
Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene.
Cytogenetics and cell genetics 2001;93(1-2):77-82.
2001: Davisson M T; Gardiner K; Costa A C
Report and abstracts of the ninth international workshop on the molecular biology of human chromosome 21 and Down syndrome. Bar Harbor, Maine, USA. 23-26 September 2000.
Cytogenetics and cell genetics 2001;92(1-2):1-22.
2001: Anderson M G; Smith R S; Savinova O V; Hawes N L; Chang B; Zabaleta A; Wilpan R; Heckenlively J R; Davisson M; John S W
Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice.
BMC genetics 2001;2():1.
2000: Davisson M T; Johnson K R; Bronson R T; Ward-Bailey P F; Cook S A; Harris B S; Donahue L R
Grey intense: a new mouse mutation affecting pigmentation.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(12):1139-41.
2000: Chrast R; Scott H S; Papasavvas M P; Rossier C; Antonarakis E S; Barras C; Davisson M T; Schmidt C; Estivill X; Dierssen M; Pritchard M; Antonarakis S E
The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals.
Genome research 2000;10(12):2006-21.
2000: Ward-Bailey P F; Wood B; Johnson K R; Bronson R T; Donahue L R; Davisson M T
Neuromuscular ataxia: a new spontaneous mutation in the mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(10):820-3.
2000: Hawes N L; Chang B; Hageman G S; Nusinowitz S; Nishina P M; Schneider B S; Smith R S; Roderick T H; Davisson M T; Heckenlively J R
Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens.
Investigative ophthalmology & visual science 2000;41(10):3149-57.
2000: Akhmedov N B; Piriev N I; Chang B; Rapoport A L; Hawes N L; Nishina P M; Nusinowitz S; Heckenlively J R; Roderick T H; Kozak C A; Danciger M; Davisson M T; Farber D B
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(10):5551-6.
2000: Smith R S; Hawes N L; Chang B; Roderick T H; Akeson E C; Heckenlively J R; Gong X; Wang X; Davisson M T
Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract.
Genomics 2000;63(3):314-20.
2000: Smith R S; John S W; Zabeleta A; Davisson M T; Hawes N L; Chang B
The bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(5):2191-5.
2000: Blake J A; Eppig J T; Richardson J E; Davisson M T
The Mouse Genome Database (MGD): expanding genetic and genomic resources for the laboratory mouse. The Mouse Genome Database Group.
Nucleic acids research 2000;28(1):108-11.
1999: Costa A C; Walsh K; Davisson M T
Motor dysfunction in a mouse model for Down syndrome.
Physiology & behavior 1999;68(1-2):211-20.
1999: Hawes N L; Smith R S; Chang B; Davisson M; Heckenlively J R; John S W
Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypes.
Molecular vision 1999;5():22.
1999: Chang B; Hawes N L; Roderick T H; Smith R S; Heckenlively J R; Horwitz J; Davisson M T
Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouse.
Molecular vision 1999;5():21.
1999: Festing M F; Simpson E M; Davisson M T; Mobraaten L E
Revised nomenclature for strain 129 mice.
Mammalian genome : official journal of the International Mammalian Genome Society 1999;10(8):836.
1999: Chang B; Smith R S; Hawes N L; Anderson M G; Zabaleta A; Savinova O; Roderick T H; Heckenlively J R; Davisson M T; John S W
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice.
Nature genetics 1999;21(4):405-9.
1999: Smith R S; Johnson K R; Hawes N L; Harris B S; Sundberg J P; Davisson M T
Lens epithelial proliferation cataract in segmental trisomy involving mouse Chromosomes 4 and 17.
Mammalian genome : official journal of the International Mammalian Genome Society 1999;10(2):102-6.
1999: Blake J A; Richardson J E; Davisson M T; Eppig J T
The Mouse Genome Database (MGD): genetic and genomic information about the laboratory mouse. The Mouse Genome Database Group.
Nucleic acids research 1999;27(1):95-8.
1998: Korobova O; Lane P W; Perry J; Palmer S; Ashworth A; Davisson M T; Arnheim N
Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, maps to the pseudoautosomal boundary region.
Genomics 1998;54(3):556-9.
1998: Sweet H O; Brilliant M H; Cook S A; Johnson K R; Davisson M T
A new allelic series for the underwhite gene on mouse chromosome 15.
The Journal of heredity 1998;89(6):546-51.
1998: Johnson K R; Sweet H O; Donahue L R; Ward-Bailey P; Bronson R T; Davisson M T
A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly.
Human molecular genetics 1998;7(6):1033-8.
1998: Lane P W; Bronson R T; Cook S A; Ward-Bailey P; Donahue L R; Davisson M T
Juvenile bare: a new hair loss mutation on chromosome 7 of the mouse.
The Journal of heredity 1998;89(3):254-7.
1998: John S W; Smith R S; Savinova O V; Hawes N L; Chang B; Turnbull D; Davisson M; Roderick T H; Heckenlively J R
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice.
Investigative ophthalmology & visual science 1998;39(6):951-62.
1998: Eppig J T; Blake J A; Davisson M T; Richardson J E
Informatics for mouse genetics and genome mapping.
Methods (San Diego, Calif.) 1998;14(2):179-90.
1998: Blake J A; Eppig J T; Richardson J E; Davisson M T
The Mouse Genome Database (MGD): a community resource. Status and enhancements. The Mouse Genome Informatics Group.
Nucleic acids research 1998;26(1):130-7.
1998: Johnson K R; Davisson M T
Encyclopedia of the mouse genome VII. Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;8 Spec No():S343-52.
1997: González J L; Russo C J; Goldowitz D; Sweet H O; Davisson M T; Walsh C A
Birthdate and cell marker analysis of scrambler: a novel mutation affecting cortical development with a reeler-like phenotype.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1997;17(23):9204-11.
1997: Goldowitz D; Cushing R C; Laywell E; D'Arcangelo G; Sheldon M; Sweet H O; Davisson M; Steindler D; Curran T
Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of reelin.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1997;17(22):8767-77.
1997: Maltais L J; Blake J A; Eppig J T; Davisson M T
Rules and guidelines for mouse gene nomenclature: a condensed version. International Committee on Standardized Genetic Nomenclature for Mice.
Genomics 1997;45(2):471-6.
1997: Rice D S; Tang Q; Williams R W; Harris B S; Davisson M T; Goldowitz D
Decreased retinal ganglion cell number and misdirected axon growth associated with fissure defects in Bst/+ mutant mice.
Investigative ophthalmology & visual science 1997;38(10):2112-24.
1997: Cook S; Johnson K; Davisson M
The mouse urate oxidase gene, Uox, maps to distal chromosome 3.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(8):623-4.
1997: Letts V A; Valenzuela A; Kirley J P; Sweet H O; Davisson M T; Frankel W N
Genetic and physical maps of the stargazer locus on mouse chromosome 15.
Genomics 1997;43(1):62-8.
1997: Simpson E M; Linder C C; Sargent E E; Davisson M T; Mobraaten L E; Sharp J J
Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice.
Nature genetics 1997;16(1):19-27.
1997: Harris B S; Franz T; Ullrich S; Cook S; Bronson R T; Davisson M T
Forebrain overgrowth (fog): a new mutation in the mouse affecting neural tube development.
Teratology 1997;55(4):231-40.
1997: Janaswami P M; Birkenmeier E H; Cook S A; Rowe L B; Bronson R T; Davisson M T
Identification and genetic mapping of a new polycystic kidney disease on mouse chromosome 8.
Genomics 1997;40(1):101-7.
1997: Cook S A; Bronson R T; Donahue L R; Ben-Arie N; Davisson M T
Cerebellar deficient folia (cdf): a new mutation on mouse chromosome 6.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(2):108-12.
1997: Blake J A; Richardson J E; Davisson M T; Eppig J T
The Mouse Genome Database (MGD). A comprehensive public resource of genetic, phenotypic and genomic data. The Mouse Genome Informatics Group.
Nucleic acids research 1997;25(1):85-91.
1997: Johnson K R; Davisson M T
Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;7 Spec No():S295-304.
1996: Donahue L R; Cook S A; Johnson K R; Bronson R T; Davisson M T
Megencephaly: a new mouse mutation on chromosome 6 that causes hypertrophy of the brain.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(12):871-6.
1996: Sweet H O; Bronson R T; Johnson K R; Cook S A; Davisson M T
Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(11):798-802.
1996: Ward-Bailey P F; Johnson K R; Handel M A; Harris B S; Davisson M T
A new mouse mutation causing male sterility and histoincompatibility.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(11):793-7.
1996: Chang B; Hawes N L; Smith R S; Heckenlively J R; Davisson M T; Roderick T H
Chromosomal localization of a new mouse lens opacity gene (lop18)
Genomics 1996;36(1):171-3.
1996: Heine D; Passmore H C; Patel V; Shultz L D; Ward-Bailey P; Cook S A; Davisson M T
Effect of the mouse scid mutation on meiotic recombination.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(7):497-500.
1996: Sweet H O; Bronson R T; Donahue L R; Davisson M T
Mesenchymal dysplasia: a recessive mutation on chromosome 13 of the mouse.
The Journal of heredity 1996;87(2):87-95.
1996: Sweet H O; Marks S C; MacKay C A; Johnson K R; Davisson M T
Dense incisors (din): a new mouse mutation on chromosome 16 affecting tooth eruption and body size.
The Journal of heredity 1996;87(2):162-7.
1996: Johnson K R; Davisson M T
Encyclopedia of the mouse genome V. Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;6 Spec No():S300-8.
1995: Reeves R H; Irving N G; Moran T H; Wohn A; Kitt C; Sisodia S S; Schmidt C; Bronson R T; Davisson M T
A mouse model for Down syndrome exhibits learning and behaviour deficits.
Nature genetics 1995;11(2):177-84.
1995: Johnson K R; Lane P W; Ward-Bailey P; Davisson M T
Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac.
Genomics 1995;29(2):457-64.
1995: Rice D S; Williams R W; Ward-Bailey P; Johnson K R; Harris B S; Davisson M T; Goldowitz D
Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophy.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(8):546-8.
1995: Cook S A; Johnson K R; Bronson R T; Davisson M T
Neuromuscular degeneration (nmd): a mutation on mouse chromosome 19 that causes motor neuron degeneration.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(3):187-91.
1994: Johnson K R; Cook S A; Davisson M T
Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5(11):670-87.
1994: Frankel W N; Sweet H O; Davisson M T
The stumbler mutation maps to proximal mouse chromosome 2.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5(11):659-62.
1994: Beamer W G; Sweet H O; Bronson R T; Shire J G; Orth D N; Davisson M T
Adrenocortical dysplasia: a mouse model system for adrenocortical insufficiency.
The Journal of endocrinology 1994;141(1):33-43.
1994: Davisson M T; Cook S A; Johnson K R; Eicher E M
Balding: a new mutation on mouse chromosome 18 causing hair loss and immunological defects.
The Journal of heredity 1994;85(2):134-6.
1994: Johnson K R; Davisson M T
Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5 Spec No():S259-65.
1993: Davisson M T; Akeson E C
Recombination suppression by heterozygous Robertsonian chromosomes in the mouse.
Genetics 1993;133(3):649-67.
1993: Davisson M T; Johnson K R
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4 Spec No():S253-60.
1993: Davisson M T; Schmidt C; Reeves R H; Irving N G; Akeson E C; Harris B S; Bronson R T
Segmental trisomy as a mouse model for Down syndrome.
Progress in clinical and biological research 1993;384():117-33.
1993: Johnson K R; Cook S A; Ward-Bailey P; Bustin M; Davisson M T
Identification and genetic mapping of the murine gene and 20 related sequences encoding chromosomal protein HMG-17.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(2):83-9.
1993: Johnson K R; Cook S A; Ward-Bailey P; Davisson M T
Genetic mapping of variable length rDNA segments to centromeric regions of mouse chromosomes 11, 12, 15, 16, and 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(1):49-52.
1992: Johnson K R; Lu S; Murtha M T; Ruddle F H; Davisson M T
Genetic mapping of a new homeobox gene to mouse chromosome 7.
Genomics 1992;14(4):1107-9.
1992: Johnson K R; Davisson M T
A multipoint genetic linkage map of mouse chromosome 18.
Genomics 1992;13(4):1143-9.
1992: Bronson R T; Sweet H O; Spencer C A; Davisson M T
Genetic and age related models of neurodegeneration in mice: dystrophic axons.
Journal of neurogenetics 1992;8(2):71-83.
1992: Johnson K R; Cook S A; Davisson M T
Chromosomal localization of the murine gene and two related sequences encoding high-mobility-group I and Y proteins.
Genomics 1992;12(3):503-9.
1992: Davisson M T; Johnson K R
Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3 Spec No():S261-5.
1992: Nadeau J H; Davisson M T; Doolittle D P; Grant P; Hillyard A L; Kosowsky M R; Roderick T H
Comparative map for mice and humans.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3(9):480-536.
1992: Johnson K R; Cook S A; Bustin M; Davisson M T
Genetic mapping of the murine gene and 14 related sequences encoding chromosomal protein HMG-14.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3(11):625-32.
1991: Davisson M T; Guay-Woodford L M; Harris H W; D'Eustachio P
The mouse polycystic kidney disease mutation (cpk) is located on proximal chromosome 12.
Genomics 1991;9(4):778-81.
1991: Nadeau J H; Davisson M T; Doolittle D P; Grant P; Hillyard A L; Kosowsky M; Roderick T H
Comparative map for mice and humans.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1 Spec No():S461-515.
1991: Davisson M T; Johnson K R; Seldin M F; Suzuki H; Watanabe T
Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1 Spec No():S301-5.
1991: Akeson E C; Davisson M T
C-band polymorphisms in exotic inbred strains of mice: a method for mapping centromeric ends of chromosomes.
Cytogenetics and cell genetics 1991;57(4):217-20.
1990: Davisson M T; Roderick T H; Akeson E C; Hawes N L; Sweet H O
The hairy ears (Eh) mutation is closely associated with a chromosomal rearrangement in mouse chromosome 15.
Genetical research 1990;56(2-3):167-78.
1990: Davisson M T; Cattanach B M
The mouse mutation ulnaless on chromosome 2.
The Journal of heredity 1990;81(2):151-3.
1990: Lane P W; Davisson M T
Patchy fur (Paf), a semidominant X-linked gene associated with a high level of X-Y nondisjunction in male mice.
The Journal of heredity 1990;81(1):43-50.
1990: Roderick T H; Hillyard A L; Doolittle D P; Davisson M T
The use of comparative mapping to identify loci involved in human carcinogenesis.
Birth defects original article series 1990;26(1):141-78.
1990: Davisson M T; Schmidt C; Akeson E C
Segmental trisomy of murine chromosome 16: a new model system for studying Down syndrome.
Progress in clinical and biological research 1990;360():263-80.
1990: Davisson M T; Lalley P A; Peters J; Doolittle D P; Hillyard A L; Searle A G
Report of the comparative subcommittee for human and mouse homologies.
Cytogenetics and cell genetics 1990;55(1-4):434-56.
1989: Nadeau J H; Berger F G; Cox D R; Crosby J L; Davisson M T; Ferrara D; Fuchs E; Hart C; Hunihan L; Lalley P A
A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11.
Genomics 1989;5(3):454-62.
1988: Lalley P A; Davisson M T; Graves J A; O'Brien S J; Roderick T H; Doolittle D P; Hillyard A L
Report of the committee on comparative mapping.
Cytogenetics and cell genetics 1988;49(1-3):227-35.
1987: Davisson M T
X-linked genetic homologies between mouse and man.
Genomics 1987;1(3):213-27.
1987: Davisson M T; Akeson E C
An improved method for preparing G-banded chromosomes from mouse peripheral blood.
Cytogenetics and cell genetics 1987;45(2):70-4.
1987: Lalley P A; O'Brien S J; Créau-Goldberg N; Davisson M T; Roderick T H; Echard G; Womack J E; Graves J M; Doolittle D P; Guidi J N
Report on the committee on comparative mapping.
Cytogenetics and cell genetics 1987;46(1-4):367-89.
1984: Roderick T H; Lalley P A; Davisson M T; O'Brien S J; Womack J E; Créau-Goldberg N; Echard G; Moore K L
Report of the Committee on Comparative Mapping.
Cytogenetics and cell genetics 1984;37(1-4):312-39.

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