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Muriel Davisson

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Leah Rae Donahue; Craig Franklin; Michael Hagn; Andreas Hörlein; Martin Hrabe de Angelis; K C Kent Lloyd; Terry Magnuson; Colin McKerlie; Naomi Nakagata; Yuichi Obata; Stuart Read; Wolfgang Wurst; Muriel T Davisson
Centralized mouse repositories.
Md Mahiuddin Ahmed; Muriel T Davisson; Misoo Ellison; Xiaolu Sturgeon; Katheleen J Gardiner
Loss of correlations among proteins in brains of the Ts65Dn mouse model of down syndrome.
Laura G Reinholdt; Randall J Roper; Jeffrey P Solzak; Griffith J Gilbert; Yueming Ding; Leah Rae Donahue; Griffith T Gilbert; Mark T Johnson; Cathleen Lutz; Anne Czechanski; Muriel T Davisson
Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn.

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2012: Leah Rae Donahue; Craig Franklin; Michael Hagn; Andreas Hörlein; Martin Hrabe de Angelis; K C Kent Lloyd; Terry Magnuson; Colin McKerlie; Naomi Nakagata; Yuichi Obata; Stuart Read; Wolfgang Wurst; Muriel T Davisson
Centralized mouse repositories.
Mammalian genome : official journal of the International Mammalian Genome Society 2012;23(9-10):559-71.
2012: Md Mahiuddin Ahmed; Muriel T Davisson; Misoo Ellison; Xiaolu Sturgeon; Katheleen J Gardiner
Loss of correlations among proteins in brains of the Ts65Dn mouse model of down syndrome.
Journal of proteome research 2012;11(2):1251-63.
2011: Laura G Reinholdt; Randall J Roper; Jeffrey P Solzak; Griffith J Gilbert; Yueming Ding; Leah Rae Donahue; Griffith T Gilbert; Mark T Johnson; Cathleen Lutz; Anne Czechanski; Muriel T Davisson
Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn.
Mammalian genome : official journal of the International Mammalian Genome Society 2011;22(11-12):685-91.
2011: Charlotte Lindfors; Jan Mulder; Ida A K Nilsson; Derry C Roopenian; Martin Schalling; Mathias Uhlén; Aamir R Zuberi; Muriel T Davisson; Leah Rae Donahue; Tomas J Ekström; Pablo M Garcia-Roves; Tomas G M Hökfelt; Mohsen Karimi; Jeanette E Johansen
Hypothalamic mitochondrial dysfunction associated with anorexia in the anx/anx mouse.
Proceedings of the National Academy of Sciences of the United States of America 2011;108(44):18108-13.
2010: Jonah Jacob Scott-McKean; Bo Chang; Ronald E Hurd; Steven Nusinowitz; Cecilia Schmidt; Muriel T Davisson; Alberto Costa
The mouse model of Down syndrome Ts65Dn presents visual deficits as assessed by pattern visual evoked potentials.
Investigative ophthalmology & visual science 2010;51(6):3300-8.
2010: Alberto Costa; Melissa R Stasko; Cecilia Schmidt; Muriel T Davisson
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: Fengchan Han; Heping Yu; Jiangping Zhang; Cong Tian; Cecilia Schmidt; Casey Nava; Muriel T Davisson; Qing Y Zheng
Otitis media in a mouse model for Down syndrome.
International journal of experimental pathology 2009;90(5):480-8.
2009: Susan A Cook; Gayle B Collin; Roderick T Bronson; Jürgen K Naggert; Dong P Liu; Ellen C Akeson; Muriel T Davisson
A mouse model for Meckel syndrome type 3.
Journal of the American Society of Nephrology : JASN 2009;20(4):753-64.
2008: Sergey V Voronov; Samuel G Frere; Silvia Giovedi; Elizabeth A Pollina; Christelle Borel; Hong Zhang; Cecilia Schmidt; Ellen C Akeson; Markus R Wenk; Laurent Cimasoni; Ottavio Arancio; Muriel T Davisson; Stylianos E Antonarakis; Katheleen Gardiner; Pietro De Camilli; Gilbert Di Paolo
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: Yunzhi Du; Melissa R Stasko; Alberto Costa; Muriel T Davisson; Katheleen J Gardiner
Editing of the serotonin 2C receptor pre-mRNA: Effects of the Morris Water Maze.
Gene 2007;391(1-2):186-97.
2007: Bo Chang; Norman L Hawes; Machelle T Pardue; A M German; Ronald E Hurd; Muriel T Davisson; Steven Nusinowitz; Kalpana Rengarajan; A P Boyd; Sheree S Sidney; M J Phillips; Rachael E Stewart; R Chaudhury; John M Nickerson; John R Heckenlively; Jeffrey H Boatright
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: Muriel T Davisson; Ellen C Akeson; C Schmidt; B Harris; J Farley; Mary Ann Handel
Impact of trisomy on fertility and meiosis in male mice.
Human reproduction (Oxford, England) 2007;22(2):468-76.
2006: Robert A Taft; Muriel T Davisson; Michael V Wiles
Know thy mouse.
Trends in genetics : TIG 2006;22(12):649-53.
2006: Yunzhi Du; Muriel T Davisson; Karen Kafadar; Katheleen Gardiner
A-to-I pre-mRNA editing of the serotonin 2C receptor: comparisons among inbred mouse strains.
Gene 2006;382():39-46.
2006: Jeong Woong Lee; Kirk Beebe; Leslie A Nangle; Jaeseon Jang; Chantal M Longo-Guess; Susan A Cook; Muriel T Davisson; John P Sundberg; Paul Schimmel; Susan L Ackerman
Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration.
Nature 2006;443(7107):50-5.
2006: Muriel T Davisson; Robert A Taft
Strategies for managing an ever increasing mutant mouse repository.
Brain research 2006;1091(1):255-7.
2006: Muriel T Davisson
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: Dominique Simon-Chazottes; Sylvie Tutois; Michael Kuehn; Martin Evans; Franck Bourgade; Sue Cook; Muriel T Davisson; Jean-Louis Guénet
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: Sandra L Gilbert; Li Zhang; Michele L Forster; Jeffrey R Anderson; Tamaki Iwase; Betty Soliven; Leah Rae Donahue; Hope O Sweet; Roderick T Bronson; Muriel T Davisson; Robert Wollmann; Bruce T Lahn
Trak1 mutation disrupts GABA(A) receptor homeostasis in hypertonic mice.
Nature genetics 2006;38(2):245-50.
2006: Ellen C Akeson; Leah Rae Donahue; Wesley G Beamer; Kathryn L Shultz; Cheryl L Ackert-Bicknell; Clifford J Rosen; Jennifer Corrigan; Muriel T Davisson
Chromosomal inversion discovered in C3H/HeJ mice.
Genomics 2006;87(2):311-3.
2006: Bo Chang; John R Heckenlively; Philippa R Bayley; Nicholas Brecha; Muriel T Davisson; Norman L Hawes; Arlene A Hirano; Ronald E Hurd; Akihiro Ikeda; Britt A Johnson; Maureen A McCall; Catherine W Morgans; Steven Nusinowitz; Neal S Peachey; Dennis S Rice; Kirstan A Vessey; Ronald G Gregg
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: Carmen Martínez-Cué; Noemí Rueda; Eva García; Muriel T Davisson; Cecilia Schmidt; Jesús Flórez
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: Bo Chang; Norman L Hawes; Ronald E Hurd; J Wang; D Howell; Muriel T Davisson; TH Roderick; Steven Nusinowitz; John R Heckenlively
Mouse models of ocular diseases.
Visual neuroscience 2005;22(5):587-93.
2005: Ji-Jing Pang; Bo Chang; Norman L Hawes; Ronald E Hurd; Muriel T Davisson; Jie Li; Syed M Noorwez; Ritu Malhotra; J Hugh McDowell; Shalesh Kaushal; William W Hauswirth; Steven Nusinowitz; Debra A Thompson; John R Heckenlively
Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).
Molecular vision 2005;11():152-62.
2005: Muriel T Davisson
Discovery genetics: serendipity in basic research.
ILAR journal / National Research Council, Institute of Laboratory Animal Resources 2005;46(4):338-45.
2005: Katheleen Gardiner; Muriel T Davisson; M Pritchard; David Patterson; Y Groner; Linda S Crnic; Stylianos E Antonarakis; William C. Mobley
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: Katheleen Gardiner; Muriel T Davisson; Linda S Crnic
Building protein interaction maps for Down's syndrome.
Briefings in functional genomics & proteomics 2004;3(2):142-56.
2004: Bettina Lorenz-Depiereux; Victoria E Guido; Kenneth R Johnson; Qing Yin Zheng; Leona H Gagnon; Joiel D Bauschatz; Muriel T Davisson; Linda L Washburn; Leah Rae Donahue; Tim M Strom; Eva M Eicher
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: Galen R Wenger; Cecilia Schmidt; Muriel T Davisson
Operant conditioning in the Ts65Dn mouse: learning.
Behavior genetics 2004;34(1):105-19.
2003: Dong P Liu; Cecilia Schmidt; Timothy Billings; Muriel T Davisson
Quantitative PCR genotyping assay for the Ts65Dn mouse model of Down syndrome.
BioTechniques 2003;35(6):1170-4, 1176, 1178 passim.
2003: Katheleen Gardiner; Andrew Fortna; Lawrence Bechtel; Muriel T Davisson
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: Leah Rae Donahue; Bo Chang; Subburaman Mohan; Naohisa Miyakoshi; Jon E Wergedal; David J Baylink; Norman L Hawes; Clifford J Rosen; Patricia Ward-Bailey; Qing Yin Zheng; Roderick T Bronson; Kenneth R Johnson; Muriel T Davisson
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: John R Heckenlively; Norman L Hawes; Martin Friedlander; Steven Nusinowitz; Ronald Hurd; Muriel T Davisson; Bo Chang
Mouse model of subretinal neovascularization with choroidal anastomosis.
Retina (Philadelphia, Pa.) 2003;23(4):518-22.
2003: Joiel D Bauschatz; Michelle M Curtain; Muriel T Davisson; Priscilla W Lane; Leah Rae Donahue
In collaboration: the Jackson Laboratory Craniofacial Resource.
Critical reviews in eukaryotic gene expression 2003;13(2-4):107-8.
2003: Kenneth R Johnson; Priscilla W Lane; Susan A Cook; Belinda S Harris; Patricia Ward-Bailey; Roderick T Bronson; Bonnie L Lyons; Leonard D Shultz; Muriel T Davisson
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.
2002: Timothy H Moran; George T Capone; Susan Knipp; Muriel T Davisson; Roger H Reeves; John D Gearhart
The effects of piracetam on cognitive performance in a mouse model of Down's syndrome.
Physiology & behavior 2002;77(2-3):403-9.
2002: Carmen Martínez-Cué; Carmela Baamonde; Marian Lumbreras; Jesús Paz; Muriel T Davisson; Cecilia Schmidt; Mara Dierssen; Jesús Flórez
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: Katheleen Gardiner; Dobromir Slavov; Lawrence Bechtel; Muriel T Davisson
Annotation of human chromosome 21 for relevance to Down syndrome: gene structure and expression analysis.
Genomics 2002;79(6):833-43.
2002: Teresa H Chae; Kristina M Allen; Muriel T Davisson; Hope O Sweet; Christopher Walsh
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: Bo Chang; Xin Wang; Norman L Hawes; Ryan Ojakian; Muriel T Davisson; Woo-Kuen Lo; Xiaohua Gong
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: Bo Chang; Norman L Hawes; Ronald E Hurd; Muriel T Davisson; Steven Nusinowitz; John R Heckenlively
Retinal degeneration mutants in the mouse.
Vision research 2002;42(4):517-25.
2001: Muriel T Davisson; Lawrence Bechtel; Ellen C Akeson; Andrew Fortna; Dobromir Slavov; Katheleen Gardiner
Evolutionary breakpoints on human chromosome 21.
Genomics 2001;78(1-2):99-106.
2001: A V Anagnostopoulos; John J Sharp; LE Mobraaten; Janan T Eppig; Muriel T Davisson
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: J M Newton; Orit Cohen-Barak; Nobuko Hagiwara; JM Gardner; Muriel T Davisson; Richard A King; Murray H Brilliant
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: A V Anagnostopoulos; LE Mobraaten; John J Sharp; Muriel T Davisson
Transgenic and knockout databases: behavioral profiles of mouse mutants.
Physiology & behavior 2001;73(5):675-89.
2001: Ellen C Akeson; Muriel T Davisson
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: Ellen C Akeson; J P Lambert; S Narayanswami; Katheleen Gardiner; Lawrence Bechtel; Muriel T Davisson
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: Susan A Cook; Ellen C Akeson; CJ Calvano; Kenneth R Johnson; J Mandell; Norman L Hawes; Roderick T Bronson; TH Roderick; Muriel T Davisson
Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene.
Cytogenetics and cell genetics 2001;93(1-2):77-82.
2001: Muriel T Davisson; Katheleen Gardiner; Alberto Costa
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: Michael G Anderson; Richard S Smith; Olga V Savinova; Norman L Hawes; Bo Chang; Adriana Zabaleta; R Wilpan; John R Heckenlively; Muriel T Davisson; Simon W M John
Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice.
BMC genetics 2001;2():1.
2000: Muriel T Davisson; Kenneth R Johnson; Roderick T Bronson; Patricia Ward-Bailey; Susan A Cook; Belinda S Harris; Leah Rae Donahue
Grey intense: a new mouse mutation affecting pigmentation.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(12):1139-41.
2000: R Chrast; Hamish Scott; MP Papasavvas; Colette Rossier; E S Antonarakis; C Barras; Muriel T Davisson; C Schmidt; Xavier Estivill; Mara Dierssen; M Pritchard; Stylianos E Antonarakis
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: Patricia Ward-Bailey; B Wood; Kenneth R Johnson; Roderick T Bronson; Leah Rae Donahue; Muriel T Davisson
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: Norman L Hawes; Bo Chang; G S Hageman; Steven Nusinowitz; Patsy M Nishina; B S Schneider; Richard S Smith; TH Roderick; Muriel T Davisson; John R Heckenlively
Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens.
Investigative ophthalmology & visual science 2000;41(10):3149-57.
2000: Novrouz B Akhmedov; Natik I Piriev; Bo Chang; A L Rapoport; Norman L Hawes; Patsy M Nishina; Steven Nusinowitz; John R Heckenlively; TH Roderick; CA Kozak; Michael Danciger; Muriel T Davisson; Debora B Farber
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: Richard S Smith; Simon W M John; A Zabeleta; Muriel T Davisson; Norman L Hawes; Bo Chang
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: Richard S Smith; Norman L Hawes; Bo Chang; TH Roderick; Ellen C Akeson; John R Heckenlively; X Gong; X Wang; Muriel T Davisson
Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract.
Genomics 2000;63(3):314-20.
2000: Judith A Blake; Janan T Eppig; Joel E Richardson; Muriel T Davisson
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: Alberto Costa; K Walsh; Muriel T Davisson
Motor dysfunction in a mouse model for Down syndrome.
Physiology & behavior 1999;68(1-2):211-20.
1999: Norman L Hawes; Richard S Smith; Bo Chang; Muriel T Davisson; John R Heckenlively; Simon W M John
Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypes.
Molecular vision 1999;5():22.
1999: Bo Chang; Norman L Hawes; TH Roderick; Richard S Smith; John R Heckenlively; J Horwitz; Muriel T Davisson
Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouse.
Molecular vision 1999;5():21.
1999: Michael F W Festing; Elizabeth M Simpson; Muriel T Davisson; LE Mobraaten
Revised nomenclature for strain 129 mice.
Mammalian genome : official journal of the International Mammalian Genome Society 1999;10(8):836.
1999: Bo Chang; Richard S Smith; Norman L Hawes; Michael G Anderson; Adriana Zabaleta; Olga V Savinova; TH Roderick; John R Heckenlively; Muriel T Davisson; Simon W M John
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice.
Nature genetics 1999;21(4):405-9.
1999: R S Smith; Kenneth R Johnson; Norman L Hawes; Belinda S Harris; John P Sundberg; Muriel T Davisson
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: Judith A Blake; Joel E Richardson; Muriel T Davisson; Janan T Eppig
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: O Korobova; Priscilla W Lane; J Perry; S Palmer; Alan Ashworth; Muriel T Davisson; Norman Arnheim
Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, maps to the pseudoautosomal boundary region.
Genomics 1998;54(3):556-9.
1998: Hope O Sweet; Murray H Brilliant; Susan A Cook; Kenneth R Johnson; Muriel T Davisson
A new allelic series for the underwhite gene on mouse chromosome 15.
The Journal of heredity 1998;89(6):546-51.
1998: Kenneth R Johnson; Hope O Sweet; Leah Rae Donahue; Patricia Ward-Bailey; Roderick T Bronson; Muriel T Davisson
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: Priscilla W Lane; Roderick T Bronson; Susan A Cook; Patricia Ward-Bailey; Leah Rae Donahue; Muriel T Davisson
Juvenile bare: a new hair loss mutation on chromosome 7 of the mouse.
The Journal of heredity 1998;89(3):254-7.
1998: Simon W M John; Richard S Smith; Olga V Savinova; Norman L Hawes; Bo Chang; Daniel Turnbull; Muriel T Davisson; TH Roderick; John R Heckenlively
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice.
Investigative ophthalmology & visual science 1998;39(6):951-62.
1998: Janan T Eppig; Judith A Blake; Muriel T Davisson; Joel E Richardson
Informatics for mouse genetics and genome mapping.
Methods (San Diego, Calif.) 1998;14(2):179-90.
1998: Kenneth R Johnson; Muriel T Davisson
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.
1998: Judith A Blake; Janan T Eppig; Joel E Richardson; Muriel T Davisson
The Mouse Genome Database (MGD): a community resource. Status and enhancements. The Mouse Genome Informatics Group.
Nucleic acids research 1998;26(1):130-7.
1997: J L González; C J Russo; Dan Goldowitz; Hope O Sweet; Muriel T Davisson; Christopher Walsh
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: Dan Goldowitz; R C Cushing; Eric D Laywell; Gabriella D'Arcangelo; Michael Sheldon; Hope O Sweet; Muriel T Davisson; Dennis A Steindler; Tom Curran
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: Lois J Maltais; Judith A Blake; Janan T Eppig; Muriel T Davisson
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: Dennis S Rice; Q Tang; Robert Williams; Belinda S Harris; Muriel T Davisson; Dan Goldowitz
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: S Cook; K Johnson; Muriel T Davisson
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: Verity A Letts; A Valenzuela; J P Kirley; Hope O Sweet; Muriel T Davisson; Wayne N Frankel
Genetic and physical maps of the stargazer locus on mouse chromosome 15.
Genomics 1997;43(1):62-8.
1997: Elizabeth M Simpson; C C Linder; E E Sargent; Muriel T Davisson; LE Mobraaten; John J Sharp
Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice.
Nature genetics 1997;16(1):19-27.
1997: Belinda S Harris; T Franz; S Ullrich; S Cook; Roderick T Bronson; Muriel T Davisson
Forebrain overgrowth (fog): a new mutation in the mouse affecting neural tube development.
Teratology 1997;55(4):231-40.
1997: P M Janaswami; EH Birkenmeier; Susan A Cook; L B Rowe; Roderick T Bronson; Muriel T Davisson
Identification and genetic mapping of a new polycystic kidney disease on mouse chromosome 8.
Genomics 1997;40(1):101-7.
1997: Susan A Cook; Roderick T Bronson; Leah Rae Donahue; N Ben-Arie; Muriel T Davisson
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: K R Johnson; Muriel T Davisson
Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;7 Spec No():S295-304.
1997: Judith A Blake; Joel E Richardson; Muriel T Davisson; Janan T Eppig
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.
1996: Leah Rae Donahue; Susan A Cook; Kenneth R Johnson; Roderick T Bronson; Muriel T Davisson
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: Hope O Sweet; Roderick T Bronson; Kenneth R Johnson; Susan A Cook; Muriel T Davisson
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: Patricia Ward-Bailey; Kenneth R Johnson; M A Handel; B S Harris; Muriel T Davisson
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: Bo Chang; Norman L Hawes; Richard S Smith; John R Heckenlively; Muriel T Davisson; TH Roderick
Chromosomal localization of a new mouse lens opacity gene (lop18)
Genomics 1996;36(1):171-3.
1996: D Heine; H C Passmore; V Patel; L D Shultz; Patricia Ward-Bailey; Susan A Cook; Muriel T Davisson
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: Hope O Sweet; Roderick T Bronson; Leah Rae Donahue; Muriel T Davisson
Mesenchymal dysplasia: a recessive mutation on chromosome 13 of the mouse.
The Journal of heredity 1996;87(2):87-95.
1996: H O Sweet; S C Marks; C A MacKay; Kenneth R Johnson; Muriel T Davisson
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: Kenneth R Johnson; Muriel T Davisson
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: Roger H Reeves; N G Irving; Timothy H Moran; A Wohn; C Kitt; Sangram S Sisodia; C Schmidt; R T Bronson; Muriel T Davisson
A mouse model for Down syndrome exhibits learning and behaviour deficits.
Nature genetics 1995;11(2):177-84.
1995: Kenneth R Johnson; Priscilla W Lane; Patricia Ward-Bailey; Muriel T Davisson
Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac.
Genomics 1995;29(2):457-64.
1995: Dennis S Rice; Robert Williams; Patricia Ward-Bailey; Kenneth R Johnson; B S Harris; Muriel T Davisson; Dan Goldowitz
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: Susan A Cook; Kenneth R Johnson; Roderick T Bronson; Muriel T Davisson
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: Kenneth R Johnson; Susan A Cook; Muriel T Davisson
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: Wayne N Frankel; Hope O Sweet; Muriel T Davisson
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: Wesley G Beamer; Hope O Sweet; Roderick T Bronson; J G Shire; D N Orth; Muriel T Davisson
Adrenocortical dysplasia: a mouse model system for adrenocortical insufficiency.
The Journal of endocrinology 1994;141(1):33-43.
1994: Muriel T Davisson; S A Cook; K R Johnson; E M Eicher
Balding: a new mutation on mouse chromosome 18 causing hair loss and immunological defects.
The Journal of heredity 1994;85(2):134-6.
1994: Kenneth R Johnson; Muriel T Davisson
Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5 Spec No():S259-65.
1993: Muriel T Davisson; E C Akeson
Recombination suppression by heterozygous Robertsonian chromosomes in the mouse.
Genetics 1993;133(3):649-67.
1993: Muriel T Davisson; Kenneth R Johnson
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: Muriel T Davisson; C Schmidt; Roger H Reeves; N G Irving; E C Akeson; B S Harris; R T Bronson
Segmental trisomy as a mouse model for Down syndrome.
Progress in clinical and biological research 1993;384():117-33.
1993: Kenneth R Johnson; Susan A Cook; Patricia Ward-Bailey; M Bustin; Muriel T Davisson
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: Kenneth R Johnson; Susan A Cook; Patricia Ward-Bailey; Muriel T Davisson
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: Kenneth R Johnson; S Lu; M T Murtha; F H Ruddle; Muriel T Davisson
Genetic mapping of a new homeobox gene to mouse chromosome 7.
Genomics 1992;14(4):1107-9.
1992: Kenneth R Johnson; Muriel T Davisson
A multipoint genetic linkage map of mouse chromosome 18.
Genomics 1992;13(4):1143-9.
1992: R T Bronson; H O Sweet; C A Spencer; Muriel T Davisson
Genetic and age related models of neurodegeneration in mice: dystrophic axons.
Journal of neurogenetics 1992;8(2):71-83.
1992: Kenneth R Johnson; Susan A Cook; Muriel T Davisson
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: Muriel T Davisson; Kenneth R Johnson
Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3 Spec No():S261-5.
1992: Joseph H Nadeau; Muriel T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Comparative map for mice and humans.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3(9):480-536.
1992: Kenneth R Johnson; Susan A Cook; M Bustin; Muriel T Davisson
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: Muriel T Davisson; Lisa M Guay-Woodford; H W Harris; P D'Eustachio
The mouse polycystic kidney disease mutation (cpk) is located on proximal chromosome 12.
Genomics 1991;9(4):778-81.
1991: Joseph H Nadeau; Muriel T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Comparative map for mice and humans.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1 Spec No():S461-515.
1991: Muriel T Davisson; K R Johnson; Michael F Seldin; H Suzuki; T Watanabe
Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1 Spec No():S301-5.
1991: E C Akeson; Muriel T Davisson
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: Muriel T Davisson; TH Roderick; E C Akeson; Norman L Hawes; H O Sweet
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: Muriel T Davisson; B M Cattanach
The mouse mutation ulnaless on chromosome 2.
The Journal of heredity 1990;81(2):151-3.
1990: P W Lane; Muriel T Davisson
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: T H Roderick; A L Hillyard; D P Doolittle; Muriel T Davisson
The use of comparative mapping to identify loci involved in human carcinogenesis.
Birth defects original article series 1990;26(1):141-78.
1990: Muriel T Davisson; C Schmidt; E C Akeson
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: Muriel T Davisson; P A Lalley; J Peters; D P Doolittle; A L Hillyard; A G Searle
Report of the comparative subcommittee for human and mouse homologies.
Cytogenetics and cell genetics 1990;55(1-4):434-56.
1989: Joseph H Nadeau; F G Berger; D R Cox; J L Crosby; Muriel T Davisson; D Ferrara; E Fuchs; C Hart; L Hunihan; P A Lalley
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: P A Lalley; Muriel T Davisson; J A Graves; S J O'Brien; T H Roderick; D P Doolittle; A L Hillyard
Report of the committee on comparative mapping.
Cytogenetics and cell genetics 1988;49(1-3):227-35.
1987: Muriel T Davisson
X-linked genetic homologies between mouse and man.
Genomics 1987;1(3):213-27.
1987: Muriel T Davisson; E C Akeson
An improved method for preparing G-banded chromosomes from mouse peripheral blood.
Cytogenetics and cell genetics 1987;45(2):70-4.
1987: P A Lalley; S J O'Brien; N Créau-Goldberg; Muriel T Davisson; T H Roderick; G Echard; J E Womack; J M Graves; D P Doolittle; J N Guidi
Report on the committee on comparative mapping.
Cytogenetics and cell genetics 1987;46(1-4):367-89.
1984: T H Roderick; P A Lalley; Muriel T Davisson; S J O'Brien; J E Womack; N Créau-Goldberg; G Echard; K L Moore
Report of the Committee on Comparative Mapping.
Cytogenetics and cell genetics 1984;37(1-4):312-39.