Two mouse retinal degenerations caused by missense mutations in the β-subunit of rod cGMP phosphodiesterase gene
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.
Published in Vision research (Oxford) (01.03.2007)
Published in Vision research (Oxford) (01.03.2007)
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Retinal degeneration mutants in the mouse
Chang, B., Hawes, N.L., Hurd, R.E., Davisson, M.T., Nusinowitz, S., Heckenlively, J.R.
Published in Vision research (Oxford) (01.02.2002)
Published in Vision research (Oxford) (01.02.2002)
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Journal Article
Mouse models of ocular diseases
CHANG, B., HAWES, N.L., HURD, R.E., WANG, J., HOWELL, D., DAVISSON, M.T., RODERICK, T.H., NUSINOWITZ, S., HECKENLIVELY, J.R.
Published in Visual neuroscience (01.09.2005)
Published in Visual neuroscience (01.09.2005)
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Journal Article
A mouse model for Down syndrome exhibits learning and behaviour deficits
Reeves, Roger H, Irving, Nicholas G, Moran, Timothy H, Wohn, Anny, Kitt, Cheryl, Sisodia, Sangram S, Schmidt, Cecilia, Bronson, Roderick T, Davisson, Muriel T
Published in Nature genetics (01.10.1995)
Published in Nature genetics (01.10.1995)
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Journal Article
Motor dysfunction in a mouse model for Down syndrome
Costa, Alberto C.S, Walsh, Kathryn, Davisson, Muriel T
Published in Physiology & behavior (01.12.1999)
Published in Physiology & behavior (01.12.1999)
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Journal Article
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice
John, Simon W M, Chang, Bo, Smith, Richard S, Hawes, Norman L, Anderson, Michael G, Zabaleta, Adriana, Savinova, Olga, Roderick, Thomas H, Heckenlively, John R, Davisson, Muriel T
Published in Nature genetics (01.04.1999)
Published in Nature genetics (01.04.1999)
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Retinal Degeneration 6 (rd6): A New Mouse Model for Human Retinitis Punctata Albescens
Hawes, Norman L, Chang, Bo, Hageman, Gregory S, Nusinowitz, Steven, Nishina, Patsy M, Schneider, Bobbie S, Smith, Richard S, Roderick, Thomas H, Davisson, Muriel T, Heckenlively, John R
Published in Investigative ophthalmology & visual science (01.09.2000)
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Published in Investigative ophthalmology & visual science (01.09.2000)
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Ts65Dn – localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome
Akeson, E.C., Lambert, J.P., Narayanswami, S., Gardiner, K., Bechtel, L.J., Davisson, M.T.
Published in Cytogenetic and genome research (01.01.2001)
Published in Cytogenetic and genome research (01.01.2001)
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Conference Proceeding
Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta
S D Chipman, H O Sweet, D J McBride, Jr, M T Davisson, S C Marks, Jr, A R Shuldiner, R J Wenstrup, D W Rowe, J R Shapiro
Published in Proceedings of the National Academy of Sciences - PNAS (01.03.1993)
Published in Proceedings of the National Academy of Sciences - PNAS (01.03.1993)
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A New Spontaneous Mouse Mutation of Hoxd13 with a Polyalanine Expansion and Phenotype Similar to Human Synpolydactyly
Johnson, Kenneth R., Sweet, Hope O., Donahue, Leah Rae, Ward-Bailey, Pat, Bronson, Roderick T., Davisson, Muriel T.
Published in Human molecular genetics (01.06.1998)
Published in Human molecular genetics (01.06.1998)
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Journal Article
Murine mucopolysaccharidosis type VII: characterization of a mouse with β-glucuronidase deficiency
BIRKENMEIER, E. H, DAVISSON, M. T, BEAMER, W. G, GANSCHOW, R. E, VOGLER, C. A, GWYNN, B, LYFORT, K. A, MALTAIS, L. M, WAWRZYNIAK, C. J
Published in The Journal of clinical investigation (01.04.1989)
Published in The Journal of clinical investigation (01.04.1989)
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Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration
Sweet, H O, Bronson, R T, Johnson, K R, Cook, S A, Davisson, M T
Published in Mammalian genome (01.11.1996)
Published in Mammalian genome (01.11.1996)
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Molecular analysis of reverse mutations from nonagouti (a) to black-and-tan (at) and white-bellied agouti (AW) reveals alternative forms of agouti transcripts
BULTMAN, S. J, KLEBIG, M. L, MICHAUD, E. J, SWEET, H. O, DAVISSON, M. T, WOYCHIK, R. P
Published in Genes & development (15.02.1994)
Published in Genes & development (15.02.1994)
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Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis
Sundberg, JP, Boggess, D, Hogan, ME, Sundberg, BA, Rourk, MH, Harris, B, Johnson, K, Dunstan, RW, Davisson, MT
Published in The American journal of pathology (01.07.1997)
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Published in The American journal of pathology (01.07.1997)
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Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease)
Bronson, R T, Lake, B D, Cook, S, Taylor, S, Davisson, M T
Published in Annals of neurology (01.04.1993)
Published in Annals of neurology (01.04.1993)
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The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities
LANGNER, C. A, BIRKENMEIER, E. H, BEN-ZEEV, O, SCHOTZ, M. C, SWEET, H. O, DAVISSON, M. T, GORDON, J. I
Published in The Journal of biological chemistry (15.05.1989)
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Published in The Journal of biological chemistry (15.05.1989)
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