Two mouse retinal degenerations caused by missense mutations in the β-subunit of rod cGMP phosphodiesterase gene von 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.

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Retinal degeneration mutants in the mouse von Chang, B., Hawes, N.L., Hurd, R.E., Davisson, M.T., Nusinowitz, S., Heckenlively, J.R.

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Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice von Simpson, Elizabeth M., Linder, Carol C., Sargent, Evelyn E., Davisson, Muriel T., Mobraaten, Larry E., Sharp, John J.

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Mouse models of ocular diseases von CHANG, B., HAWES, N.L., HURD, R.E., WANG, J., HOWELL, D., DAVISSON, M.T., RODERICK, T.H., NUSINOWITZ, S., HECKENLIVELY, J.R.

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Motor dysfunction in a mouse model for Down syndrome von Costa, Alberto C.S, Walsh, Kathryn, Davisson, Muriel T

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Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice von Chang, Bo, Smith, Richard S, Hawes, Norman L, Anderson, Michael G, Zabaleta, Adriana, Savinova, Olga, Roderick, Thomas H, Heckenlively, John R., Davisson, Muriel T, John, Simon W M

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A mouse model for Down syndrome exhibits learning and behaviour deficits von Reeves, Roger H., Irving, Nicholas G., Moran, Timothy H., Wohn, Anny, Kitt, Cheryl, Sisodia, Sangram S., Schmidt, Cecilia, Bronson, Roderick T., Davisson, Muriel T.

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Retinal Degeneration 6 (rd6): A New Mouse Model for Human Retinitis Punctata Albescens von 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

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Ts65Dn – localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome von Akeson, E.C., Lambert, J.P., Narayanswami, S., Gardiner, K., Bechtel, L.J., Davisson, M.T.

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Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions von Gardiner, Katheleen, Fortna, Andrew, Bechtel, Lawrence, Davisson, Muriel T

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Mutations in the Human Orthologue of the Mouse underwhite Gene ( uw) Underlie a New Form of Oculocutaneous Albinism, OCA4 von Newton, J.M., Cohen-Barak, Orit, Hagiwara, Nobuko, Gardner, John M., Davisson, Muriel T., King, Richard A., Brilliant, Murray H.

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Discovery genetics: Serendipity in basic research von Davisson, M.T

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A New Spontaneous Mouse Mutation of Hoxd13 with a Polyalanine Expansion and Phenotype Similar to Human Synpolydactyly von Johnson, Kenneth R., Sweet, Hope O., Donahue, Leah Rae, Ward-Bailey, Pat, Bronson, Roderick T., Davisson, Muriel T.

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Recombination Suppression by Heterozygous Robertsonian Chromosomes in the Mouse von Davisson, M. T, Akeson, E. C

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Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta von 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

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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 von BULTMAN, S. J, KLEBIG, M. L, MICHAUD, E. J, SWEET, H. O, DAVISSON, M. T, WOYCHIK, R. P

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Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis von Sundberg, JP, Boggess, D, Hogan, ME, Sundberg, BA, Rourk, MH, Harris, B, Johnson, K, Dunstan, RW, Davisson, MT

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Murine mucopolysaccharidosis type VII: characterization of a mouse with β-glucuronidase deficiency von 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

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Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration von Sweet, H O, Bronson, R T, Johnson, K R, Cook, S A, Davisson, M T

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Differential effects of environmental enrichment on behavior and learning of male and female Ts65Dn mice, a model for Down syndrome von Martı́nez-Cué, Carmen, Baamonde, Carmela, Lumbreras, Marian, Paz, Jesús, Davisson, Muriel T, Schmidt, Cecilia, Dierssen, Mara, Flórez, Jesús

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