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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Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice von John, Simon W.M, Anderson, Michael G, Smith, Richard S, Hawes, Norman L, Zabaleta, Adriana, Chang, Bo, Wiggs, Janey L

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CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina von Mehalow, Adrienne K., Kameya, Shuhei, Smith, Richard S., Hawes, Norman L., Denegre, James M., Young, James A., Bechtold, Lesley, Haider, Neena B., Tepass, Ulrich, Heckenlively, John R., Chang, Bo, Naggert, Jürgen K., Nishina, Patsy M.

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Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene von Johnson, Kenneth R., Gagnon, Leona H., Webb, Lisa S., Peters, Luanne L., Hawes, Norman L., Chang, Bo, Zheng, Qing Yin

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Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA) von 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

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Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice [published erratum appears in Invest Ophthalmol Vis Sci 1998 Aug;39(9):1641] von John, SW, Smith, RS, Savinova, OV, Hawes, NL, Chang, B, Turnbull, D, Davisson, M, Roderick, TH, Heckenlively, JR

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Mouse model of subretinal neovascularization with choroidal anastomosis von Heckenlively, John R, Hawes, Norman L, Friedlander, Martin, Nusinowitz, Steven, Hurd, Ronald, Davisson, Muriel, Chang, Bo

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Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice von 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

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The nob2 mouse, a null mutation in Cacnalf : Anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses von BO CHANG, HECKENLIVELY, John R, MCCALL, Maureen A, MORGANS, Catherine W, NUSINOWITZ, Steve, PEACHEY, Neal S, RICE, Dennis S, VESSEY, Kirstan A, GREGG, Ronald G, BAYLEY, Philippa R, BRECHA, Nicholas C, DAVISSON, Muriel T, HAWES, Norm L, HIRANO, Arlene A, HURD, Ronald E, IKEDA, Akihiro, JOHNSON, Britt A

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Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation von Burmeister, Margit, Novak, Jakub, Liang, Mei-Ying, Basu, Sharmila, Ploder, Lynda, Hawes, Norman L, Vidgen, Danka, Hoover, Frank, Goldman, Daniel, Kalnins, Vitauts I, Roderick, Thomas H, Taylor, Benjamin A, Hankin, Mark H, Mclnnes, Roderick R

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A Deletion in a Photoreceptor-Specific Nuclear Receptor mRNA Causes Retinal Degeneration in the rd7 Mouse von Akhmedov, Novrouz B., Piriev, Natik I., Chang, Bo, Rapoport, Ana Lia, Hawes, Norman L., Nishina, Patsy M., Nusinowitz, Steven, Heckenlively, John R., Roderick, Thomas H., Kozak, Christine A., Danciger, Michael, Davisson, Muriel T., Farber, Debora B.

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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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Fierce: a new mouse deletion of Nr2e1; violent behaviour and ocular abnormalities are background-dependent von Young, Kelly A, Berry, Melissa L, Mahaffey, Connie L, Saionz, Jennifer R, Hawes, Norman L, Chang, Bo, Zheng, Qing Yin, Smith, Richard S, Bronson, Roderick T, Nelson, Randy J, Simpson, Elizabeth M

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A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice von Chang, Bo, Wang, Xin, Hawes, Norman L, Ojakian, Ryan, Davisson, Muriel T, Lo, Woo-Kuen, Gong, Xiaohua

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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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Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6 von Kameya, Shuhei, Hawes, Norman L., Chang, Bo, Heckenlively, John R., Naggert, Jürgen K., Nishina, Patsy M.

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Deficiency of SHP-1 Protein-Tyrosine Phosphatase in "Viable Motheaten" Mice Results in Retinal Degeneration von Lyons, Bonnie L, Smith, Richard S, Hurd, Ron E, Hawes, Norman L, Burzenski, Lisa M, Nusinowitz, Steven, Hasham, Muneer G, Chang, Bo, Shultz, Leonard D

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Severe Ocular Abnormalities in C57BL/6 but Not in 129/Sv p53-Deficient Mice von Ikeda, Sakae, Hawes, Norman L, Chang, Bo, Avery, Cindy S, Smith, Richard S, Nishina, Patsy M

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Characterization of the mouse Prox1 gene von Tomarev, S I, Zinovieva, R D, Chang, B, Hawes, N L

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Lop12, a Mutation in Mouse Crygd Causing Lens Opacity Similar to Human Coppock Cataract von Smith, Richard S., Hawes, Norman L., Chang, Bo, Roderick, Thomas H., Akeson, Ellen C., Heckenlively, John R., Gong, Xiaohua, Wang, Xin, Davisson, Muriel T.

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