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

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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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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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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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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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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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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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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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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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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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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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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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A New Dominant Retinal Degeneration (Rd4) Associated with a Chromosomal Inversion in the Mouse von Roderick, Thomas H., Chang, Bo, Hawes, Norman L., Heckenlively, John 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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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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Autosomal dominant mouse cataract (Lop-10). Consistent differences of expression in heterozygotes von Runge, PE, Hawes, NL, Heckenlively, JR, Langley, SH, Roderick, TH

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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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Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene von 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.

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