Restoration of cone vision in a mouse model of achromatopsia von Hauswirth, William W, Alexander, John J, Umino, Yumiko, Everhart, Drew, Chang, Bo, Min, Seok H, Li, Qiuhong, Timmers, Adrian M, Hawes, Norman L, Pang, Ji-jing, Barlow, Robert B

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Premature Truncation of a Novel Protein, RD3, Exhibiting Subnuclear Localization Is Associated with Retinal Degeneration von Friedman, James S., Chang, Bo, Kannabiran, Chitra, Chakarova, Christina, Singh, Hardeep P., Jalali, Subhadra, Hawes, Norman L., Branham, Kari, Othman, Mohammad, Filippova, Elena, Thompson, Debra A., Webster, Andrew R., Andréasson, Sten, Jacobson, Samuel G., Bhattacharya, Shomi S., Heckenlively, John R., Swaroop, Anand

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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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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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Iris phenotypes and pigment dispersion caused by genes influencing pigmentation von Anderson, Michael G., Hawes, Norman L., Trantow, Colleen M., Chang, Bo, John, Simon W.M.

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AAV-Mediated Gene Therapy for Retinal Degeneration in the rd10 Mouse Containing a Recessive PDEβ Mutation von PANG, Ji-Jing, BOYE, Sanford L, HAWES, Norman L, BOATRIGHT, Jeffrey H, HAUSWIRTH, William W, KUMAR, Ashok, DINCULESCU, Astra, WENTAO DENG, JIE LI, QIUHONG LI, RANI, Asha, FOSTER, Thomas C, BO CHANG

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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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A Missense Mutation in the Mouse Col2a1 Gene Causes Spondyloepiphyseal Dysplasia Congenita, Hearing Loss, and Retinoschisis von Donahue, Leah Rae, Chang, BO, Mohan, Subburaman, Miyakoshi, Nao, Wergedal, Jon E, Baylink, David J, Hawes, Norman L, Rosen, Clifford J, Ward‐Bailey, Patricia, Zheng, Qing Y, Bronson, Roderick T, Johnson, Kenneth R, Davisson, Muriel T

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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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Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses von Maddox, Dennis M., Vessey, Kirstan A., Yarbrough, Gary L., Invergo, Brandon M., Cantrell, Donald R., Inayat, Samsoon, Balannik, Victoria, Hicks, Wanda L., Hawes, Norman L., Byers, Shannon, Smith, Richard S., Hurd, Ron, Howell, Douglas, Gregg, Ronald G., Chang, Bo, Naggert, Jürgen K., Troy, John B., Pinto, Lawrence H., Nishina, Patsy M., McCall, Maureen 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 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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Genetic Background Modifies Inner Ear and Eye Phenotypes of Jag1 Heterozygous Mice von Kiernan, Amy E, Li, Renhua, Hawes, Norman L, Churchill, Gary A, Gridley, Thomas

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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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Dense Nuclear Cataract Caused by the γB-Crystallin S11R Point Mutation von LIN LI, BO CHANG, CHENG, Catherine, DA CHANG, HAWES, Norman L, XIA, Chun-Hong, XIAOHUA GONG

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Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene von Chang, Bo, Mandal, Md Nawajes A., Chavali, Venkata R.M., Hawes, Norman L., Khan, Naheed W., Hurd, Ronald E., Smith, Richard S., Davisson, Muriel L., Kopplin, Laura, Klein, Barbara E.K., Klein, Ronald, Iyengar, Sudha K., Heckenlively, John R., Ayyagari, Radha

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A Gja8 (Cx50) point mutation causes an alteration of α3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice von BO CHANG, XIN WANG, HAWES, Norman L, OJAKIAN, Ryan, DAVISSON, Muriel T, LO, Woo-Kuen, XIAOHUA GONG

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Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice von Talamas, Elijah, Jackson, Lavinia, Koeberl, Matthew, Jackson, Todd, McElwee, John L., Hawes, Norman L., Chang, Bo, Jablonski, Monica M., Sidjanin, D.J.

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