Loss-of-Function Mutations in TBC1D20 Cause Cataracts and Male Infertility in blind sterile Mice and Warburg Micro Syndrome in Humans von Liegel, Ryan P., Handley, Mark T., Ronchetti, Adam, Brown, Stephen, Langemeyer, Lars, Linford, Andrea, Chang, Bo, Morris-Rosendahl, Deborah J., Carpanini, Sarah, Posmyk, Renata, Harthill, Verity, Sheridan, Eamonn, Abdel-Salam, Ghada M.H., Terhal, Paulien A., Faravelli, Francesca, Accorsi, Patrizia, Giordano, Lucio, Pinelli, Lorenzo, Hartmann, Britta, Ebert, Allison D., Barr, Francis A., Aligianis, Irene A., Sidjanin, Duska J.

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Functional analysis of HSF4 mutations found in patients with autosomal recessive congenital cataracts von Merath, Kate, Ronchetti, Adam, Sidjanin, Duska J

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Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation von Handley, Mark T., Carpanini, Sarah M., Mali, Girish R., Sidjanin, Duska J., Aligianis, Irene A., Jackson, Ian J., FitzPatrick, David R.

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ADAM17 transactivates EGFR signaling during embryonic eyelid closure von Hassemer, Eryn L, Endres, Bradley, Toonen, Joseph A, Ronchetti, Adam, Dubielzig, Richard, Sidjanin, Duska J

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Type I Interferon Counteracts Antiviral Effects of Statins in the Context of Gammaherpesvirus Infection von Lange, Philip T, Darrah, Eric J, Vonderhaar, Emily P, Mboko, Wadzanai P, Rekow, Michaela M, Patel, Shailendra B, Sidjanin, Duska J, Tarakanova, Vera L

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Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3 von Sidjanin, Duska J., Lowe, Jennifer K., McElwee, John L., Milne, Bruce S., Phippen, Taryn M., Sargan, David R., Aguirre, Gustavo D., Acland, Gregory M., Ostrander, Elaine A.

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spontaneous mutation in Srebf2 leads to cataracts and persistent skin wounds in the lens opacity 13 (lop13) mouse von Merath, Kate M, Chang, Bo, Dubielzig, Richard, Jeannotte, Richard, Sidjanin, Duska J

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Linkage disequilibrium mapping in domestic dog breeds narrows the progressive rod–cone degeneration interval and identifies ancestral disease-transmitting chromosome von Goldstein, Orly, Zangerl, Barbara, Pearce-Kelling, Sue, Sidjanin, Duska J., Kijas, James W., Felix, Jeanette, Acland, Gregory M., Aguirre, Gustavo D.

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Waved with open eyelids 2 (woe2) is a novel spontaneous mouse mutation in the protein phosphatase 1, regulatory (inhibitor) subunit 13 like (Ppp1r13l) gene von Toonen, Joseph, Liang, Lina, Sidjanin, Duska J

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Radiation hybrid mapping of cataract genes in the dog von Hunter, Linda S, Sidjanin, Duska J, Johnson, Jennifer L, Zangerl, Barbara, Galibert, Francis, Andre, Catherine, Kirkness, Ewen, Talamas, Elijah, Acland, Gregory M, Aguirre, Gustavo D

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Targeted disruption of Tbc1d20 with zinc-finger nucleases causes cataracts and testicular abnormalities in mice von Park, Anna Kyunglim, Liegel, Ryan P, Ronchetti, Adam, Ebert, Allison D, Geurts, Aron, Sidjanin, Duska J

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Cloning and characterization of canine PAX6 and evaluation as a candidate gene in a canine model of aniridia von Hunter, Linda S, Sidjanin, Duska J, Hijar, Manuel Villagrasa, Johnson, Jennifer L, Kirkness, Ewen, Acland, Gregory M, Aguirre, Gustavo D

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Targeted disruption of Tbc1d20with zinc-finger nucleases causes cataracts and testicular abnormalities in mice von Park, Anna Kyunglim, Liegel, Ryan P, Ronchetti, Adam, Ebert, Allison D, Geurts, Aron, Sidjanin, Duska J

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Identification of two novel mutations in families with X-linked ocular albinism von Iannaccone, Alessandro, Gallaher, Kevin T, Buchholz, Janda, Jennings, Barbara J, Neitz, Maureen, Sidjanin, D J

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Cloning of the galactokinase cDNA and identification of mutations in two families with cataracts von Stambolian, Dwight, Ai, Yunjun, Sidjanin, Duska, Nesburn, Kristin, Sathe, Ganesh, Rosenberg, Martin, Bergsma, Derk J.

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Waved with open eyelids 2 gene von Toonen, Joseph, Liang, Lina, Sidjanin, Duska J

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DNA damage and repair in rabbit lens epithelial cells following UVA radiation von Sidjanin, Duska, Zigman, Seymour, Reddan, John

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Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16 von Sidjanin, DJ, Grimes, PA, Pretsch, W, Neuhauser-Klaus, A, Favor, J, Stambolian, DE

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METHOD FOR IDENTIFYING PROGRESSIVE ROD-CONE DEGENERATION IN DOGS von FELIX, JEANETTE S, SIDJANIN, DUSKA J, PEARCE-KELLING, SUSAN, GOLDSTEIN, ORLY, AGUIRRE, GUSTAVO D, ACLAND, GREGORY M, ZANGERL, BARBARA

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IDENTIFICATION OF THE GENE AND MUTATION FOR PROGRESSIVE ROD-CONE DEGENERATION IN DOG AND A METHOD FOR TESTING SAME von FELIX, JEANETTE S, AGUIRRE, GUSTAVO, SIDJANIN, DUSKA J, PEARCE-KELLING, SUSAN, GOLDSTEIN, ORLY, ACLAND, GREGORY M, ZANGERL, BARBARA

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