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Mouse model resources for vision research.
Won J, Shi LY, Hicks W, Wang J, Hurd R, Naggert JK, Chang B, Nishina PM. Won J, et al. Among authors: hicks w. J Ophthalmol. 2011;2011:391384. doi: 10.1155/2011/391384. Epub 2010 Oct 31. J Ophthalmol. 2011. PMID: 21052544 Free PMC article.
Translational vision research models program.
Won J, Shi LY, Hicks W, Wang J, Naggert JK, Nishina PM. Won J, et al. Among authors: hicks w. Adv Exp Med Biol. 2012;723:391-7. doi: 10.1007/978-1-4614-0631-0_50. Adv Exp Med Biol. 2012. PMID: 22183357
A Chemical Mutagenesis Screen Identifies Mouse Models with ERG Defects.
Charette JR, Samuels IS, Yu M, Stone L, Hicks W, Shi LY, Krebs MP, Naggert JK, Nishina PM, Peachey NS. Charette JR, et al. Among authors: hicks w. Adv Exp Med Biol. 2016;854:177-83. doi: 10.1007/978-3-319-17121-0_24. Adv Exp Med Biol. 2016. PMID: 26427409 Free PMC article.
Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity.
Saksens NT, Krebs MP, Schoenmaker-Koller FE, Hicks W, Yu M, Shi L, Rowe L, Collin GB, Charette JR, Letteboer SJ, Neveling K, van Moorsel TW, Abu-Ltaif S, De Baere E, Walraedt S, Banfi S, Simonelli F, Cremers FP, Boon CJ, Roepman R, Leroy BP, Peachey NS, Hoyng CB, Nishina PM, den Hollander AI. Saksens NT, et al. Among authors: hicks w. Nat Genet. 2016 Feb;48(2):144-51. doi: 10.1038/ng.3474. Epub 2015 Dec 21. Nat Genet. 2016. PMID: 26691986 Free PMC article.
Alms1-disrupted mice recapitulate human Alström syndrome.
Collin GB, Cyr E, Bronson R, Marshall JD, Gifford EJ, Hicks W, Murray SA, Zheng QY, Smith RS, Nishina PM, Naggert JK. Collin GB, et al. Among authors: hicks w. Hum Mol Genet. 2005 Aug 15;14(16):2323-33. doi: 10.1093/hmg/ddi235. Epub 2005 Jul 6. Hum Mol Genet. 2005. PMID: 16000322 Free PMC article.
314 results