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Page 1
Mouse models of human ocular disease for translational research.
Krebs MP, Collin GB, Hicks WL, Yu M, Charette JR, Shi LY, Wang J, Naggert JK, Peachey NS, Nishina PM. Krebs MP, et al. Among authors: peachey ns. PLoS One. 2017 Aug 31;12(8):e0183837. doi: 10.1371/journal.pone.0183837. eCollection 2017. PLoS One. 2017. PMID: 28859131 Free PMC article.
Attenuation of oscillatory potentials in nob2 mice.
Yu M, Peachey NS. Yu M, et al. Among authors: peachey ns. Doc Ophthalmol. 2007 Nov;115(3):173-86. doi: 10.1007/s10633-007-9058-9. Epub 2007 May 4. Doc Ophthalmol. 2007. PMID: 17479213 Free PMC article.
Mutations in Lama1 disrupt retinal vascular development and inner limiting membrane formation.
Edwards MM, Mammadova-Bach E, Alpy F, Klein A, Hicks WL, Roux M, Simon-Assmann P, Smith RS, Orend G, Wu J, Peachey NS, Naggert JK, Lefebvre O, Nishina PM. Edwards MM, et al. Among authors: peachey ns. J Biol Chem. 2010 Mar 5;285(10):7697-711. doi: 10.1074/jbc.M109.069575. Epub 2010 Jan 4. J Biol Chem. 2010. PMID: 20048158 Free PMC article.
Photoreceptor degeneration, azoospermia, leukoencephalopathy, and abnormal RPE cell function in mice expressing an early stop mutation in CLCN2.
Edwards MM, Marín de Evsikova C, Collin GB, Gifford E, Wu J, Hicks WL, Whiting C, Varvel NH, Maphis N, Lamb BT, Naggert JK, Nishina PM, Peachey NS. Edwards MM, et al. Among authors: peachey ns. Invest Ophthalmol Vis Sci. 2010 Jun;51(6):3264-72. doi: 10.1167/iovs.09-4887. Epub 2010 Jan 13. Invest Ophthalmol Vis Sci. 2010. PMID: 20071672 Free PMC article.
Mutations of the opsin gene (Y102H and I307N) lead to light-induced degeneration of photoreceptors and constitutive activation of phototransduction in mice.
Budzynski E, Gross AK, McAlear SD, Peachey NS, Shukla M, He F, Edwards M, Won J, Hicks WL, Wensel TG, Naggert JK, Nishina PM. Budzynski E, et al. Among authors: peachey ns. J Biol Chem. 2010 May 7;285(19):14521-33. doi: 10.1074/jbc.M110.112409. Epub 2010 Mar 5. J Biol Chem. 2010. PMID: 20207741 Free PMC article.
GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.
Peachey NS, Ray TA, Florijn R, Rowe LB, Sjoerdsma T, Contreras-Alcantara S, Baba K, Tosini G, Pozdeyev N, Iuvone PM, Bojang P Jr, Pearring JN, Simonsz HJ, van Genderen M, Birch DG, Traboulsi EI, Dorfman A, Lopez I, Ren H, Goldberg AF, Nishina PM, Lachapelle P, McCall MA, Koenekoop RK, Bergen AA, Kamermans M, Gregg RG. Peachey NS, et al. Am J Hum Genet. 2012 Feb 10;90(2):331-9. doi: 10.1016/j.ajhg.2011.12.006. Am J Hum Genet. 2012. PMID: 22325362 Free PMC article.
220 results