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Plos Genetics|June 8, 2022
Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse modelSonia M Weatherly, Gayle B Collin, Jeremy R Charette, et al.
International Journal of Molecular Sciences|February 26, 2022
A Splicing Mutation in Slc4a5 Results in Retinal Detachment and Retinal Pigment Epithelium DysfunctionGayle B Collin, Lanying Shi, Minzhong Yu, et al.
International Journal of Molecular Sciences|October 14, 2022
A Dpagt1 Missense Variant Causes Degenerative Retinopathy without Myasthenic Syndrome in MiceLillian F Hyde, Yang Kong, Lihong Zhao, et al.
Nature Communications|January 22, 2015
Numerical chromosomal instability mediates susceptibility to radiation treatmentSamuel F Bakhoum, Lilian Kabeche, Matthew D Wood, et al.
Investigative Ophthalmology & Visual Science|January 15, 2010
Photoreceptor degeneration, azoospermia, leukoencephalopathy, and abnormal RPE cell function in mice expressing an early stop mutation in CLCN2Malia M Edwards, Caralina Marín de Evsikova, Gayle B Collin, et al.
The American Journal of Pathology|May 22, 2016
Mouse Models of NMNAT1-Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human DiseaseScott H Greenwald, Jeremy R Charette, Magdalena Staniszewska, et al.
Human Mutation|June 28, 2007
Spectrum of ALMS1 variants and evaluation of genotype-phenotype correlations in Alström syndromeJan D Marshall, Elizabeth G Hinman, Gayle B Collin, et al.
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