Showing results (51-60 of 66) with videos related to
Sort By:
Pageof 7
The Journal of General Physiology|April 26, 2006
The light peak of the electroretinogram is dependent on voltage-gated calcium channels and antagonized by bestrophin (best-1)Lihua Y Marmorstein, Jiang Wu, Precious McLaughlin, et al.Plos One|September 9, 2010
Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndromeAriel M Pani, Holly H Hobart, Colleen A Morris, et al.American Journal of Physiology. Gastrointestinal and Liver Physiology|September 24, 2016
A novel transgenic mouse model of lysosomal storage disorderSonia Ortiz-Miranda, Rui Ji, Agata Jurczyk, et al.Developmental Dynamics : an Official Publication of the American Association of Anatomists|April 2, 2011
Loss of Lrp2 in zebrafish disrupts pronephric tubular clearance but not forebrain developmentEsther Kur, Anna Christa, Kerry N Veth, et al.Plos One|December 19, 2009
Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD)Yuanquan Song, Mary A Selak, Corey T Watson, et al.American Journal of Human Genetics|November 10, 2009
Mutations in TRPM1 are a common cause of complete congenital stationary night blindnessMaria M van Genderen, Mieke M C Bijveld, Yvonne B Claassen, et al.Plos Genetics|March 8, 2011
Mutations in zebrafish lrp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucomaKerry N Veth, Jason R Willer, Ross F Collery, et al.Journal of Neurophysiology|August 17, 2012
Depolarizing bipolar cell dysfunction due to a Trpm1 point mutationNeal S Peachey, Jillian N Pearring, Pasano Bojang, et al.American Journal of Medical Genetics. Part A|October 14, 2003
GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome regionColleen A Morris, Carolyn B Mervis, Holly H Hobart, et al.Human Molecular Genetics|August 28, 2015
Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindnessMiranda L Scalabrino, Sanford L Boye, Kathryn M H Fransen, et al.Pageof 7