Showing results (181-190 of 403) with videos related to
Sort By:
Pageof 41
Bioinformatics (Oxford, England)|June 22, 2021
Embeddings of genomic region sets capture rich biological associations in lower dimensionsErfaneh Gharavi, Aaron Gu, Guangtao Zheng, et al.Journal of Neurodevelopmental Disorders|May 7, 2011
Novel copy number variants in children with autism and additional developmental anomaliesL K Davis, K J Meyer, D S Rudd, et al.Behavioral Neuroscience|November 3, 2010
Light aversion in mice depends on nonimage-forming irradiance detectionStewart Thompson, Ana Recober, Timothy W Vogel, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 12, 2021
Gene therapy rescues olfactory perception in a clinically relevant ciliopathy model of Bardet-Biedl syndromeChao Xie, Julien C Habif, Cedric R Uytingco, et al.Vision Research|September 4, 2012
Phenotypic expression of Bardet-Biedl syndrome in patients homozygous for the common M390R mutation in the BBS1 geneKyle F Cox, Natalie C Kerr, Marina Kedrov, et al.The Journal of Clinical Investigation|March 5, 2008
Leptin resistance contributes to obesity and hypertension in mouse models of Bardet-Biedl syndromeKamal Rahmouni, Melissa A Fath, Seongjin Seo, et al.Human Genetics|March 7, 2008
Pax6 3' deletion results in aniridia, autism and mental retardationL K Davis, K J Meyer, D S Rudd, et al.Human Genetics|February 1, 1994
Linkage analysis of autosomal dominant atrioventricular canal defects: exclusion of chromosome 21A J Cousineau, R M Lauer, M E Pierpont, et al.STAR Protocols|June 8, 2026
Protocol to evaluate markers of reactiveoxygen species and labile iron from a single sample across in vitro and in in vivo lung cancer modelsJennifer A Petsche, Sunny C Huang, Danielle J Foster, et al.Human Molecular Genetics|December 1, 1992
Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13E M Stone, A E Kimura, J C Folk, et al.Pageof 41