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Human Mutation|July 22, 2014
Mutation of POC1B in a severe syndromic retinal ciliopathyBodo B Beck, Jennifer B Phillips, Malte P Bartram, et al.Human Molecular Genetics|August 23, 2022
Expression and subcellular localization of USH1C/harmonin in human retina provides insights into pathomechanisms and therapyKerstin Nagel-Wolfrum, Benjamin R Fadl, Mirjana M Becker, et al.Nature Communications|May 14, 2016
An organelle-specific protein landscape identifies novel diseases and molecular mechanismsKarsten Boldt, Jeroen van Reeuwijk, Qianhao Lu, et al.Annals of the New York Academy of Sciences|June 7, 2019
The expanding functional roles and signaling mechanisms of adhesion G protein-coupled receptorsRory K Morgan, Garret R Anderson, Demet Araç, et al.Annals of the New York Academy of Sciences|November 27, 2014
New functions and signaling mechanisms for the class of adhesion G protein-coupled receptorsInes Liebscher, Brian Ackley, Demet Araç, et al.Genome Biology|December 31, 2015
KIAA0556 is a novel ciliary basal body component mutated in Joubert syndromeAnna A W M Sanders, Erik de Vrieze, Anas M Alazami, et al.Nature Genetics|June 5, 2007
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosisAnneke I den Hollander, Robert K Koenekoop, Moin D Mohamed, et al.EMBO Molecular Medicine|March 7, 2022
Early disruption of photoreceptor cell architecture and loss of vision in a humanized pig model of usher syndromesSophia Grotz, Jessica Schäfer, Kirsten A Wunderlich, et al.Nature Cell Biology|July 14, 2015
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genesGabrielle Wheway, Miriam Schmidts, Dorus A Mans, et al.Pharmacological Reviews|March 27, 2026
Adhesion G protein-coupled receptorsTobias Langenhan, Garret R Anderson, Demet Araç, et al.Pageof 16