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Plos One|November 10, 2010
Neural and synaptic defects in slytherin, a zebrafish model for human congenital disorders of glycosylationYuanquan Song, Jason R Willer, Paul C Scherer, et al.Genetics|October 16, 2014
A novel ribosomopathy caused by dysfunction of RPL10 disrupts neurodevelopment and causes X-linked microcephaly in humansSusan S Brooks, Alissa L Wall, Christelle Golzio, et al.Proceedings of the National Academy of Sciences of the United States of America|January 5, 2011
rnaset2 mutant zebrafish model familial cystic leukoencephalopathy and reveal a role for RNase T2 in degrading ribosomal RNANoémie Haud, Firat Kara, Simone Diekmann, et al.BMC Developmental Biology|November 25, 2011
Maternal topoisomerase II alpha, not topoisomerase II beta, enables embryonic development of zebrafish top2a-/- mutantsBeata Sapetto-Rebow, Sarah C McLoughlin, Lynne C O'Shea, et al.Nature Communications|September 13, 2023
The tectonic complex regulates membrane protein composition in the photoreceptor ciliumHanh M Truong, Kevin O Cruz-Colón, Jorge Y Martínez-Márquez, et al.Human Genomics|April 18, 2019
Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansionRossella Spataro, Maria Kousi, Sali M K Farhan, et al.American Journal of Human Genetics|March 21, 2017
Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal SyndromeAsaf Ta-Shma, Tahir N Khan, Asaf Vivante, 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 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.American Journal of Human Genetics|August 4, 2016
Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl SyndromeAnna Lindstrand, Stephan Frangakis, Claudia M B Carvalho, et al.Pageof 3