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Nature Genetics|April 6, 2010
Genome-wide association study of intracranial aneurysm identifies three new risk lociKatsuhito Yasuno, Kaya Bilguvar, Philippe Bijlenga, et al.
Nature Communications|May 19, 2018
Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatmentShazia Ashraf, Hiroki Kudo, Jia Rao, et al.
Journal of the American Society of Nephrology : JASN|August 26, 2018
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary TractAmelie T van der Ven, Dervla M Connaughton, Hadas Ityel, et al.
Plos Biology|September 15, 2010
Multi-platform next-generation sequencing of the domestic turkey (Meleagris gallopavo): genome assembly and analysisRami A Dalloul, Julie A Long, Aleksey V Zimin, et al.
American Journal of Human Genetics|January 28, 2021
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosisPatricia L Weng, Amar J Majmundar, Kamal Khan, et al.
Evolution and Human Behavior : Official Journal of the Human Behavior and Evolution Society|October 11, 2022
Family still matters: Human social motivation across 42 countries during a global pandemicCari M Pick, Ahra Ko, Alexandra S Wormley, et al.
Nature Communications|November 17, 2023
Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformationsShujuan Zhao, Kedous Y Mekbib, Martijn A van der Ent, et al.
Biorxiv : the Preprint Server for Biology|March 30, 2023
Genetic dysregulation of an endothelial Ras signaling network in vein of Galen malformationsShujuan Zhao, Kedous Y Mekbib, Martijn A van der Ent, et al.
Nature Genetics|December 28, 2010
The genome of woodland strawberry (Fragaria vesca)Vladimir Shulaev, Daniel J Sargent, Ross N Crowhurst, et al.
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