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Current Biology : CB|April 23, 2002
Gene flow from the Indian subcontinent to Australia: evidence from the Y chromosomeAlan J Redd, June Roberts-Thomson, Tatiana Karafet, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 18, 2013
Multistate structural modeling and voltage-clamp analysis of epilepsy/autism mutation Kv10.2-R327H demonstrate the role of this residue in stabilizing the channel closed stateYang Yang, Dmytro V Vasylyev, Fadia Dib-Hajj, et al.Epilepsy Research|June 14, 2019
Altered expression of signaling pathways regulating neuronal excitability in hippocampal tissue of temporal lobe epilepsy patients with low and high seizure frequencyMichael F Hammer, Ryan Sprissler, Robert W Bina, et al.Proceedings of the National Academy of Sciences of the United States of America|June 6, 2012
Religion as a means to assure paternityBeverly I Strassmann, Nikhil T Kurapati, Brendan F Hug, et al.Journal of Human Genetics|August 1, 2014
Isolation, contact and social behavior shaped genetic diversity in West TimorMeryanne K Tumonggor, Tatiana M Karafet, Sean Downey, et al.American Journal of Human Genetics|December 7, 2002
A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo populationZanhua Yi, Nanibaa' Garrison, Orit Cohen-Barak, et al.Clinical Nutrition (Edinburgh, Scotland)|March 17, 2022
Development of age-dependent micronutrient centile charts and their utility in children with chronic gastrointestinal conditions at risk of deficiencies: A proof-of-concept studyMaha Al Fify, Ben Nichols, Lefkothea Arailoudi Alexiadou, et al.Genetics|March 15, 2015
Examining phylogenetic relationships among gibbon genera using whole genome sequence data using an approximate bayesian computation approachKrishna R Veeramah, August E Woerner, Laurel Johnstone, et al.Molecular Biology and Evolution|September 29, 2017
Complex Patterns of Admixture across the Indonesian ArchipelagoGeorgi Hudjashov, Tatiana M Karafet, Daniel J Lawson, et al.Plos One|July 8, 2017
Rare variants of small effect size in neuronal excitability genes influence clinical outcome in Japanese cases of SCN1A truncation-positive Dravet syndromeMichael F Hammer, Atsushi Ishii, Laurel Johnstone, et al.Pageof 22