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Proceedings of the National Academy of Sciences of the United States of America|August 1, 2002
A strong signature of balancing selection in the 5' cis-regulatory region of CCR5Michael J Bamshad, Srinivas Mummidi, Enrique Gonzalez, et al.
Human Antibodies|November 29, 2013
Developing and mature human granulocytes express ELP 6 in the cytoplasmLori A Wagner, Shuping Wang, Elizabeth A Wayner, et al.
European Journal of Human Genetics : EJHG|March 20, 2023
A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severityKevin M Flanigan, Megan A Waldrop, Paul T Martin, et al.
Neuromuscular Disorders : NMD|October 2, 2009
DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophyKevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.
Genome Biology and Evolution|January 11, 2014
Genome degeneration and adaptation in a nascent stage of symbiosisKelly F Oakeson, Rosario Gil, Adam L Clayton, et al.
Annals of Neurology|March 28, 2012
Evidence-based path to newborn screening for Duchenne muscular dystrophyJerry R Mendell, Chris Shilling, Nancy D Leslie, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco|May 14, 2009
Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypesTimothy B Baker, Robert B Weiss, Daniel Bolt, et al.
Annals of Neurology|February 27, 2013
LTBP4 genotype predicts age of ambulatory loss in Duchenne muscular dystrophyKevin M Flanigan, Ermelinda Ceco, Kay-Marie Lamar, et al.
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