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JMIR Infodemiology|January 15, 2024
The Use of Social Media to Express and Manage Medical Uncertainty in Dyskeratosis Congenita: Content AnalysisEmily Pearce, Hannah Raj, Ngozika Emezienna, et al.
Genes & Development|January 6, 2011
Disruption of telomerase trafficking by TCAB1 mutation causes dyskeratosis congenitaFranklin Zhong, Sharon A Savage, Marina Shkreli, et al.
Journal of the American Society of Nephrology : JASN|February 10, 2006
A genome-wide DNA microsatellite association screen to identify chromosomal regions harboring candidate genes in diabetic nephropathyAmy Jayne McKnight, A Peter Maxwell, Stephen Sawcer, et al.
Plos One|September 9, 2017
Effect of pre-analytic variables on the reproducibility of qPCR relative telomere length measurementCasey L Dagnall, Belynda Hicks, Kedest Teshome, et al.
Clinical Genetics|July 23, 2014
Carrier screening of RTEL1 mutations in the Ashkenazi Jewish populationA M Fedick, L Shi, C Jalas, et al.
Journal of the American Society of Nephrology : JASN|February 13, 2010
A GREM1 gene variant associates with diabetic nephropathyAmy Jayne McKnight, Christopher C Patterson, Kerry A Pettigrew, et al.
Nature Communications|June 18, 2024
Digital telomere measurement by long-read sequencing distinguishes healthy aging from diseaseSantiago E Sanchez, Yuchao Gu, Yan Wang, et al.
Mutation Research|September 1, 1993
The mutator mut7-1 of Saccharomyces cerevisiaeR C von Borstel, R W Ord, S P Stewart, et al.
The American Journal of Geriatric Psychiatry : Official Journal of the American Association for Geriatric Psychiatry|February 14, 2017
Neuronal Loss and Α-Synuclein Pathology in the Superior Colliculus and Its Relationship to Visual Hallucinations in Dementia with Lewy BodiesDaniel Erskine, Alan J Thomas, John-Paul Taylor, et al.
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