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Journal of Diabetes and Its Complications|April 17, 2008
Association of insulin sensitivity and glucose tolerance with the c.825C>T variant of the G protein beta-3 subunit geneDaniel Kopf, Li S-C Cheng, Petra Blandau, et al.
Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
New Gain-of-Function Mutations Prioritize Mechanisms of HER2 ActivationChristopher J Giacoletto, Liz J Valente, Lancer Brown, et al.
American Journal of Human Genetics|November 1, 1983
The Tay-Sachs disease gene in North American Jewish populations: geographic variations and originG M Petersen, J I Rotter, R M Cantor, et al.
Nature Genetics|July 1, 1993
Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafnessT R Prezant, J V Agapian, M C Bohlman, et al.
Nature Genetics|October 25, 2022
A combined polygenic score of 21,293 rare and 22 common variants improves diabetes diagnosis based on hemoglobin A1C levelsPeter Dornbos, Ryan Koesterer, Andrew Ruttenburg, et al.
Human Genetics|August 2, 2011
Analysis of family- and population-based samples in cohort genome-wide association studiesAni Manichaikul, Wei-Min Chen, Kayleen Williams, et al.
Investigative Ophthalmology & Visual Science|June 5, 2012
Variation in the lysyl oxidase (LOX) gene is associated with keratoconus in family-based and case-control studiesYelena Bykhovskaya, Xiaohui Li, Irina Epifantseva, et al.
Metabolic Syndrome and Related Disorders|November 8, 2011
Electrocardiographic abnormalities associated with the metabolic syndrome and its components: the multi-ethnic study of atherosclerosisImo A Ebong, Alain G Bertoni, Elsayed Z Soliman, et al.
Human Heredity|January 1, 1984
Estimating the recombination frequency for the MN and the Ss lociM A Spence, L L Field, M L Marazita, et al.
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