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Diabetes|August 29, 2006
Association of transcription factor 7-like 2 (TCF7L2) variants with type 2 diabetes in a Finnish sampleLaura J Scott, Lori L Bonnycastle, Cristen J Willer, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2006
Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson-Gilford progeria syndromeRenee Varga, Maria Eriksson, Michael R Erdos, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 28, 2010
Cardiovascular pathology in Hutchinson-Gilford progeria: correlation with the vascular pathology of agingMichelle Olive, Ingrid Harten, Richard Mitchell, et al.
Human Genetics|September 6, 2005
Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in FinnsKaren L Mohlke, Anne U Jackson, Laura J Scott, et al.
Science (New York, N.Y.)|March 20, 2010
Heritable individual-specific and allele-specific chromatin signatures in humansRyan McDaniell, Bum-Kyu Lee, Lingyun Song, et al.
Human Molecular Genetics|July 16, 2009
Tissue-specific alternative splicing of TCF7L2Ludmila Prokunina-Olsson, Cullan Welch, Ola Hansson, et al.
Genomics|October 15, 1996
Characterization of EZH1, a human homolog of Drosophila Enhancer of zeste near BRCA1K J Abel, L C Brody, J M Valdes, et al.
Biorxiv : the Preprint Server for Biology|February 12, 2026
Donor-matched iPSC model reveals context-dependent T2D genetic signals in fibro-adipogenic progenitorsChrista Ventresca, Arushi Varshney, Peter Orchard, et al.
Cell Reports|July 30, 2025
Integrative single-cell multi-omics profiling of human pancreatic islets identifies T1D-associated genes and regulatory signalsRicardo D'Oliveira Albanus, Xiaoshan Zhang, Zeping Zhao, et al.
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