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The Journal of Clinical Endocrinology and Metabolism|January 30, 2014
The influence of rare genetic variation in SLC30A8 on diabetes incidence and β-cell functionLiana K Billings, Kathleen A Jablonski, Rachel J Ackerman, et al.
Diabetes|March 1, 2007
Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjectsKatharine R Owen, Christopher J Groves, Robert L Hanson, et al.
Nature Communications|May 15, 2023
DNA methylation markers for kidney function and progression of diabetic kidney diseaseKelly Yichen Li, Claudia Ha Ting Tam, Hongbo Liu, et al.
Scientific Reports|January 22, 2021
Further evidence supporting a potential role for ADH1B in obesityLiza D Morales, Douglas T Cromack, Devjit Tripathy, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 29, 2011
Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathyMeredith A Bostrom, W H Linda Kao, Man Li, et al.
Investigative Ophthalmology & Visual Science|September 4, 2008
Heritability of the severity of diabetic retinopathy: the FIND-Eye studyNedal H Arar, Barry I Freedman, Sharon G Adler, et al.
Diabetes|April 25, 2009
Linkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1qInga Prokopenko, Eleftheria Zeggini, Robert L Hanson, et al.
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