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Diabetologia|December 1, 1995
Human hexokinase II gene: exon-intron organization, mutation screening in NIDDM, and its relationship to muscle hexokinase activityM Lehto, X Huang, E M Davis, et al.Diabetologia|May 20, 2008
Age influences DNA methylation and gene expression of COX7A1 in human skeletal muscleT Rönn, P Poulsen, O Hansson, et al.American Journal of Nephrology|October 22, 2010
Genetic polymorphisms in nitric oxide synthase 3 gene and implications for kidney disease: a meta-analysisA J McKnight, C C Patterson, N Sandholm, et al.Diabetologia|October 10, 2009
Lipid abnormalities predict progression of renal disease in patients with type 1 diabetesN Tolonen, C Forsblom, L Thorn, et al.Diabetologia|December 24, 2004
Increased levels of mannan-binding lectin in type 1 diabetic patients with incipient and overt nephropathyM Saraheimo, C Forsblom, T K Hansen, et al.Diabetologia|August 14, 1999
High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetesM Lehto, C Wipemo, S A Ivarsson, et al.Diabetic Medicine : a Journal of the British Diabetic Association|April 23, 2014
Coffee consumption and the risk of latent autoimmune diabetes in adults--results from a Swedish case-control studyJ E Löfvenborg, T Andersson, P-O Carlsson, et al.Diabetologia|February 14, 2008
Epigenetic regulation of PPARGC1A in human type 2 diabetic islets and effect on insulin secretionC Ling, S Del Guerra, R Lupi, et al.Journal of Internal Medicine|September 1, 1992
Metabolic control and progression of complications in insulin-dependent diabetic patients after kidney transplantationA Ekstrand, L Groop, E Pettersson, et al.The Journal of Clinical Endocrinology and Metabolism|December 1, 1995
A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency--a clinical research center studyJ D Cogan, B Ramel, M Lehto, et al.Pageof 28