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L Groop

Showing results (201-210 of 242) with videos related to

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Diabetologia|April 18, 2009
Assessing the effect of interaction between an FTO variant (rs9939609) and physical activity on obesity in 15,925 Swedish and 2,511 Finnish adultsA Jonsson, F Renström, V Lyssenko, et al.
Diabetologia|October 16, 2007
Polymorphisms in the gene encoding the voltage-dependent Ca(2+) channel Ca (V)2.3 (CACNA1E) are associated with type 2 diabetes and impaired insulin secretionJ Holmkvist, D Tojjar, P Almgren, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 30, 2016
Use of Swedish smokeless tobacco (snus) and the risk of Type 2 diabetes and latent autoimmune diabetes of adulthood (LADA)B Rasouli, T Andersson, P-O Carlsson, et al.
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.
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 25

Showing results (201-210 of 242) with videos related to

Sort By:
Pageof 25
Diabetologia|April 18, 2009
Assessing the effect of interaction between an FTO variant (rs9939609) and physical activity on obesity in 15,925 Swedish and 2,511 Finnish adultsA Jonsson, F Renström, V Lyssenko, et al.
Diabetologia|October 16, 2007
Polymorphisms in the gene encoding the voltage-dependent Ca(2+) channel Ca (V)2.3 (CACNA1E) are associated with type 2 diabetes and impaired insulin secretionJ Holmkvist, D Tojjar, P Almgren, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 30, 2016
Use of Swedish smokeless tobacco (snus) and the risk of Type 2 diabetes and latent autoimmune diabetes of adulthood (LADA)B Rasouli, T Andersson, P-O Carlsson, et al.
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.
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 25