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Nature Genetics|February 2, 2000
LMNA, encoding lamin A/C, is mutated in partial lipodystrophyS Shackleton, D J Lloyd, S N Jackson, et al.Diabetologia|September 1, 2005
Large-scale studies of the association between variation at the TNF/LTA locus and susceptibility to type 2 diabetesE Zeggini, C J Groves, J R C Parkinson, et al.Journal of Internal Medicine|March 14, 2018
Defective glucose and lipid metabolism in rheumatoid arthritis is determined by chronic inflammation in metabolic tissuesI Arias de la Rosa, A Escudero-Contreras, S Rodríguez-Cuenca, et al.Diabetologia|January 22, 2005
Analysis of the contribution to type 2 diabetes susceptibility of sequence variation in the gene encoding stearoyl-CoA desaturase, a key regulator of lipid and carbohydrate metabolismC F Liew, C J Groves, S Wiltshire, et al.The Journal of Endocrinology|April 24, 2016
Loss of Mrap2 is associated with Sim1 deficiency and increased circulating cholesterolT V Novoselova, R Larder, D Rimmington, et al.Science (New York, N.Y.)|October 8, 2011
An activating mutation of AKT2 and human hypoglycemiaK Hussain, B Challis, N Rocha, et al.Diabetes|August 13, 2014
Clinical and molecular characterization of a novel PLIN1 frameshift mutation identified in patients with familial partial lipodystrophyK Kozusko, Vhm Tsang, W Bottomley, et al.Diabetologia|February 15, 2011
Founder effect in the Horn of Africa for an insulin receptor mutation that may impair receptor recyclingE Raffan, M A Soos, N Rocha, et al.Diabetes|September 10, 1999
Genetic and physiologic analysis of the role of uncoupling protein 3 in human energy homeostasisW K Chung, A Luke, R S Cooper, et al.Journal of Neuroendocrinology|January 1, 2010
The effects of neurokinin B upon gonadotrophin release in male rodentsM P Corander, B G Challis, E L Thompson, et al.Pageof 20