T Rankinen, A Zuberi, YC Chagnon, SJ … - Obesity, 2006 - pbrc.edu Abstract RANKINEN, TUOMO, AAMIR ZUBERI, YVON C. CHAGNON, S. JOHN WEISNAGEL,
GEORGE ARGYROPOULOS, BRANDON WALTS, LOUIS PE´RUSSE, AND CLAUDE BOUCHARD. The
human obesity gene map: the 2005 update. Obesity. 2006;14: 529–644. This ... Cited by 335 - Related articles - View as HTML - All 6 versions
- ►shouxi.net A Garg - The New England journal of medicine, 2004 - nejm.org Lipodystrophies are clinically heterogeneous acquired or inherited disorders
characterized by the selective loss of adipose tissue. Affected patients are
predisposed to insulin resistance and its attendant complications, ... Cited by 251 - Related articles - BL Direct - All 10 versions
- ►unc.edu [PDF] RA Coleman, DP Lee - Progress in Lipid Research, 2004 - Elsevier Since the pathways of glycerolipid biosynthesis were elucidated in the 1950's,
considerable knowledge has been gained about the enzymes that catalyze the lipid
biosynthetic reactions and the factors that regulate triacylglycerol ... Cited by 184 - Related articles - All 8 versions
B Lu, YJ Jiang, Y Zhou, FY Xu, GM Hatch, PC … - Biochemical Journal, 2005 - pubmedcentral.nih.gov AGPAT (1-acyl-sn-glycerol 3-phosphate acyltransferase) exists in at least five
isoforms in humans, termed as AGPAT1, AGPAT2, AGPAT3, AGPAT4 and AGPAT5.
Although they catalyse the same biochemical reaction, their relative ... Cited by 40 - Related articles - All 9 versions
- ►endojournals.org CA Kim, M Delepine, E Boutet, H El Mourabit, … - Journal of Clinical Endocrinology & Metabolism, 2008 - Endocrine Soc Results: A homozygous nonsense mutation (p.Glu38X) was identified in CAV1 in a
patient with BSCL born from a consanguineous union. This mutation affects both
the - and β-CAV1 isoforms and ablates CAV1 expression in skin fibroblasts. ... Cited by 28 - Related articles - BL Direct - All 3 versions
- ►jlr.org [PDF] AP Beigneux, L Vergnes, X Qiao, S Quatela, … - The Journal of Lipid Research, 2006 - ASBMB Anne P. Beigneux,1,* Laurent Vergnes,† Xin Qiao,* Steven Quatela,§ Ryan
Davis,** Steven M. Watkins,** Rosalind A. Coleman,†† Rosemary L. Walzem,**
Mark Philips,§ Karen Reue,† and Stephen G. Young* Division of ... Cited by 26 - Related articles - BL Direct - All 6 versions
L Vergnes, AP Beigneux, R Davis, SM … - Journal of lipid research, 2006 - ASBMB Page 1. Agpat6 deficiency causes subdermal lipodystrophy and resistance
to obesity Laurent Vergnes*, Anne P. Beigneux † , Ryan ... Cited by 26 - Related articles - BL Direct - All 6 versions
AK Agarwal, A Garg - Trends in Molecular Medicine, 2004 - Elsevier In 2001, a locus for autosomal-recessive congenital generalized lipodystrophy
was identified on chromosome 11q13 and mutations in a novel gene named
Berardinelli–Seip congenital lipodystrophy 2 (BSCL2) were reported. ... Cited by 18 - Related articles - All 5 versions
AK Agarwal, RI Barnes, A Garg - International Journal of Obesity, 2003 - nature.com Congenital generalized lipodystrophy (CGL) is an autosomal recessive disorder
characterized by extreme lack of body fat and severe insulin resistance since
birth. Recently, mutations have been reported in 1-acylglycerol-3-phosphate- ... Cited by 18 - Related articles - BL Direct - All 4 versions
SI Anghel, W Wahli - Cell Research, 2007 - nature.com Adipose tissue is not an inert cell mass contributing only to the storage of
fat, but a sophisticated ensemble of cellular components with highly specialized
and complex functions. In addition to managing the most important energy ... Cited by 17 - Related articles - BL Direct - All 6 versions
