About: Perilipin deficiency and autosomal dominant partial lipodystrophy

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About: Perilipin deficiency and autosomal dominant partial lipodystrophy Goto Sponge NotDistinct Permalink

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scientific article published on February 2011

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2011 (ast) наукова стаття, опублікована в лютому 2011 (uk) مقالة علمية نشرت في فبراير 2011 (ar) scientific article published on February 2011 (en)
publication date	wds:Q37173608-A22EAACA-FE72-42D4-A1E6-47BEFBD35511
publication date	2011-02-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37173608-2360813E-D097-4753-8F0A-63B10340BD1D
language of work or name	English
cites work	wds:Q37173608-08D4FC7F-478A-4CE1-8F3E-16B8FD66A01B wds:Q37173608-2DEC80EE-2A3A-41F8-BA6A-D18C7E6DD2B4 wds:Q37173608-2FE8D746-04D6-4357-A9DC-4BBBD7F4644B wds:Q37173608-314EF982-1457-434B-9094-CDE4101D19BD wds:Q37173608-502B31F1-1F84-4648-81F9-B9F5BAF54972 wds:Q37173608-503043D8-8466-423C-8BDC-42DB51B3C3E7 wds:Q37173608-57824342-B6B4-43D4-927F-3E4E3EC218C2 wds:Q37173608-79961649-DCC9-4B2D-ABB7-8BAAAE274AAD wds:Q37173608-82C66BB9-4671-4129-9C2D-0AA10EDAD795 wds:Q37173608-8540AC71-CA03-466F-9F5A-D4AAD031686B wds:Q37173608-89E7F1AE-8602-44DC-95EB-C7DEE5A71E31 wds:Q37173608-93F12B87-5B3F-409C-BFAF-270DA9BB414C wds:Q37173608-97165BDE-437F-4762-9C5A-E33532041FFB wds:Q37173608-9B326A6E-6C25-47EC-A2D7-6190402866CA wds:Q37173608-AB70031F-CEAA-437F-B794-AEFA133C42B7 wds:Q37173608-ADFBA062-F081-4735-924C-C946E654CDA6 wds:Q37173608-B26AF249-A184-423C-91BA-F63DFB49DA84 wds:Q37173608-B7EB1EFB-BD3B-4D91-A8E4-A69E1D9AD62C wds:Q37173608-BA1CF3FC-C532-4C70-91CA-6E3ED759E4B1 wds:Q37173608-BC7B9D3A-3181-495F-9530-1E0CF5887022 wds:Q37173608-C40BD65D-15B6-4EBE-9CB6-B31B308516CA wds:Q37173608-C6C92160-E1C3-48F0-9E64-54E7654C12E1 wds:Q37173608-DED03040-156E-406E-B6E5-63524B9CEDB0 wds:Q37173608-EE0E5EEE-D975-4353-90A3-C1F7ECA92B2C wds:Q37173608-FDE0DF86-B7C6-4210-94D8-2B9046BB17B5
cites work	Higher adiponectin levels in patients with Berardinelli-Seip congenital lipodystrophy due to seipin as compared with 1-acylglycerol-3-phosphate-o-acyltransferase-2 deficiency Partial lipodystrophy and insulin resistant diabetes in a patient with a homozygous nonsense mutation in CIDEC Perilipin A and the control of triacylglycerol metabolism The Amino and Carboxyl Termini of Perilipin A Facilitate the Storage of Triacylglycerols Acquired and inherited lipodystrophies Hydrophobic sequences target and anchor perilipin A to lipid droplets Thematic review series: adipocyte biology. The perilipin family of structural lipid droplet proteins: stabilization of lipid droplets and control of lipolysis Perilipin ablation results in a lean mouse with aberrant adipocyte lipolysis, enhanced leptin production, and resistance to diet-induced obesity Hypoxia-inducible factor 1alpha induces fibrosis and insulin resistance in white adipose tissue. Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy. Adipose tissue as a buffer for daily lipid flux Dual-energy x-ray absorptiometry for total-body and regional bone-mineral and soft-tissue composition Serum adiponectin and leptin levels in patients with lipodystrophies Lipase-selective functional domains of perilipin A differentially regulate constitutive and protein kinase A-stimulated lipolysis Disordered lipid metabolism and the pathogenesis of insulin resistance The lipodystrophy protein seipin is found at endoplasmic reticulum lipid droplet junctions and is important for droplet morphology Fld1p, a functional homologue of human seipin, regulates the size of lipid droplets in yeast Fatal cardiac arrhythmia and long-QT syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (CGL4) due to PTRF-CAVIN mutations Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy Absence of perilipin results in leanness and reverses obesity in Lepr(db/db) mice Metabolic adaptations in the absence of perilipin: increased beta-oxidation and decreased hepatic glucose production associated with peripheral insulin resistance but normal glucose tolerance in perilipin-null mice. Perilipin controls lipolysis by regulating the interactions of AB-hydrolase containing 5 (Abhd5) and adipose triglyceride lipase (Atgl). Adipose tissue transcriptomic signature highlights the pathological relevance of extracellular matrix in human obesity Seipin deficiency alters fatty acid Delta9 desaturation and lipid droplet formation in Berardinelli-Seip congenital lipodystrophy New metabolic phenotypes in laminopathies: LMNA mutations in patients with severe metabolic syndrome.
author name string	wds:Q37173608-3A8D5151-DD6E-43EB-80C5-CA2F089B0BE2 wds:Q37173608-4D584226-3283-4A2C-9087-885F6346D141 wds:Q37173608-5FC028F4-AEB9-4573-AF84-F04E6BCDA5CA wds:Q37173608-64948E73-409F-4C3C-8D7C-FACB604C677C wds:Q37173608-6737C2BC-DD5B-46B4-9A32-F5F70B617C3E wds:Q37173608-6E3D02BC-5C23-494D-8D79-C14DF8DE0272 wds:Q37173608-73C9B890-8FA4-4A3F-BC2E-EF179D38EB95 wds:Q37173608-AF63334A-971A-4050-9189-C019F7CFAC71 wds:Q37173608-B50F5D24-F5C7-4C66-A9A6-3884A1B8ED83 wds:Q37173608-DD913427-E01C-4D29-A8AF-94158874A441 wds:Q37173608-FC9B027E-5E7C-4B91-95E5-74A8B1F28781
author name string	Guillaume Charpentier Sheetal Gandotra Corinne Vigouroux Jacqueline Capeau Philippe Giral Pascale Cervera Yves Reznik Martine Auclair Caroline Le Dour Marc Delépine William Bottomley
rdfs:label	Perilipin deficiency and autosomal dominant partial lipodystrophy (en) Perilipin deficiency and autosomal dominant partial lipodystrophy (nl) Perilipin deficiency and autosomal dominant partial lipodystrophy (ast)
skos:prefLabel	Perilipin deficiency and autosomal dominant partial lipodystrophy (en) Perilipin deficiency and autosomal dominant partial lipodystrophy (nl) Perilipin deficiency and autosomal dominant partial lipodystrophy (ast)
name	Perilipin deficiency and autosomal dominant partial lipodystrophy (en)

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