Functional relationship between mTERF4 and GUN1 in retrograde signaling.
Martinsried, Germany. In J Exp Bot, Jan 2016
Comparative analysis revealed that in gun1 and coe1/mterf4, but not in wild-type, gun4, or gun5 plants, the processing of plastid transcripts and expression levels of Lhcb1 mRNA were affected in opposite ways when plants were grown in the presence of LIN or SPE.
Topiramate effects lipolysis in 3T3-L1 adipocytes.
Criciúma, Brazil. In Biomed Rep, Nov 2015
The phosphorylation of protein kinase A (PKA), hormone-sensitive lipase (HSL), adipocyte triglyceride lipase (ATGL) and perilipin A, as well as the protein levels of comparative genetic identification 58 (CGI-58) were assessed.
Pathophysiology of lipid droplet proteins in liver diseases.
Philadelphia, United States. In Exp Cell Res, Nov 2015
Five proteins of the perilipin (PLIN) family (PLIN1 (perilipin), PLIN2 (adipose differentiation-related protein), PLIN3 (tail-interacting protein of 47kDa), PLIN4 (S3-12), and PLIN5 (myocardial lipid droplet protein)), are associated with LD formation.
Regulation of adipocyte lipolysis.
Pamplona, Spain. In Nutr Res Rev, 2014
Perilipin, comparative gene identification-58 (CGI-58) and other proteins of the lipid droplet surface are currently known to be key regulators of the lipolytic machinery, protecting or exposing the TAG core of the droplet to lipases.
Perilipin deficiency and autosomal dominant partial lipodystrophy.
Cambridge, United Kingdom. In N Engl J Med, 2011
Identified two heterozygous frameshift mutations in the perilipin gene (PLIN1) in three families with partial lipodystrophy, severe dyslipidemia, and insulin-resistant diabetes; findings define a novel dominant form of inherited lipodystrophy.