Literature DB >> 17493868

The PPAR resource page.

John P Vanden Heuvel1.   

Abstract

Peroxisome proliferator-activated receptors (PPARs) are nuclear receptors (NRs) that control many cellular and metabolic processes. These proteins are ligand-activated transcription factors and three isotypes called PPARalpha, PPARbeta/delta and PPARgamma have been identified in lower vertebrates and mammals. They display differential tissue distribution and each of the three subtypes fulfills specific functions; however, all three PPARs affect energy homoeostasis and inflammatory responses. In addition, their activity can be modulated by drugs such as the hypolipidemic fibrates and the insulin sensitizing thiazolidinediones. Thus, understanding the biology and identifying small molecule modulators of the PPARs is an active area of research and may impact chronic diseases such as diabetes, obesity, heart disease and atherosclerosis. The PPAR Resource Page (http://ppar.cas.psu.edu) is a website devoting to keeping scientists up-to-date with the latest research on these proteins and provides links to a variety of public databases. The site was launched in 1998 to disseminate information about PPAR including cDNA sequences, protein alignments, DNA response elements (PPREs), and sources of cDNAs, proteins and antibodies. Recent additions include bioinformatics support such as gene expression microarray and pathway analysis links. As part of the Nuclear Receptor Resource (NRR, http://nrr.georgetown.edu/NRR/nrrhome.htm) some tools are shared with other constituents of this larger project. These include electronic publication, and a listing of scientists interested in the steroid and thyroid hormone superfamily. Receiving greater than 300 unique visits per week, the PPAR resource page has become a useful tool for researchers of these important NRs.

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Year:  2007        PMID: 17493868     DOI: 10.1016/j.bbalip.2007.03.007

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  6 in total

Review 1.  The potential for chemical mixtures from the environment to enable the cancer hallmark of sustained proliferative signalling.

Authors:  Wilhelm Engström; Philippa Darbre; Staffan Eriksson; Linda Gulliver; Tove Hultman; Michalis V Karamouzis; James E Klaunig; Rekha Mehta; Kim Moorwood; Thomas Sanderson; Hideko Sone; Pankaj Vadgama; Gerard Wagemaker; Andrew Ward; Neetu Singh; Fahd Al-Mulla; Rabeah Al-Temaimi; Amedeo Amedei; Anna Maria Colacci; Monica Vaccari; Chiara Mondello; A Ivana Scovassi; Jayadev Raju; Roslida A Hamid; Lorenzo Memeo; Stefano Forte; Rabindra Roy; Jordan Woodrick; Hosni K Salem; Elizabeth P Ryan; Dustin G Brown; William H Bisson
Journal:  Carcinogenesis       Date:  2015-06       Impact factor: 4.944

2.  Dysregulation of gene expression within the peroxisome proliferator activated receptor pathway in morbidly obese patients.

Authors:  A Katharine Hindle; Jadd Koury; Tim McCaffrey; Sidney W Fu; Fred Brody
Journal:  Surg Endosc       Date:  2008-10-15       Impact factor: 4.584

Review 3.  Peroxisome proliferator activated receptor gamma and oxidized docosahexaenoic acids as new class of ligand.

Authors:  Toshimasa Itoh; Keiko Yamamoto
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2008-01-08       Impact factor: 3.000

4.  Reactivation of adiponectin expression in obese patients after bariatric surgery.

Authors:  A Katharine Hindle; Claire Edwards; Tim McCaffrey; Sidney W Fu; Fred Brody
Journal:  Surg Endosc       Date:  2009-12-24       Impact factor: 4.584

5.  Screening for PPAR Responsive Regulatory Modules in Cancer.

Authors:  Merja Heinäniemi; Carsten Carlberg
Journal:  PPAR Res       Date:  2008       Impact factor: 4.964

6.  Does Pro(12)Ala Polymorphism Enhance the Physiological Role of PPARγ2?

Authors:  A C Pereira; R Oliveira; A C Castro; R Fernandes
Journal:  PPAR Res       Date:  2013-07-31       Impact factor: 4.964

  6 in total

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