Literature DB >> 25460295

PPARγ mutations, lipodystrophy and diabetes.

Olga Astapova, Todd Leff.   

Abstract

The focus of this review is the lipodystrophy syndrome caused by mutation in the PPARγ nuclear receptor - partial familial lipodystrophy FPLD3. To provide a broader context for how these mutations act to generate the clinical features of partial lipodystrophy we will review the basic biology of PPARγ and also survey the set PPARγ genetic variants that do not cause lipodystrophy, but are nonetheless associated with clinically related syndromes, specifically type 2 diabetes.

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Year:  2014        PMID: 25460295     DOI: 10.1515/hmbci-2014-0033

Source DB:  PubMed          Journal:  Horm Mol Biol Clin Investig        ISSN: 1868-1883


  3 in total

Review 1.  PPARs: regulators of metabolism and as therapeutic targets in cardiovascular disease. Part II: PPAR-β/δ and PPAR-γ.

Authors:  Lu Han; Wen-Jun Shen; Stefanie Bittner; Fredric B Kraemer; Salman Azhar
Journal:  Future Cardiol       Date:  2017-06-05

2.  Obesity-induced endoplasmic reticulum stress suppresses nuclear factor-Y expression.

Authors:  Yulan Liu; Yuwei Zhang; Yanjie Zhang; Jinlong Zhang; Yin Liu; Peiqun Feng; Zhiguang Su
Journal:  Mol Cell Biochem       Date:  2016-11-12       Impact factor: 3.396

3.  New Transcriptional Reporters to Quantify and Monitor PPARγ Activity.

Authors:  Séverine A Degrelle; Hussein Shoaito; Thierry Fournier
Journal:  PPAR Res       Date:  2017-11-01       Impact factor: 4.964

  3 in total

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