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Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS

  • Published:2016-11 Issue:3 Volume:17 Page:526-530
  • ISSN:1873-5061
  • Container-title:Stem Cell Research
  • language:en
  • Short-container-title:Stem Cell Research

Author:

Burnett Lisa C.,LeDuc Charles A.,Sulsona Carlos R.,Paull Daniel,Eddiry Sanaa,Levy Brynn,Salles Jean Pierre,Tauber Maithe,Driscoll Daniel J.,Egli Dieter,Leibel Rudolph L.

Funder

FPWR

FPWR/PWSA

Rudin Foundation

NYSCF

Helmsley Foundation

Russell Berrie Foundation

NIH

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology,General Medicine

Reference13 articles.

1. Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings;Angulo;J. Endocrinol. Investig.,2015

2. Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi syndrome;Bieth;Eur. J. Hum. Genet.,2015

3. Management of Prader-Willi Syndrome;Butler,2006

4. Prader–Willi syndrome;Cassidy;Eur. J. Hum. Genet.,2009

5. Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader–Willi syndromes;Chamberlain;Proc. Natl. Acad. Sci.,2010
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