Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader–Willi syndromes

Angelman syndrome (AS) and Prader–Willi syndrome (PWS) are neurodevelopmental disorders of genomic imprinting. AS results from loss of function of the ubiquitin protein ligase E3A (UBE3A) gene, whereas the genetic defect in PWS is unknown. Although induced pluripotent stem cells (iPSCs) provide inva...

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Main Authors: Chamberlain, Stormy J., Chen, Pin-Fang, Ng, Khong Y., Bourgois-Rocha, Fany, Lemtiri-Chlieh, Fouad, Levine, Eric S., Lalande, Marc
Formáid: Artigo
Teanga:Inglês
Foilsithe: National Academy of Sciences 2010
Ábhair:
Biological Sciences
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2955112/
https://ncbi.nlm.nih.gov/pubmed/20876107
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1004487107
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