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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Detalhes bibliográficos
Main Authors: Chamberlain, Stormy J., Chen, Pin-Fang, Ng, Khong Y., Bourgois-Rocha, Fany, Lemtiri-Chlieh, Fouad, Levine, Eric S., Lalande, Marc
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2010
Assuntos:
Biological Sciences
Acesso em linha: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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