Loss of hierarchical imprinting regulation at the Prader–Willi/Angelman syndrome locus in human iPSCs

The human chr15q11-q13 imprinted cluster is linked to several disorders, including Prader–Willi (PWS) and Angelman (AS) syndromes. Recently, disease modeling approaches based on induced pluripotent stem cells (iPSCs) have been used to study these syndromes. A concern regarding the use of these cells...

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Detalles Bibliográficos
Autores principales: Pólvora-Brandão, Duarte, Joaquim, Mariana, Godinho, Inês, Aprile, Domenico, Álvaro, Ana Rita, Onofre, Isabel, Raposo, Ana Cláudia, Pereira de Almeida, Luís, Duarte, Sofia T, da Rocha, Simão T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
General Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240739/
https://www.ncbi.nlm.nih.gov/pubmed/30102380
http://dx.doi.org/10.1093/hmg/ddy274

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240739/
https://www.ncbi.nlm.nih.gov/pubmed/30102380
http://dx.doi.org/10.1093/hmg/ddy274

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