Generation of a human induced pluripotent stem cell line via CRISPR-Cas9 mediated integration of a site-specific homozygous mutation in CHMP2B

Frontotemporal dementia (FTD) is an early onset neurodegenerative disease. Mutations in several genes cause familial FTD and one of them is charged multivesicular body protein 2B (CHMP2B) on chromosome 3 (FTD3), a component of the endosomal sorting complex required for transport III (ESCRT-III). We...

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Egile Nagusiak: Yu Zhang, Benjamin Schmid, Troels T. Nielsen, Jørgen E. Nielsen, Christian Clausen, Poul Hyttel, Bjørn Holst, Kristine K. Freude
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Elsevier 2016-07-01
Saila:Stem Cell Research
Sarrera elektronikoa:http://www.sciencedirect.com/science/article/pii/S187350611630068X
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