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Establishment of a human iPSC line, IISHDOi004-A, from a patient with Usher syndrome associated with the mutation c.2276G > T; p.Cys759Phe in the USH2A gene

Autores

ZURITA DIAZ, FRANCISCO, del Carmen Ortuno-Costela, Maria , Moreno-Izquierdo, Ana , Galbis, Liliana , Maria Millan, Jose , Ayuso, Carmen , Garesse, Rafael , Esther Gallardo, M.

Publicación externa

No

Medio

Stem Cell Res.

Alcance

Article

Naturaleza

Científica

Cuartil JCR

1

Cuartil SJR

2

Impacto JCR

3.929

Fecha de publicacion

01/08/2018

ISI

000444011900024

Abstract

A human iPSC line, IISH DOi 004-A, from fibroblasts obtained from a patient with Usher syndrome, harboring a homozygous mutation in the USH2A gene (c.2276G > T; p.Cys759Phe) has been generated. Reprogramming factors Oct3/4, Sox2, Klf4, and c-Myc were delivered using Sendai virus.

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