Generation and characterization of two iPSC lines carrying heterozygous or homozygous nonsense mutation in PROM1 gene from a single family.

Xu, Ping; Guo, Fuying; Xie, Bingbing; Zhong, Xiufeng

Xu, Ping; Guo, Fuying; Xie, Bingbing; Zhong, Xiufeng.

Afiliación

Xu P; State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University; Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangzhou 510060, China.
Guo F; State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University; Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangzhou 510060, China.
Xie B; State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University; Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangzhou 510060, China.
Zhong X; State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University; Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangzhou 510060, China. Electronic address: zhongxf7@mail.sysu.edu.cn.

Stem Cell Res ; 64: 102913, 2022 10.

Article en En | MEDLINE | ID: mdl-36191543

Asunto(s)

Antígeno AC133; Células Madre Pluripotentes Inducidas; Distrofias Retinianas; Humanos; Antígeno AC133/genética; Antígeno AC133/metabolismo; Codón sin Sentido/genética; Heterocigoto; Homocigoto; Células Madre Pluripotentes Inducidas/metabolismo; Mutación; Distrofias Retinianas/genética; Distrofias Retinianas/metabolismo

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre Pluripotentes Inducidas / Distrofias Retinianas / Antígeno AC133 Límite: Humans Idioma: En Revista: Stem Cell Res Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google