Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200.

Zhang, Dan; McLenachan, Samuel; Chen, Shang-Chih; Zaw, Khine; Alziyadat, Yaqin; Zhang, Xiao; Lamey, Tina M; Thompson, Jennifer A; McLaren, Terri L; Mellough, Carla; De Roach, John N; Chen, Fred K

Zhang, Dan; McLenachan, Samuel; Chen, Shang-Chih; Zaw, Khine; Alziyadat, Yaqin; Zhang, Xiao; Lamey, Tina M; Thompson, Jennifer A; McLaren, Terri L; Mellough, Carla; De Roach, John N; Chen, Fred K.

Afiliação

Zhang D; Lions Eye Institute, Nedlands, Western Australia, Australia.
McLenachan S; Lions Eye Institute, Nedlands, Western Australia, Australia; Centre for Ophthalmology and Visual Science, The University of Western Australia, Perth, Western Australia, Australia.
Chen SC; Lions Eye Institute, Nedlands, Western Australia, Australia.
Zaw K; Lions Eye Institute, Nedlands, Western Australia, Australia.
Alziyadat Y; Centre for Ophthalmology and Visual Science, The University of Western Australia, Perth, Western Australia, Australia.
Zhang X; Lions Eye Institute, Nedlands, Western Australia, Australia.
Lamey TM; Centre for Ophthalmology and Visual Science, The University of Western Australia, Perth, Western Australia, Australia; Australian Inherited Retinal Disease Registry and DNA Bank, Department of Medical Technology and Physics, Sir Charles Gairdner Hospital, Perth, Western Australia, Australia.
Thompson JA; Australian Inherited Retinal Disease Registry and DNA Bank, Department of Medical Technology and Physics, Sir Charles Gairdner Hospital, Perth, Western Australia, Australia.
McLaren TL; Centre for Ophthalmology and Visual Science, The University of Western Australia, Perth, Western Australia, Australia; Australian Inherited Retinal Disease Registry and DNA Bank, Department of Medical Technology and Physics, Sir Charles Gairdner Hospital, Perth, Western Australia, Australia.
Mellough C; Lions Eye Institute, Nedlands, Western Australia, Australia; Centre for Ophthalmology and Visual Science, The University of Western Australia, Perth, Western Australia, Australia.
De Roach JN; Centre for Ophthalmology and Visual Science, The University of Western Australia, Perth, Western Australia, Australia; Australian Inherited Retinal Disease Registry and DNA Bank, Department of Medical Technology and Physics, Sir Charles Gairdner Hospital, Perth, Western Australia, Australia.
Chen FK; Lions Eye Institute, Nedlands, Western Australia, Australia; Centre for Ophthalmology and Visual Science, The University of Western Australia, Perth, Western Australia, Australia; Australian Inherited Retinal Disease Registry and DNA Bank, Department of Medical Technology and Physics, Sir Charles Ga

Stem Cell Res ; 51: 102154, 2021 03.

Article em En | MEDLINE | ID: mdl-33429167

Assuntos

Células-Tronco Pluripotentes Induzidas; Doenças Retinianas; Diferenciação Celular; Linhagem Celular; Fibroblastos; Humanos; Fator 4 Semelhante a Kruppel; Mutação; Ribonucleoproteínas Nucleares Pequenas

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Células-Tronco Pluripotentes Induzidas Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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