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Generation of TWO G51D SNCA missense mutation iPSC lines (CRICKi011-A, CRICKi012-A) from two individuals at risk of Parkinson's disease.
Devito, Liani G; Zanjani, Zeinab Shadman; Evans, James R; Scardamaglia, Annarita; Houlden, Henry; Gandhi, Sonia; Healy, Lyn.
Afiliação
  • Devito LG; Human Embryo and Stem Cell Unit, The Francis Crick Institute, London, UK. Electronic address: liani.devito@crick.ac.uk.
  • Zanjani ZS; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, UK; The Francis Crick Institute, 1 Midland Road, London, UK.
  • Evans JR; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, UK; The Francis Crick Institute, 1 Midland Road, London, UK.
  • Scardamaglia A; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.
  • Houlden H; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.
  • Gandhi S; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, UK; The Francis Crick Institute, 1 Midland Road, London, UK.
  • Healy L; Human Embryo and Stem Cell Unit, The Francis Crick Institute, London, UK. Electronic address: lyn.healy@crick.ac.uk.
Stem Cell Res ; 71: 103134, 2023 09.
Article em En | MEDLINE | ID: mdl-37336145
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Atrofia de Múltiplos Sistemas / Células-Tronco Pluripotentes Induzidas Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Atrofia de Múltiplos Sistemas / Células-Tronco Pluripotentes Induzidas Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article