Lab resource: Single cell line generation and characterization of a human-derived induced pluripotent stem cell line (IGIBi005-A) from a patient with spastic paraplegia/ataxia/ALS phenotype due to the mutation of the gene Kinesin Family Member 5A (KIF5A).

Ahmad, Istaq; Goel, Divya; Ghosh, Anindita; Kapoor, Himanshi; Kumar, Deepak; Srivastava, Achal K; Faruq, Mohammed

Ahmad, Istaq; Goel, Divya; Ghosh, Anindita; Kapoor, Himanshi; Kumar, Deepak; Srivastava, Achal K; Faruq, Mohammed.

Afiliação

Ahmad I; Genomics and Molecular Medicine Division, CSIR - Institute of Genomics and Integrative Biology, New Delhi 110007, India; Department of Neurology, Neurosciences Centre, All India Institute of Medical Sciences, New Delhi 110029, India.
Goel D; Genomics and Molecular Medicine Division, CSIR - Institute of Genomics and Integrative Biology, New Delhi 110007, India; Department of Pharmacology, SPER, Jamia Hamdard, New Delhi 110062, India.
Ghosh A; Genomics and Molecular Medicine Division, CSIR - Institute of Genomics and Integrative Biology, New Delhi 110007, India; Division of Investigations of Human Pathology by Application Genomics-Exomics&Stem Cells (StemAppGenE SAGE), CSIR-IGIB, Delhi 110007, India.
Kapoor H; Genomics and Molecular Medicine Division, CSIR - Institute of Genomics and Integrative Biology, New Delhi 110007, India.
Kumar D; Genomics and Molecular Medicine Division, CSIR - Institute of Genomics and Integrative Biology, New Delhi 110007, India; Department of Zoology, University of Allahabad, Prayagraj, Uttar Pradesh 211002, India.
Srivastava AK; Department of Neurology, Neurosciences Centre, All India Institute of Medical Sciences, New Delhi 110029, India.
Faruq M; Genomics and Molecular Medicine Division, CSIR - Institute of Genomics and Integrative Biology, New Delhi 110007, India; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India; Division of Investigations of Human Pathology by Application Genomics-Exomics&Stem Cells (StemA

Stem Cell Res ; 64: 102904, 2022 10.

Article em En | MEDLINE | ID: mdl-36055117

Assuntos

Esclerose Lateral Amiotrófica; Células-Tronco Pluripotentes Induzidas; Ataxias Espinocerebelares; Humanos; Esclerose Lateral Amiotrófica/genética; Esclerose Lateral Amiotrófica/metabolismo; Células-Tronco Pluripotentes Induzidas/metabolismo; Cinesinas/genética; Proteína Coestimuladora de Linfócitos T Induzíveis/genética; Proteína Coestimuladora de Linfócitos T Induzíveis/metabolismo; Ataxias Espinocerebelares/metabolismo; Linhagem Celular; Mutação/genética; Fenótipo; Paraplegia/metabolismo; Família

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxias Espinocerebelares / Células-Tronco Pluripotentes Induzidas / Esclerose Lateral Amiotrófica Limite: Humans Idioma: En Revista: Stem Cell Res Ano de publicação: 2022 Tipo de documento: Article

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