Generation and characterization of human-derived induced pluripotent stem cell line (IGIBi010-A) from a patient with neurodegenerative disease phenotype carrying mutation in SQSTM1/p62 gene
Author:
Funder
Council of Scientific and Industrial Research, India
Indian Council of Medical Research
Publisher
Elsevier BV
Reference5 articles.
1. 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;Stem Cell Res.,2022
2. Generation of two induced pluripotent stem cell (iPSC) lines from patients with Duchenne muscular dystrophy (IGIBi006-A and IGIBi008-A) carrying exonic deletions in the dystrophin gene;Ahmad;Stem Cell Res.,2022
3. Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy;Haack;Am. J. Hum. Genet.,2016
4. A more efficient method to generate integration-free human iPS cells;Okita;Nat. Meth.,2011
5. The role of SQSTM1 (p62) in mitochondrial function and clearance in human cortical neurons;Poon;Stem Cell Rep.,2021
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