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Stem Cell Res ; 71: 103170, 2023 09.
Article in English | MEDLINE | ID: mdl-37494850

ABSTRACT

Uncovering the molecular mechanisms of autism spectrum disorder (autism) necessitates development of relevant experimental models that are capable of recapitulating features of the clinical phenotype. Using non-integrative episomal vectors, peripheral blood mononuclear cells derived from three unrelated individuals diagnosed with autism were reprogrammed to induced pluripotent stem cells (iPSCs). The resultant lines exhibited the expected cellular morphology, karyotype, and evidence of pluripotency. These iPSCs constitute a valuable resource to support investigations of the underlying aetiology of autism.


Subject(s)
Autism Spectrum Disorder , Autistic Disorder , Induced Pluripotent Stem Cells , Humans , Induced Pluripotent Stem Cells/metabolism , Autism Spectrum Disorder/genetics , Autism Spectrum Disorder/metabolism , Leukocytes, Mononuclear/metabolism , Karyotype , Cell Differentiation , Cellular Reprogramming
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