Generation of induced pluripotent stem cell line, ICGi007-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease.
Stem Cell Res
; 34: 101382, 2019 01.
Article
en En
| MEDLINE
| ID: mdl-30658253
ABSTRACT
Huntington's disease (HD) is an autosomal dominant neurodegenerative disease caused by mutation in the HTT gene encoding HTT protein. The mutant protein leads to the neuronal death through dysregulation of multiple cellular processes. HD human induced pluripotent stem cells (iPSCs) represent a useful and valid model for the disease study. iPSC line from HD patient with 47 CAG repeats in HTT was generated from blood mononuclear cells by non-integrating episomal vectors. The iPSC line retained the mutation, expressed pluripotency markers, had a normal karyotype and displayed in vitro differentiation to the three germ layers. Resource table.
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Leucocitos Mononucleares
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Enfermedad de Huntington
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Técnicas de Cultivo de Célula
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Reprogramación Celular
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Células Madre Pluripotentes Inducidas
Límite:
Adult
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Female
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Humans
Idioma:
En
Revista:
Stem Cell Res
Año:
2019
Tipo del documento:
Article