The mRNA-based reprogramming of fibroblasts from a SOD1E101G familial amyotrophic lateral sclerosis patient to induced pluripotent stem cell line UOWi007.
Stem Cell Res
; 42: 101701, 2020 01.
Article
in En
| MEDLINE
| ID: mdl-32006803
Dermal fibroblasts were donated by a 43 year old male patient with clinically diagnosed familial amyotrophic lateral sclerosis (ALS), carrying the SOD1E101G mutation. The induced pluripotent stem cell (iPSC) line UOWi007-A was generated using repeated mRNA transfections for pluripotency transcription factors Oct4, Klf4, Sox2, c-Myc, Lin28 and Nanog. The iPSCs carried the SOD1E101G genotype and had a normal karyotype, expressed expected pluripotency markers and were capable of in vitro differentiation into endodermal, mesodermal and ectodermal lineages. This iPSC line may be useful for investigating familial ALS resulting from a SOD1E101G mutation.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Fibroblasts
/
Superoxide Dismutase-1
/
Amyotrophic Lateral Sclerosis
Limits:
Humans
Language:
En
Journal:
Stem Cell Res
Year:
2020
Document type:
Article
Affiliation country:
Australia
Country of publication:
United kingdom