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In vitro modeling of amyotrophic lateral sclerosis with induced pluripotent stem cell technology-derived cell line ORIONi002-A
J. Strnadel, HM. Dumortier, D. Hajduchova, R. Zahumenska, V. Nosal, M. Smolar, J. Marcinek, M. Kalman, S. Mersakova, D. Brany, S. Juhas, J. Juhasova, H. Studenovska, B. Mitruskova, S. Suroviakova, S. Novakova, H. Skovierova, E. Kurca, R. Pecova,...
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2014
Open Access Digital Library
od 2007-10-01
Open Access Digital Library
od 2014-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2007
- MeSH
- amyotrofická laterální skleróza * patologie MeSH
- buněčná diferenciace MeSH
- buněčné linie MeSH
- fibroblasty metabolismus MeSH
- indukované pluripotentní kmenové buňky * metabolismus MeSH
- lidé MeSH
- technologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
We present here a new iPS cell line for modeling sporadic form of ALS. Cell line was generated by reprogramming skin fibroblasts isolated with explant culture technology from skin biopsy, donated by ALS patient. For reprogramming, polycistronic self-replicating RNA vector was used and derived iPS cells were characterized by immunocytochemistry and FACS (pluripotent factors expression), karyotyping, STR fingerprinting analysis and in vitro differentiation assay. New cell line showed normal (46, XY) karyotype and differentiated in vitro into cells from three germ layers. STR analysis proved the origin and originality of the cell line.
Citace poskytuje Crossref.org
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