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Clinical-Grade Human Pluripotent Stem Cells for Cell Therapy: Characterization Strategy
D. Rehakova, T. Souralova, I. Koutna
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články, přehledy
Grantová podpora
CZ.02.1.01/0.0/0.0/16_019/0000868
European Regional Development Fund
CZ.02.1.01/0.0/0.0/15_003/0000492
European Regional Development Fund
NV18-08-00412
Ministerstvo Zdravotnictví Ceské Republiky
NLK
Free Medical Journals
od 2000
Freely Accessible Science Journals
od 2000
PubMed Central
od 2007
Europe PubMed Central
od 2007
ProQuest Central
od 2000-03-01
Open Access Digital Library
od 2000-01-01
Open Access Digital Library
od 2007-01-01
Health & Medicine (ProQuest)
od 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
od 2000
PubMed
32244538
DOI
10.3390/ijms21072435
Knihovny.cz E-zdroje
- MeSH
- Bacteria MeSH
- buněčná a tkáňová terapie metody MeSH
- endotoxiny MeSH
- indukované pluripotentní kmenové buňky MeSH
- lidé MeSH
- lidské embryonální kmenové buňky MeSH
- Mycoplasma MeSH
- pluripotentní kmenové buňky * MeSH
- viry MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Human pluripotent stem cells have the potential to change the way in which human diseases are cured. Clinical-grade human embryonic stem cells and human induced pluripotent stem cells have to be created according to current good manufacturing practices and regulations. Quality and safety must be of the highest importance when humans' lives are at stake. With the rising number of clinical trials, there is a need for a consensus on hPSCs characterization. Here, we summarize mandatory and 'for information only' characterization methods with release criteria for the establishment of clinical-grade hPSC lines.
Citace poskytuje Crossref.org
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