Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 gene

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SYSNO ASEP	0493025
Document Type	J - Journal Article
R&D Document Type	Journal Article
Subsidiary J	Článek ve WOS
Title	Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 gene
Author(s)	Bolinches-Amorós, A. (ES) Lukovic, D. (ES) Castro, A.A. (ES) León, M. (ES) Kamenarova, K. (BG) Kaneva, R. (BG) Jendelová, Pavla (UEM-P)_{RID, ORCID} Blanco-Kelly, F. (ES) Ayuso, C. (ES) Cortón, M. (ES) Erceg, Slaven (UEM-P)_{RID, ORCID}
Source Title	Stem Cell Research. - : Elsevier - ISSN 1873-5061 Roč. 28, apr (2018), s. 96-99
Number of pages	4 s.
Language	eng - English
Country	NL - Netherlands
Keywords	cytochrome P450 1B1 ; fibroblast growth factor 4 ; growth differentiation factor 3
Subject RIV	FH - Neurology
OECD category	Cell biology
R&D Projects	EF15_003/0000419 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
	GBP304/12/G069 GA ČR - Czech Science Foundation (CSF)
Institutional support	UEM-P - RVO:68378041
UT WOS	000428799700018
EID SCOPUS	85041919429
DOI	10.1016/j.scr.2018.01.004
Annotation	The human iPSC cell line, GLC-FiPS4F1 (ESi047-A), derived from dermal fibroblast from the patient with congenital glaucoma caused by the mutation of the gene CYP1B1, was generated by non-integrative reprogramming technology using OCT3/4, SOX2, CMYC and KLF4 reprogramming factors.
Workplace	Institute of Experimental Medicine
Contact	Lenka Koželská, lenka.kozelska@iem.cas.cz, Tel.: 241 062 218, 296 442 218
Year of Publishing	2019

Number of the records: 1