Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/34183
Title: Generation of induced pluripotent stem cell (iPSC) lines carrying a heterozygous (UKWMPi002-A-1) and null mutant knockout (UKWMPi002-A-2) of Cadherin 13 associated with neurodevelopmental disorders using CRISPR/Cas9
Authors: Vitale, Maria Rosaria
Zoeller, Johanna Eva Maria
Jansch, Charline
Janz, Anna
Edenhofer, Frank
Klopocki, Eva
van den Hove, Daniel
VANMIERLO, Tim 
Rivero, Olga
Kasri, Nael Nadif
Ziegler, Georg Christoph
Lesch, Klaus-Peter
Issue Date: 2021
Publisher: ELSEVIER
Source: Stem Cell Research, 51 (Art N° 102169)
Abstract: Fibroblasts isolated from a skin biopsy of a healthy 46-year-old female were infected with Sendai virus containing the Yamanaka factors to produce transgene-free human induced pluripotent stem cells (iPSCs). CRISPR/Cas9 was used to generate isogenic cell lines with a gene dose-dependent deficiency of CDH13, a risk gene associated with neurodevelopmental and psychiatric disorders. Thereby, a heterozygous CDH13 knockout (CDH13(+/-)) and a CDH13 null mutant (CDH13(-/-)) iPSC line was obtained. All three lines showed expression of pluripotency-associated markers, the ability to differentiate into cells of the three germ layers in vitro, and a normal female karyotype.
Notes: Vitale, MR; Lesch, KP (corresponding author), Univ Hosp Wurzburg, Ctr Mental Hlth, Div Mol Psychiat, Margarete Hoppel Pl 1, D-97080 Wurzburg, Germany.
Vitale_M@ukw.de; kplesch@mail.uni-wuerzburg.de
Other: Vitale, MR; Lesch, KP (corresponding author), Univ Hosp Wurzburg, Ctr Mental Hlth, Div Mol Psychiat, Margarete Hoppel Pl 1, D-97080 Wurzburg, Germany. Vitale_M@ukw.de; kplesch@mail.uni-wuerzburg.de
Keywords: CRISPR-Cas Systems;Cadherins;Female;Heterozygote;Humans;Middle Aged;Induced Pluripotent Stem Cells;Neurodevelopmental Disorders
Document URI: http://hdl.handle.net/1942/34183
ISSN: 1873-5061
e-ISSN: 1876-7753
DOI: 10.1016/j.scr.2021.102169
ISI #: WOS:000629039100019
Rights: 2021 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
Category: A1
Type: Journal Contribution
Validations: ecoom 2022
Appears in Collections:Research publications

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