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XACHi013-A
Registration Summary
:
A
P
E
C
The cell line is
not submitted
yet.
(only basic data is shown)
General
Cell Line
hPSCreg name
XACHi013-A
Cite as:
When citing this cell line, please use the hPSCreg name (see
Naming Tool
) and the corresponding Research Resource ID (RRID).
XACHi013-A (RRID:CVCL_A8WM)
Cell line type
Human induced pluripotent stem cell (hiPSC)
Similar lines
No similar lines found.
Last update
26th November 2020
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Provider
Generator
Xi'an children's hospital (XACH)
External Databases
Cellosaurus
CVCL_A8WM
Wikidata
Q108821530
General Information
Publications
Zhou Y et al. Establishment of iPSC line from a Chinese infant (XACHi012-A) with Jervell and Lange-Nielsen syndrome carrying combined KCNQ1 frameshift c.431delC(p.I145Sfs*92) and nonsense c.1175G > A (p.W392X) variants and two iPSC lines from the parents (XACHi013-A, XACHi014-A). Stem cell research. 2021 May;53:102391.
Wang T et al. Generation of induced pluripotent stem cells (iPSCs) from a Chinese infant (XACHi015-A) with type 2 Long QT syndrome carrying the heterozygous mutation c.1814C>T(p.P605L) in KCNH2. Stem cell research. 2021 Oct;56:102509.
Zhou Yafei et al. Wnt pathway activation unlocks disease-neutral proliferative potential in human iPSC-derived cardiomyocytes: A comparative study across healthy and inherited cardiac disease models. Tissue and Cell. 2026-02-00.
hIPSC Derivation
General
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