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SDQLCHi004-A
Registration Summary
:
A
P
E
C
The cell line is
not submitted
yet.
(only basic data is shown)
General
Cell Line
hPSCreg name
SDQLCHi004-A
Cite as:
When citing this cell line, please use the hPSCreg name (see
Naming Tool
) and the corresponding Research Resource ID (RRID).
SDQLCHi004-A (RRID:CVCL_XI74)
Cell line type
Human induced pluripotent stem cell (hiPSC)
Similar lines
No similar lines found.
Last update
22nd July 2019
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Provider
Generator
Children’s Hospital affiliated to Shandong University (SDQLCH)
External Databases
Cellosaurus
CVCL_XI74
Wikidata
Q98129450
General Information
Publications
Ma Y et al. Establishment of a human induced pluripotent stem cell line (SDQLCHi004-A) from a patient with nemaline myopathy-4 disease carrying heterozygous mutation in TPM2 gene. Stem cell research. 2019 Oct;40:101559.
Zumwalt M et al. Stem Cells for Treatment of Musculoskeletal Conditions - Orthopaedic/Sports Medicine Applications. Biochimica et biophysica acta. Molecular basis of disease. 2020 Apr 1;1866(4):165624.
Zhang W et al. Multifunctional polyphenol-based silk hydrogel alleviates oxidative stress and enhances endogenous regeneration of osteochondral defects. Materials today. Bio. 2022 Mar;14:100251.
Gartz M et al. ACTA1 H40Y mutant iPSC-derived skeletal myocytes display mitochondrial defects in an in vitro model of nemaline myopathy. Experimental cell research. 2023 Mar 15;424(2):113507.
Chen Genghua et al. Bulk and single‐cell alternative splicing analyses reveal roles of
TRA2B
in myogenic differentiation. Cell Proliferation. 2024-02-00.
hIPSC Derivation
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