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CPGHi002-A
Registration Summary
:
A
P
E
C
The cell line is
not submitted
yet.
(only basic data is shown)
General
Cell Line
hPSCreg name
CPGHi002-A
Cite as:
When citing this cell line, please use the hPSCreg name (see
Naming Tool
) and the corresponding Research Resource ID (RRID).
CPGHi002-A (RRID:CVCL_A1AZ)
Cell line type
Human induced pluripotent stem cell (hiPSC)
Similar lines
No similar lines found.
Last update
9th September 2020
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Provider
Generator
Chinese PLA General Hospital (CPGH)
External Databases
BioSamples
SAMEA7340582
Cellosaurus
CVCL_A1AZ
Wikidata
Q102113716
General Information
Publications
Gao X et al. Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1B2. Stem cell research. 2020 Oct;48:101986.
Gao X et al. Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with heterozygous c.1516 C>T mutation in the ATP6V1B2 gene. Stem cell research. 2021 May;53:102271.
Durán-Alonso MB et al. Induced Pluripotent Stem Cells, a Stepping Stone to In Vitro Human Models of Hearing Loss. Cells. 2022 Oct 21;11(20).
Amore Greta et al. ATP6V1B2-related disorders featuring Lennox-Gastaut-syndrome: A case-based overview. Brain and Development. 2023-11-00.
Subclones
CPGHi002-A-1
hIPSC Derivation
General
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