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SDQLCHi010-A
Registration Summary
:
A
P
E
C
The cell line is
not submitted
yet.
(only basic data is shown)
General
Cell Line
hPSCreg name
SDQLCHi010-A
Cite as:
When citing this cell line, please use the hPSCreg name (see
Naming Tool
) and the corresponding Research Resource ID (RRID).
SDQLCHi010-A (RRID:CVCL_YK74)
Cell line type
Human induced pluripotent stem cell (hiPSC)
Similar lines
No similar lines found.
Last update
22nd October 2019
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Provider
Generator
Children’s Hospital affiliated to Shandong University (SDQLCH)
External Databases
Cellosaurus
CVCL_YK74
Wikidata
Q98129467
General Information
Publications
Zhang H et al. Establishment of a human iPSC line (SDQLCHi010-A) from a patient with optic nerve malformation carrying a heterozygous mutation in PAX6 gene. Stem cell research. 2019 Dec;41:101611.
Abdolkarimi D et al. PAX6 disease models for aniridia. Indian journal of ophthalmology. 2022 Dec;70(12):4119-4129.
Tamayo A et al. Minigene Splicing Assays and Long-Read Sequencing to Unravel Pathogenic Deep-Intronic Variants in PAX6 in Congenital Aniridia. International journal of molecular sciences. 2023 Jan 13;24(2).
Koc AC et al. Patient-derived cornea organoid model to study metabolomic characterization of rare disease: aniridia-associated keratopathy. BMC ophthalmology. 2025 Jan 10;25(1):14.
hIPSC Derivation
General
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