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UCLi014-A
Registration Summary
:
A
P
E
C
RDH12 AD
The cell line is
not submitted
yet.
(only basic data is shown)
General
Cell Line
hPSCreg name
UCLi014-A
Cite as:
When citing this cell line, please use the hPSCreg name (see
Naming Tool
) and the corresponding Research Resource ID (RRID).
UCLi014-A (RRID:CVCL_A0KB)
Alternative name(s)
RDH12 AD
Cell line type
Human induced pluripotent stem cell (hiPSC)
Similar lines
No similar lines found.
Last update
16th April 2020
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Provider
Generator
University College London (UCL)
External Databases
Wikidata
Q105511316
Cellosaurus
CVCL_A0KB
General Information
Publications
Sarkar H et al. Generation of two human iPSC lines from patients with autosomal dominant retinitis pigmentosa (UCLi014-A) and autosomal recessive Leber congenital amaurosis (UCLi015-A), associated with RDH12 variants. Stem cell research. 2021 Jul;54:102449.
Hosseini Shabanan S et al. Stem cell transplantation as a progressing treatment for retinitis pigmentosa. Cell and tissue research. 2022 Feb;387(2):177-205.
Liang Yuqin et al. Application of patient-derived induced pluripotent stem cells and organoids in inherited retinal diseases. Stem Cell Research & Therapy. 2023-11-27.
Guo Fuying et al. Generation of two hiPSC lines carrying compound heterozygous RDH12 mutations in a LCA patient. Stem Cell Research. 2024-12-00.
hIPSC Derivation
General
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