UCLi015-A

Registration Summary:

A P E C

RDH12 AR

The cell line is not submitted yet.

(only basic data is shown)

General

Cell Line
hPSCreg name	UCLi015-A
Cite as:	UCLi015-A (RRID:CVCL_A0KC)
Alternative name(s)	RDH12 AR
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	Q105511320
Cellosaurus	CVCL_A0KC
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. Holtes Lara K. et al. Dual inheritance patterns: A spectrum of non-syndromic inherited retinal disease phenotypes with varying molecular mechanisms. Progress in Retinal and Eye Research. 2025-01-00.

hIPSC Derivation

General