INMi003-A

Registration Summary:

A P E C

CRX-CRD-iPSC

The cell line is not submitted yet.

(only basic data is shown)

General

Cell Line
hPSCreg name	INMi003-A
Cite as:	INMi003-A (RRID:CVCL_WR01)
Alternative name(s)	CRX-CRD-iPSC
Cell line type	Human induced pluripotent stem cell (hiPSC)
Similar lines	No similar lines found.
Last update	8th March 2019
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Provider
Generator	Institute for Neurosciences of Montpellier (INM)
External Databases
Cellosaurus	CVCL_WR01
Wikidata	Q94317998
General Information
Publications	Erkilic N et al. Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophy. Stem cell research. 2019 Jul;38:101478. Erkilic N et al. A Novel Chromosomal Translocation Identified due to Complex Genetic Instability in iPSC Generated for Choroideremia. Cells. 2019 Sep 11;8(9). Diakatou M et al. Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3. International journal of molecular sciences. 2021 Mar 5;22(5). Pushp P et al. A Concise Review on Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Personalized Regenerative Medicine. Stem cell reviews and reports. 2021 Jun;17(3):748-776. Cui H et al. Various phenotypes of autosomal dominant cone-rod dystrophy with cone-rod homeobox mutation in two Chinese families. International journal of ophthalmology. 2022;15(12):1915-1923. Chien Y et al. Nanoparticles-mediated CRISPR-Cas9 gene therapy in inherited retinal diseases: applications, challenges, and emerging opportunities. Journal of nanobiotechnology. 2022 Dec 3;20(1):511.

hIPSC Derivation

General