INMi005-A

Registration Summary:

A P E C

USH2A-RP-2-iPSC

The cell line is not submitted yet.

(only basic data is shown)

General

Cell Line
hPSCreg name	INMi005-A
Cite as:	INMi005-A (RRID:CVCL_B7MC)
Alternative name(s)	USH2A-RP-2-iPSC
Cell line type	Human induced pluripotent stem cell (hiPSC)
Similar lines	No similar lines found.
Last update	27th October 2021
User feedback	Written by on No feedback available yet. Login to share your feedback, experiences or results with the research community.
Provider
Generator	Institute for Neurosciences of Montpellier (INM)
External Databases
Cellosaurus	CVCL_B7MC
Wikidata	Q112929865
General Information
Publications	Sanjurjo-Soriano C et al. Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosa. Stem cell research. 2022 Apr;60:102738. Zaw K et al. Pathogenesis and Treatment of Usher Syndrome Type IIA. Asia-Pacific journal of ophthalmology (Philadelphia, Pa.). 2022 Jul-Aug 01;11(4):369-379. Sanjurjo-Soriano Carla et al. USH2A variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids. Human Genetics and Genomics Advances. 2023-10-00. Chen Yi et al. The occurrence and development of induced pluripotent stem cells. Frontiers in Genetics. 2024-04-18.

hIPSC Derivation

General