IISHDOi004-A

Registration Summary:

A P E C

RPAB16-FiPS4F3

The cell line is not submitted yet.

(only basic data is shown)

General

iPSC Line
hPSCreg name	IISHDOi004-A
Cite as:	IISHDOi004-A (RRID:CVCL_VN42)
Alternative name(s)	RPAB16-FiPS4F3
iPSC line type	Human induced pluripotent stem cell (hiPSC)
Similar iPSC lines	No similar lines found.
Last update	9th May 2018
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Provider
Generator	Instituto de Investigación Sanitaria Hospital 12 de Octubre, i+12 (IISHDO)
External iPSC Databases
Cellosaurus	CVCL_VN42
Wikidata	Q94315429
General iPSC Information
Publications	Zurita-Díaz F et al. Establishment of a human iPSC line, IISHDOi004-A, from a patient with Usher syndrome associated with the mutation c.2276G>T; p.Cys759Phe in the USH2A gene. Stem cell research. 2018 Aug;31:152-156. Liu X et al. Generation and Genetic Correction of USH2A c.2299delG Mutation in Patient-Derived Induced Pluripotent Stem Cells. Genes. 2021 May 25;12(6). 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. Ladero Miguel et al. Hereditary Optic Neuropathies: A Systematic Review on the Interplay between Biomaterials and Induced Pluripotent Stem Cells. Bioengineering. 2024-01-03. Leith Fiona K. et al. Current approaches for Usher syndrome disease models and developing therapies. Frontiers in Cell and Developmental Biology. 2025-06-20.

iPSC Derivation

General