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IISHDOi004-A
Registration Summary
:
A
P
E
C
RPAB16-FiPS4F3
The cell line is
not submitted
yet.
(only basic data is shown)
General
Cell Line
hPSCreg name
IISHDOi004-A
Cite as:
When citing this cell line, please use the hPSCreg name (see
Naming Tool
) and the corresponding Research Resource ID (RRID).
IISHDOi004-A (RRID:CVCL_VN42)
Alternative name(s)
RPAB16-FiPS4F3
Cell line type
Human induced pluripotent stem cell (hiPSC)
Similar 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 Databases
Cellosaurus
CVCL_VN42
Wikidata
Q94315429
General 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.
hIPSC Derivation
General
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