IISHDOi001-A

Registration Summary:

A P E C

MA5622-FiPS4F1

The cell line is not submitted yet.

(only basic data is shown)

General

Cell Line
hPSCreg name	IISHDOi001-A
Cite as:	IISHDOi001-A (RRID:CVCL_QX71)
Alternative name(s)	MA5622-FiPS4F1
Cell line type	Human induced pluripotent stem cell (hiPSC)
Similar lines	No similar lines found.
Last update	10th July 2017
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Provider
Generator	Instituto de Investigación Sanitaria Hospital 12 de Octubre, i+12 (IISHDO)
External Databases
Cellosaurus	CVCL_QX71
Wikidata	Q54897442
General Information
Publications	Ortuño-Costela MDC et al. Establishment of a human iPSC line (IISHDOi001-A) from a patient with McArdle disease. Stem cell research. 2017 Aug;23:188-192. Del Carmen Ortuño-Costela M et al. iPSCs: A powerful tool for skeletal muscle tissue engineering. Journal of cellular and molecular medicine. 2019 Jun;23(6):3784-3794. Hu T et al. Insight into cellular dedifferentiation in regenerative medicine. Science China. Life sciences. 2020 Feb;63(2):301-304. Ortuño-Costela MDC et al. Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology. International journal of molecular sciences. 2022 Nov 12;23(22). Ladero Miguel et al. Hereditary Optic Neuropathies: A Systematic Review on the Interplay between Biomaterials and Induced Pluripotent Stem Cells. Bioengineering. 2024-01-03. García-López Marta et al. Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861C>T (p.Gln621Ter) in the OPA1 Gene. International Journal of Molecular Sciences. 2024-06-30.

hIPSC Derivation

General