IISHDOi001-A

Registration Summary:

A P E C

MA5622-FiPS4F1

The cell line is not submitted yet.

(only basic data is shown)

General

iPSC Line
hPSCreg name	IISHDOi001-A
Cite as:	IISHDOi001-A (RRID:CVCL_QX71)
Alternative name(s)	MA5622-FiPS4F1
iPSC line type	Human induced pluripotent stem cell (hiPSC)
Similar iPSC lines	No similar lines found.
Last update	10th July 2017
User feedback	Written by on No feedback available yet. Login to share your feedback, experiences or results with the research community.
Provider
Generator	Instituto de Investigación Sanitaria Hospital 12 de Octubre, i+12 (IISHDO)
External iPSC Databases
Cellosaurus	CVCL_QX71
Wikidata	Q54897442
General iPSC 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 M 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 Jun 30;25(13).

iPSC Derivation

General