FINCBi002-A

Registration Summary:

A P E C

mt8742#118

The cell line is not submitted yet.

(only basic data is shown)

General

Cell Line
hPSCreg name	FINCBi002-A
Cite as:	FINCBi002-A (RRID:CVCL_A4XD)
Alternative name(s)	mt8742#118
Cell line type	Human induced pluripotent stem cell (hiPSC)
Similar lines	No similar lines found.
Last update	15th October 2020
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Provider
Generator	Fondazione IRCCS Istituto Neurologico C. Besta (FINCB)
Owner	Fondazione IRCCS Istituto Neurologico C. Besta (FINCB)
Distributors	Fondazione IRCCS Istituto Neurologico C. Besta (FINCB)
External Databases
Cellosaurus	CVCL_A4XD
Wikidata	Q107115013
General Information
Publications	Peron C et al. Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives. Frontiers in neurology. 2021;12:648916. Peron C et al. Generation of two human iPSC lines, FINCBi002-A and FINCBi003-A, carrying heteroplasmic macrodeletion of mitochondrial DNA causing Pearson's syndrome. Stem cell research. 2021 Jan 4;50:102151. McKnight CL et al. Modelling Mitochondrial Disease in Human Pluripotent Stem Cells: What Have We Learned?. International journal of molecular sciences. 2021 Jul 20;22(14). Hernández-Ainsa C et al. Development and characterization of cell models harbouring mtDNA deletions for in vitro study of Pearson syndrome. Disease models & mechanisms. 2022 Mar 1;15(3). Tolle I et al. Modeling mitochondrial DNA diseases: from base editing to pluripotent stem-cell-derived organoids. EMBO reports. 2023 Apr 5;24(4):e55678.
* Is the cell line readily obtainable for third parties?	Yes Research use: allowed Clinical use: allowed Commercial use: not allowed

hIPSC Derivation

General