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
User feedback	Written by on No feedback available yet. Login to share your feedback, experiences or results with the research community.
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. Fasano C et al. Protocol for evaluating mitochondrial respiration in iPSC-derived neurons by the Seahorse XF analyzer. STAR protocols. 2024 Sep 20;5(3):103127.
* Is the cell line readily obtainable for third parties?	Yes Research use: allowed Clinical use: allowed Commercial use: not allowed

hIPSC Derivation

General