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pcDNA3.1-hFrataxin-HA Citations (3)

Originally described in: Mitochondrial frataxin interacts with ISD11 of the NFS1/ISCU complex and multiple mitochondrial chaperones.
Shan Y, Napoli E, Cortopassi G Hum Mol Genet. 2007 Apr 15;16(8):929-41. Epub 2007 Mar 1. PubMed Journal

Articles Citing pcDNA3.1-hFrataxin-HA

Articles
Selected missense mutations impair frataxin processing in Friedreich ataxia. Clark E, Butler JS, Isaacs CJ, Napierala M, Lynch DR. Ann Clin Transl Neurol. 2017 Jun 29;4(8):575-584. doi: 10.1002/acn3.433. eCollection 2017 Aug. PubMed
Identification of a novel missense mutation in Friedreich's ataxia -FXN(W) (168R). Clark E, Strawser C, Schadt K, Lynch DR. Ann Clin Transl Neurol. 2019 Feb 21;6(4):812-816. doi: 10.1002/acn3.728. eCollection 2019 Apr. PubMed
Frataxin deficiency alters gene expression in Friedreich ataxia derived IPSC-neurons and cardiomyocytes. Angulo MB, Bertalovitz A, Argenziano MA, Yang J, Patel A, Zesiewicz T, McDonald TV. Mol Genet Genomic Med. 2023 Jan;11(1):e2093. doi: 10.1002/mgg3.2093. Epub 2022 Nov 11. PubMed

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