Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Robbie L. Conley"'
Autor:
Daniel Fil, Robbie L. Conley, Aamir R. Zuberi, Cathleen M. Lutz, Terry Gemelli, Marek Napierala, Jill S. Napierala
Publikováno v:
Neurobiology of Disease, Vol 177, Iss , Pp 105996- (2023)
Friedreich's ataxia (FRDA) is a neurodegenerative disease caused by reduced expression of the mitochondrial protein frataxin (FXN). Most FRDA patients are homozygous for large expansions of GAA repeats in intron 1 of FXN, while some are compound hete
Externí odkaz:
https://doaj.org/article/27a0bb7b0e1b457a91ff01f2e3b6068c
Autor:
Gobinath Shanmugam, Madhusudhanan Narasimhan, Robbie L. Conley, Thiagarajan Sairam, Ashutosh Kumar, Ronald P. Mason, Ramalingam Sankaran, John R. Hoidal, Namakkal S. Rajasekaran
Publikováno v:
Frontiers in Physiology, Vol 8 (2017)
Nuclear factor erythroid 2 related factor 2 (Nrf2) signaling maintains the redox homeostasis and its activation is shown to suppress cardiac maladaptation. Earlier we reported that acute endurance exercise (2 days) evoked antioxidant cytoprotection i
Externí odkaz:
https://doaj.org/article/11e39344db80426d982f74f6513c2585
Autor:
Victor M. Darley-Usmar, Daniel Fil, Xiaosen Ouyang, Jianhua Zhang, Jill S. Napierala, Balu K. Chacko, Marek Napierala, Cathleen M. Lutz, Robbie L. Conley, Aamir Zuberi
Publikováno v:
Disease Models & Mechanisms
article-version (VoR) Version of Record
Disease Models & Mechanisms, Vol 13, Iss 7 (2020)
article-version (VoR) Version of Record
Disease Models & Mechanisms, Vol 13, Iss 7 (2020)
Friedreich's ataxia (FRDA) is an autosomal recessive neurodegenerative disease caused by reduced expression of the mitochondrial protein frataxin (FXN). Most FRDA patients are homozygous for large expansions of GAA repeat sequences in intron 1 of FXN