These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
8. Cardiolipin metabolism and the role it plays in heart failure and mitochondrial supercomplex formation. Mejia EM; Cole LK; Hatch GM Cardiovasc Hematol Disord Drug Targets; 2014; 14(2):98-106. PubMed ID: 24801725 [TBL] [Abstract][Full Text] [Related]
9. Mitochondria-targeted antioxidant prevents cardiac dysfunction induced by tafazzin gene knockdown in cardiac myocytes. He Q; Harris N; Ren J; Han X Oxid Med Cell Longev; 2014; 2014():654198. PubMed ID: 25247053 [TBL] [Abstract][Full Text] [Related]
11. Overexpression of mitochondrial oxodicarboxylate carrier (ODC1) preserves oxidative phosphorylation in a yeast model of Barth syndrome. de Taffin de Tilques M; Tribouillard-Tanvier D; Tétaud E; Testet E; di Rago JP; Lasserre JP Dis Model Mech; 2017 Apr; 10(4):439-450. PubMed ID: 28188263 [TBL] [Abstract][Full Text] [Related]
13. The Function of Tafazzin, a Mitochondrial Phospholipid-Lysophospholipid Acyltransferase. Schlame M; Xu Y J Mol Biol; 2020 Aug; 432(18):5043-5051. PubMed ID: 32234310 [TBL] [Abstract][Full Text] [Related]
14. Cardiolipin deficiency in Barth syndrome is not associated with increased superoxide/H Goncalves RLS; Schlame M; Bartelt A; Brand MD; Hotamışlıgil GS FEBS Lett; 2021 Feb; 595(3):415-432. PubMed ID: 33112430 [TBL] [Abstract][Full Text] [Related]
15. SS-31 treatment ameliorates cardiac mitochondrial morphology and defective mitophagy in a murine model of Barth syndrome. Russo S; De Rasmo D; Rossi R; Signorile A; Lobasso S Sci Rep; 2024 Jun; 14(1):13655. PubMed ID: 38871974 [TBL] [Abstract][Full Text] [Related]
16. Cardiolipin remodeling by TAZ/tafazzin is selectively required for the initiation of mitophagy. Hsu P; Liu X; Zhang J; Wang HG; Ye JM; Shi Y Autophagy; 2015 Apr; 11(4):643-52. PubMed ID: 25919711 [TBL] [Abstract][Full Text] [Related]
17. Cardiolipin metabolism and its causal role in the etiology of the inherited cardiomyopathy Barth syndrome. Gaspard GJ; McMaster CR Chem Phys Lipids; 2015 Dec; 193():1-10. PubMed ID: 26415690 [TBL] [Abstract][Full Text] [Related]
18. Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients. McKenzie M; Lazarou M; Thorburn DR; Ryan MT J Mol Biol; 2006 Aug; 361(3):462-9. PubMed ID: 16857210 [TBL] [Abstract][Full Text] [Related]
19. Substantial Decrease in Plasmalogen in the Heart Associated with Tafazzin Deficiency. Kimura T; Kimura AK; Ren M; Berno B; Xu Y; Schlame M; Epand RM Biochemistry; 2018 Apr; 57(14):2162-2175. PubMed ID: 29557170 [TBL] [Abstract][Full Text] [Related]
20. Dysfunctional cardiac mitochondrial bioenergetic, lipidomic, and signaling in a murine model of Barth syndrome. Kiebish MA; Yang K; Liu X; Mancuso DJ; Guan S; Zhao Z; Sims HF; Cerqua R; Cade WT; Han X; Gross RW J Lipid Res; 2013 May; 54(5):1312-25. PubMed ID: 23410936 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]