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.
28. Only one splice variant of the human TAZ gene encodes a functional protein with a role in cardiolipin metabolism. Vaz FM; Houtkooper RH; Valianpour F; Barth PG; Wanders RJ J Biol Chem; 2003 Oct; 278(44):43089-94. PubMed ID: 12930833 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. A novel mutation of the TAZ gene in Barth syndrome: acute exacerbation after contrast-dye injection. Kim GB; Kwon BS; Bae EJ; Noh CI; Seong MW; Park SS J Korean Med Sci; 2013 May; 28(5):784-7. PubMed ID: 23678274 [TBL] [Abstract][Full Text] [Related]
31. Mutation characterization and genotype-phenotype correlation in Barth syndrome. Johnston J; Kelley RI; Feigenbaum A; Cox GF; Iyer GS; Funanage VL; Proujansky R Am J Hum Genet; 1997 Nov; 61(5):1053-8. PubMed ID: 9345098 [TBL] [Abstract][Full Text] [Related]
32. Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype. Bowron A; Honeychurch J; Williams M; Tsai-Goodman B; Clayton N; Jones L; Shortland GJ; Qureshi SA; Heales SJ; Steward CG J Inherit Metab Dis; 2015 Mar; 38(2):279-86. PubMed ID: 25112388 [TBL] [Abstract][Full Text] [Related]
33. Intra-individual plasticity of the TAZ gene leading to different heritable mutations in siblings with Barth syndrome. Ferri L; Donati MA; Funghini S; Cavicchi C; Pensato V; Gellera C; Natacci F; Spaccini L; Gasperini S; Vaz FM; Cooper DN; Guerrini R; Morrone A Eur J Hum Genet; 2015 Dec; 23(12):1708-12. PubMed ID: 25782672 [TBL] [Abstract][Full Text] [Related]
34. Barth syndrome: an X-linked cardiomyopathy with a novel mutation. Aljishi E; Ali F Indian J Pediatr; 2010 Dec; 77(12):1432-3. PubMed ID: 20981509 [TBL] [Abstract][Full Text] [Related]
35. Delayed appearance of 3-methylglutaconic aciduria in neonates with early onset metabolic cardiomyopathies: A potential pitfall for the diagnosis. Baban A; Adorisio R; Corica B; Rizzo C; Calì F; Semeraro M; Taurisano R; Magliozzi M; Carrozzo R; Parisi F; Dallapiccola B; Vaz FM; Drago F; Dionisi-Vici C Am J Med Genet A; 2020 Jan; 182(1):64-70. PubMed ID: 31729175 [TBL] [Abstract][Full Text] [Related]
36. AAV Gene Therapy Prevents and Reverses Heart Failure in a Murine Knockout Model of Barth Syndrome. Wang S; Li Y; Xu Y; Ma Q; Lin Z; Schlame M; Bezzerides VJ; Strathdee D; Pu WT Circ Res; 2020 Apr; 126(8):1024-1039. PubMed ID: 32146862 [TBL] [Abstract][Full Text] [Related]