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.
23. Complex expression pattern of the Barth syndrome gene product tafazzin in human cell lines and murine tissues. Lu B; Kelher MR; Lee DP; Lewin TM; Coleman RA; Choy PC; Hatch GM Biochem Cell Biol; 2004 Oct; 82(5):569-76. PubMed ID: 15499385 [TBL] [Abstract][Full Text] [Related]
24. Structural and functional analyses of Barth syndrome-causing mutations and alternative splicing in the tafazzin acyltransferase domain. Hijikata A; Yura K; Ohara O; Go M Meta Gene; 2015 Jun; 4():92-106. PubMed ID: 25941633 [TBL] [Abstract][Full Text] [Related]
25. Increased mtDNA Abundance and Improved Function in Human Barth Syndrome Patient Fibroblasts Following AAV- Suzuki-Hatano S; Sriramvenugopal M; Ramanathan M; Soustek M; Byrne BJ; Cade WT; Kang PB; Pacak CA Int J Mol Sci; 2019 Jul; 20(14):. PubMed ID: 31336787 [TBL] [Abstract][Full Text] [Related]
27. 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]
28. A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth Syndrome. Fan Y; Steller J; Gonzalez IL; Kulik W; Fox M; Chang R; Westerfield BA; Batra AS; Wang RY; Gallant NM; Pena LS; Wang H; Huang T; Bhuta S; Penny DJ; McCabe ER; Kimonis VE JIMD Rep; 2013; 11():99-106. PubMed ID: 23606313 [TBL] [Abstract][Full Text] [Related]
29. BARTH SYNDROME IN MALE AND FEMALE SIBLINGS CAUSED BY A NOVEL MUTATION IN THE TAZ GENE. Avdjieva-Tzavella DM; Todorova AP; Kathom H M ; Ivanova MB; Yordanova IT; Todorov TP; Litvinenko IO; Dasheva-Dimitrova AT; Tincheva RS Genet Couns; 2016; 27(4):495-501. PubMed ID: 30226969 [TBL] [Abstract][Full Text] [Related]
35. Seven functional classes of Barth syndrome mutation. Whited K; Baile MG; Currier P; Claypool SM Hum Mol Genet; 2013 Feb; 22(3):483-92. PubMed ID: 23100323 [TBL] [Abstract][Full Text] [Related]
36. A Drosophila model of Barth syndrome. Xu Y; Condell M; Plesken H; Edelman-Novemsky I; Ma J; Ren M; Schlame M Proc Natl Acad Sci U S A; 2006 Aug; 103(31):11584-8. PubMed ID: 16855048 [TBL] [Abstract][Full Text] [Related]
37. 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]
38. Identification of TAZ mutations in pediatric patients with cardiomyopathy by targeted next-generation sequencing in a Chinese cohort. Wang J; Guo Y; Huang M; Zhang Z; Zhu J; Liu T; Shi L; Li F; Huang H; Fu L Orphanet J Rare Dis; 2017 Feb; 12(1):26. PubMed ID: 28183324 [TBL] [Abstract][Full Text] [Related]
39. AAV-Mediated TAZ Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome. Suzuki-Hatano S; Saha M; Rizzo SA; Witko RL; Gosiker BJ; Ramanathan M; Soustek MS; Jones MD; Kang PB; Byrne BJ; Cade WT; Pacak CA Hum Gene Ther; 2019 Feb; 30(2):139-154. PubMed ID: 30070157 [TBL] [Abstract][Full Text] [Related]
40. TAZ encodes tafazzin, a transacylase essential for cardiolipin formation and central to the etiology of Barth syndrome. Garlid AO; Schaffer CT; Kim J; Bhatt H; Guevara-Gonzalez V; Ping P Gene; 2020 Feb; 726():144148. PubMed ID: 31647997 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]