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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 17241629)

  • 21. Gonadal mosaicism of a TAZ (G4.5) mutation in a Japanese family with Barth syndrome and left ventricular noncompaction.
    Chang B; Momoi N; Shan L; Mitomo M; Aoyagi Y; Endo K; Takeda I; Chen R; Xing Y; Yu X; Watanabe S; Yoshida T; Kanegane H; Tsubata S; Bowles NE; Ichida F; Miyawaki T;
    Mol Genet Metab; 2010 Jun; 100(2):198-203. PubMed ID: 20303308
    [TBL] [Abstract][Full Text] [Related]  

  • 22. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update.
    Barth PG; Valianpour F; Bowen VM; Lam J; Duran M; Vaz FM; Wanders RJ
    Am J Med Genet A; 2004 May; 126A(4):349-54. PubMed ID: 15098233
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel TAZ gene mutation and mosaicism in a Polish family with Barth syndrome.
    Zapała B; Płatek T; Wybrańska I
    Ann Hum Genet; 2015 May; 79(3):218-24. PubMed ID: 25776009
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. X-linked fetal cardiomyopathy caused by a novel mutation in the TAZ gene.
    Brady AN; Shehata BM; Fernhoff PM
    Prenat Diagn; 2006 May; 26(5):462-5. PubMed ID: 16548007
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Obstetric outcomes in donor oocyte pregnancies compared with advanced maternal age in in vitro fertilization pregnancies.
    Krieg SA; Henne MB; Westphal LM
    Fertil Steril; 2008 Jul; 90(1):65-70. PubMed ID: 17727845
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. 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]  

  • 30. The 'immunologic theory' of preeclampsia revisited: a lesson from donor oocyte gestations.
    Levron Y; Dviri M; Segol I; Yerushalmi GM; Hourvitz A; Orvieto R; Mazaki-Tovi S; Yinon Y
    Am J Obstet Gynecol; 2014 Oct; 211(4):383.e1-5. PubMed ID: 24657130
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. 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]  

  • 33. Identification of novel mitochondrial localization signals in human Tafazzin, the cause of the inherited cardiomyopathic disorder Barth syndrome.
    Dinca AA; Chien WM; Chin MT
    J Mol Cell Cardiol; 2018 Jan; 114():83-92. PubMed ID: 29129703
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel Alu-mediated Xq28 microdeletion ablates TAZ and partially deletes DNL1L in a patient with Barth syndrome.
    Singh HR; Yang Z; Siddiqui S; Peña LS; Westerfield BH; Fan Y; Towbin JA; Vatta M
    Am J Med Genet A; 2009 May; 149A(5):1082-5. PubMed ID: 19396829
    [No Abstract]   [Full Text] [Related]  

  • 35. Tafazzin splice variants and mutations in Barth syndrome.
    Kirwin SM; Manolakos A; Barnett SS; Gonzalez IL
    Mol Genet Metab; 2014 Jan; 111(1):26-32. PubMed ID: 24342716
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome.
    Ichida F; Tsubata S; Bowles KR; Haneda N; Uese K; Miyawaki T; Dreyer WJ; Messina J; Li H; Bowles NE; Towbin JA
    Circulation; 2001 Mar; 103(9):1256-63. PubMed ID: 11238270
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Differing clinical courses and outcomes in two siblings with Barth syndrome and left ventricular noncompaction.
    Momoi N; Chang B; Takeda I; Aoyagi Y; Endo K; Ichida F
    Eur J Pediatr; 2012 Mar; 171(3):515-20. PubMed ID: 21987083
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Barth syndrome, a human disorder of cardiolipin metabolism.
    Schlame M; Ren M
    FEBS Lett; 2006 Oct; 580(23):5450-5. PubMed ID: 16973164
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Defining functional classes of Barth syndrome mutation in humans.
    Lu YW; Galbraith L; Herndon JD; Lu YL; Pras-Raves M; Vervaart M; Van Kampen A; Luyf A; Koehler CM; McCaffery JM; Gottlieb E; Vaz FM; Claypool SM
    Hum Mol Genet; 2016 May; 25(9):1754-70. PubMed ID: 26908608
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A novel mutation in TAZ causes mitochondrial respiratory chain disorder without cardiomyopathy.
    Borna NN; Kishita Y; Ishikawa K; Nakada K; Hayashi JI; Tokuzawa Y; Kohda M; Nyuzuki H; Yamashita-Sugahara Y; Nasu T; Takeda A; Murayama K; Ohtake A; Okazaki Y
    J Hum Genet; 2017 Apr; 62(5):539-547. PubMed ID: 28123175
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.