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Journal Abstract Search

436 related items for PubMed ID: 19962311

  • 1. Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndrome.
    Gebert N, Joshi AS, Kutik S, Becker T, McKenzie M, Guan XL, Mooga VP, Stroud DA, Kulkarni G, Wenk MR, Rehling P, Meisinger C, Ryan MT, Wiedemann N, Greenberg ML, Pfanner N.
    Curr Biol; 2009 Dec 29; 19(24):2133-9. PubMed ID: 19962311
    [Abstract] [Full Text] [Related]

  • 2. Cardiolipin remodeling in Barth syndrome and other hereditary cardiomyopathies.
    Bertero E, Kutschka I, Maack C, Dudek J.
    Biochim Biophys Acta Mol Basis Dis; 2020 Aug 01; 1866(8):165803. PubMed ID: 32348916
    [Abstract] [Full Text] [Related]

  • 3. Mechano-energetic aspects of Barth syndrome.
    Dudek J, Maack C.
    J Inherit Metab Dis; 2022 Jan 01; 45(1):82-98. PubMed ID: 34423473
    [Abstract] [Full Text] [Related]

  • 4. Cardiolipin function in the yeast S. cerevisiae and the lessons learned for Barth syndrome.
    Ji J, Greenberg ML.
    J Inherit Metab Dis; 2022 Jan 01; 45(1):60-71. PubMed ID: 34626131
    [Abstract] [Full Text] [Related]

  • 5. A simple mechanistic explanation for Barth syndrome and cardiolipin remodeling.
    Xu Y, Phoon CKL, Ren M, Schlame M.
    J Inherit Metab Dis; 2022 Jan 01; 45(1):51-59. PubMed ID: 34611930
    [Abstract] [Full Text] [Related]

  • 6. Experimental models of Barth syndrome.
    Pu WT.
    J Inherit Metab Dis; 2022 Jan 01; 45(1):72-81. PubMed ID: 34370877
    [Abstract] [Full Text] [Related]

  • 7. Barth syndrome: cellular compensation of mitochondrial dysfunction and apoptosis inhibition due to changes in cardiolipin remodeling linked to tafazzin (TAZ) gene mutation.
    Gonzalvez F, D'Aurelio M, Boutant M, Moustapha A, Puech JP, Landes T, Arnauné-Pelloquin L, Vial G, Taleux N, Slomianny C, Wanders RJ, Houtkooper RH, Bellenguer P, Møller IM, Gottlieb E, Vaz FM, Manfredi G, Petit PX.
    Biochim Biophys Acta; 2013 Aug 01; 1832(8):1194-206. PubMed ID: 23523468
    [Abstract] [Full Text] [Related]

  • 8. Cardiolipin metabolism and its causal role in the etiology of the inherited cardiomyopathy Barth syndrome.
    Gaspard GJ, McMaster CR.
    Chem Phys Lipids; 2015 Dec 01; 193():1-10. PubMed ID: 26415690
    [Abstract] [Full Text] [Related]

  • 9. Unremodeled and remodeled cardiolipin are functionally indistinguishable in yeast.
    Baile MG, Sathappa M, Lu YW, Pryce E, Whited K, McCaffery JM, Han X, Alder NN, Claypool SM.
    J Biol Chem; 2014 Jan 17; 289(3):1768-78. PubMed ID: 24285538
    [Abstract] [Full Text] [Related]

  • 10. Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients.
    McKenzie M, Lazarou M, Thorburn DR, Ryan MT.
    J Mol Biol; 2006 Aug 18; 361(3):462-9. PubMed ID: 16857210
    [Abstract] [Full Text] [Related]

  • 11. Cardiolipin-deficient cells have decreased levels of the iron-sulfur biogenesis protein frataxin.
    Li Y, Lou W, Grevel A, Böttinger L, Liang Z, Ji J, Patil VA, Liu J, Ye C, Hüttemann M, Becker T, Greenberg ML.
    J Biol Chem; 2020 Aug 14; 295(33):11928-11937. PubMed ID: 32636300
    [Abstract] [Full Text] [Related]

  • 12. An essential role for cardiolipin in the stability and function of the mitochondrial calcium uniporter.
    Ghosh S, Basu Ball W, Madaris TR, Srikantan S, Madesh M, Mootha VK, Gohil VM.
    Proc Natl Acad Sci U S A; 2020 Jul 14; 117(28):16383-16390. PubMed ID: 32601238
    [Abstract] [Full Text] [Related]

  • 13. Role of Cardiolipin in Mitochondrial Function and Dynamics in Health and Disease: Molecular and Pharmacological Aspects.
    Paradies G, Paradies V, Ruggiero FM, Petrosillo G.
    Cells; 2019 Jul 16; 8(7):. PubMed ID: 31315173
    [Abstract] [Full Text] [Related]

  • 14. Cardiolipin deficiency leads to the destabilization of mitochondrial magnesium channel MRS2 in Barth syndrome.
    Joshi A, Gohil VM.
    Hum Mol Genet; 2023 Dec 01; 32(24):3353-3360. PubMed ID: 37721533
    [Abstract] [Full Text] [Related]

  • 15. Taz1, an outer mitochondrial membrane protein, affects stability and assembly of inner membrane protein complexes: implications for Barth Syndrome.
    Brandner K, Mick DU, Frazier AE, Taylor RD, Meisinger C, Rehling P.
    Mol Biol Cell; 2005 Nov 01; 16(11):5202-14. PubMed ID: 16135531
    [Abstract] [Full Text] [Related]

  • 16. Cardiolipin remodeling: a regulatory hub for modulating cardiolipin metabolism and function.
    Ye C, Shen Z, Greenberg ML.
    J Bioenerg Biomembr; 2016 Apr 01; 48(2):113-23. PubMed ID: 25432572
    [Abstract] [Full Text] [Related]

  • 17. Barth Syndrome: Connecting Cardiolipin to Cardiomyopathy.
    Ikon N, Ryan RO.
    Lipids; 2017 Feb 01; 52(2):99-108. PubMed ID: 28070695
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 10(4):439-450. PubMed ID: 28188263
    [Abstract] [Full Text] [Related]

  • 19. Clinical presentation and natural history of Barth Syndrome: An overview.
    Taylor C, Rao ES, Pierre G, Chronopoulou E, Hornby B, Heyman A, Vernon HJ.
    J Inherit Metab Dis; 2022 Jan 01; 45(1):7-16. PubMed ID: 34355402
    [Abstract] [Full Text] [Related]

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