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 *

430 related articles for article (PubMed ID: 23523468)

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

  • 22. New C-Terminal Conserved Regions of Tafazzin, a Catalyst of Cardiolipin Remodeling.
    Shilovsky GA; Zverkov OA; Seliverstov AV; Ashapkin VV; Putyatina TS; Rubanov LI; Lyubetsky VA
    Oxid Med Cell Longev; 2019; 2019():2901057. PubMed ID: 31781330
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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; 1866(8):165803. PubMed ID: 32348916
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cardiolipin provides an essential activating platform for caspase-8 on mitochondria.
    Gonzalvez F; Schug ZT; Houtkooper RH; MacKenzie ED; Brooks DG; Wanders RJ; Petit PX; Vaz FM; Gottlieb E
    J Cell Biol; 2008 Nov; 183(4):681-96. PubMed ID: 19001123
    [TBL] [Abstract][Full Text] [Related]  

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

  • 26. 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; 295(33):11928-11937. PubMed ID: 32636300
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Barth syndrome in a female patient.
    Cosson L; Toutain A; Simard G; Kulik W; Matyas G; Guichet A; Blasco H; Maakaroun-Vermesse Z; Vaillant MC; Le Caignec C; Chantepie A; Labarthe F
    Mol Genet Metab; 2012 May; 106(1):115-20. PubMed ID: 22410210
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. N-oleoylethanolamide treatment of lymphoblasts deficient in Tafazzin improves cell growth and mitochondrial morphology and dynamics.
    Chan JZ; Fernandes MF; Steckel KE; Bradley RM; Hashemi A; Groh MR; Sciaini G; Stark KD; Duncan RE
    Sci Rep; 2022 Jun; 12(1):9466. PubMed ID: 35676289
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Aberrant cardiolipin metabolism is associated with cognitive deficiency and hippocampal alteration in tafazzin knockdown mice.
    Cole LK; Kim JH; Amoscato AA; Tyurina YY; Bay R H; Karimi B; Siddiqui TJ; Kagan VE; Hatch GM; Kauppinen TM
    Biochim Biophys Acta Mol Basis Dis; 2018 Oct; 1864(10):3353-3367. PubMed ID: 30055293
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The lipid environment modulates cardiolipin and phospholipid constitution in wild type and tafazzin-deficient cells.
    Oemer G; Koch J; Wohlfarter Y; Lackner K; Gebert REM; Geley S; Zschocke J; Keller MA
    J Inherit Metab Dis; 2022 Jan; 45(1):38-50. PubMed ID: 34494285
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Blocking phosphatidylglycerol degradation in yeast defective in cardiolipin remodeling results in a new model of the Barth syndrome cellular phenotype.
    Káňovičová P; Čermáková P; Kubalová D; Bábelová L; Veselá P; Valachovič M; Zahumenský J; Horváth A; Malínský J; Balážová M
    J Biol Chem; 2022 Jan; 298(1):101462. PubMed ID: 34864056
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Cardiac mitochondrial structure and function in tafazzin-knockdown mice.
    Kim J; Lee K; Fujioka H; Tandler B; Hoppel CL
    Mitochondrion; 2018 Nov; 43():53-62. PubMed ID: 30389594
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Deletion of the cardiolipin-specific phospholipase Cld1 rescues growth and life span defects in the tafazzin mutant: implications for Barth syndrome.
    Ye C; Lou W; Li Y; Chatzispyrou IA; Hüttemann M; Lee I; Houtkooper RH; Vaz FM; Chen S; Greenberg ML
    J Biol Chem; 2014 Feb; 289(6):3114-25. PubMed ID: 24318983
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Long-chain fatty acid oxidation and respiratory complex I deficiencies distinguish Barth Syndrome from idiopathic pediatric cardiomyopathy.
    Chatfield KC; Sparagna GC; Specht KS; Whitcomb LA; Omar AK; Miyamoto SD; Wolfe LM; Chicco AJ
    J Inherit Metab Dis; 2022 Jan; 45(1):111-124. PubMed ID: 34821394
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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; 289(3):1768-78. PubMed ID: 24285538
    [TBL] [Abstract][Full Text] [Related]  

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

  • 39. 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]  

  • 40. 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; 45(1):7-16. PubMed ID: 34355402
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 22.