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Journal Abstract Search

294 related items for PubMed ID: 24316278

  • 1. Defining the impact on yeast ATP synthase of two pathogenic human mitochondrial DNA mutations, T9185C and T9191C.
    Kabala AM, Lasserre JP, Ackerman SH, di Rago JP, Kucharczyk R.
    Biochimie; 2014 May; 100():200-6. PubMed ID: 24316278
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  • 2. A yeast model of the neurogenic ataxia retinitis pigmentosa (NARP) T8993G mutation in the mitochondrial ATP synthase-6 gene.
    Rak M, Tetaud E, Duvezin-Caubet S, Ezkurdia N, Bietenhader M, Rytka J, di Rago JP.
    J Biol Chem; 2007 Nov 23; 282(47):34039-47. PubMed ID: 17855363
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  • 4. Biochemical consequences in yeast of the human mitochondrial DNA 8993T>C mutation in the ATPase6 gene found in NARP/MILS patients.
    Kucharczyk R, Rak M, di Rago JP.
    Biochim Biophys Acta; 2009 May 23; 1793(5):817-24. PubMed ID: 19269308
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  • 7. [Molecular bases of diseases caused by mutations in genes encoding subunits of ATP synthase].
    Baranowska E, Rytka J, Kucharczyk R.
    Postepy Biochem; 2018 Dec 29; 64(4):304-317. PubMed ID: 30656915
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  • 8. ATP Synthase Subunit a Supports Permeability Transition in Yeast Lacking Dimerization Subunits and Modulates yPTP Conductance.
    Niedzwiecka K, Baranowska E, Panja C, Kucharczyk R.
    Cell Physiol Biochem; 2020 Feb 27; 54(2):211-229. PubMed ID: 32100973
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  • 9. Functional investigation of an universally conserved leucine residue in subunit a of ATP synthase targeted by the pathogenic m.9176 T>G mutation.
    Kucharczyk R, Dautant A, Godard F, Tribouillard-Tanvier D, di Rago JP.
    Biochim Biophys Acta Bioenerg; 2019 Jan 27; 1860(1):52-59. PubMed ID: 30414414
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  • 10. Deregulating mitochondrial metabolite and ion transport has beneficial effects in yeast and human cellular models for NARP syndrome.
    Su X, Rak M, Tetaud E, Godard F, Sardin E, Bouhier M, Gombeau K, Caetano-Anollés D, Salin B, Chen H, di Rago JP, Tribouillard-Tanvier D.
    Hum Mol Genet; 2019 Nov 15; 28(22):3792-3804. PubMed ID: 31276579
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  • 11. Yeast cells lacking the mitochondrial gene encoding the ATP synthase subunit 6 exhibit a selective loss of complex IV and unusual mitochondrial morphology.
    Rak M, Tetaud E, Godard F, Sagot I, Salin B, Duvezin-Caubet S, Slonimski PP, Rytka J, di Rago JP.
    J Biol Chem; 2007 Apr 13; 282(15):10853-64. PubMed ID: 17261589
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  • 13. Yeast models of mutations in the mitochondrial ATP6 gene found in human cancer cells.
    Niedzwiecka K, Kabala AM, Lasserre JP, Tribouillard-Tanvier D, Golik P, Dautant A, di Rago JP, Kucharczyk R.
    Mitochondrion; 2016 Jul 13; 29():7-17. PubMed ID: 27083309
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  • 14. Yeast cells depleted in Atp14p fail to assemble Atp6p within the ATP synthase and exhibit altered mitochondrial cristae morphology.
    Goyon V, Fronzes R, Salin B, di-Rago JP, Velours J, Brèthes D.
    J Biol Chem; 2008 Apr 11; 283(15):9749-58. PubMed ID: 18252710
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  • 17. The pathogenic m.8993 T > G mutation in mitochondrial ATP6 gene prevents proton release from the subunit c-ring rotor of ATP synthase.
    Su X, Dautant A, Rak M, Godard F, Ezkurdia N, Bouhier M, Bietenhader M, Mueller DM, Kucharczyk R, di Rago JP, Tribouillard-Tanvier D.
    Hum Mol Genet; 2021 Apr 27; 30(5):381-392. PubMed ID: 33600551
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  • 18. Pathogenesis of primary defects in mitochondrial ATP synthesis.
    Schon EA, Santra S, Pallotti F, Girvin ME.
    Semin Cell Dev Biol; 2001 Dec 27; 12(6):441-8. PubMed ID: 11735378
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  • 19. Role of gamma-subunit N- and C-termini in assembly of the mitochondrial ATP synthase in yeast.
    Dian EA, Papatheodorou P, Emmrich K, Randel O, Geissler A, Kölling R, Rassow J, Motz C.
    J Mol Biol; 2008 Apr 11; 377(5):1314-23. PubMed ID: 18328502
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  • 20. ATP6 homoplasmic mutations inhibit and destabilize the human F1F0-ATP synthase without preventing enzyme assembly and oligomerization.
    Cortés-Hernández P, Vázquez-Memije ME, García JJ.
    J Biol Chem; 2007 Jan 12; 282(2):1051-8. PubMed ID: 17121862
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