Tribouillard-Tanvier D - Search Results

1

ATP Synthase Diseases of Mitochondrial Genetic Origin.

Dautant A, Meier T, Hahn A, Tribouillard-Tanvier D, di Rago JP, Kucharczyk R. Dautant A, et al. Front Physiol. 2018 Apr 4;9:329. doi: 10.3389/fphys.2018.00329. eCollection 2018. Front Physiol. 2018. PMID: 29670542 Free PMC article. Review.

2

Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies.

Lasserre JP, Dautant A, Aiyar RS, Kucharczyk R, Glatigny A, Tribouillard-Tanvier D, Rytka J, Blondel M, Skoczen N, Reynier P, Pitayu L, Rötig A, Delahodde A, Steinmetz LM, Dujardin G, Procaccio V, di Rago JP. Lasserre JP, et al. Dis Model Mech. 2015 Jun;8(6):509-26. doi: 10.1242/dmm.020438. Dis Model Mech. 2015. PMID: 26035862 Free PMC article. Review.

3

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. Niedzwiecka K, et al. Mitochondrion. 2016 Jul;29:7-17. doi: 10.1016/j.mito.2016.04.003. Epub 2016 Apr 12. Mitochondrion. 2016. PMID: 27083309

4

Identification of G8969>A in mitochondrial ATP6 gene that severely compromises ATP synthase function in a patient with IgA nephropathy.

Wen S, Niedzwiecka K, Zhao W, Xu S, Liang S, Zhu X, Xie H, Tribouillard-Tanvier D, Giraud MF, Zeng C, Dautant A, Kucharczyk R, Liu Z, di Rago JP, Chen H. Wen S, et al. Sci Rep. 2016 Nov 4;6:36313. doi: 10.1038/srep36313. Sci Rep. 2016. PMID: 27812026 Free PMC article.

5

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. de Taffin de Tilques M, et al. Dis Model Mech. 2017 Apr 1;10(4):439-450. doi: 10.1242/dmm.027540. Epub 2017 Feb 10. Dis Model Mech. 2017. PMID: 28188263 Free PMC article.

6

Molecular basis of diseases caused by the mtDNA mutation m.8969G>A in the subunit a of ATP synthase.

Skoczeń N, Dautant A, Binko K, Godard F, Bouhier M, Su X, Lasserre JP, Giraud MF, Tribouillard-Tanvier D, Chen H, di Rago JP, Kucharczyk R. Skoczeń N, et al. Biochim Biophys Acta Bioenerg. 2018 Aug;1859(8):602-611. doi: 10.1016/j.bbabio.2018.05.009. Epub 2018 May 18. Biochim Biophys Acta Bioenerg. 2018. PMID: 29778688 Free article.

7

Decreasing cytosolic translation is beneficial to yeast and human Tafazzin-deficient cells.

de Taffin de Tilques M, Lasserre JP, Godard F, Sardin E, Bouhier M, Le Guedard M, Kucharczyk R, Petit PX, Testet E, di Rago JP, Tribouillard-Tanvier D. de Taffin de Tilques M, et al. Microb Cell. 2018 Feb 18;5(5):220-232. doi: 10.15698/mic2018.05.629. Microb Cell. 2018. PMID: 29796387 Free PMC article.

8

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. Kucharczyk R, et al. Biochim Biophys Acta Bioenerg. 2019 Jan;1860(1):52-59. doi: 10.1016/j.bbabio.2018.11.005. Epub 2018 Nov 7. Biochim Biophys Acta Bioenerg. 2019. PMID: 30414414 Free article.

9

The pathogenic MT-ATP6 m.8851T>C mutation prevents proton movements within the n-side hydrophilic cleft of the membrane domain of ATP synthase.

Kucharczyk R, Dautant A, Gombeau K, Godard F, Tribouillard-Tanvier D, di Rago JP. Kucharczyk R, et al. Biochim Biophys Acta Bioenerg. 2019 Jul 1;1860(7):562-572. doi: 10.1016/j.bbabio.2019.06.002. Epub 2019 Jun 8. Biochim Biophys Acta Bioenerg. 2019. PMID: 31181185 Free article.

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. Su X, et al. Hum Mol Genet. 2019 Nov 15;28(22):3792-3804. doi: 10.1093/hmg/ddz160. Hum Mol Genet. 2019. PMID: 31276579

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