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	Pour les 24 documents Envoyer sur ORCID RSS ATOM Exporter BibTeX XML-TEI CSV RTF EndNote PDF HTML Export avancé	Page :	triés par Pertinence Auteur A→Z Auteur Z→A Titre A→Z Titre Z→A Date de publication croissante Date de publication décroissante Date de dépôt croissante Date de dépôt décroissante

		Defining the impact on yeast ATP synthase of two pathogenic human mitochondrial DNA mutations, T9185C and T9191C. Anna Magdalena Kabala , Jean-Paul Lasserre , Sharon H Ackerman , Jean-Paul Di Rago , Roza Kucharczyk Biochimie, 2014, epub ahead of print. ⟨10.1016/j.biochi.2013.11.024⟩ Article dans une revue hal-00940330v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Flavonoids as Potential Drugs for VPS13-Dependent Rare Neurodegenerative Diseases Jean-Paul Di Rago Genes, 2020, 11 (7), pp.828. ⟨10.3390/genes11070828⟩ Article dans une revue hal-03103175v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Regulation of Aerobic Energy Metabolism in Podospora anserina by Two Paralogous Genes Encoding Structurally Different c-Subunits of ATP Synthase Carole H. Sellem , Jean-Paul Di Rago , Jean-Paul Lasserre , Sharon H. Ackerman , Annie Sainsard-Chanet PLoS Genetics, 2016, 12 (7), ⟨10.1371/journal.pgen.1006161⟩ Article dans une revue hal-01412332v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		The Unique Cysteine of F-ATP Synthase OSCP Subunit Participates in Modulation of the Permeability Transition Pore Michela Carraro , Kristen Jones , Geppo Sartori , Marco Schiavone , Salvatore Antonucci , et al. Cell Reports, 2020, 32 (9), pp.108095. ⟨10.1016/j.celrep.2020.108095⟩ Article dans une revue hal-03103150v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		The depletion of F1 subunit {varepsilon} in yeast leads to an uncoupled respiratory phenotype that is rescued by mutations in the proton translocating subunits of F0. Emmanuel Tetaud , François Godard , Marie-France Giraud , Sharon H Ackerman , Jean-Paul Di Rago Molecular Biology of the Cell, 2014, 25 (6), pp.791-99. ⟨10.1091/mbc.E13-02-0112⟩ Article dans une revue hal-00940281v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		TMEM70 forms oligomeric scaffolds within mitochondrial cristae promoting in situ assembly of mammalian ATP synthase proton channel Hela Bahri , Jeremie Buratto , Manuel Rojo , Jim Paul Dompierre , Bénédicte Salin , et al. Biochimica et Biophysica Acta - Molecular Cell Research, 2020, pp.118942. ⟨10.1016/j.bbamcr.2020.118942⟩ Article dans une revue hal-03103088v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		ATP Synthase Diseases of Mitochondrial Genetic Origin Alain Dautant , Thomas Meier , Alexander Hahn , Deborah Tribouillard-Tanvier , Jean-Paul Di Rago , et al. Frontiers in Physiology, 2018, 9, ⟨10.3389/fphys.2018.00329⟩ Article dans une revue hal-02398397v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Case Report: Identification of a Novel Variant (m.8909T>C) of Human Mitochondrial ATP6 Gene and Its Functional Consequences on Yeast ATP Synthase Qiuju Ding , Róża Kucharczyk , Weiwei Zhao , Alain Dautant , Shutian Xu , et al. Life, 2020, 10, ⟨10.3390/life10090215⟩ Article dans une revue hal-02988793v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		TMEM70 forms oligomeric scaffolds within mitochondrial cristae promoting in situ assembly of mammalian ATP synthase proton channel Hela Bahri , Jérémie Buratto , Manuel Rojo , Jim Dompierre , Bénédicte Salin , et al. 2020 Pré-publication, Document de travail hal-03034356v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Experimental Relocation of the Mitochondrial ATP9 Gene to the Nucleus Reveals Forces Underlying Mitochondrial Genome Evolution. Maïlis Bietenhader , Alexandre Martos , Emmanuel Tetaud , Raeka S Aiyar , Carole H Sellem , et al. PLoS Genetics, 2012, 8 (8), pp.e1002876. ⟨10.1371/journal.pgen.1002876⟩ Article dans une revue hal-00735337v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		The energetic state of mitochondria modulates complex III biogenesis through the ATP-dependent activity of Bcs1. Jelena Ostojić , Cristina Panozzo , Jean-Paul Lasserre , Cécile Nouet , Florence Courtin , et al. Cell Metab, 2013, 18 (4), pp.567-77. ⟨10.1016/j.cmet.2013.08.017⟩ Article dans une revue hal-00905852v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		The pathogenic MT-ATP6 m.8851T>C mutation prevents proton movements within the n-side hydrophilic cleft of the membrane domain of ATP synthase Alain Dautant , Roza Kucharczyk , Kewin Gombeau , François Godard , Déborah Tribouillard-Tanvier , et al. Biochimica biophysica acta (BBA) - Bioenergetics, 2019, 1860 (7), pp.562-572. ⟨10.1016/j.bbabio.2019.06.002⟩ Article dans une revue hal-02988559v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Assigning mitochondrial localization of dual localized proteins using a yeast Bi-Genomic Mitochondrial-Split-GFP Gaétan Bader , Ludovic Enkler , Yuhei Araiso , Marine Hemmerle , Krystyna Binko , et al. eLife, 2020, 9, ⟨10.7554/eLife.56649⟩ Article dans une revue hal-02898815v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Two nuclear life-cycle-regulated genes encode interchangeable subunits c of mitochondrial ATP synthase in Podospora anserina. Michelle Déquard-Chablat , Carole H Sellem , Pawel Golik , Frédérique Bidard , Alexandre Martos , et al. Molecular Biology and Evolution, 2011, epub ahead of print. ⟨10.1093/molbev/msr025⟩ Article dans une revue hal-00574233v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Functional investigation of an universally conserved leucine residue in subunit a of ATP synthase targeted by the pathogenic m.9176 T>G mutation Roza Kucharczyk , Alain Dautant , François Godard , Deborah Tribouillard-Tanvier , Jean-Paul Di Rago Biochimica biophysica acta (BBA) - Bioenergetics, 2019, 1860 (1), pp.52-59. ⟨10.1016/j.bbabio.2018.11.005⟩ Article dans une revue hal-02404981v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Molecular Basis of the Pathogenic Mechanism Induced by the m.9191T>C Mutation in Mitochondrial ATP6 Gene Alain Dautant , Xin Su , François Godard , Marine Bouhier , Teresa Zoladek , et al. International Journal of Molecular Sciences, 2020, 21, ⟨10.3390/ijms21145083⟩ Article dans une revue hal-02988568v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Decreasing cytosolic translation is beneficial to yeast and human tafazzin-deficient cells Maxence de Taffin de Tilques , Jean-Paul Lasserre , François Godard , Elodie Sardin , Marine Bouhier , et al. Microbial Cell , 2018, 5 (5), pp.1-13. ⟨10.15698/mic2018.05.629⟩ Article dans une revue hal-02628099v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Molecular basis of diseases caused by the mtDNA mutation m.8969G>A in the subunit a of ATP synthase Natalia Skoczen , Alain Dautant , Krystyna Binko , François Godard , Marine Bouhier , et al. Biochimica biophysica acta (BBA) - Bioenergetics, 2018, 1859 (8), pp.602-611. ⟨10.1016/j.bbabio.2018.05.009⟩ Article dans une revue hal-02398396v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Overexpression of mitochondrial oxodicarboxylate carrier (ODC1) preserves oxidative phosphorylation in a yeast model of Barth syndrome Maxence de Taffin de Tilques , Deborah Tribouillard-Tanvier , Emmanuel Tetaud , Eric Testet , Jean-Paul Di Rago , et al. Disease Models & Mechanisms, 2017, 10 (4), pp.439-450. ⟨10.1242/dmm.027540⟩ Article dans une revue hal-01600647v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		A "petite obligate" mutant of Saccharomyces cerevisiae: functional mtDNA is lethal in cells lacking the delta subunit of mitochondrial F1-ATPase. Stéphane Duvezin-Caubet , Malgorzata Rak , Linnka Lefebvre-Legendre , Emmanuel Tetaud , Nathalie Bonnefoy , et al. Journal of Biological Chemistry, 2006, 281 (24), pp.16305-13. ⟨10.1074/jbc.M513805200⟩ Article dans une revue hal-00132178v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies. Jean-Paul Lasserre , Alain Dautant , Raeka S Aiyar , Roza Kucharczyk , Annie Glatigny , et al. Disease Models & Mechanisms, 2015, 8 (6), pp.509-26. ⟨10.1242/dmm.020438⟩ Article dans une revue hal-01199669v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Deregulating mitochondrial metabolite and ion transport has beneficial effects in yeast and human cellular models for NARP syndrome Xin Su , Malgorzata Rak , Emmanuel Tetaud , François Godard , Elodie Sardin , et al. Human Molecular Genetics, 2019, 28 (22), pp.3792-3804. ⟨10.1093/hmg/ddz160⟩ Article dans une revue hal-02362008v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Mitochondrial DNA mutations provoke dominant inhibition of mitochondrial inner membrane fusion. Cécile Sauvanet , Stéphane Duvezin-Caubet , Bénédicte Salin , Claudine David , Aurélie Massoni-Laporte , et al. PLoS ONE, 2012, 7 (11), pp.e49639. ⟨10.1371/journal.pone.0049639⟩ Article dans une revue hal-00757387v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Defining the pathogenesis of human mtDNA mutations using a yeast model: The case of T8851C. Roza Kucharczyk , Marie-France Giraud , Daniel Brèthes , Monica Wysocka-Kapcinska , Nahia Ezkurdia , et al. International Journal of Biochemistry and Cell Biology, 2013, 45 (1), pp.130-40. ⟨10.1016/j.biocel.2012.07.001⟩ Article dans une revue istex hal-00735756v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More

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Defining the impact on yeast ATP synthase of two pathogenic human mitochondrial DNA mutations, T9185C and T9191C.

Flavonoids as Potential Drugs for VPS13-Dependent Rare Neurodegenerative Diseases

Regulation of Aerobic Energy Metabolism in Podospora anserina by Two Paralogous Genes Encoding Structurally Different c-Subunits of ATP Synthase

The Unique Cysteine of F-ATP Synthase OSCP Subunit Participates in Modulation of the Permeability Transition Pore

The depletion of F1 subunit {varepsilon} in yeast leads to an uncoupled respiratory phenotype that is rescued by mutations in the proton translocating subunits of F0.

TMEM70 forms oligomeric scaffolds within mitochondrial cristae promoting in situ assembly of mammalian ATP synthase proton channel

ATP Synthase Diseases of Mitochondrial Genetic Origin

Case Report: Identification of a Novel Variant (m.8909T>C) of Human Mitochondrial ATP6 Gene and Its Functional Consequences on Yeast ATP Synthase

TMEM70 forms oligomeric scaffolds within mitochondrial cristae promoting in situ assembly of mammalian ATP synthase proton channel

Experimental Relocation of the Mitochondrial ATP9 Gene to the Nucleus Reveals Forces Underlying Mitochondrial Genome Evolution.

The energetic state of mitochondria modulates complex III biogenesis through the ATP-dependent activity of Bcs1.

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

Assigning mitochondrial localization of dual localized proteins using a yeast Bi-Genomic Mitochondrial-Split-GFP

Two nuclear life-cycle-regulated genes encode interchangeable subunits c of mitochondrial ATP synthase in Podospora anserina.

Functional investigation of an universally conserved leucine residue in subunit a of ATP synthase targeted by the pathogenic m.9176 T>G mutation

Molecular Basis of the Pathogenic Mechanism Induced by the m.9191T>C Mutation in Mitochondrial ATP6 Gene

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

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

Overexpression of mitochondrial oxodicarboxylate carrier (ODC1) preserves oxidative phosphorylation in a yeast model of Barth syndrome

A "petite obligate" mutant of Saccharomyces cerevisiae: functional mtDNA is lethal in cells lacking the delta subunit of mitochondrial F1-ATPase.

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

Deregulating mitochondrial metabolite and ion transport has beneficial effects in yeast and human cellular models for NARP syndrome

Mitochondrial DNA mutations provoke dominant inhibition of mitochondrial inner membrane fusion.

Defining the pathogenesis of human mtDNA mutations using a yeast model: The case of T8851C.

Functional investigation of an universally conserved leucine residue in subunit a of ATP synthase targeted by the pathogenic m.9176 T>G mutation