Torthaí cuardaigh - Goudenège, David

CoBaltDB: Complete bacterial and archaeal orfeomes subcellular localization database and associated resources de réir Goudenège, David, Avner, Stéphane, Lucchetti-Miganeh, Céline, Barloy-Hubler, Frédérique

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SORGOdb: Superoxide Reductase Gene Ontology curated DataBase de réir Lucchetti-Miganeh, Céline, Goudenège, David, Thybert, David, Salbert, Gilles, Barloy-Hubler, Frédérique

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Populations, not clones, are the unit of vibrio pathogenesis in naturally infected oysters de réir Lemire, Astrid, Goudenège, David, Versigny, Typhaine, Petton, Bruno, Calteau, Alexandra, Labreuche, Yannick, Le Roux, Frédérique

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Comparative genomics of pathogenic lineages of Vibrio nigripulchritudo identifies virulence-associated traits de réir Goudenège, David, Labreuche, Yannick, Krin, Evelyne, Ansquer, Dominique, Mangenot, Sophie, Calteau, Alexandra, Médigue, Claudine, Mazel, Didier, Polz, Martin F, Le Roux, Frédérique

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Bioinformatics Tools and Databases to Assess the Pathogenicity of Mitochondrial DNA Variants in the Field of Next Generation Sequencing de réir Bris, Céline, Goudenege, David, Desquiret-Dumas, Valérie, Charif, Majida, Colin, Estelle, Bonneau, Dominique, Amati-Bonneau, Patrizia, Lenaers, Guy, Reynier, Pascal, Procaccio, Vincent

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High‐throughput sequencing revealed a novel SETX mutation in a Hungarian patient with amyotrophic lateral sclerosis de réir Tripolszki, Kornélia, Török, Dóra, Goudenège, David, Farkas, Katalin, Sulák, Adrienn, Török, Nóra, Engelhardt, József I., Klivényi, Péter, Procaccio, Vincent, Nagy, Nikoletta, Széll, Márta

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Use of Next-Generation Sequencing for the Molecular Diagnosis of 1,102 Patients With a Autosomal Optic Neuropathy de réir Charif, Majida, Bris, Céline, Goudenège, David, Desquiret-Dumas, Valérie, Colin, Estelle, Ziegler, Alban, Procaccio, Vincent, Reynier, Pascal, Bonneau, Dominique, Lenaers, Guy, Amati-Bonneau, Patrizia

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Novel NDUFS4 gene mutation in an atypical late-onset mitochondrial form of multifocal dystonia de réir Bris, Celine, Rouaud, Tiphaine, Desquiret-Dumas, Valerie, Gueguen, Naig, Goudenege, David, Barth, Magalie, Bonneau, Dominique, Amati-Bonneau, Patrizia, Lenaers, Guy, Reynier, Pascal, Lebre, Anne-Sophie, Procaccio, Vincent

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Mitochondrial DNA Instability Is Common in HIV-Exposed Uninfected Newborns de réir Monnin, Audrey, Desquiret-Dumas, Valérie, Méda, Nicolas, Goudenège, David, Bris, Céline, Kankasa, Chipepo, Singata-Madliki, Mandisa, Tylleskar, Thorkild, Procaccio, Vincent, Nagot, Nicolas, Van de Perre, Philippe, Reynier, Pascal, Molès, Jean-Pierre

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Cancer/Testis Antigen 55 is required for cancer cell proliferation and mitochondrial DNA maintenance de réir Aurrière, Jade, Goudenege, David, Baechler, Simone A, Huang, Shar-Yin N, Gueguen, Naig, Desquiret-Dumas, Valerie, Chabrun, Floris, Perrot, Rodolphe, Chevrollier, Arnaud, Charif, Majida, Baris, Olivier, Pommier, Yves, Lenaers, Guy, Khiati, Salim

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Long-Term Persistence of Mitochondrial DNA Instability in HIV-Exposed Uninfected Children during and after Exposure to Antiretroviral Drugs and HIV de réir Desquiret-Dumas, Valérie, D’Ottavi, Morgana, Monnin, Audrey, Goudenège, David, Méda, Nicolas, Vizeneux, Amélie, Kankasa, Chipepo, Tylleskar, Thorkild, Bris, Céline, Procaccio, Vincent, Nagot, Nicolas, Van de Perre, Philippe, Reynier, Pascal, Molès, Jean-Pierre

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First characterization of LHON pedigrees in North Africa de réir Bouzidi, Aymane, Aboussair, Nisrine, Charif, Majida, Amalou, Ghita, Goudenège, David, Desquiret-Dumas, Valérie, Bris, Céline, Sifeddine, Najat, Nahili, Halima, Elqabli, Meriem, Dafir, Kenza, Kandil, Mostafa, Amati-Bonneau, Patrizia, Procaccio, Vincent, Barakat, Abdelhamid, Lenaers, Guy

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Next-Generation Sequencing Identifies Novel PMPCA Variants in Patients with Late-Onset Dominant Optic Atrophy de réir Charif, Majida, Chevrollier, Arnaud, Gueguen, Naïg, Kane, Selma, Bris, Céline, Goudenège, David, Desquiret-Dumas, Valerie, Meunier, Isabelle, Mochel, Fanny, Jeanjean, Luc, Varenne, Fanny, Procaccio, Vincent, Reynier, Pascal, Bonneau, Dominique, Amati-Bonneau, Patrizia, Lenaers, Guy

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Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy de réir Piro-Mégy, Camille, Sarzi, Emmanuelle, Tarrés-Solé, Aleix, Péquignot, Marie, Hensen, Fenna, Quilès, Mélanie, Manes, Gaël, Chakraborty, Arka, Sénéchal, Audrey, Bocquet, Béatrice, Cazevieille, Chantal, Roubertie, Agathe, Müller, Agnès, Charif, Majida, Goudenège, David, Lenaers, Guy, Wilhelm, Helmut, Kellner, Ulrich, Weisschuh, Nicole, Wissinger, Bernd, Zanlonghi, Xavier, Hamel, Christian, Spelbrink, Johannes N., Sola, Maria, Delettre, Cécile

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Glutamate-Induced Deregulation of Krebs Cycle in Mitochondrial Encephalopathy Lactic Acidosis Syndrome Stroke-Like Episodes (MELAS) Syndrome Is Alleviated by Ketone Body Exposure de réir Belal, Sophie, Goudenège, David, Bocca, Cinzia, Dumont, Florent, Chao De La Barca, Juan Manuel, Desquiret-Dumas, Valérie, Gueguen, Naïg, Geffroy, Guillaume, Benyahia, Rayane, Kane, Selma, Khiati, Salim, Bris, Céline, Aranyi, Tamas, Stockholm, Daniel, Inisan, Aurore, Renaud, Aurélie, Barth, Magalie, Simard, Gilles, Reynier, Pascal, Letournel, Franck, Lenaers, Guy, Bonneau, Dominique, Chevrollier, Arnaud, Procaccio, Vincent

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Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy de réir Charif, Majida, Chevrollier, Arnaud, Gueguen, Naïg, Bris, Céline, Goudenège, David, Desquiret-Dumas, Valérie, Leruez, Stéphanie, Colin, Estelle, Meunier, Audrey, Vignal, Catherine, Smirnov, Vasily, Defoort-Dhellemmes, Sabine, Drumare Bouvet, Isabelle, Goizet, Cyril, Votruba, Marcela, Jurkute, Neringa, Yu-Wai-Man, Patrick, Tagliavini, Francesca, Caporali, Leonardo, La Morgia, Chiara, Carelli, Valerio, Procaccio, Vincent, Zanlonghi, Xavier, Meunier, Isabelle, Reynier, Pascal, Bonneau, Dominique, Amati-Bonneau, Patrizia, Lenaers, Guy

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Co-Exposure of Cardiomyocytes to IFN-γ and TNF-α Induces Mitochondrial Dysfunction and Nitro-Oxidative Stress: Implications for the Pathogenesis of Chronic Chagas Disease Cardiomyo... de réir Nunes, João Paulo Silva, Andrieux, Pauline, Brochet, Pauline, Almeida, Rafael Ribeiro, Kitano, Eduardo, Honda, André Kenji, Iwai, Leo Kei, Andrade-Silva, Débora, Goudenège, David, Alcântara Silva, Karla Deysiree, Vieira, Raquel de Souza, Levy, Débora, Bydlowski, Sergio Paulo, Gallardo, Frédéric, Torres, Magali, Bocchi, Edimar Alcides, Mano, Miguel, Santos, Ronaldo Honorato Barros, Bacal, Fernando, Pomerantzeff, Pablo, Laurindo, Francisco Rafael Martins, Teixeira, Priscila Camillo, Nakaya, Helder I., Kalil, Jorge, Procaccio, Vincent, Chevillard, Christophe, Cunha-Neto, Edecio

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Dominant ACO2 mutations are a frequent cause of isolated optic atrophy de réir Charif, Majida, Gueguen, Naïg, Ferré, Marc, Elkarhat, Zouhair, Khiati, Salim, LeMao, Morgane, Chevrollier, Arnaud, Desquiret-Dumas, Valerie, Goudenège, David, Bris, Céline, Kane, Selma, Alban, Jennifer, Chupin, Stéphanie, Wetterwald, Céline, Caporali, Leonardo, Tagliavini, Francesca, LaMorgia, Chiara, Carbonelli, Michele, Jurkute, Neringa, Barakat, Abdelhamid, Gohier, Philippe, Verny, Christophe, Barth, Magalie, Procaccio, Vincent, Bonneau, Dominique, Zanlonghi, Xavier, Meunier, Isabelle, Weisschuh, Nicole, Schimpf-Linzenbold, Simone, Tonagel, Felix, Kellner, Ulrich, Yu-Wai-Man, Patrick, Carelli, Valerio, Wissinger, Bernd, Amati-Bonneau, Patrizia, Reynier, Pascal, Lenaers, Guy

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Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults de réir Charif, Majida, Nasca, Alessia, Thompson, Kyle, Gerber, Sylvie, Makowski, Christine, Mazaheri, Neda, Bris, Céline, Goudenège, David, Legati, Andrea, Maroofian, Reza, Shariati, Gholamreza, Lamantea, Eleonora, Hopton, Sila, Ardissone, Anna, Moroni, Isabella, Giannotta, Melania, Siegel, Corinna, Strom, Tim M., Prokisch, Holger, Vignal-Clermont, Catherine, Derrien, Sabine, Zanlonghi, Xavier, Kaplan, Josseline, Hamel, Christian P., Leruez, Stephanie, Procaccio, Vincent, Bonneau, Dominique, Reynier, Pascal, White, Frances E., Hardy, Steven A., Barbosa, Inês A., Simpson, Michael A., Vara, Roshni, Perdomo Trujillo, Yaumara, Galehdari, Hamind, Deshpande, Charu, Haack, Tobias B., Rozet, Jean-Michel, Taylor, Robert W., Ghezzi, Daniele, Amati-Bonneau, Patrizia, Lenaers, Guy

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