Resultats de la cerca - Goudenège, David

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

Novel NDUFS4 gene mutation in an atypical late-onset mitochondrial form of multifocal dystonia per 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

Obtenir text complet Obtenir text complet Obtenir text complet

Mitochondrial DNA Instability Is Common in HIV-Exposed Uninfected Newborns per 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

Obtenir text complet Obtenir text complet Obtenir text complet

Cancer/Testis Antigen 55 is required for cancer cell proliferation and mitochondrial DNA maintenance per 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

Obtenir text complet Obtenir text complet Obtenir text complet

Long-Term Persistence of Mitochondrial DNA Instability in HIV-Exposed Uninfected Children during and after Exposure to Antiretroviral Drugs and HIV per 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

Obtenir text complet Obtenir text complet Obtenir text complet

First characterization of LHON pedigrees in North Africa per 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

Obtenir text complet Obtenir text complet Obtenir text complet

Next-Generation Sequencing Identifies Novel PMPCA Variants in Patients with Late-Onset Dominant Optic Atrophy per 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

Obtenir text complet Obtenir text complet Obtenir text complet

Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy per 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

Obtenir text complet Obtenir text complet Obtenir text complet

Glutamate-Induced Deregulation of Krebs Cycle in Mitochondrial Encephalopathy Lactic Acidosis Syndrome Stroke-Like Episodes (MELAS) Syndrome Is Alleviated by Ketone Body Exposure per 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

Obtenir text complet Obtenir text complet Obtenir text complet

Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy per 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

Obtenir text complet Obtenir text complet Obtenir text complet

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... per 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

Obtenir text complet Obtenir text complet Obtenir text complet

Dominant ACO2 mutations are a frequent cause of isolated optic atrophy per 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

Obtenir text complet Obtenir text complet Obtenir text complet

Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults per 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

Obtenir text complet Obtenir text complet Obtenir text complet