检索结果 - Lombès, Anne

Kinetic analysis of ATP hydrolysis by complex V in four murine tissues: Towards an assay suitable for clinical diagnosis 由 Haraux, Francis, Lombès, Anne

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Mitochondrial Fusion in Human Cells Is Efficient, Requires the Inner Membrane Potential, and Is Mediated by Mitofusins 由 Legros, Frédéric, Lombès, Anne, Frachon, Paule, Rojo, Manuel

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Use of H(2)O(2) to Cause Oxidative Stress, the Catalase Issue 由 Ransy, Céline, Vaz, Clément, Lombès, Anne, Bouillaud, Frédéric

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HK2 Recruitment to Phospho-BAD Prevents Its Degradation, Promoting Warburg Glycolysis by Theileria-Transformed Leukocytes 由 Haidar, Malak, Lombès, Anne, Bouillaud, Frédéric, Kennedy, Eileen J., Langsley, Gordon

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Hypoxia Promotes Mitochondrial Complex I Abundance via HIF-1α in Complex III and Complex IV Deficient Cells 由 Saldana-Caboverde, Amy, Nissanka, Nadee, Garcia, Sofia, Lombès, Anne, Diaz, Francisca

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PGC-1α/β induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders 由 Srivastava, Sarika, Diaz, Francisca, Iommarini, Luisa, Aure, Karine, Lombes, Anne, Moraes, Carlos T.

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Separate fusion of outer and inner mitochondrial membranes 由 Malka, Florence, Guillery, Olwenn, Cifuentes-Diaz, Carmen, Guillou, Emmanuelle, Belenguer, Pascale, Lombès, Anne, Rojo, Manuel

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Mutations in C12orf62, a Factor that Couples COX I Synthesis with Cytochrome c Oxidase Assembly, Cause Fatal Neonatal Lactic Acidosis 由 Weraarpachai, Woranontee, Sasarman, Florin, Nishimura, Tamiko, Antonicka, Hana, Auré, Karine, Rötig, Agnès, Lombès, Anne, Shoubridge, Eric A.

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Mitochondrial DNA Content, an Inaccurate Biomarker of Mitochondrial Alteration in Human Immunodeficiency Virus-Related Lipodystrophy 由 Kim, Min Ji, Jardel, Claude, Barthélémy, Cyrille, Jan, Véronique, Bastard, Jean Philippe, Fillaut-Chapin, Sandrine, Houry, Sydney, Capeau, Jacqueline, Lombès, Anne

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Nitroso-Redox Balance and Mitochondrial Homeostasis Are Regulated by STOX1, a Pre-Eclampsia-Associated Gene 由 Doridot, Ludivine, Châtre, Laurent, Ducat, Aurélien, Vilotte, Jean-Luc, Lombès, Anne, Méhats, Céline, Barbaux, Sandrine, Calicchio, Rosamaria, Ricchetti, Miria, Vaiman, Daniel

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Unravelling the Effects of the Mutation m.3571insC/MT-ND1 on Respiratory Complexes Structural Organization 由 Iommarini, Luisa, Ghelli, Anna, Tropeano, Concetta Valentina, Kurelac, Ivana, Leone, Giulia, Vidoni, Sara, Lombes, Anne, Zeviani, Massimo, Gasparre, Giuseppe, Porcelli, Anna Maria

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Mitochondrial targeting of recombinant RNAs modulates the level of a heteroplasmic mutation in human mitochondrial DNA associated with Kearns Sayre Syndrome 由 Comte, Caroline, Tonin, Yann, Heckel-Mager, Anne-Marie, Boucheham, Abdeldjalil, Smirnov, Alexandre, Auré, Karine, Lombès, Anne, Martin, Robert P., Entelis, Nina, Tarassov, Ivan

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Mitochondrial myopathy and myoclonic epilepsy 由 Arruda, Walter O., Torres, Luiz F. B., lombes, Anne, Dimauro, Salvatore, Cardoso, Belkiss A., Teive, Hélio A. G., Paola, Duilton de, Seixas, Ricardo R.

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Homoplasmic mitochondrial tRNA(Pro) mutation causing exercise-induced muscle swelling and fatigue 由 Auré, Karine, Fayet, Guillemette, Chicherin, Ivan, Rucheton, Benoit, Filaut, Sandrine, Heckel, Anne-Marie, Eichler, Julie, Caillon, Florence, Péréon, Yann, Entelis, Nina, Tarassov, Ivan, Lombès, Anne

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CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures 由 Mollet, Julie, Delahodde, Agnès, Serre, Valérie, Chretien, Dominique, Schlemmer, Dimitri, Lombes, Anne, Boddaert, Nathalie, Desguerre, Isabelle, de Lonlay, Pascale, Ogier de Baulny, Hélène, Munnich, Arnold, Rötig, Agnès

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Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts 由 Procaccio, Vincent, Mousson, Bénédicte, Beugnot, Réjane, Duborjal, Hervé, Feillet, François, Putet, Guy, Pignot-Paintrand, Isabelle, Lombès, Anne, Coo, René De, Smeets, Hubert, Lunardi, Joël, Issartel, Jean-Paul

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Identifying mitotane-induced mitochondria-associated membranes dysfunctions: metabolomic and lipidomic approaches 由 Hescot, Ségolène, Amazit, Larbi, Lhomme, Marie, Travers, Simon, DuBow, Anais, Battini, Stephanie, Boulate, Geoffrey, Namer, Izzie Jacques, Lombes, Anne, Kontush, Anatol, Imperiale, Alessio, Baudin, Eric, Lombes, Marc

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Correction of the consequences of mitochondrial 3243A>G mutation in the MT-TL1 gene causing the MELAS syndrome by tRNA import into mitochondria 由 Karicheva, Olga Z., Kolesnikova, Olga A., Schirtz, Tom, Vysokikh, Mikhail Y., Mager-Heckel, Anne-Marie, Lombès, Anne, Boucheham, Abdeldjalil, Krasheninnikov, Igor A., Martin, Robert P., Entelis, Nina, Tarassov, Ivan

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Tissue- and Cell-Specific Mitochondrial Defect in Parkin-Deficient Mice 由 Damiano, Maria, Gautier, Clément A., Bulteau, Anne-Laure, Ferrando-Miguel, Rosa, Gouarne, Caroline, Paoli, Marc Giraudon, Pruss, Rebecca, Auchère, Françoise, L'Hermitte-Stead, Caroline, Bouillaud, Frédéric, Brice, Alexis, Corti, Olga, Lombès, Anne

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Severe respiratory complex III defect prevents liver adaptation to prolonged fasting 由 Kremer, Laura, L 'hermitte-Stead, Caroline, Lesimple, Pierre, Gilleron, Mylène, Filaut, Sandrine, Jardel, Claude, Haack, Tobias, Strom, Tim, Meitinger, Thomas, Azzouz, Hatem, Tebib, Neji, Ogier De Baulny, Hélène, Touati, Guy, Prokisch, Holger, Lombès, Anne

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