Ngā hua rapu - Lombès, Anne

Kinetic analysis of ATP hydrolysis by complex V in four murine tissues: Towards an assay suitable for clinical diagnosis mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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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