Secondary Mitochondrial Respiratory Chain Defect Can Delay Accurate PFIC2 Diagnosis

por Davit-Spraul, Anne, Beinat, Marine, Debray, Dominique, Rötig, Agnes, Slama, Abdelhamid, Jacquemin, Emmanuel
Publicado em 2013

Three human aminoacyl-tRNA synthetases have distinct sub-mitochondrial localizations that are unaffected by disease-associated mutations

por González-Serrano, Ligia Elena, Karim, Loukmane, Pierre, Florian, Schwenzer, Hagen, Rötig, Agnès, Munnich, Arnold, Sissler, Marie
Publicado no J Biol Chem (2018)

Mutations in C12orf62, a Factor that Couples COX I Synthesis with Cytochrome c Oxidase Assembly, Cause Fatal Neonatal Lactic Acidosis

por Weraarpachai, Woranontee, Sasarman, Florin, Nishimura, Tamiko, Antonicka, Hana, Auré, Karine, Rötig, Agnès, Lombès, Anne, Shoubridge, Eric A.
Publicado em 2012

Mitochondrial activities in human cultured skin fibroblasts contaminated by Mycoplasma hyorhinis

por Darin, Niklas, Kadhom, Norman, Brière, Jean-Jacques, Chretien, Dominique, Bébéar, Cécile M, Rötig, Agnès, Munnich, Arnold, Rustin, Pierre
Publicado em 2003

Mutations in mitochondrial ribosomal protein MRPL12 leads to growth retardation, neurological deterioration and mitochondrial translation deficiency()

por Serre, Valérie, Rozanska, Agata, Beinat, Marine, Chretien, Dominique, Boddaert, Nathalie, Munnich, Arnold, Rötig, Agnès, Chrzanowska-Lightowlers, Zofia M.
Publicado em 2013

Unusual clinical expression and long survival of a pseudouridylate synthase (PUS1) mutation into adulthood

por Metodiev, Metodi D, Assouline, Zahra, Landrieu, Pierre, Chretien, Dominique, Bader-Meunier, Brigitte, Guitton, Corinne, Munnich, Arnold, Rötig, Agnès
Publicado no Eur J Hum Genet (2015)

Expanding the clinical spectrum of MTTF mutations

por Barcia, Giulia, Assouline, Zahra, Pennisi, Alessandra, Steffann, Julie, Boddaert, Nathalie, Gitiaux, Cyril, Rötig, Agnès, Bonnefont, Jean-Paul, Munnich, Arnold
Publicado no Mol Genet Metab Rep (2019)

Mitochondrial myopathy plus due to the variant m.586G > A in MT-TF

por Barcia, Giulia, Assouline, Zahra, Pennisi, Alessandra, Steffann, Julie, Boddaert, Nathalie, Gitiaux, Cyril, Rötig, Agnès, Bonnefont, Jean-Paul, Munnich, Arnold
Publicado no Mol Genet Metab Rep (2019)

Cytochrome c oxidase deficiency caused by biallelic SCO2 mutations in two sibs with cerebellar ataxia and progressive peripheral axonal neuropathy

por Barcia, Giulia, Assouline, Zahra, Pennisi, Alessandra, Gitiaux, Cyril, Schiff, Manuel, Boddaert, Nathalie, Munnich, Arnold, Bonnefont, Jean-Paul, Rötig, Agnès
Publicado no Mol Genet Metab Rep (2019)

The R22X Mutation of the SDHD Gene in Hereditary Paraganglioma Abolishes the Enzymatic Activity of Complex II in the Mitochondrial Respiratory Chain and Activates the Hypoxia Pathw...

por Gimenez-Roqueplo, Anne-Paule, Favier, Judith, Rustin, Pierre, Mourad, Jean-Jacques, Plouin, Pierre-François, Corvol, Pierre, Rötig, Agnès, Jeunemaitre, Xavier
Publicado em 2001

Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders

por Mollet, Julie, Giurgea, Irina, Schlemmer, Dimitri, Dallner, Gustav, Chretien, Dominique, Delahodde, Agnès, Bacq, Delphine, de Lonlay, Pascale, Munnich, Arnold, Rötig, Agnès
Publicado em 2007

Nonsense mutations in the COX1 subunit impair the stability of respiratory chain complexes rather than their assembly

por Hornig-Do, Hue-Tran, Tatsuta, Takashi, Buckermann, Angela, Bust, Maria, Kollberg, Gittan, Rötig, Agnes, Hellmich, Martin, Nijtmans, Leo, Wiesner, Rudolf J
Publicado em 2012

Modeling of Antigenomic Therapy of Mitochondrial Diseases by Mitochondrially Addressed RNA Targeting a Pathogenic Point Mutation in Mitochondrial DNA

por Tonin, Yann, Heckel, Anne-Marie, Vysokikh, Mikhail, Dovydenko, Ilya, Meschaninova, Mariya, Rötig, Agnès, Munnich, Arnold, Venyaminova, Alya, Tarassov, Ivan, Entelis, Nina
Publicado em 2014

Mutations of the SCO1 Gene in Mitochondrial Cytochrome c Oxidase Deficiency with Neonatal-Onset Hepatic Failure and Encephalopathy

por Valnot, Isabelle, Osmond, Sandrine, Gigarel, Nadine, Mehaye, Blandine, Amiel, Jeanne, Cormier-Daire, Valérie, Munnich, Arnold, Bonnefont, Jean-Paul, Rustin, Pierre, Rötig, Agnès
Publicado em 2000

Large-Scale Deletion and Point Mutations of the Nuclear NDUFV1 and NDUFS1 Genes in Mitochondrial Complex I Deficiency

por Bénit, Paule, Chretien, Dominique, Kadhom, Nohman, de Lonlay-Debeney, Pascale, Cormier-Daire, Valérie, Cabral, Aguinaldo, Peudenier, Sylviane, Rustin, Pierre, Munnich, Arnold, Rötig, Agnès
Publicado em 2001

Phenotypic variability and identification of novel YARS2 mutations in YARS2 mitochondrial myopathy, lactic acidosis and sideroblastic anaemia

por Riley, Lisa G, Menezes, Minal J, Rudinger-Thirion, Joëlle, Duff, Rachael, de Lonlay, Pascale, Rotig, Agnes, Tchan, Michel C, Davis, Mark, Cooper, Sandra T, Christodoulou, John
Publicado em 2013

Defects in Galactose Metabolism and Glycoconjugate Biosynthesis in a UDP-Glucose Pyrophosphorylase-Deficient Cell Line Are Reversed by Adding Galactose to the Growth Medium

por Durrant, Christelle, Fuehring, Jana I., Willemetz, Alexandra, Chrétien, Dominique, Sala, Giusy, Ghidoni, Riccardo, Katz, Abram, Rötig, Agnès, Thelestam, Monica, Ermonval, Myriam, Moore, Stuart E. H.
Publicado no Int J Mol Sci (2020)

CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures

por 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
Publicado em 2008

Mutation in PNPT1, which Encodes a Polyribonucleotide Nucleotidyltransferase, Impairs RNA Import into Mitochondria and Causes Respiratory-Chain Deficiency

por Vedrenne, Vanessa, Gowher, Ali, De Lonlay, Pascale, Nitschke, Patrick, Serre, Valérie, Boddaert, Nathalie, Altuzarra, Cecilia, Mager-Heckel, Anne-Marie, Chretien, Florence, Entelis, Nina, Munnich, Arnold, Tarassov, Ivan, Rötig, Agnès
Publicado em 2012

Refractory epilepsy and mitochondrial dysfunction due to GM3 synthase deficiency

por Fragaki, Konstantina, Ait-El-Mkadem, Samira, Chaussenot, Annabelle, Gire, Catherine, Mengual, Raymond, Bonesso, Laurent, Bénéteau, Marie, Ricci, Jean-Ehrland, Desquiret-Dumas, Valérie, Procaccio, Vincent, Rötig, Agnès, Paquis-Flucklinger, Véronique
Publicado em 2013