Correlation between genetic polymorphisms and stroke recovery: Analysis of the GAIN Americas and GAIN International Studies von Cramer, S. C., Procaccio, V.

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The mitochondrial DNA content of cumulus granulosa cells is linked to embryo quality von Desquiret-Dumas, V., Clément, A., Seegers, V., Boucret, L., Ferré-L'Hotellier, V., Bouet, P.E., Descamps, P., Procaccio, V., Reynier, P., May-Panloup, P.

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Relationship between diminished ovarian reserve and mitochondrial biogenesis in cumulus cells von Boucret, L., Chao de la Barca, J.M., Morinière, C., Desquiret, V., Ferré-L'Hôtellier, V., Descamps, P., Marcaillou, C., Reynier, P., Procaccio, V., May-Panloup, P.

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The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype von Rouzier, Cécile, Bannwarth, Sylvie, Chaussenot, Annabelle, Chevrollier, Arnaud, Verschueren, Annie, Bonello-Palot, Nathalie, Fragaki, Konstantina, Cano, Aline, Pouget, Jean, Pellissier, Jean-François, Procaccio, Vincent, Chabrol, Brigitte, Paquis-Flucklinger, Véronique

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Highly asymmetrical distribution of muscle wasting correlates to the heteroplasmy in a patient carrying a large-scale mitochondrial DNA deletion: a novel pathophysiological mechani... von Masingue, M., Rucheton, B., Bris, C., Romero, N.B., Procaccio, V., Eymard, B

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Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases von Koene, S., Rodenburg, R. J., van der Knaap, M. S., Willemsen, M. A. A. P., Sperl, W., Laugel, V., Ostergaard, E., Tarnopolsky, M., Martin, M. A., Nesbitt, V., Fletcher, J., Edvardson, S., Procaccio, V., Slama, A., van den Heuvel, L. P. W. J., Smeitink, J. A. M.

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Deep sequencing shows that oocytes are not prone to accumulate mtDNA heteroplasmic mutations during ovarian ageing von Boucret, L., Bris, C., Seegers, V., Goudenège, D., Desquiret-Dumas, V., Domin-Bernhard, M., Ferré-L'Hotellier, V., Bouet, P.E., Descamps, P., Reynier, P., Procaccio, V., May-Panloup, P.

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Targeted metabolomics reveals reduced levels of polyunsaturated choline plasmalogens and a smaller dimethylarginine/arginine ratio in the follicular fluid of patients with a dimini... von de la Barca, J M Chao, Boueilh, T, Simard, G, Boucret, L, Ferré-L’Hotellier, V, Tessier, L, Gadras, C, Bouet, P E, Descamps, P, Procaccio, V, Reynier, P, May-Panloup, P

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The mitochondrial DNA content of cumulus cells may help predict embryo implantation von Taugourdeau, A., Desquiret-Dumas, V., Hamel, J. F., Chupin, S., Boucret, L., Ferré-L’Hotellier, V., Bouet, P. E., Descamps, P., Procaccio, V., Reynier, P., May-Panloup, P.

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Perspectives of drug-based neuroprotection targeting mitochondria von Procaccio, V., Bris, C., Chao de la Barca, J.M., Oca, F., Chevrollier, A., Amati-Bonneau, P., Bonneau, D., Reynier, P.

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Mitochondrial complex I defect resulting from exercise-induced lower-limb ischemia in patients with peripheral arterial disease von Signolet, Isabelle, Abraham, Pierre, Chupin, Stéphanie, Ammi, Myriam, Gueguen, Naïg, Letournel, Franck, Picquet, Jean, Baufreton, Christophe, Daligault, Mickael, Procaccio, Vincent, Reynier, Pascal, Henni, Samir

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Key Role of Estrogens and Endothelial Estrogen Receptor α in Blood Flow–Mediated Remodeling of Resistance Arteries von Tarhouni, K, Guihot, A L, Freidja, M L, Toutain, B, Henrion, B, Baufreton, C, Pinaud, F, Procaccio, V, Grimaud, L, Ayer, A, Loufrani, L, Lenfant, F, Arnal, J F, Henrion, D

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Multiethnic involvement in autosomal-dominant optic atrophy in Singapore von Loo, J L, Singhal, S, Rukmini, A V, Tow, S, Amati-Bonneau, P, Procaccio, V, Bonneau, D, Gooley, J J, Reynier, P, Ferré, M, Milea, D

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SIMULTANEOUS MFN2 AND GDAP1 MUTATIONS CAUSE MAJOR MITOCHONDRIAL DEFECTS IN A PATIENT WITH CMT von CASSEREAU, J, CASASNOVAS, C, PROCACCIO, V, CHEVROLLIER, A, GUEGUEN, N, MALINGE, M.-C, GUILLET, V, REYNIER, P, BONNEAU, D, AMATI-BONNEAU, P, BANCHS, I, VOLPINI, V

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Deep Sequencing Shows That Oocytes Are Not Prone to Accumulate mtDNA Heteroplasmic Mutations During Ovarian Ageing von Boucret, L, Bris, C, Seegers, V, Goudenège, D, Desquiret-Dumas, V, Domin-Bernhard, M, Ferré-L’Hotellier, V, Bouet, P E, Descamps, P, Reynier, P, Procaccio, V, May-Panloup, P

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Estrogens are needed for the improvement in endothelium-mediated dilation induced by a chronic increase in blood flow in rat mesenteric arteries von Tarhouni, K, Guihot, A.L, Vessieres, E, Procaccio, V, Grimaud, L, Abraham, P, Lenfant, F, Arnal, J.F, Favre, J, Loufrani, L, Henrion, D

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Early‐onset Behr syndrome due to compound heterozygous mutations in OPA1 von Bonneau, D., Lenaers, G., Procaccio, V., Amati‐Bonneau, P., Reynier, P.

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Novel pathophysiological mechanisms in dominant optic atrophy beyond the mitochondrial dynamics equilibrium von Lenaers, G., Charif, M., Amati‐Bonneau, P., la Barca, J. Chao, Procaccio, V., Chevrollier, A., Leruez, S., Bonneau, D., Reynier, P.

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Mitochondrial macro-haplogroup JT may play a protective role in ovarian ageing von May-Panloup, P, Desquiret, V, Morinière, C, Ferré-L'Hôtellier, V, Lemerle, S, Boucret, L, Lehais, S, Chao de la Barca, J M, Descamps, P, Procaccio, V, Reynier, P

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Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndrome von Cano, A., Rouzier, C., Monnot, S., Chabrol, B., Conrath, J., Lecomte, P., Delobel, B., Boileau, P., Valero, R., Procaccio, V., Paquis-Flucklinger, V., Vialettes, B.

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