Skeletal muscle effects of electrostimulation after COPD exacerbation: a pilot study von ABDELLAOUI, A, PREFAUT, C, HAYOT, M, GOUZI, F, COUILLARD, A, COISY-QUIVY, M, HUGON, G, MOLINARI, N, LAFONTAINE, T, JONQUET, O, LAOUDJ-CHENIVESSE, D

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P177 Profil d’insulino-sécrétion des patients atteints de dystrophie facio-scapulo-humérale (FSHD) von Laoudj-Chenivesse, D, Fédou, C, Dmitriev, P, Raynaud de Mauverger, E, Brun, J, Jacques, M

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Sécrétion inappropriée d’insuline chez des patients atteints de dystrophie facio-scapulo-humérale (FSHD) von Laoudj-Chenivesse, D, Dmitriev, M.P, Fédou, C, Raynaud de Mauverger, E, Mercier, J, Brun, J.-F

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Chromatin Loop Domain Organization within the 4q35 Locus in Facioscapulohumeral Dystrophy Patients versus Normal Human Myoblasts von Petrov, Andrei, Pirozhkova, Iryna, Carnac, Gilles, Laoudj, Dalila, Lipinski, Marc, Vassetzky, Yegor S.

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Increased levels of adenine nucleotide translocator 1 protein and response to oxidative stress are early events in facioscapulohumeral muscular dystrophy muscle von LAOUDJ-CHENIVESSE, Dalila, CARNAC, Gilles, BISBAL, Catherine, HUGON, Gerald, BOUILLOT, Sandrine, DESNUELLE, Claude, VASSETZKY, Yegor, FERNANDEZ, Anne

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Follicle retinol binding protein levels accurately predict human oocyte fertilization potential von Anahory, T, Laoudj, D, Dechaud, H, Fernandez, A, Lamb, N.J.C, Hamamah, S

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Surface potential mapping of dispersed proteins von Laoudj, Dalila, Guasch, Cathy, Renault, Eric, Bennes, René, Bonnet, Jacques

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Antisense strategies targeting DUX4 and DUX4c as therapeutic approaches for facioscapulohumeral muscular dystrophy (FSHD) von Vanderplanck, C, Tassin, A, Ansseau, E, Lancelot, C, Derenne, A, Conotte, S, Dudome, V, Leroy, B, Wilton, S, Laoudj-Chenivesse, D, Wattiez, R, Legrand, A, Belayew, A, Coppée, F

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Refined localization of the gene for Clouston syndrome (hidrotic ectodermal dysplasia) in a large French family von Lamartine, J., Laoudj, D., Blanchet-Bardon, C., Kibar, Z., Soularue, P., Ridoux, V., Dubertret, L., Rouleau, G.A., Waksman, G.

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Mutations in GJB6 cause hidrotic ectodermal dysplasia von Laoudj, Dalila, Christianson, Arnold L, Kelsell, David P, Callouet, Edwige, Hand, Colette, Pitaval, Amandine, Lamartine, Jérôme, Radhakrishna, Uppala, Rouleau, Guy A, Waksman, Gilles, Antonarakis, Stylianos, Kibar, Zoha, Munhoz Essenfelder, Guilherme, Zonana, Jonathan, Blanchet-Bardon, Claudine, Fraser, Clarke, Lanneluc, Isabelle, Lemaître, Gilles, Hayflick, Susan J, Der Kaloustian, Vazken

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Cloning and analysis of the entire Escherichia coli ams gene : ams is identical to hmp1 and encodes a 114 kDa protein that migrates as a 180 kDa protein von Casarégola, S., Jacq, A., Laoudj, D., McGurk, G., Margarson, S., Tempête, M., Norris, V., Holland, I.B.

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The FSHD atrophic myotube phenotype is caused by DUX4 expression von Vanderplanck, Céline, Ansseau, Eugénie, Charron, Sébastien, Stricwant, Nadia, Tassin, Alexandra, Laoudj-Chenivesse, Dalila, Wilton, Steve D, Coppée, Frédérique, Belayew, Alexandra

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Reduced myotube diameter, atrophic signalling and elevated oxidative stress in cultured satellite cells from COPD patients von Pomiès, Pascal, Rodriguez, Julie, Blaquière, Marine, Sedraoui, Sami, Gouzi, Fares, Carnac, Gilles, Laoudj‐Chenivesse, Dalila, Mercier, Jacques, Préfaut, Christian, Hayot, Maurice

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DUX4 expression in FSHD muscle cells: how could such a rare protein cause a myopathy? von Tassin, Alexandra, Laoudj‐Chenivesse, Dalila, Vanderplanck, Céline, Barro, Marietta, Charron, Sébastien, Ansseau, Eugénie, Chen, Yi‐Wen, Mercier, Jacques, Coppée, Frédérique, Belayew, Alexandra

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Myoblasts from affected and non‐affected FSHD muscles exhibit morphological differentiation defects von Barro, Marietta, Carnac, Gilles, Flavier, Sébastien, Mercier, Jacques, Vassetzky, Yegor, Laoudj‐Chenivesse, Dalila

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Effects of vitamin C, vitamin E, zinc gluconate, and selenomethionine supplementation on muscle function and oxidative stress biomarkers in patients with facioscapulohumeral dystro... von Passerieux, Emilie, Hayot, Maurice, Jaussent, Audrey, Carnac, Gilles, Gouzi, Fares, Pillard, Fabien, Picot, Marie-Christine, Böcker, Koen, Hugon, Gerald, Pincemail, Joel, Defraigne, Jean O., Verrips, Theo, Mercier, Jacques, Laoudj-Chenivesse, Dalila

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Mutations in GJB6 cause hidrotic ectodermal dysplasia von Lamartine, J, Munhoz Essenfelder, G, Kibar, Z, Lanneluc, I, Callouet, E, Laoudj, D, Lemaître, G, Hand, C, Hayflick, S J, Zonana, J, Antonarakis, S, Radhakrishna, U, Kelsell, D P, Christianson, A L, Pitaval, A, Der Kaloustian, V, Fraser, C, Blanchet-Bardon, C, Rouleau, G A, Waksman, G

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FSHD myoblasts fail to downregulate intermediate filament protein vimentin during myogenic differentiation von Dmitriev, P. V., Barat, A. L., Cochet, E., Ogryzko, V. V., Laoudj-Chenivesse, D., Lipinski, M., Vassetzky, Y. S.

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On the flexibility and the dynamics of DNA von Laoudj-Chenivesse, Dalila, Bennes, René, Tronel-Peyroz, Emmanuel

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Functional muscle impairment in facioscapulohumeral muscular dystrophy is correlated with oxidative stress and mitochondrial dysfunction von Turki, Ahmed, Hayot, Maurice, Carnac, Gilles, Pillard, Fabien, Passerieux, Emilie, Bommart, Sébastien, de Mauverger, Eric Raynaud, Hugon, Gérald, Pincemail, Joel, Pietri, Sylvia, Lambert, Karen, Belayew, Alexandra, Vassetzky, Yegor, Juntas Morales, Raul, Mercier, Jacques, Laoudj-Chenivesse, Dalila

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