Resultats de la cerca - Bonne, Gisèle

The Treatabolome, an emerging concept per Bonne, Gisèle

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“Laminopathies:” a wide spectrum of human diseases per Worman, Howard J., Bonne, Gisèle

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199th ENMC international workshop: FHL1 related myopathies, June 7–9, 2013, Naarden, The Netherlands per Bertrand, Anne T., Bönnemann, Carsten G., Bonne, Gisèle

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Targeted therapies for congenital myasthenic syndromes: systematic review and steps towards a treatabolome per Thompson, Rachel, Bonne, Gisèle, Missier, Paolo, Lochmüller, Hanns

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Effect of genetic background on the cardiac phenotype in a mouse model of Emery-Dreifuss muscular dystrophy per Vignier, Nicolas, Mougenot, Nathalie, Bonne, Gisèle, Muchir, Antoine

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Pharmacological inhibition of c-Jun N-terminal kinase signaling prevents cardiomyopathy caused by mutation in LMNA gene per Wu, Wei, Shan, Jian, Bonne, Gisèle, Worman, Howard J., Muchir, Antoine

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Mitogen Activated Protein Kinase Inhibitors Improve Heart Function and Prevent Fibrosis in Cardiomyopathy Caused by Mutation in Lamin A/C Gene per Wu, Wei, Muchir, Antoine, Shan, Jian, Bonne, Gisèle, Worman, Howard J.

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The Pathogenesis and Therapies of Striated Muscle Laminopathies per Brull, Astrid, Morales Rodriguez, Blanca, Bonne, Gisèle, Muchir, Antoine, Bertrand, Anne T.

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Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins per Muchir, Antoine, Shan, Jian, Bonne, Gisèle, Lehnart, Stephan E., Worman, Howard J.

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ColVI myopathies: where do we stand, where do we go? per Allamand, Valérie, Briñas, Laura, Richard, Pascale, Stojkovic, Tanya, Quijano-Roy, Susana, Bonne, Gisèle

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Preclinical Advances of Therapies for Laminopathies per Benarroch, Louise, Cohen, Enzo, Atalaia, Antonio, Ben Yaou, Rabah, Bonne, Gisèle, Bertrand, Anne T

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The (13)C hyperpolarized pyruvate generated by ParaHydrogen detects the response of the heart to altered metabolism in real time per Cavallari, Eleonora, Carrera, Carla, Sorge, Matteo, Bonne, Gisèle, Muchir, Antoine, Aime, Silvio, Reineri, Francesca

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Proteasome-mediated degradation of integral inner nuclear membrane protein emerin in fibroblasts lacking A-type lamins per Muchir, Antoine, Massart, Catherine, van Engelen, Baziel G., Lammens, Martin, Bonne, Gisèle, Worman, Howard J.

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Targeting the histone demethylase LSD1 prevents cardiomyopathy in a mouse model of laminopathy per Guénantin, Anne-Claire, Jebeniani, Imen, Leschik, Julia, Watrin, Erwan, Bonne, Gisèle, Vignier, Nicolas, Pucéat, Michel

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Laminopathies’ Treatments Systematic Review: A Contribution Towards a ‘Treatabolome’ per Atalaia, Antonio, Ben Yaou, Rabah, Wahbi, Karim, De Sandre-Giovannoli, Annachiara, Vigouroux, Corinne, Bonne, Gisèle

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Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy per Muchir, Antoine, Pavlidis, Paul, Decostre, Valérie, Herron, Alan J., Arimura, Takuro, Bonne, Gisèle, Worman, Howard J.

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Deficiency of emerin contributes differently to the pathogenesis of skeletal and cardiac muscles in Lmna(H222P/H222P) mutant mice per Wada, Eiji, Kato, Megumi, Yamashita, Kaori, Kokuba, Hiroko, Liang, Wen-Chen, Bonne, Gisèle, Hayashi, Yukiko K.

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A Muscle Hybrid Promoter as a Novel Tool for Gene Therapy per Piekarowicz, Katarzyna, Bertrand, Anne T., Azibani, Feriel, Beuvin, Maud, Julien, Laura, Machowska, Magdalena, Bonne, Gisèle, Rzepecki, Ryszard

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Lamin A/C Mutants Disturb Sumo1 Localization and Sumoylation in Vitro and in Vivo per Boudreau, Émilie, Labib, Sarah, Bertrand, Anne T., Decostre, Valérie, Bolongo, Pierrette M., Sylvius, Nicolas, Bonne, Gisèle, Tesson, Frédérique

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Muscle dystrophy-causing ΔK32 lamin A/C mutant does not impair functions of nucleoplasmic LAP2α - lamin A/C complexes in mice per Pilat, Ursula, Dechat, Thomas, Bertrand, Anne T, Woisetschläger, Nikola, Gotic, Ivana, Spilka, Rita, Biadasiewicz, Katarzyna, Bonne, Gisèle, Foisner, Roland

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