Rezultati - Bonne, Gisèle

The Treatabolome, an emerging concept od Bonne, Gisèle

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

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199th ENMC international workshop: FHL1 related myopathies, June 7–9, 2013, Naarden, The Netherlands od 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 od 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 od 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 od 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 od Wu, Wei, Muchir, Antoine, Shan, Jian, Bonne, Gisèle, Worman, Howard J.

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The Pathogenesis and Therapies of Striated Muscle Laminopathies od 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 od 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? od Allamand, Valérie, Briñas, Laura, Richard, Pascale, Stojkovic, Tanya, Quijano-Roy, Susana, Bonne, Gisèle

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Preclinical Advances of Therapies for Laminopathies od 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 od 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 od 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 od 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’ od 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 od 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 od 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 od 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 od 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 od Pilat, Ursula, Dechat, Thomas, Bertrand, Anne T, Woisetschläger, Nikola, Gotic, Ivana, Spilka, Rita, Biadasiewicz, Katarzyna, Bonne, Gisèle, Foisner, Roland

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