Search Results - "Christel, Gentil"

Clathrin plaques and associated actin anchor intermediate filaments in skeletal muscle by Franck, Agathe, Lainé, Jeanne, Moulay, Gilles, Lemerle, Eline, Trichet, Michaël, Gentil, Christel, Benkhelifa-Ziyyat, Sofia, Lacène, Emmanuelle, Bui, Mai Thao, Brochier, Guy, Guicheney, Pascale, Romero, Norma, Bitoun, Marc, Vassilopoulos, Stéphane

“…Clathrin plaques are stable features of the plasma membrane observed in several cell types. They are abundant in muscle, where they localize at costameres that…”
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GDF5 as a rejuvenating treatment for age-related neuromuscular failure by Massiré, Traoré, Chiara, Noviello, Amélie, Vergnol, Christel, Gentil, Marius, Halliez, Lucile, Saillard, Maxime, Gelin, Anne, Forand, Mégane, Lemaitre, Zoheir, Guesmia, Bruno, Cadot, Eriky, Caldas, Benjamin, Marty, Nathalie, Mougenot, Julien, Messéant, Laure, Strochlic, Jeremy, Sadoine, Lofti, Slimani, Ariane, Jolly, Pierre, De la Grange, Jean-Yves, Hogrel, France, Pietri-Rouxel, Sestina, Falcone

“…Sarcopenia involves a progressive loss of skeletal muscle force, quality and mass during ageing, which results in increased inability and death; however, no…”
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Actin scaffolding by clathrin heavy chain is required for skeletal muscle sarcomere organization by Vassilopoulos, Stéphane, Gentil, Christel, Lainé, Jeanne, Buclez, Pierre-Olivier, Franck, Agathe, Ferry, Arnaud, Précigout, Guillaume, Roth, Robyn, Heuser, John E, Brodsky, Frances M, Garcia, Luis, Bonne, Gisèle, Voit, Thomas, Piétri-Rouxel, France, Bitoun, Marc

“…The ubiquitous clathrin heavy chain (CHC), the main component of clathrin-coated vesicles, is well characterized for its role in intracellular membrane traffic…”
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Duchenne muscular dystrophy trajectory in R-DMDdel52 preclinical rat model identifies COMP as biomarker of fibrosis by Taglietti, Valentina, Kefi, Kaouthar, Bronisz-Budzyńska, Iwona, Mirciloglu, Busra, Rodrigues, Mathilde, Cardone, Nastasia, Coulpier, Fanny, Periou, Baptiste, Gentil, Christel, Goddard, Melissa, Authier, François-Jérôme, Pietri-Rouxel, France, Malfatti, Edoardo, Lafuste, Peggy, Tiret, Laurent, Relaix, Frederic

“…Duchenne muscular dystrophy (DMD) is a fatal muscle-wasting disorder caused by mutations in the Dystrophin gene and for which there is currently no cure. To…”
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Dystrophin Threshold Level Necessary for Normalization of Neuronal Nitric Oxide Synthase, Inducible Nitric Oxide Synthase, and Ryanodine Receptor-Calcium Release Channel Type 1 Nitrosylation in Golden Retriever Muscular Dystrophy Dystrophinopathy by Gentil, Christel, Le Guiner, Caroline, Falcone, Sestina, Hogrel, Jean-Yves, Peccate, Cécile, Lorain, Stéphanie, Benkhelifa-Ziyyat, Sofia, Guigand, Lydie, Montus, Marie, Servais, Laurent, Voit, Thomas, Piétri-Rouxel, France

“…At present, the clinically most advanced strategy to treat Duchenne muscular dystrophy (DMD) is the exon-skipping strategy. Whereas antisense…”
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NR1D1 controls skeletal muscle calcium homeostasis through myoregulin repression by Boulinguiez, Alexis, Duhem, Christian, Mayeuf-Louchart, Alicia, Pourcet, Benoit, Sebti, Yasmine, Kondratska, Kateryna, Montel, Valérie, Delhaye, Stéphane, Thorel, Quentin, Beauchamp, Justine, Hebras, Aurore, Gimenez, Marion, Couvelaere, Marie, Zecchin, Mathilde, Ferri, Lise, Prevarskaya, Natalia, Forand, Anne, Gentil, Christel, Ohana, Jessica, Piétri-Rouxel, France, Bastide, Bruno, Staels, Bart, Duez, Helene, Lancel, Steve

“…The sarcoplasmic reticulum (SR) plays an important role in calcium homeostasis. SR calcium mishandling is described in pathological conditions, such as…”
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miR-708-5p and miR-34c-5p are involved in nNOS regulation in dystrophic context by Guilbaud, Marine, Gentil, Christel, Peccate, Cécile, Gargaun, Elena, Holtzmann, Isabelle, Gruszczynski, Carole, Falcone, Sestina, Mamchaoui, Kamel, Ben Yaou, Rabah, Leturcq, France, Jeanson-Leh, Laurence, Piétri-Rouxel, France

“…Duchenne (DMD) and Becker (BMD) muscular dystrophies are caused by mutations in the DMD gene coding for dystrophin, a protein being part of a large sarcolemmal…”
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Is oxygen a key factor in the lipodystrophy phenotype? by Gentil, Christel, Le Jan, Sébastien, Philippe, Josette, Leibowitch, Jacques, Sonigo, Pierre, Germain, Stéphane, Piétri-Rouxel, France

“…The lipodystrophic syndrome (LD) is a disorder resulting from selective damage of adipose tissue by antiretroviral drugs included in therapy controlling…”
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Progressive cardiomyopathy with intercalated disc disorganization in a rat model of Becker dystrophy by Taglietti, Valentina, Kefi, Kaouthar, Mirciloglu, Busra, Bastu, Sultan, Masson, Jean-Daniel, Bronisz-Budzyńska, Iwona, Gouni, Vassiliki, Ferri, Carlotta, Jorge, Alan, Gentil, Christel, Pietri-Rouxel, France, Malfatti, Edoardo, Lafuste, Peggy, Tiret, Laurent, Relaix, Frederic

“…Becker muscular dystrophy (BMD) is an X-linked disorder due to in-frame mutations in the DMD gene, leading to a less abundant and truncated dystrophin. BMD is…”
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Progressive cardiomyopathy with intercalated disc disorganization in a rat model of Becker dystrophy by Taglietti, Valentina, Kefi, Kaouthar, Mirciloglu, Busra, Bastu, Sultan, Masson, Jean-Daniel, Bronisz-Budzyńska, Iwona, Gouni, Vassiliki, Ferri, Carlotta, Jorge, Alan, Gentil, Christel, Piétri‐rouxel, France, Malfatti, Edoardo, Lafuste, Peggy, Tiret, Laurent, Relaix, Frederic

“…Becker muscular dystrophy (BMD) is an X-linked disorder due to in-frame mutations in the DMD gene, leading to a less abundant and truncated dystrophin. BMD is…”
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Pannexin-1 and CaV1.1 show reciprocal interaction during excitation–contraction and excitation–transcription coupling in skeletal muscle by Jaque-Fernández, Francisco, Jorquera, Gonzalo, Troc-Gajardo, Jennifer, Pietri-Rouxel, France, Gentil, Christel, Buvinic, Sonja, Allard, Bruno, Jaimovich, Enrique, Jacquemond, Vincent, Casas, Mariana

“…One of the most important functions of skeletal muscle is to respond to nerve stimuli by contracting. This function ensures body movement but also participates…”
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Pannexin-1 and Ca V 1.1 show reciprocal interaction during excitation-contraction and excitation-transcription coupling in skeletal muscle by Jaque-Fernández, Francisco, Jorquera, Gonzalo, Troc-Gajardo, Jennifer, Pietri-Rouxel, France, Gentil, Christel, Buvinic, Sonja, Allard, Bruno, Jaimovich, Enrique, Jacquemond, Vincent, Casas, Mariana

“…One of the most important functions of skeletal muscle is to respond to nerve stimuli by contracting. This function ensures body movement but also participates…”
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DHPR α1S subunit controls skeletal muscle mass and morphogenesis by Piétri-Rouxel, France, Gentil, Christel, Vassilopoulos, Stéphane, Baas, Dominique, Mouisel, Etienne, Ferry, Arnaud, Vignaud, Alban, Hourdé, Christophe, Marty, Isabelle, Schaeffer, Laurent, Voit, Thomas, Garcia, Luis

“…The α1S subunit has a dual function in skeletal muscle: it forms the L‐type Ca 2+ channel in T‐tubules and is the voltage sensor of excitation–contraction…”
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Variable phenotype of del45-55 Becker patients correlated with nNOSμ mislocalization and RYR1 hypernitrosylation by GENTIL, Christel, LETURCQ, France, BEN YAOU, Rabah, KAPLAN, Jean-Claude, LAFORET, Pascal, PENISSON-BESNIER, Isabelle, ESPIL-TARIS, Caroline, VOIT, Thomas, GARCIA, Luis, PIETRI-ROUXE, France

“…Duchenne and Becker muscular dystrophies (DMD and BMD) are muscle-wasting diseases caused by mutations in the DMD gene-encoding dystrophin. Usually,…”
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Duchenne muscular dystrophy trajectory in R-DMDdel52 preclinical rat model identifies COMP as biomarker of fibrosis by Taglietti, Valentina, Kefi, Kaouthar, Bronisz-Budzyńska, Iwona, Mirciloglu, Busra, Rodrigues, Mathilde, Cardone, Nastasia, Coulpier, Fanny, Periou, Baptiste, Gentil, Christel, Goddard, Melissa, Authier, François-Jérôme, Pietri-Rouxel, France, Malfatti, Edoardo, Lafuste, Peggy, Tiret, Laurent, Relaix, Frederic

“…Abstract Duchenne muscular dystrophy (DMD) is a fatal muscle-wasting disorder caused by mutations in the Dystrophin gene and for which there is currently no…”
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Cav1.1 Controls ATP Release in Adult Muscle Fibers by Jorquera, Gonzalo, Piétri-Rouxel, France, Allard, Bruno, Jacquemond, Vincent, Gentil, Christel, Jaimovich, Enrique, Casas, Mariana

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Variable phenotype of del45-55 Becker patients correlated with nNOSµ mislocalization and RYR1 hypernitrosylation by Gentil, Christel, Leturcq, France, Ben Yaou, Rabah, Kaplan, Jean-Claude, Laforet, Pascal, Pénisson-Besnier, Isabelle, Espil-Taris, Caroline, Voit, Thomas, Garcia, Luis, Piétri-Rouxel, France

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DHPR alpha1S subunit controls skeletal muscle mass and morphogenesis by Piétri-Rouxel, France, Gentil, Christel, Vassilopoulos, Stéphane, Baas, Dominique, Mouisel, Etienne, Ferry, Arnaud, Vignaud, Alban, Hourdé, Christophe, Marty, Isabelle, Schaeffer, Laurent, Voit, Thomas, Garcia, Luis

“…The alpha1S subunit has a dual function in skeletal muscle: it forms the L-type Ca(2+) channel in T-tubules and is the voltage sensor of excitation-contraction…”
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DHPR a1S subunit controls skeletal muscle mass and morphogenesis by Pietri-Rouxel, France, Gentil, Christel, Vassilopoulos, Stephane, Baas, Dominique, Mouisel, Etienne, Ferry, Arnaud, Vignaud, Alban, Hourde, Christophe, Marty, Isabelle, Schaeffer, Laurent, Voit, Thomas, Garcia, Luis

“…The a1S subunit has a dual function in skeletal muscle: it forms the L-type Ca super(2+) channel in T-tubules and is the voltage sensor of…”
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DHPR [alpha]1S subunit controls skeletal muscle mass and morphogenesis by Piétri-rouxel, France, Gentil, Christel, Vassilopoulos, Stéphane, Baas, Dominique, Mouisel, Etienne, Ferry, Arnaud, Vignaud, Alban, Hourdé, Christophe, Marty, Isabelle, Schaeffer, Laurent, Voit, Thomas, Garcia, Luis

“…The alpha1S subunit has a dual function in skeletal muscle: it forms the L-type Ca(2+) channel in T-tubules and is the voltage sensor of excitation-contraction…”
Get full text