Dysferlin-deficient immortalized human myoblasts and myotubes as a useful tool to study dysferlinopathy

Por Philippi, Susanne, Bigot, Anne, Marg, Andreas, Mouly, Vincent, Spuler, Simone, Zacharias, Ute
Publicado em 2012

Large CTG Repeats Trigger p16-Dependent Premature Senescence in Myotonic Dystrophy Type 1 Muscle Precursor Cells

Por Bigot, Anne, Klein, Arnaud F., Gasnier, Erwan, Jacquemin, Virginie, Ravassard, Philippe, Butler-Browne, Gillian, Mouly, Vincent, Furling, Denis
Publicado em 2009

The absence of dysferlin induces the expression of functional connexin-based hemichannels in human myotubes

Por Cea, Luis A., Bevilacqua, Jorge A., Arriagada, Christian, Cárdenas, Ana María, Bigot, Anne, Mouly, Vincent, Sáez, Juan C., Caviedes, Pablo
Publicado no BMC Cell Biol (2016)

Skeletal muscle characteristics are preserved in hTERT/cdk4 human myogenic cell lines

Por Thorley, Matthew, Duguez, Stéphanie, Mazza, Emilia Maria Cristina, Valsoni, Sara, Bigot, Anne, Mamchaoui, Kamel, Harmon, Brennan, Voit, Thomas, Mouly, Vincent, Duddy, William
Publicado no Skelet Muscle (2016)

Quiescence of human muscle stem cells is favored by culture on natural biopolymeric films

Por Monge, Claire, DiStasio, Nicholas, Rossi, Thomas, Sébastien, Muriel, Sakai, Hiroshi, Kalman, Benoit, Boudou, Thomas, Tajbakhsh, Shahragim, Marty, Isabelle, Bigot, Anne, Mouly, Vincent, Picart, Catherine
Publicado no Stem Cell Res Ther (2017)

Age-dependent alteration in muscle regeneration: the critical role of tissue niche

Por Barberi, Laura, Scicchitano, Bianca Maria, De Rossi, Manuela, Bigot, Anne, Duguez, Stephanie, Wielgosik, Aurore, Stewart, Claire, McPhee, Jamie, Conte, Maria, Narici, Marco, Franceschi, Claudio, Mouly, Vincent, Butler-Browne, Gillian, Musarò, Antonio
Publicado em 2013

Regenerative potential of human muscle stem cells in chronic inflammation

Por Duijnisveld, Bouke J, Bigot, Anne, Beenakker, Karel GM, Portilho, Débora M, Raz, Vered, van der Heide, Huub JL, Visser, Cornelis PJ, Chaouch, Soraya, Mamchaoui, Kamel, Westendorp, Rudi GJ, Mouly, Vincent, Butler-Browne, Gillian S, Nelissen, Rob GHH, Maier, Andrea B
Publicado em 2011

Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders

Por Mamchaoui, Kamel, Trollet, Capucine, Bigot, Anne, Negroni, Elisa, Chaouch, Soraya, Wolff, Annie, Kandalla, Prashanth K, Marie, Solenne, Di Santo, James, St Guily, Jean Lacau, Muntoni, Francesco, Kim, Jihee, Philippi, Susanne, Spuler, Simone, Levy, Nicolas, Blumen, Sergiu C, Voit, Thomas, Wright, Woodring E, Aamiri, Ahmed, Butler-Browne, Gillian, Mouly, Vincent
Publicado em 2011

A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss

Por Servián‐Morilla, Emilia, Takeuchi, Hideyuki, Lee, Tom V, Clarimon, Jordi, Mavillard, Fabiola, Area‐Gómez, Estela, Rivas, Eloy, Nieto‐González, Jose L, Rivero, Maria C, Cabrera‐Serrano, Macarena, Gómez‐Sánchez, Leonardo, Martínez‐López, Jose A, Estrada, Beatriz, Márquez, Celedonio, Morgado, Yolanda, Suárez‐Calvet, Xavier, Pita, Guillermo, Bigot, Anne, Gallardo, Eduard, Fernández‐Chacón, Rafael, Hirano, Michio, Haltiwanger, Robert S, Jafar‐Nejad, Hamed, Paradas, Carmen
Publicado no EMBO Mol Med (2016)