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Lamin A/C-mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy. [electronic resource] by
- Méjat, Alexandre
- Decostre, Valérie
- Li, Juan
- Renou, Laure
- Kesari, Akanchha
- Hantaï, Daniel
- Stewart, Colin L
- Xiao, Xiao
- Hoffman, Eric
- Bonne, Gisèle
- Misteli, Tom
Producer: 20090213
In:
The Journal of cell biology vol. 184
Availability: No items available.
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9.
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SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells. [electronic resource] by
- Janin, Alexandre
- Bauer, Delphine
- Ratti, Francesca
- Valla, Camille
- Bertrand, Anne
- Christin, Emilie
- Chopin, Emilie
- Streichenberger, Nathalie
- Bonne, Gisèle
- Gache, Vincent
- Cohen, Tatiana
- Méjat, Alexandre
Producer: 20191023
In:
Scientific reports vol. 8
Availability: No items available.
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Calcineurin-NFAT signaling, together with GABP and peroxisome PGC-1{alpha}, drives utrophin gene expression at the neuromuscular junction. [electronic resource] by
- Angus, Lindsay M
- Chakkalakal, Joe V
- Méjat, Alexandre
- Eibl, Joe K
- Bélanger, Guy
- Megeney, Lynn A
- Chin, Eva R
- Schaeffer, Laurent
- Michel, Robin N
- Jasmin, Bernard J
Producer: 20051019
In:
American journal of physiology. Cell physiology vol. 289
Availability: No items available.
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Histone deacetylase 6 is a FoxO transcription factor-dependent effector in skeletal muscle atrophy. [electronic resource] by
- Ratti, Francesca
- Ramond, Francis
- Moncollin, Vincent
- Simonet, Thomas
- Milan, Giulia
- Méjat, Alexandre
- Thomas, Jean-Luc
- Streichenberger, Nathalie
- Gilquin, Benoit
- Matthias, Patrick
- Khochbin, Saadi
- Sandri, Marco
- Schaeffer, Laurent
Producer: 20150508
In:
The Journal of biological chemistry vol. 290
Availability: No items available.
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"Be an ambassador for change that you would like to see": a call to action to all stakeholders for co-creation in healthcare and medical research to improve quality of life of people with a neuromuscular disease. [electronic resource] by
- Ambrosini, Anna
- Quinlivan, Ros
- Sansone, Valeria A
- Meijer, Ingeborg
- Schrijvers, Guus
- Tibben, Aad
- Padberg, George
- de Wit, Maarten
- Sterrenburg, Ellen
- Mejat, Alexandre
- Breukel, Alexandra
- Rataj, Michal
- Lochmüller, Hanns
- Willmann, Raffaella
Producer: 20200330
In:
Orphanet journal of rare diseases vol. 14
Availability: No items available.
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