1702 documents
- Sylvie Besse, Valérie Allamand, Jean-Thomas Vilquin, Zhenlin Li, Christophe Poirier, et al.. Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin α2 chain gene. Neuromuscular Disorders, 2003, 13 (3), pp.216-222. ⟨10.1016/s0960-8966(02)00278-x⟩. ⟨hal-03824380⟩
- L.T. Guo, X.U. Zhang, W. Kuang, H. Xu, L.A. Liu, et al.. Laminin α2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice. Neuromuscular Disorders, 2003, 13 (3), pp.207-215. ⟨10.1016/s0960-8966(02)00266-3⟩. ⟨hal-03824384⟩
- Albert Hagège, Claire Carrion, Philippe Menasché, Jean-Thomas Vilquin, Denis Duboc, et al.. Viability and differentiation of autologous skeletal myoblast grafts in ischaemic cardiomyopathy. The Lancet, 2003, 361 (9356), pp.491-492. ⟨10.1016/S0140-6736(03)12458-0⟩. ⟨hal-03824092⟩
- Rozen Le Panse, Louis Dubertret, Bernard Coulomb. p38 Mitogen-activated Protein Kinase Activation by Ultraviolet A Radiation in Human Dermal Fibroblasts¶. Photochemistry and Photobiology, 2003, 78 (2), pp.168. <a target="_blank" href="https://dx.doi.org/10.1562/0031-8655(2003)0782.0.co;2">⟨10.1562/0031-8655(2003)0782.0.co;2⟩. ⟨hal-03442095⟩
- Claudine Laurent, Dana Niehaus, Stéphanie Bauché, Douglas Levinson, Stéphane Soubigou, et al.. CAG repeat polymorphisms in KCNN3 (HSKCa3) and PPP2R2B show no association or linkage to schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2003, 116B (1), pp.45-50. ⟨10.1002/ajmg.b.10797⟩. ⟨hal-03863965⟩
- Bruno Pitard, Hélène Pollard, Onnik Agbulut, Olivier Lambert, Jean-Thomas Vilquin, et al.. A Nonionic Amphiphile Agent Promotes Gene Delivery In Vivo to Skeletal and Cardiac Muscles. Human Gene Therapy, 2002, 13 (14), pp.1767-1775. ⟨10.1089/104303402760293592⟩. ⟨hal-03824393⟩
- Ana Buj-Bello, Furling D, Helene Tronchere, Jocelyn Laporte, Thierry Lerouge, et al.. Muscle-specific alternative splicing of myotubularin-related 1 gene is impaired in DM1 muscle cells. Human Molecular Genetics, 2002, 11 (19), pp.2297-2307. ⟨10.1093/hmg/11.19.2297⟩. ⟨hal-04481805⟩
- Daniel Skuk, Jean Thomas Vilquin, Jacques Tremblay. Experimental and therapeutic approaches to muscular dystrophies. Current Opinion in Neurology, 2002, 15 (5), pp.563-569. ⟨10.1097/00019052-200210000-00007⟩. ⟨hal-03824399⟩
- Bruno Pouzet, Saïd Ghostine, Jean-Thomas Vilquin, Isabelle Garcin, Marcio Scorsin, et al.. Is Skeletal Myoblast Transplantation Clinically Relevant in the Era of Angiotensin-Converting Enzyme Inhibitors?. Circulation, 2001, 104 (suppl 1), pp.I-223-I-228. ⟨10.1161/hc37t1.094593⟩. ⟨hal-03824409⟩
- Jt Vilquin, Pf Kennel, M Paturneau-Jouas, P Chapdelaine, N Boissel, et al.. Electrotransfer of naked DNA in the skeletal muscles of animal models of muscular dystrophies. Gene Therapy, 2001, 8 (14), pp.1097-1107. ⟨10.1038/sj.gt.3301484⟩. ⟨hal-03824098⟩
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