Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors
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Published in Human molecular genetics (01.06.2005)
Published in Human molecular genetics (01.06.2005)
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Calpainopathy in Chile, first cases reported
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Published in Neuromuscular disorders : NMD (01.10.2016)
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Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndrome
Badens, C, Lacoste, C, Philip, N, Martini, N, Courrier, S, Giuliano, F, Verloes, A, Munnich, A, Leheup, B, Burglen, L, Odent, S, Van Esch, H, Levy, N
Published in Clinical genetics (01.07.2006)
Published in Clinical genetics (01.07.2006)
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Survival in the soil of the ectomycorrhizal fungus Laccaria bicolor and the effects of a mycorrhiza helper Pseudomonas fluorescens
Brulé, C, Frey-Klett, P, Pierrat, J.C, Courrier, S, Gérard, F, Lemoine, M.C, Rousselet, J.L, Sommer, G, Garbaye, J
Published in Soil biology & biochemistry (01.10.2001)
Published in Soil biology & biochemistry (01.10.2001)
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Immunolabelling and flow cytometry as new tools to explore dysferlinopathies
Wein, N, Krahn, M, Courrier, S, Bartoli, M, Salort-Campana, E, Nguyen, K, Fernandez, C, Pouget, J, Fossat, C, Depetris, D, Leturcq, F, Cau, P, Levy, N
Published in Neuromuscular disorders : NMD (01.01.2010)
Published in Neuromuscular disorders : NMD (01.01.2010)
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O.17 Efficient bypass of mutations in dysferlin deficient patient cells by antisense-induced exon skipping
Wein, N, Avril, A, Krahn, M, Navarro, C, Barthelemy, F, Courrier, S, Leturcq, F, Garcia, L, Bartoli, M, Lévy, N
Published in Neuromuscular disorders : NMD (01.10.2010)
Published in Neuromuscular disorders : NMD (01.10.2010)
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G.O.5 Partial functionality of a Mini-dysferlin molecule identified in a patient affected with moderately severe primary dysferlinopathy
Krahn, M, Wein, N, Lostal, W, Bourg-Alibert, N, Nguyen, K, Courrier, S, Vial, C, Labelle, V, Petris, D. De, Borges, A, Mattei, M.G, Roudaut, C, Miyake, K, McNeil, P, Cau, P, Leturcq, F, Bartoli, M, Lévy, N, Richard, I
Published in Neuromuscular disorders : NMD (01.10.2008)
Published in Neuromuscular disorders : NMD (01.10.2008)
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FROM THE SPINAL CORD TO THE MUSCLE
Ballouhey, O., Courrier, S., Krahn, M., Levy, N., Bartoli, M.
Published in Neuromuscular disorders : NMD (01.10.2020)
Published in Neuromuscular disorders : NMD (01.10.2020)
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FROM THE SPINAL CORD TO THE MUSCLE: O.12 Midi-Dysferlin gene therapy for dysferlinopathies
Ballouhey, O., Courrier, S., Krahn, M., Levy, N., Bartoli, M.
Published in Neuromuscular disorders : NMD (01.10.2020)
Published in Neuromuscular disorders : NMD (01.10.2020)
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G.P.4.10 Functional evaluation of a putative mini-dysferlin identified in a patient with moderate Miyoshi myopathy phenotype
Krahn, M, Wein, N, Nguyen, K, Vial, C, Courrier, S, Lostal, W, Bartoli, M, Labelle, V, Leturcq, F, Cau, P, Richard, I, Levy, N
Published in Neuromuscular disorders : NMD (2007)
Published in Neuromuscular disorders : NMD (2007)
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New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update
Navarro, Claire Laure, Esteves-Vieira, Vera, Courrier, Sébastien, Boyer, Amandine, Duong Nguyen, Thuy, Huong, Le Thi Thanh, Meinke, Peter, Schröder, Winnie, Cormier-Daire, Valérie, Sznajer, Yves, Amor, David J, Lagerstedt, Kristina, Biervliet, Martine, van den Akker, Peter C, Cau, Pierre, Roll, Patrice, Lévy, Nicolas, Badens, Catherine, Wehnert, Manfred, De Sandre-Giovannoli, Annachiara
Published in European journal of human genetics : EJHG (01.08.2014)
Published in European journal of human genetics : EJHG (01.08.2014)
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Ectomycorrhizal symbiosis affects functional diversity of rhizosphere fluorescent pseudomonads
Frey-Klett, P, Chavatte, M, Clausse, M.L, Courrier, S, Le Roux, C, Raaijmakers, J, Martinotti, M.G, Pierrat, J.C, Garbaye, J
Published in The New phytologist (01.01.2005)
Published in The New phytologist (01.01.2005)
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P.1 - Calpainopathy in Chile, first cases reported
Bevilacqua, J., Mathieu, Y., Krahn, M., Bartoli, M., Castiglioni, C., Kleinsteuber, K., Díaz, J., Puppo, F., Cerino, M., Courrier, S., Gorokhova, S., Miranda, N., Trangulao, A., González-Hormazábal, P., Avaria, M., Urtizberea, J., Caviedes, P., Jara, L., Levy, N.
Published in Neuromuscular disorders : NMD (01.10.2016)
Published in Neuromuscular disorders : NMD (01.10.2016)
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Cavéoline 3 et lamines A/C : une même voie physiologique ?
Simon, J.-P., Barthelemy, F., Puppo, F., Courrier, S., Bartoli, M., Krahn, M.
Published in Revue neurologique (01.04.2014)
Published in Revue neurologique (01.04.2014)
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Short Report: Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndrome
Badens, C, Lacoste, C, Philip, N, Martini, N, Courrier, S, Giuliano, F, Verloes, A, Munnich, A, Leheup, B, Burglen, L, Odent, S, H Van Esch, Levy, N
Published in Clinical genetics (01.07.2006)
Published in Clinical genetics (01.07.2006)
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Ectomycorrhizal symbiosis affects functional diversity of rhizosphere fluorescent pseudomonas
Frey-Klett, Pascale, Chavatte, M., Clausse, M.L., Courrier, S., Le Roux, C., Raaijmakers, Jos, Martinotti, M.G., Pierrat, J.C., Garbaye, Jean
Published in The New phytologist (2004)
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Published in The New phytologist (2004)
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G.P.6.09 Immunolabelling and FACS as new tools to explore dysferlinopathies
Wein, W.N, Krahn, K.M, Courrier, C.S, Salort-Campana, S.C.E, Nguyen, N.K, Fernandez, F.C, Pouget, P.J, Fossat, F.C, Depetris, D.D, Leturcq, L.F, Lévy, L.N
Published in Neuromuscular disorders : NMD (01.09.2009)
Published in Neuromuscular disorders : NMD (01.09.2009)
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Desensitization of children to television violence
Cline, V B, Croft, R G, Courrier, S
Published in Journal of personality and social psychology (01.09.1973)
Published in Journal of personality and social psychology (01.09.1973)
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