Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease
Fontés, Michel, Passage, Edith, Norreel, Jean Chrétien, Noack-Fraissignes, Pauline, Sanguedolce, Véronique, Pizant, Josette, Thirion, Xavier, Robaglia-Schlupp, Andrée, Pellissier, Jean François
Published in Nature medicine (01.04.2004)
Published in Nature medicine (01.04.2004)
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Correlation Between Varying Levels of PMP22 Expression and the Degree of Demyelination and Reduction in Nerve Conduction Velocity in Transgenic Mice
Huxley, C., Passage, E., Robertson, A. M., Youl, B., Huston, S., Manson, A., Sabéran-Djoniedi, D., Figarella-Branger, D., Pellissier, J. F., Thomas, P. K., Fontés, M.
Published in Human molecular genetics (01.03.1998)
Published in Human molecular genetics (01.03.1998)
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PMP22 overexpression causes dysmyelination in mice
Robaglia‐Schlupp, A., Pizant, J., Norreel, J.‐C., Passage, E., Sabéran‐Djoneidi, D., Ansaldi, J.‐L., Vinay, L., Figarella‐Branger, D., Lévy, N., Clarac, F., Cau, P., Pellissier, J.‐F., Fontés, M.
Published in Brain (London, England : 1878) (01.10.2002)
Published in Brain (London, England : 1878) (01.10.2002)
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Behavioural profiling of a murine Charcot-Marie-Tooth disease type 1A model
Norreel, J. C., Jamon, M., Riviere, G., Passage, E., Fontes, M., Clarac, F.
Published in The European journal of neuroscience (01.04.2001)
Published in The European journal of neuroscience (01.04.2001)
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DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome
Mattei, M G, Philip, N, Passage, E, Moisan, J P, Mandel, J L, Mattei, J F
Published in Human genetics (01.03.1985)
Published in Human genetics (01.03.1985)
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Assignment of microsatellite sequences to the region duplicated in CMT1A (17p12): a useful tool for diagnosis
Cudrey, C, Chevillard, C, Le Paslier, D, Vignal, A, Passage, E, Fontes, M
Published in Journal of medical genetics (01.03.1995)
Published in Journal of medical genetics (01.03.1995)
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Cloning and chromosomal localization of human genes encoding the three chains of type VI collagen
WEIL, D, MATTEI, M.-G, PASSAGE, E, N'GUYEN VAN CONG, PRIBULA-CONWAY, D, MANN, K, DEUTZMANN, R, TIMPL, R, MON-LI CHU
Published in American journal of human genetics (01.03.1988)
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Published in American journal of human genetics (01.03.1988)
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The Human Inward Rectifying K+Channel Kir 2.2 (KCNJ12) Gene: Gene Structure, Assignment to Chromosome 17p11.1, and Identification of a Simple Tandem Repeat Polymorphism
Hugnot, J.P., Pedeutour, F., Le Calvez, C., Grosgeorge, J., Passage, E., Fontes, M., Lazdunski, M.
Published in Genomics (San Diego, Calif.) (01.01.1997)
Published in Genomics (San Diego, Calif.) (01.01.1997)
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The human calbindin D28k (CALB1) and calretinin (CALB2) genes are located at 8q21.3----q22.1 and 16q22----q23, respectively, suggesting a common duplication with the carbonic anhydrase isozyme loci
Parmentier, M, Passage, E, Vassart, G, Mattei, M G
Published in Cytogenetics and cell genetics (1991)
Published in Cytogenetics and cell genetics (1991)
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The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosome
Mattei, M G, Alliel, P M, Dautigny, A, Passage, E, Pham-Dinh, D, Mattei, J F, Jollès, P
Published in Human genetics (01.04.1986)
Published in Human genetics (01.04.1986)
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Assignment of the human gamma-glutamyl transferase gene to the long arm of chromosome 22
Bulle, F, Mattei, M G, Siegrist, S, Pawlak, A, Passage, E, Chobert, M N, Laperche, Y, Guellaën, G
Published in Human genetics (01.07.1987)
Published in Human genetics (01.07.1987)
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The gene encoding the large human neurofilament subunit (NF-H) maps to the q121-q131 region on human chromosome 22
Mattei, M G, Dautigny, A, Pham-Dinh, D, Passage, E, Mattei, J F, Jollès, P
Published in Human genetics (01.11.1988)
Published in Human genetics (01.11.1988)
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Chromosomal localization of human aspartate aminotransferase genes by in situ hybridization
Pol, S, Bousquet-Lemercier, B, Pavé-Preux, M, Bulle, F, Passage, E, Hanoune, J, Mattei, M G, Barouki, R
Published in Human genetics (01.09.1989)
Published in Human genetics (01.09.1989)
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In situ mapping of the muscle-specific form of phosphoglycerate mutase gene to human chromosome 7p12-7p13
Castella-Escola, J, Mattei, M G, Ojcius, D M, Passage, E, Valentin, C, Cohen-Solal, M
Published in Human genetics (01.01.1990)
Published in Human genetics (01.01.1990)
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Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridization
Pellissier, M C, Laffage, M, Philip, N, Passage, E, Mattei, M G, Mattei, J F
Published in Human genetics (01.11.1988)
Published in Human genetics (01.11.1988)
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