De Novo and Inherited Deletions of the 5q13 Region in Spinal Muscular Atrophies
Melki, Judith, Lefebvre, Suzie, Burglen, Lydie, Burlet, Philippe, Clermont, Olivier, Millasseau, Philippe, Reboullet, Sophie, Bénichou, Bernard, Zeviani, Massimo, Le Paslier, Denis, Cohen, Daniel, Weissenbach, Jean, Munnich, Arnold
Published in Science (American Association for the Advancement of Science) (03.06.1994)
Published in Science (American Association for the Advancement of Science) (03.06.1994)
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Isolation of 10 Differentially Expressed cDNAs in p53-Induced Apoptosis: Activation of the Vertebrate Homologue of the Drosophila Seven in Absentia Gene
Amson, Robert B., Nemani, Mona, Roperch, Jean-Pierre, Israeli, David, Bougueleret, Lydie, Le Gall, Isabelle, Medhioub, Monia, Linares-Cruz, Gustavo, Lethrosne, Florence, Pasturaud, Patricia, Piouffre, Laurence, Prieur, Sylvie, Susini, Laurent, Alvaro, Véronique, Millasseau, Philippe, Guidicelli, Catherine, Bui, Hung, Massart, Catherine, Cazes, Lucien, Dufour, Fabienne, Bruzzoni-Giovanelli, Heriberto, Owadi, Houman, Hennion, Claude, Charpak, Georges, Dausset, Jean, Calvo, Fabien, Oren, Moshe, Cohen, Daniel, Telerman, Adam
Published in Proceedings of the National Academy of Sciences - PNAS (30.04.1996)
Published in Proceedings of the National Academy of Sciences - PNAS (30.04.1996)
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E-box- and MEF-2-independent muscle-specific expression, positive autoregulation, and cross-activation of the chicken MyoD (CMD1) promoter reveal an indirect regulatory pathway
Dechesne, C A, Wei, Q, Eldridge, J, Gannoun-Zaki, L, Millasseau, P, Bougueleret, L, Caterina, D, Paterson, B M
Published in Molecular and Cellular Biology (01.08.1994)
Published in Molecular and Cellular Biology (01.08.1994)
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Journal Article
Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 in Xq13.3
Gecz, J, Pollard, H, Consalez, G, Villard, L, Stayton, C, Millasseau, P, Khrestchatisky, M, Fontes, M
Published in Human molecular genetics (01.01.1994)
Published in Human molecular genetics (01.01.1994)
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Journal Article
Genetic and Physiological Data Implicating the New Human Gene G72 and the Gene for D-Amino Acid Oxidase in Schizophrenia
Chumakov, Ilya, Blumenfeld, Marta, Guerassimenko, Oxana, Cavarec, Laurent, Palicio, Marta, Abderrahim, Hadi, Bougueleret, Lydie, Barry, Caroline, Tanaka, Hiroaki, La Rosa, Philippe, Puech, Anne, Tahri, Nadia, Cohen-Akenine, Annick, Delabrosse, Sylvain, Lissarrague, Sébastien, Picard, Françoise-Pascaline, Maurice, Karelle, Essioux, Laurent, Millasseau, Philippe, Grel, Pascale, Debailleul, Virginie, Simon, Anne-Marie, Caterina, Dominique, Dufaure, Isabelle, Malekzadeh, Kattayoun, Belova, Maria, Luan, Jian-Jian, Bouillot, Michel, Sambucy, Jean-Luc, Primas, Gwenael, Saumier, Martial, Boubkiri, Nadia, Martin-Saumier, Sandrine, Nasroune, Myriam, Peixoto, Hélène, Delaye, Arnaud, Pinchot, Virginie, Bastucci, Mariam, Guillou, Sophie, Chevillon, Magali, Sainz-Fuertes, Ricardo, Meguenni, Said, Aurich-Costa, Joan, Cherif, Dorra, Gimalac, Anne, van Duijn, Cornelia, Gauvreau, Denis, Ouelette, Gail, Fortier, Isabel, Realson, John, Sherbatich, Tatiana, Riazanskaia, Nadejda, Rogaev, Evgeny, Raeymaekers, Peter, Aerssens, Jeroen, Konings, Frank, Luyten, Walter, Macciardi, Fabio, Sham, Pak C., Straub, Richard E., Weinberger, Daniel R., Cohen, Nadine, Cohen, Daniel
Published in Proceedings of the National Academy of Sciences - PNAS (15.10.2002)
Published in Proceedings of the National Academy of Sciences - PNAS (15.10.2002)
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Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations
Plassart, E, Reboul, J, Rime, C S, Recan, D, Millasseau, P, Eymard, B, Pelletier, J, Thomas, C, Chapon, F, Desnuelle, C
Published in European journal of human genetics : EJHG (1994)
Published in European journal of human genetics : EJHG (1994)
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Journal Article
A comprehensive genetic map of the human genome based on 5,264 microsatellites
Dib, Colette, Fauré, Sabine, Fizames, Cécile, Samson, Delphine, Drouot, Nathalie, Vignal, Alain, Millasseau, Philippe, Marc, Sophie, Kazan, Jamile, Seboun, Eric, Lathrop, Mark, Gyapay, Gabor, Morissette, Jean, Weissenbach, Jean
Published in Nature (London) (14.03.1996)
Published in Nature (London) (14.03.1996)
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Journal Article
The 1993-94 Généthon human genetic linkage map
Bernardi, Giorgio, Vignal, Alain, Morissette, Jean, Marc, Sophie, Millasseau, Philippe, Weissenbach, Jean, Fizames, Cécile, Lathrop, Mark, Gyapay, Gabor, Dib, Colette
Published in Nature genetics (01.06.1994)
Published in Nature genetics (01.06.1994)
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Journal Article
Identification and characterization of a spinal muscular atrophy-determining gene
Lefebvre, Suzie, Bürglen, Lydie, Reboullet, Sophie, Clermont, Olivier, Burlet, Philippe, Viollet, Louis, Benichou, Bernard, Cruaud, Corinne, Millasseau, Philippe, Zeviani, Massimo, Le Paslier, Denis, Frézal, Jean, Cohen, Daniel, Weissenbach, Jean, Munnich, Arnold, Melki, Judith
Published in Cell (13.01.1995)
Published in Cell (13.01.1995)
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Journal Article
A second-generation linkage map of the human genome
Weissenbach, Jean, Gyapay, Gabor, Dib, Colette, Vignal, Alain, Morissette, Jean, Millasseau, Philippe, Vaysseix, Guy, Lathrop, Mark
Published in Nature (London) (29.10.1992)
Published in Nature (London) (29.10.1992)
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Journal Article
Two DRβ Allelic Series Defined by Exon II-Specific Synthetic Oligonucleotide Genomic Hybridization: A Method of HLA Typing?
Le Gall, Isabelle, Millasseau, Philippe, Dausset, Jean, Cohen, Daniel
Published in Proceedings of the National Academy of Sciences - PNAS (01.10.1986)
Published in Proceedings of the National Academy of Sciences - PNAS (01.10.1986)
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Journal Article
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
Legouis, Renaud, Hardelin, Jean-Pierre, Levilliers, Jacqueline, Claverie, Jean-Michel, Compain, Sylvia, Wunderle, Véronique, Millasseau, Philippe, Le Paslier, Denis, Cohen, Daniel, Caterina, Dominique, Bougueleret, Lydie, Delemarre-Van de Waal, Henriette, Lutfalla, Georges, Weissenbach, Jean, Petit, Christine
Published in Cell (18.10.1991)
Published in Cell (18.10.1991)
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Predisposing Gene for Early-Onset Prostate Cancer, Localized on Chromosome 1q42.2-43
Berthon, Philippe, Valeri, Antoine, Cohen-Akenine, Annick, Drelon, Eric, Paiss, Thomas, Wöhr, Gudrun, Latil, Alain, Millasseau, Philippe, Mellah, Imène, Cohen, Nadine, Blanché, Hélène, Bellané-Chantelot, Christine, Demenais, Florence, Teillac, Pierre, Le Duc, Alain, de Petriconi, Robert, Hautmann, Richard, Chumakov, Ilya, Bachner, Lucien, Maitland, Norman J., Lidereau, Rosette, Vogel, Walther, Fournier, Georges, Mangin, Philippe, Cohen, Daniel, Cussenot, Olivier
Published in American journal of human genetics (01.06.1998)
Published in American journal of human genetics (01.06.1998)
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Journal Article
New methods for detection of HLA genes polymorphism useful for associated diseases studies
Le Gall, I, Chausse, A M, Marcadet, A, Millasseau, P, Beaud'Huy-Lancelin, D, Font, M P, Paul, P, Sayagh, B, Masse, M, Massart, C
Published in Pathologie biologie (Paris) (01.06.1986)
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Published in Pathologie biologie (Paris) (01.06.1986)
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Survey of CAG/CTG Repeats in Human cDNAs Representing New Genes: Candidates for Inherited Neurological Disorders
Néri, Christian, Albanèse, Véronique, Lebre, Anne-Sophie, Holbert, Sébastien, Saada, Claudine, Bougueleret, Lydie, Meier-Ewert, Sebastian, Le Gall, Isabelle, Millasseau, Philippe, Bui, Hung, Giudicelli, Catherine, Massart, Catherine, Guillou, Sophie, Gervy, Patricia, Poullier, Eric, Rigault, Philippe, Weissenbach, Jean, Lennon, Greg, Chumakov, Ilya, Dausset, Jean, Lehrach, Hans, Cohen, Daniel, Cann, Howard M.
Published in Human molecular genetics (01.07.1996)
Published in Human molecular genetics (01.07.1996)
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Journal Article
Down-regulation of mitochondrial mRNAs in the mdx mouse model for Duchenne muscular dystrophy
Gannoun-Zaki, L, Fournier-Bidoz, S, Le Cam, G, Chambon, C, Millasseau, Ph, Léger, J.J, Dechesne, C.A
Published in FEBS letters (20.11.1995)
Published in FEBS letters (20.11.1995)
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Journal Article
Illegitimate transcription of the phenylalanine hydroxylase gene in lymphocytes for identification of mutations in phenylketonuria
Abadie, V, Jaruzelska, J, Lyonnet, S, Millasseau, P, Berthelon, M, Rey, F, Munnich, A, Rey, J
Published in Human molecular genetics (01.01.1993)
Published in Human molecular genetics (01.01.1993)
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Journal Article
Physical and transcriptional mapping of DXS56-PGK1 1 Mb region: identification of three new transcripts
Gecz, J, Villard, L, Lossi, A M, Millasseau, P, Djabali, M, Fontes, M
Published in Human molecular genetics (01.09.1993)
Published in Human molecular genetics (01.09.1993)
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Journal Article
The 1993-94 Généthon human genetic linkage map
GYAPAY, G, MORISSETTE, J, VIGNAL, A, DIB, C, FIZAMES, C, MILLASSEAU, P, MARC, S, BERNARDI, G, LATHROP, M, WEISSENBACH, J
Published in Nature genetics (1994)
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Published in Nature genetics (1994)
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