PML nuclear bodies are highly organised DNA-protein structures with a function in heterochromatin remodelling at the G2 phase von Luciani, J.J, Depetris, D, Usson, Y, Metzler-Guillemain, C, Mignon-Ravix, C, Mitchell, M.J, Megarbane, A, Sarda, P, Sirma, H, Moncla, A, Feunteun, J, Mattei, M.-G

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Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations von Luciani, J J, de Mas, P, Depetris, D, Mignon-Ravix, C, Bottani, A, Prieur, M, Jonveaux, P, Philippe, A, Bourrouillou, G, de Martinville, B, Delobel, B, Vallee, L, Croquette, M-F, Mattei, M-G

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Disruption of a new X linked gene highly expressed in brain in a family with two mentally retarded males von Cantagrel, V, Lossi, A-M, Boulanger, S, Depetris, D, Mattei, M-G, Gecz, J, Schwartz, C E, Van Maldergem, L, Villard, L

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Immunolabelling and flow cytometry as new tools to explore dysferlinopathies von 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

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Assignment of a new congenital fibrosis of extraocular muscles type 3 (CFEOM3) locus, FEOM4, based on a balanced translocation t(2;13) (q37.3;q12.11) and identification of candidat... von Aubourg, P, Krahn, M, Bernard, R, Nguyen, K, Forzano, O, Boccaccio, I, Delague, V, De Sandre-Giovannoli, A, Pouget, J, Depétris, D, Mattei, M-G, Philip, N, Lévy, N

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ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X protein von Cardoso, Carlos, Lutz, Yves, Mignon, Cecile, Compe, Emmanuel, Depetris, Danielle, Mattei, Marie-Geneviève, Fontes, Michel, Colleaux, Laurence

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SRPX2 mutations in disorders of language cortex and cognition von Roll, Patrice, Rudolf, Gabrielle, Pereira, Sandrine, Royer, Barbara, Scheffer, Ingrid E., Massacrier, Annick, Valenti, Maria-Paola, Roeckel-Trevisiol, Nathalie, Jamali, Sarah, Beclin, Christophe, Seegmuller, Caroline, Metz-Lutz, Marie-Noëlle, Lemainque, Arnaud, Delepine, Marc, Caloustian, Christophe, Martin, Anne de Saint, Bruneau, Nadine, Depétris, Danièle, Mattéi, Marie-Geneviève, Flori, Elisabeth, Robaglia-Schlupp, Andrée, Lévy, Nicolas, Neubauer, Bernd A., Ravid, Rivka, Marescaux, Christian, Berkovic, Samuel F., Hirsch, Edouard, Lathrop, Mark, Cau, Pierre, Szepetowski, Pierre

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Definition of a T-Cell Receptor β Gene Core Enhancer of V(D)J Recombination by Transgenic Mapping von Tripathi, Raj Kamal, Mathieu, Noëlle, Spicuglia, Salvatore, Payet, Dominique, Verthuy, Christophe, Bouvier, Gaëlle, Depetris, Danielle, Mattei, Marie-Geneviève, HempeL, William M., Ferrier, Pierre

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Evaluation of the genotoxic activity of paclitaxel by the in vitro micronucleus test in combination with fluorescent in situ hybridization of a DNA centromeric probe and the alkali... von Digue, L., Orsière, T., De Méo, M., Mattéi, M. G., Depetris, D., Duffaud, F., Favre, R., Botta, A.

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Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation von Lossi, A-M, Laugier-Anfossi, F, Depetris, D, Gecz, J, Gedeon, A, Kooy, F, Schwartz, C, Mattei, M-G, Croquette, M-F, Villard, L

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Dual-targeted therapy with trastuzumab and lapatinib in treatment-refractory, KRAS codon 12/13 wild-type, HER2-positive metastatic colorectal cancer (HERACLES): a proof-of-concept,... von Sartore-Bianchi, Andrea, MD, Trusolino, Livio, MD, Martino, Cosimo, PhD, Bencardino, Katia, MD, Lonardi, Sara, MD, Bergamo, Francesca, MD, Zagonel, Vittorina, MD, Leone, Francesco, MD, Depetris, Ilaria, MD, Martinelli, Erika, MD, Troiani, Teresa, MD, Ciardiello, Fortunato, Prof, Racca, Patrizia, MD, Bertotti, Andrea, MD, Siravegna, Giulia, MSc, Torri, Valter, MD, Amatu, Alessio, MD, Ghezzi, Silvia, MSc, Marrapese, Giovanna, PhD, Palmeri, Laura, MD, Valtorta, Emanuele, PhD, Cassingena, Andrea, MSc, Lauricella, Calogero, PhD, Vanzulli, Angelo, MD, Regge, Daniele, MD, Veronese, Silvio, MSc, Comoglio, Paolo M, Prof, Bardelli, Alberto, PhD, Marsoni, Silvia, Dr, Siena, Salvatore, Prof

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Assignment of the tumor protein p53 induced nuclear protein 2 (TP53INP2) gene to human chromosome band 20q11.2 by in situ hybridization von Nowak, J., Depetris, D., Iovanna, J.-L., Mattei, M.-G., Pébusque, M.-J.

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Clinical heterogeneity in 16 patients with inv dup 15 chromosome: cytogenetic and molecular studies, search for an imprinting effect von Mignon, C, Malzac, P, Moncla, A, Depetris, D, Roeckel, N, Croquette, M F, Mattei, M G

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Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome von Levy, Annie, Demczuk, Suzanne, Aurias, Alain, Depétris, Danièle, Mattei, Marie-Geneviève, Philip, Nicole

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Maternally inherited duplication of the possible imprinted 14q31 region von Mignon-Ravix, Cécile, Mugneret, Francine, Stavropoulou, Christiana, Depetris, Danielle, Van Kien, Philippe Khau, Mattei, Marie-Geneviève

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Cloning, structural analysis, and mapping of the B30 and B7 multigenic families to the major histocompatibility complex (MHC) and other chromosomal regions von Henry, J, Ribouchon, M, Depetris, D, Matteï, M, Offer, C, Tazi-Ahnini, R, Pontarotti, P

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Bivalent 15 regularly associates with the sex vesicle in normal male meiosis von Metzler-Guillemain, C, Mignon, C, Depetris, D, Guichaoua, M R, Mattei, M G

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Mutation in the 5' alternatively spliced region of the XNP/ATR-X gene causes Chudley-Lowry syndrome von Abidi, Fatima E, Cardoso, Carlos, Lossi, Anne-Marie, Lowry, Robert Brian, Depetris, Danielle, Mattéi, Marie-Geneviève, Lubs, Herbert A, Stevenson, Roger E, Fontes, Michel, Chudley, Albert E, Schwartz, Charles E

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Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication study von Stavropoulou, C, Mignon, C, Delobel, B, Moncla, A, Depetris, D, Croquette, M F, Mattei, M G

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Organization of the X and Y chromosomes in human, chimpanzee and mouse pachytene nuclei using molecular cytogenetics and three-dimensional confocal analyses von Metzler-Guillemain, C, Usson, Y, Mignon, C, Depetris, D, Dubreuil, G, Guichaoua, M R, Mattei, M G

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