Not logged inIsolation and characterization of Suv39h2, a second histone H3 methyltransferase gene that displays testis-specific expression
O'Carroll, D; Scherthan, H; Peters, AHFM; Opravil, S; Haynes, AR; Laible, G; Rea, S; Schmid, M; Lebersorger, A; Jerratsch, M; Sattler, L; Mattei, MG; Denny, P; Brown, SDM; Schweizer, D; Jenuwein, T .png)
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SaveDefinition of a T-cell receptor β gene core enhancer of V(D)J recombination by transgenic mappingTripathi, RK; Mathieu, N; Spicuglia, S; Payet, D; Verthuy, C; Bouvier, G; Depetris, D; Mattei, MG; Hempel, WM; Ferrier, P Share Save Share Save Share Save Share Save Share Save Neuromuscular defects and breathing disorders in a new mouse model of spinal muscular atrophyMichaud, Magali; Arnoux, Thomas; Bielli, Serena; Durand, Estelle; Rotrou, Yann; Jablonka, Sibylle; Robert, Fabrice; Giraudon-Paoli, Marc; Riessland, Markus; Mattei, Marie-Genevieve; Andriambeloson, Emile; Wirth, Brunhilde; Sendtner, Michael; Gallego, Jorge; Pruss, Rebecca M.; Bordet, Thierry Share Save Share Save Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocationsMignon-Ravix, Cecile; Depetris, Danielle; Luciani, Judith J.; Cuoco, Cristina; Krajewska-Walasek, Malgorzata; Missirian, Chantal; Collignon, Patrick; Delobel, Bruno; Croquette, Marie-Francoise; Moncla, Anne; Kroisel, Peter M.; Mattei, Marie-Genevieve Share Save PML nuclear bodies are highly organised DNA-protein structures with a function in heterochromatin remodelling at the G2 phaseLuciani, Judith J.; Depetris, Danielle; Usson, Yves; Metzler-Guillemain, Catherine; Mignon-Ravix, Cecile; Mitchell, Michael J.; Megarbane, Andre; Sarda, Pierre; Sirma, Huseyin; Moncla, Anne; Feunteun, Jean; Mattei, Marie-Genevieve Share Save Share Save SRPX2 mutations in disorders of language cortex and cognitionRoll, P; Rudolf, G; Pereira, S; Royer, B; Scheffer, IE; Massacrier, A; Valenti, MP; Roeckel-Trevisiol, N; Jamali, S; Beclin, C; Seegmuller, C; Metz-Lutz, MN; Lemainque, A; Delepine, M; Caloustian, C; Martin, AD; Bruneau, N; Depétris, D; Mattéi, MG; Flori, E; Robaglia-Schlupp, A; Lévy, N; Neubauer, BA; Ravid, R; Marescaux, C; Berkovic, SF; Hirsch, E; Lathrop, M; Cau, P; Szepetowski, P Share Save Share Save Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertilityMachev, N; Saut, N; Longepied, G; Terriou, P; Navarro, A; Levy, N; Guichaoua, M; Metzler-Guillemain, C; Collignon, P; Frances, AM; Belougne, J; Clemente, E; Chiaroni, J; Chevillard, C; Durand, C; Ducourneau, A; Pech, N; McElreavey, K; Mattei, MG; Mitchell, MJ Share Save Mutation in the 5′ alternatively spliced region of the XNP/ATR-X gene causes Chudley-Lowry syndromeAbidi, FE; Cardoso, C; Lossi, AM; Lowry, RB; Depetris, D; Mattéi, MG; Lubs, HA; Stevenson, RE; Fontes, M; Chudley, AE; Schwartz, CE Share Save Share Save Share Save Share Save Share Save 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 retardationLossi, AM; Laugier-Anfossi, F; Depetris, D; Gecz, J; Gedeon, A; Kooy, F; Schwartz, C; Mattei, MG; Croquette, MF; Villard, L Share Save 
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