ROCCHI, Mariano

ROCCHI, Mariano  

DIPARTIMENTO DI BIOLOGIA  

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Titolo Data di pubblicazione Autore(i) File
The 14/15 association as a paradigmatic example of tracing karyotype evolution in New World monkeys 1-gen-2016 Capozzi, Oronzo; Archidiacono, Nicoletta; Lorusso, Nicola; Stanyon, Roscoe; Rocchi, Mariano
+2.71 LOD score at zero recombination is not sufficient for establishing linkage between X-linked mental retardation and X-chromosome markers 1-gen-1996 Robledo, R; Melis, P; Siniscalco, M; Marchi, J; Laficara, F; Rinaldi, A; Rocchi, Mariano; Filippi, G.
A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia chromosome translocation 1-gen-2002 Saglio, G; Storlazzi, CLELIA TIZIANA; Giugliano, E; Surace, C; Anelli, Luisa; Rege Cambrin, G; Zagaria, Antonella; Jimenez Velasco, A; Heiniger, A; Scaravaglio, P; Torres Gomez, A; Roman Gomez, J; Archidiacono, Nicoletta; Banfi, S; Rocchi, Mariano
A 76kb interchromosomal duplicon maps close to BCR gene on chromosome 22 and to ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia-chromosome translocation 1-gen-2002 G., Saglio; Storlazzi, CLELIA TIZIANA; E., Giugliano; C., Surace; Anelli, Luisa; G., REGE CAMBRIN; Zagaria, Antonella; A., JIMENEZ VELASCO; A., Heiniger; P., Scaravaglio; A., TORRES GOMEZ; J., ROMAN GOMEZ; Archidiacono, Nicoletta; S., Banfi; Rocchi, Mariano
A chronic myelocytic leukemia case bearing deletions on the three chromosomes involved in a variant t(9;22;11) 1-gen-2004 Anelli, Luisa; Albano, Francesco; Zagaria, Antonella; Liso, A.; Roberti, M. G.; Rocchi, Mariano; Specchia, Giorgina
A de novo 6p interstitial deletion and a complex translocation involving chromosomes 2, 6, and 14 in a mildly developmentally delayed patient 1-gen-2008 Misceo, D; Bjorgo, K; Ormerod, E; Ringen, O; Rocchi, Mariano; van der Hagen, Cb; Frengen, E.
A DNA fragment from Xq21 replaces a deleted region containing the entire FVIII gene in a severe hemophilia A patient 1-gen-1994 Murru, S; Casula, L; Casarino, L; Moi, P; Rocchi, Mariano; Loi, A; Figus, A; Mannella, M; Poddie, D; Kenwrick, S; Mori, P; Cao, A; Pirastu, M.
A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome 1-gen-2004 Zagaria, Antonella; Anelli, Luisa; Albano, Francesco; Storlazzi, CLELIA TIZIANA; Rocchi, Mariano; Liso, A; Roberti, Mg; Buquicchio, C; Liso, V; Specchia, Giorgina
A genome-wide comparison of recent chimpanzee and human segmental duplications 1-gen-2005 Cheng, Z; Ventura, Mario; Khaitovich, P; Graves, T; Osoegawa, K; Church, D; Dejong, P; Wilson, Rk; Paabo, S; Rocchi, Mariano; Eichler, Ee; She, X
A high resolution deletion map of the human Xp22 region 1-gen-1993 Schaefer, L; Ferrero, Gb; Grillo, A; Bassi, Mt; Roth, Ej; Wapenaar, Mc; van Ommen G., Jb; Mohandas, Tk; Rocchi, Mariano; Zoghbi, Hy; Ballabio, A.
A human alpha satellite DNA subset specific for chromosome 12 1-gen-1990 Baldini, A; Rocchi, Mariano; Archidiacono, Nicoletta; Miller, Oj; Miller, Da
A human alphoid DNA clone from the EcoRI dimeric family: genomic and internal organization and chromosomal assignment 1-gen-1989 Baldini, A; Smith, Di; Rocchi, Mariano; Miller, Oj; Miller, Da
A human chromosome 9-specific alphoid DNA repeat spatially resolvable from satellite 3 DNA by fluorescent in situ hybridization 1-gen-1991 Rocchi, Mariano; Archidiacono, Nicoletta; Ward, Dc; Baldini, A.
A human short-chain dehydrogenase/reductase gene: structure, chromosomal localization, tissue expression and subcellular localization of its product 1-gen-2002 Pellegrini, S; Censini, S; Guidotti, S; Iacopetti, P; Rocchi, Mariano; Bianchi, M; Covacci, A; Gabrielli, F.
A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH) 1-gen-2001 Nietzel, A; Rocchi, Mariano; Starke, H; Heller, A; Fiedler, W; Wlodarska, I; Loncarevic, If; Beensen, V; Claussen, U; Liehr, T.
A new translocation involving chromosomes no. 5 and no. 12 t(5;12) (5q15;12p13). 1-gen-1977 Rocchi, Mariano; Ferraro, M; Archidiacono, Nicoletta; Pelliccia, F; Valenti, C; De Capoa, A.
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1 1-gen-2003 Storlazzi, CLELIA TIZIANA; Anelli, L; Albano, Francesco; Zagaria, A; Ventura, Mario; Rocchi, Mariano; Panagopoulos, I; Pannunzio, Alessandra; Ottaviani, E; Liso, V; Specchia, Giorgina
A novel chromosomal translocation t(3;7)(q26;q21)in myeloid leukemia resulting in overexpression of EVI1 1-gen-2004 Storlazzi, CLELIA TIZIANA; Anelli, Luisa; Albano, Francesco; Zagaria, Antonella; Ventura, Mario; Rocchi, Mariano; Panagopoulos, I; Pannunzio, Alessandra; Ottaviani, E; Liso, V; Specchia, G.
A novel chromosomal translocation t(4;14)(p16.3;q32) in multiple myeloma involves the fibroblast growth-factor receptor 3 gene 1-gen-1997 Richelda, R; Ronchetti, D; Baldini, L; Cro, L; Viggiano, Luigi; Marzella, R; Rocchi, Mariano; Otsuki, T; Lombardi, L; Maiolo, At; Neri, A.
A novel FISH assay for SS18-SSX fusion type in synovial sarcoma 1-gen-2004 Surace, C; Panagopoulos, I; Palsson, E; Rocchi, Mariano; Mandahl, N; Mertens, F.