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in press
2007 ( top )
Albano F, Anelli L, Zagaria A, Archidiacono N, Liso V, Specchia G, Rocchi M: "Home-brew" FISH assay shows higher efficiency than BCR-ABL dual color, dual fusion probe in detecting microdeletions and complex rearrangements associated with t(9;22) in chronic myeloid leukemia. Cancer Genet Cytogenet 174:121-126 (2007).
Bodega B, Cardone MF, Muller S, Neusser M, Orzan F, Rossi E, Battaglioni E, Marozzi A, Riva P, Rocchi M, Meneveri R, Ginelli E: Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2). BMC Evol Biol 7:39 (2007).
Cardone MF, Lomiento M, Teti MG, Misceo D, Roberto R, Capozzi O, D'Addabbo P, Ventura M, Rocchi M, Archidiacono N: Evolutionary history of chromosome 11 featuring four distinct centromere repositioning events in Catarrhini. Genomics (2007)
Giorda R, Ciccone R, Gimelli G, Pramparo T, Beri S, Bonaglia MC, Giglio S, Genuardi M, Argente J, Rocchi M, Zuffardi O: Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2. Hum Mut 28:459-468 (2007).
Roberto R, Capozzi O, Wilson RK, Mardis ER, Lomiento M, Tuzun E, Cheng Z, Mootnick AR, Archidiacono N, Rocchi M, Eichler EE: Molecular refinement of gibbon genome rearrangement. Genome Res 17:249-257 (2007)
Storlazzi CT, Albano F, Dencic-Fekete M, Djordjevic V, Rocchi M: Late-appearing pseudocentric fission event during chronic myeloid leukemia progression. Cancer Genet Cytogenet 174:61-7 (2007).
Storlazzi CT, Albano F, Lo Cunsolo C, Doglioni C, Guastadisegni MC, Impera L, Lonoce A, Funes S, Macri E, Iuzzolino P, Panagopoulos I, Specchia G, Rocchi M. Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma. Leukemia. 2007 Jun 7; [Epub ahead of print]
Ventura A, Antonacci F, Cardone MF, Stanyon R, D'Addabbo P, Cellamare A, Sprague LJ, Eichler EE, Archidiacono N, Rocchi M: Evolutionary formation of new centromeres in macaque. Science 316:243-246 (2007).
2006 ( top )
Albano F, Specchia G, Anelli L, Zagaria A, Archidiacono N, Liso V, Rocchi M: Molecular cytogenetic findings supporting the evidence of a biclonal origin in acute myeloid leukemia. Ann Hematol 85:129-31 (2006).
Blasi P, Palmerio F, Aiello A, Rocchi M, Malaspina P, Novelletto A: SSADH Variation in Primates: Intra- and Interspecific Data on a Gene with a Potential Role in Human Cognitive Functions. J Mol Evol 63:54-68 (2006).
Bodega B, Cardone MF, Rocchi M, Meneveri R, Marozzi A, Ginelli E: The boundary of macaque rDNA is constituted by low copy sequences conserved during evolution. Genomics 88:564-571 (2006).
Carbone L, Nergadzeb SG, Magnani E, Misceo D, Cardone MF, Roberto R, Bertoni L, Attolini C, Piras MF, de Jong P, Raudseppd T, Chowdharyd BP, Guérin G, Archidiacono N, Rocchi M, Giulotto E: Evolutionary movement of centromeres in horse, donkey, and zebra. Genomics 87:777-782 (2006).
Cardone MF, Alonso A, Pazienza P, Ventura M, Montemurro G, Carbone L, de Jong PJ, Stanyon R, D'Addabbo P, Archidiacono N, She X, Eichler EE, Warburton PE, and Rocchi M: Independent centromere formation in a capricious gene-free domain of chromosome 13q21 in Old World monkeys and pigs. Genome Biol 7:R91 (2006)
Ciccone R, Mattina T, Giorda R, Bonaglia MC, Rocchi M, Pramparo T, Zuffardi O. Inversion polymorphisms and non-contiguous terminal deletions: the cause and the (unpredicted) effect of our genome architecture. J Med Genet. 2006 May;43(5):e19.
Johnson ME, Cheng Z, Morrison VA, Scherer S, Ventura M, Gibbs RA, Green ED, Eichler EE: Recurrent duplication-driven transposition of DNA during hominoid evolution. Proc Natl Acad Sci U S A 103:17626-17631 (2006)
Rocchi M, Archidiacono N, Stanyon R: Ancestral genomes reconstruction: an integrated, multi-disciplinary approach is needed. Genome Res 16:1566-1574 (2006).
Rocchi M. and Archidiacono N.: Genome Plasticity in Evolution. In “Genomic Disorders: The Genomic Basis of Disease”, pp. 153-165 P. Stankiewicz and J.R. Lupski Editors, Humana Press (2006) ISBN 1-58829-559-1
She X, Liu G, Ventura M, Zhao S, Misceo D, Roberto R, Cardone MF, Rocchi M, Comparative Sequencing Program, Green ED, Archidiacono N, Eichler EE: An initial comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications. Genome Res: 576-583 (2006)
Storlazzi CT, Albano F, Locunsolo C, Lonoce A, Funes S, Guastadisegni MC, Cimarosto L, Impera L, D'Addabbo P, Panagopoulos I, Specchia G, Rocchi M. t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene. Leukemia. 2006 Dec;20(12):2190-2. Epub 2006 Oct 5.
Storlazzi CT, Fioretos T, Surace C, Lonoce A, Mastrorilli A, Strömbeck B, D’Addabbo P, Iacovelli F, Minervini C, Aventin A, Dastugue N, Fonatsch C, Hagemeijer A, Jotterand M, Mühlematter D, Lafage-Pochitaloff M, Nguyen-Khac F, Schoch C, Slovak ML, Smith A, Solè F, Van Roy N, Johansson B, Rocchi M: MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene. Hum Mol Genet 15:933-942 (2006)
Trubia M, Albano F, Cavazzini F, Cambrin GR, Quarta G, Fabbiano F, Ciambelli F, Magro D, M. HJ, Mancini M, Diverio D, Pelicci PG, L. CF, Mecucci C, Specchia G, Rocchi M, Liso V, Cuneo A: Characterization of a recurrent translocation t(2;3)(p15–22;q26) occurring in acute myeloid leukaemia. Leukemia 20:48-54 (2006)
Van Roy N, Vandesompele J, Menten B, Nilsson, De Smet E, Rocchi M, De Paepe A, Påhlman S, Speleman F: Translocation-excision-deletion-amplification mechanism leading to non-syntenic co-amplification of MYC and ATBF1. Genes Chromosomes Cancer 45:107-117 (2006).
Zagaria A, Anelli L, Albano F, Vicari L, Schiavone EM, Annunziata M, Pane F, Liso V, Rocchi M, Specchia G. Molecular cytogenetic characterization of deletions on der(9) in chronic myelocytic leukemia. Cancer Genet Cytogenet. 2006 Jun;167(2):97-102.
2005 ( top )
Anelli L, Albano F, Zagaria A, Liso, Cuneo A, Mancini M, Liso V, Rocchi M, Specchia G. Pericentric chromosome 8 inversion associated with the 5’RUNX1/3’CBFA2T1 gene in acute myeloid leukemia cases. Ann Hematol 84:245-9 (2005).
Antonacci R., Lanave C., Del Faro L., Vaccarelli G., Ciccarese S., Massari S. Artiodactyl emergence is accompanied by the birth of an extensive pool of diverse germline TRDV1 genes. Immunogenetics 57: 254-266 (2005).
Cheng Z, Ventura M, She X, Khaitovich P, Graves T, Osoegawa K, Church D, DeJong P, Wilson RK, Paabo S, Rocchi M and Eichler EE: A Genome-wide comparison of recent human and chimpanzee segmental duplications. Nature 437:88-93 (2005)
Chimpanzee Consortium: Initial sequence of the chimpanzee genome and comparison with the human genome. Nature 437:69-87 (2005)
Horvath JE, Gulden CL, Vallente RU, Eichler MY, Ventura M, McPherson JD, Graves TA, Wilson RK, Schwartz S, Rocchi M, Eichler EE. Punctuated duplication seeding events during the evolution of human chromosome 2p11. Genome Res. 2005 Jul;15(7):914-27
Jackson MS, Oliver K, Loveland J, Humphray JS, Dunham I, Rocchi M, Viggiano V, P. Park JP, Hurles M, Santibanez-Koref M: Reticulate evolution is prevalent within recently duplicated human DNA. 77:824-840 Am J Hum Genet (2005).
Locke DP, Jiang Z, Pertz LM, Misceo D, Archidiacono N, Eichler EE. Molecular evolution of the human chromosome 15 pericentromeric region. Cytogenet Genome Res. 2005;108(1-3):73-82.
Marzella R, Carrozzo C, Chiarappa P, Miolla V, Rocchi M: Panels of somatic cell hybrids specific for chimpanzee, gorilla, orangutan, and baboon. Cytogenet Genome Res 108:223-228 (2005).
Miccoli MC, Vaccarelli G, Lanave C, Cribiu EP, Ciccarese S: Comparative analyses of sheep and human TRG joining regions: Evolution of J genes in Bovidae is driven by sequence conservation in their promoters for germline transcription. Gene 355:67-78 (2005).
Misceo D, Cardone MF, Carbone L, D'Addabbo P, de Jong PJ, Rocchi M, Archidiacono N: Evolutionary history of chromosome 20. Mol Biol Evol 22:360-366 (2005).
Newman TL, Tuzun E, Morrison VA, Hayden KE, Ventura M, McGrath SD, Rocchi M, Eichler EE: A genome-wide survey of structural variation between human and chimpanzee. Genome Res 15:1344-1356 (2005) .
Sardiello M, Tripoli G, Romito A, Minervini C, Viggiano L, Caggese C, Pesole G: Energy biogenesis: one key for coordinating two genomes. Trends Genet 21:12-6 (2005).
Schueler MG, Dunn JM, Bird CP, Ross MT, Viggiano L, Rocchi M, Willard HF, Green ED. Progressive proximal expansion of the primate X chromosome centromere. Proc Natl Acad Sci U S A. 2005 Jul 26;102(30):10563-8
Specchia G, Albano F, Anelli L, Zagaria A, Liso A, Pannunzio A, Archidiacono N, Liso V, Rocchi M: Molecular cytogenetic study of instability at 1q21 approximately q32 in adult acute lymphoblastic leukemia. Cancer Genet Cytogenet 156:54-8 (2005).
Surace C, Storlazzi CT, Engellau J, Domanski HA, Gustafson P, Panagopoulos I, D'Addabbo P, Rocchi M, Mandahl N, Mertens F: Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma. Virchows Arch 447:869-874 (2005).
Storlazzi CT, Von Steyern FV, Domanski HA, Mandahl N, Mertens F: Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma. Int J Cancer 117:1055-7 (2005).
Tripoli G, D'Elia D, Barsanti P, Caggese C: Comparison of the oxidative phosphorylation (OXPHOS) nuclear genes in the genomes of Drosophila melanogaster, Drosophila pseudoobscura and Anopheles gambiae. Genome Biol 6:R11 (2005).
Vaccarelli G, Miccoli MC, Lanave C, Massari S, Cribiu EP, Ciccarese S: Genomic organization of the sheep TRG1@ locus and comparative analyses of Bovidae and human variable genes. Gene (2005).
Wieser R, Fritz B, Ullmann R, Muller I, Galhuber M, Storlazzi CT, Ramaswamy A, Christiansen H, Shimizu N, Rehder H: Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney. Hum Mutat 26:78-83 (2005).
2004 ( top )
Anelli L., Albano F., Zagaria A., Liso A., Roberti M. G., Rocchi M., and Specchia G. (2004). A chronic myelocytic leukemia case bearing deletions on the three chromosomes involved in a variant t(9;22;11). Cancer Genet Cytogenet 148: 137-40.
Bailey JA, Church DM, Ventura M, Rocchi M, Eichler EE: An analysis of segmental duplications and genome assembly in the mouse. Genome Res. 14:789-801 (2004).
Cardone MF, Ballarati L, Ventura M, Rocchi M, Marozzi A, Ginelli E, Meneveri R: Evolution of Beta satellite DNA sequences: evidence for duplication-mediated repeat amplification and spreading. Mol Biol Evol 21:1792-9 (2004).
Nergadze S, Rocchi M, Azzalin CM, Mondello C, Giulotto E: Insertion of telomeric repeats at intrachromosomal break sites during primate evolution. Genome Res 14:1704-1710 (2004).
Panagopoulos I, Storlazzi CT, Fletcher CD, Fletcher JA, Nascimento A, Domanski HA, Wejde J, Brosjo O, Rydholm A, Isaksson M, Mandahl N, Mertens F: The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma. Genes Chromosomes Cancer 40:218-28 (2004).
She X, Horvath JE, Jiang Z, Ge L, Furey T, Christ L, Clark R, Graves T, Gulden CL, Alkan C, Bailey JA, Sahinalp C, Rocchi M, Haussler D, Wilson R, Miller W, Schwartz S, Eichler EE: The structure and evolution of centromeric transition regions within the human genome. Nature 430:857-864 (2004).
Specchia G, Albano F, Anelli L, Storlazzi CT, Zagaria A, Liso A, Pannunzio A, Pastore D, Mestice A, Greco G, Liso V, Rocchi M: Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes. Leuk Lymphoma 45:689-94 (2004).
Storlazzi CT, Anelli L, Albano F, Zagaria A, Ventura M, Rocchi M, Panagopoulos I, Pannunzio A, Ottaviani E, Liso V, Specchia G: A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1. Ann Hematol 83: 78-83 (2004).
Storlazzi CT, Fioretos T, Paulsson K, Strombeck B, Lassen C, Ahlgren T, Juliusson G, Mitelman F, Rocchi M, Johansson B: Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies. Hum Mol Genet 13:1479-85 (2004).
Surace, C., I. Panagopoulos, E. Palsson, M. Rocchi, N. Mandahl, and F. Mertens. 2004. A novel FISH assay for SS18-SSX fusion type in synovial sarcoma. Lab Invest 84: 1185-1192.
Ventura M, Boniotto M, Pazienza M, Palumbo V, Cardone MF, Rocchi M, Tossi A, Amoroso A, Crovella S: Localization of b-defensin genes in non human primates. Eur J Histochem 48:185-90 (2004).
Ventura M, Weigl S, Carbone L, Cardone MF, Misceo D, Teti M, D'Addabbo P, Wandall A, Björck E, de Jong P, She X, Eichler EE, Archidiacono N, Rocchi M: Recurrent sites for new centromere seeding. Genome Res 14:1696-1703 (2004).
Zagaria A, Anelli L, Albano F, Storlazzi CT, Liso A, Roberti MG, Buquicchio C, Liso V, Rocchi M, Specchia G: A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome. Cancer Genet Cytogenet 150:81-5 (2004).
Zollino M, Lecce R, Selicorni A, Murdolo M, Mancuso I, Marangi G, Zampino G, Garavelli L, Ferrarini A, Rocchi M, Opitz JM, Neri G: A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndrome. Eur J Hum Genet 12:797-804 (2004).
2003 ( top )
Bonaglia MC, Giorda R, Cavallini A, Pramparo T, Rocchi M, Borgatti R, Zuffardi O: Distal trisomy 6p and 20q owing to the concurrent transposition of distal 6p and 20q to the 22q telomere: a genomic polymorphism? J Med Genet 40:e94 (2003).
C.T. Storlazzi, F. Mertens, A.Nascimento, M. Isaksson, J. Wejde, O. Brosjö, N. Mandahl, I. Panagopoulos: Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma. Hum. Mol. Genet. 12: 2349-2358 (2003)
M.Ventura, J.M.Mudge, V.Palumbo, S.Burn, E.Blennow, M.Pierluigi, O.Zuffardi, N.Archidiacono, M.S.Jackson, M.Rocchi: Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25. Genome Res. 13:2059–2068 (2003)
Specchia, G., Albano, F., Storlazzi, C. T., Anelli, L., Zagaria, A. Liso, V., Rocchi, M.: t(15;17) in acute promyelocytic leukemia is not associated with submicroscopic deletions on der(17). Haematologica 87:775-777 (2003)
D.P.Locke, N.Archidiacono, D.Misceo, M.Rocchi, and E.E.Eichler: Refinement of a Chimpanzee Pericentric Inversion Breakpoint to a Site of Segmental Duplication. Genome Biol. 4(8):R50 (2003)
Horvath JE, Gulden CL, Bailey JA, Yohn C, McPherson JD, Prescott A, Roe BA, De Jong PJ, Ventura M, Misceo D, Archidiacono N, Zhao S, Schwartz S, Rocchi M, Eichler EE. Using a Pericentromeric Interspersed Repeat to Recapitulate the Phylogeny and Expansion of Human Centromeric Segmental Duplications. Mol. Biol. & Evol. 20:1463-1479 (2003)
V. Eder, M.Ventura, M.Ianigro, M.Teti, M.Rocchi, N.Archidiacono: Chromosome 6 phylogeny in primates and centromere repositioning. Mol. Biol. & Evol. 20:1506-1512 (2003)
M.-E.Brun, M.Ruault, M.Ventura, G.Roizes, A.De Sario: Juxtacentromeric region of human chromosome 21: a boundary between centromeric heterochromatin and euchromatic chromosome arms. Gene 312:41-50
D.Misceo, M.Ventura, V.Eder, M.Rocchi, and N.Archidiacono: Human chromosome 16 conservation in primates. Chromosome Res. 11:323-326 (2003)
Storlazzi CT, Mertens F, Domanski H, Fletcher CD, Wiegant J, Mandahl N. Ring chromosomes and low-grade gene amplification in an atypical lipomatous tumor with minimal nuclear atypia. Int J Oncol. 23:67-71 (2003)
S.Fabris, C.T.Storlazzi, L.Baldini, L.Nobili, L.Lombardi, A.T.Maiolo, M.Rocchi, A.Neri. Heterogeneous pattern of chromosomal breakpoints involving the MYC locus in multiple myeloma. Genes Chrom. Cancer 37:261-269 (2003)
M.Ruault, M.Ventura, N.Galtier M.-E. Brun, N.Archidiacono, G.Roizès, A.De Sario: BAGE genes generated by juxtacentromeric reshuffling in the Hominidae lineage are under selective pressure. Genomics 81:391-399 (2003)
Specchia G, Albano F, Anelli L, Storlazzi CT, Zagaria A, Mancini M, Cuneo A, Pane F, Foa R, Manolelli F, Liso V, Rocchi M. Deletions on der(9) chromosome in adult Ph-positive acute lymphoblastic leukemia occur with a frequency similar to that observed in chronic myeloid leukemia. Leukemia. 2003 Mar;17(3):528-31.
Storlazzi CT, Mertens F, Mandahl N, Gisselsson D, Isaksson M, Gustafson P, Domanski HA, Panagopoulos I. A novel fusion gene, SS18L1/SSX1, in synovial sarcoma. Genes Chromosomes Cancer. 2003 Jun;37(2):195-200.
D.P. Locke, R Segraves, LCarbone, N. Archidiacono, D.G. Albertson, D.Pinkel, and E.E. Eichler: Large-Scale Variation Among Human and Great Ape Genomes Determined by Array Comparative Genomic Hybridization. Genome Res. 2003 13: 341-346 (2003)
F.Albano, G.Specchia, L.Anelli, A.Zagaria, C.T.Storlazzi, C.Buquicchio, M.G.Roberti, V.Liso and M.Rocchi: Genomic deletions on the third chromosome involved in variant t(9;22) chronic myeloid leukemia cases. Genes Chrom Cancer 36:353–360 (2003)
FPG Silva, B Morolli, CT Storlazzi, L Anelli, H Wessels, V Bezrookove, HC Kluin-Nelemans, and M Giphart-Gassler: Identication of RUNX1/AML1 as a classical tumor suppressor gene. Oncogene 22:538-47 (2003)
F.J.Charchar, M.Svartman., N.El-Mogharbel., M.Ventura, P.Kirby, M.R.Matarazzo, A.Ciccodicola, M.Rocchi , M.D’Esposito, J.A.M.Graves: Complex events in the evolution of the human pseudoautosomal region 2 (PAR2). Genome Research 13: 281-286 (2003)
2002 ( top )
Storlazzi CT, Anelli L, Surace C, Rocchi M, Albano F, Pastore D, Liso V, Specchia G: Molecular cytogenetic characterization of a novel additional chromosomal aberration in blast crisis of a Ph-positive chronic myeloid leukemia. Cancer Genet Cytog. 134:109-13 (2002)
M.F.Cardone, M.Ventura, S.Tempesta, M.Rocchi, and N.Archidiacono: Analysis of chromosome conservation in Lemur catta studied by WCPs and BAC/PAC probes. Chromosoma 111:348-56 (2002)
L.Carbone, M.Ventura, S.Tempesta, M.Rocchi, N.Archidiacono: Evolutionary history of phylogenetic chromosome 10 in primates. Chromosoma 111: 236-255 (2002)
Boniotto M, Ventura M, Cardone MF, Boaretto F, Archidiacono N, Rocchi M, Crovella S: Localization of a new highly repeated DNA sequence of Lemur cafta (Lemuridae, Strepsirhini). Genome 45:973-6 (2002)
Ballarati L, Piccini I, Carbone L, Archidiacono N, Rollier A, Marozzi A, Meneveri R, Ginelli E.: Human genome dispersal and evolution of 4q35 duplications and interspersed LSau repeats. Gene 296(1-2):21(2002)
G.Specchia F.Albano, L.Anelli, CT.Storlazzi, A.Zagaria, M.Mancini, A.Cuneo, F.Pane, R.Foa’, V.Liso, M.Rocchi: Deletions on der(9) chromosome in adult ph-positive acute lymphoblastic leukemia occur with a frequency similar to that observed in chronic myeloid leukemia. Br J Haematol 119:488-491 (2002)
C.T.Storlazzi, G.Specchia, L.Anelli, F.Albano, D.Pastore, M.Rocchi, and V.Liso: Breakpoint Characterization of der(9) deletions in CML patients. Genes Chrom Cancer 35:271-276 (2002)
Storlazzi CT, Anelli L, Surace C, Lonoce A, Zagaria A, Nanni M, Curzi P, Rocchi M.: Molecular cytogenetic characterization of a complex rearrangement involving chromosomes 9 and 22 in a case of Ph-negative chronic myeloid leukemia. Cancer Genet Cytogenet.136:141-145 (2002)
G.Saglio, C.T. Storlazzi, E.Giugliano, C.Surace, L.Anelli, G.Rege-Cambrin, A.Zagaria, A.Jimenez Velasco, A.Heiniger, P.Scaravaglio, A.Torres Gomez, J.Roman Gomez, N.Archidiacono, S.Banfi, M.Rocchi: 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. P.N.A.S. 99:9882-9887 (2002)
G.Specchia, F.Albano, L.Anelli, C.T.Storlazzi, G.Cimino, A.Liso, A.Zagaria, V.Liso, M.Rocchi: Molecular cytogenetics characterization of a novel translocation involving chromosomes 17 and 19 in a Ph+ adult acute lymphoblastic leukaemia. British J. Haemat. 87:775-7 (2002)
S.Giglio, V.Calvari, G.Gregato, G.Gimelli, S.Camanini, R.Giorda, A.Ragusa, S.Guerneri, A.Selicorni, M.Stumm, H.Tonnies, M.Ventura, M.Zollino, G.Neri, J.Barber, D.Wieczorek, M.Rocchi, O.Zuffardii: Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation. Am. J. Hum. Genet. 71:276-285 (2002)
G.Specchia, F.Albano, C.T. Storlazzi, L.Anelli, A.Zagaria, V.Liso, M. Rocchi. t(15;17) in acute promyelocytic leukemia is not associated with submicroscopic deletions on der(17). Haematologica 87:775-7 (2002)
Sainati L, Leszl A, Surace C, Perilongo G, Rocchi M, Basso G. Fluorescence in situ hybridization improves cytogenetic results in the analysis of hepatoblastoma. Cancer Genet Cytogenet. 134:18-20 (2002)
Pellegrini S, Censini S, Guidotti S, Iacopetti P, Rocchi M, Bianchi M, Covacci A, Gabrielli F.: A human short-chain dehydrogenase/reductase gene: structure, chromosomal localization, tissue expression and subcellular localization of its product. Biochim Biophys Acta.1574:215-22 (2002)
C.T.Storlazzi, G.Specchia, L.Anelli, F.Albano, D.Pastore, M.Rocchi, and V.Liso: Breakpoint Characterization of der(9) deletions in CML patients. Genes Chrom Cancer 134: 109-113 (2002)
Denegri M, Moralli D, Rocchi M, Biggiogera M, Raimondi E, Cobianchi F, De Carli L, Riva S, Biamonti G.: Human chromosomes 9, 12, and 15 contain the nucleation sites of stress-induced nuclear bodies.Mol Biol Cell. 13: 2069-79 (2002)
Meloni, I.; Vitelli, F.; Pucci, L.; Lowry, R. B.; Tonlorenzi, R.; Rossi, E.; Ventura, M.; Rizzoni, G.; Kashtan, C. E.; Pober, B., and Renieri, A.: Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR). J Med Genet. 39:359-365 (2002)
M.Ruault, M.E.Brun, M.Ventura, G,Roizès, and A.De Sario: MLL3, a new human member of the TRX/MLL gene family, maps to 7q36, a chromosome region frequently deleted in myeloid leukemia. Gene. 284:73-81 (2002)
Specchia G, Albano F, Anelli L, Storlazzi CT, Monaco M, Capalbo S, Rocchi M, Liso V.: Concomitant tetrasomy 3q and trisomy 18 in CD5(-), CD13(+) chronic lymphocytic leukemia. Cancer Genet Cytogenet. 133:160-3 (2002)
M. Crosier, L. Viggiano , J. Guy, D. Misceo1, R. Stones, T. Hearn, M. Ventura, N. Archidiacono, M. Rocchi, and M. S. Jackson: Human paralogues of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms. Genome Res. 12: 67-80 (2002)
J.A.Bailey, A.M.Yavor, L.Viggiano, D.Misceo, J.E.Horvath, N.Archidiacono, S.Schwartz, M.Rocchi and E.E.Eichler: Recent Paralogous Structure of Human Chromosome 22. Am. J. Hum. Genet. 70:83-100 (2002)
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