Search Results - "R. La Starza"

CALM/AF10-positive leukemias show upregulation of genes involved in chromatin assembly and DNA repair processes and of genes adjacent to the breakpoint at 10p12 by Mulaw, M A, Krause, A J, Deshpande, A J, Krause, L F, Rouhi, A, La Starza, R, Borkhardt, A, Buske, C, Mecucci, C, Ludwig, W-D, Lottaz, C, Bohlander, S K

“…The t(10;11)(p12;q14) is a recurring chromosomal translocation that gives rise to the CALM/AF10 fusion gene, which is found in acute myeloid leukemia, acute…”
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FIP1L1-PDGFRA in chronic eosinophilic leukemia and BCR-ABL1 in chronic myeloid leukemia affect different leukemic cells by CRESCENZI, B, CHASE, A, JONES, A. V, CROSS, N. C. P, MARYNEN, P, MECUCCI, C, LA STARZA, R, BEACCI, D, ROSTI, V, GALLI, A, SPECCHIA, G, MARTELLI, M. F, VANDENBERGHE, P, COOLS, J

“…We investigated genetically affected leukemic cells in FIP1L1-PDGFRA+ chronic eosinophilic leukemia (CEL) and in BCR-ABL1+ chronic myeloid leukemia (CML), two…”
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A new NDE1 PDGFRB fusion transcript underlying chronic myelomonocytic leukaemia in Noonan Syndrome by La Starza, R, Rosati, R, Roti, G, Gorello, P, Bardi, A, Crescenzi, B, Pierini, V, Calabrese, O, Baens, M, Folens, C, Cools, J, Marynen, P, Martelli, M F, Mecucci, C, Cuneo, A

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TPM3 PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia by Rosati, R, La Starza, R, Luciano, L, Gorello, P, Matteucci, C, Pierini, V, Romoli, S, Crescenzi, B, Rotoli, B, Martelli, M F, Pane, F, Mecucci, C

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Different genomic imbalances in low- and high-grade HCV-related lymphomas by Matteucci, C, Bracci, M, Barba, G, Carbonari, M, Casato, M, Visentini, M, Pulsoni, A, Varasano, E, Roti, G, Starza, R La, Crescenzi, B, Martelli, M F, Fiorilli, M, Mecucci, C

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CIZ gene rearrangements in acute leukemia: report of a diagnostic FISH assay and clinical features of nine patients by La Starza, R, Aventin, A, Crescenzi, B, Gorello, P, Specchia, G, Cuneo, A, Angioni, A, Bilhou-Nabera, C, Boqué, C, Foà, R, Uyttebroeck, A, Talmant, P, Cimino, G, Martelli, M F, Marynen, P, Mecucci, C, Hagemeijer, A

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Distinct genomic events in the myeloid and lymphoid lineages in simultaneous presentation of chronic myeloid leukemia and B-chronic lymphocytic leukemia by Crescenzi, B, Sacchi, S, Marasca, R, Temperani, P, La Starza, R, Matteucci, C, Bonacorsi, G, Romoli, S, Martelli, M F, Mecucci, C, Emilia, G

“…Leukemia (2002) 16, 955-956. DOI: 10.1038/sj/leu/2402490…”
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Aberrant subcellular expression of nucleophosmin and NPM-MLF1 fusion protein in acute myeloid leukaemia carrying t(3;5): A comparison with NPMc+ AML by FALINI, B, BIGERNA, B, SUN, Y, COLOMBO, E, ARBER, D. A, PACINI, R, LA STARZA, R, GALLETTI, B. V, LISO, A, MARTELLI, M. P, DIVERIO, D, PELICCI, P-G, PUCCIARINI, A, COCO, F L, MAFLELLI, M F, TIACCI, E, MECUCCI, C, MORRIS, S. W, BOLLI, N, ROSATI, R, HANISSIAN, S, MA, Z

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A novel germline mutation in CDK4 codon 24 associated to familial melanoma by Bottillo, I., La Starza, R., Radio, F. C., Molica, C., Pedace, L., Pierini, T., De Bernardo, C., Stingeni, L., Bargiacchi, S., Paiardini, A., Janson, G., Mecucci, C., Grammatico, P.

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Incidence and significance of cryptic chromosome aberrations detected by fluorescence in situ hybridization in acute myeloid leukemia with normal karyotype by CUNEO, A, BIGONI, R, DE CUIA, R, DIVONA, M, LA STARZA, R, CRESCENZI, B, TESTONI, N, REGE CAMBRIN, G, MECUCCI, C, LO COCO, F, SAGLIO, G, CASTOLDI, G, CAVAZZINI, F, BARDI, A, ROBERTI, M. G, AGOSTINI, P, TAMMISO, E, CICCONE, N, MANCINI, M, NANNI, M

“…To better define the incidence and significance of cryptic chromosome lesions in acute myeloid leukemia (AML), fluorescence in situ hybridization (FISH)…”
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P307: DEL(17)(Q11) IS TYPICAL MARKER OF IMMATURE T‐ALL OF ADULTS, WITH NF1, UTP6, AND SUZ12 HAPLOINSUFFICIENCY, GENOME INSTABILITY, AND GENE DOWNREGULATION by Bardelli, V., Pierini, V., Arniani, S., Mvridou, E., Matteucci, C., Lema Fernandez, A. G., Moretti, M., Elia, L., Giglio, F., Forghieri, F., Cerrano, M., Fracchiolla, N., Delia, M., Sica, S., Mecucci, C., La Starza, R.

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Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia by LA STARZA, R, AVENTIN, A, DI BONA, E, LAFAGE-POCHITALOFF, M, MARTELLI, M. F, MARYNEN, P, MECUCCI, C, MATTEUCCI, C, CRESCENZI, B, ROMOLI, S, TESTONI, N, PIERINI, V, CIOLLI, S, SAMBANI, C, LOCASCIULLI, A

“…Fluorescence in situ hybridization and comparative genomic hybridization characterized 6p rearrangements in eight primary and in 10 secondary myeloid disorders…”
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Erratum: CALM/AF10-positive leukemias show upregulation of genes involved in chromatin assembly and DNA repair processes and of genes adjacent to the breakpoint at 10p12 by Mulaw, M A, Krause, A, Deshpande, A J, Krause, L F, Rouhi, A, La Starza, R, Borkhardt, A, Buske, C, Mecucci, C, Ludwig, W-D, Lottaz, C, Bohlander, S K

“…Correction to: Leukemia (2012) 26, 1012-1019; doi:10.1038/leu.2011.307 Since the publication of this article, the authors have noticed that one of the author…”
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Regions of juxtaposition in unbalanced 1q rearrangements of malignant hemopathies by La Starza, R, Aventin, A, Falzetti, D, Wlodarska, I, Fernandez Peralta, A M, Gonzalez-Aguilera, J J, Ciolli, S, Martelli, M F, Mecucci, C

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CALM/AF10-positive leukemias show upregulation of genes involved in chromatin assembly and DNA repair processes and of genes adjacent to the breakpoint at 10p12 by Mulaw, M.A, Krause, A, Deshpande, A.J, Krause, L.F, Rouhi, A, La Starza, R, Borkhardt, A, Buske, C, Mecucci, C, Ludwig, W.-D, Lottaz, C, Bohlander, S.K

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A PDGFRB-positive acute myeloid malignancy with a new t(5;12)(q33;p13.3) involving the ERC1 gene by Gorello, P, La Starza, R, Brandimarte, L, Trisolini, S M, Pierini, V, Crescenzi, B, Limongi, M Z, Nanni, M, Belloni, E, Tapinassi, C, Gerbino, E, Martelli, M F, Foà, R, Meloni, G, Pelicci, P G, Mecucci, C

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251 MN1-ETV6 fusion gene and −7: an unusual karyotypic evolution in AML after MDS with 5q by Nofrini, V, Berchicci, L, La Starza, R, Gorello, P, Di Giacomo, D, Arcioni, F, Pierini, V, Beacci, D, Crescenzi, B, Matteucci, C, Mecucci, C

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252 NPM1 haploinsufficiency in human myeloid diseases with non-isolated −5/5q by Nofrini, V, La Starza, R, Crescenzi, B, Gorello, P, Brandimarte, L, Matteucci, C, Pierini, V, Arcioni, F, Berchicci, L, Musto, P, Rosati, R, Sambani, C, Santucci, A, Aventin, A, Mecucci, C

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253 Insights on centromeric breakpoints of 5q deletions by Nofrini, V, La Starza, R, Crescenzi, B, Pierini, V, Beacci, D, Matteucci, C, Arcioni, F, Berchicci, L, Romoli, S, Musto, P, Sambani, C, Aventin, A, Mecucci, C

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C010 Commercially available Array-CGH BAC platforms: pitfalls in interpreting results by Barba, G, Matteucci, C, Brandimarte, L, La Starza, R, Pierini, V, Mecucci, C

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