Zobrazeno 1 - 10
of 55
pro vyhledávání: '"D. Falzetti"'
Autor:
Massimo F. Martelli, D Falzetti, Peter Marynen, Caterina Matteucci, Cristina Mecucci, Joris Vermeesch, Stefania Ciolli
Publikováno v:
Cancer Genetics and Cytogenetics. 118:28-34
Complex chromosomal rearrangements in malignant hemopathies frequently remain unclarified because of paucity of material for further fluorescence in situ hybridization analyses and/or lack of suitable probes. Chromosome microdissection (MD) can be an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77d6a9c71c8ddeb6e0a6372ae66a607d
https://doi.org/10.1016/s0165-4608(99)00189-2
https://doi.org/10.1016/s0165-4608(99)00189-2
Autor:
Massimo F. Martelli, Peter Marynen, D Falzetti, Caterina Matteucci, Iwona Wlodarska, Mathijs Baens, Roberta La Starza, Herman Van den Berghe, Cristina Mecucci
Publikováno v:
Genes, Chromosomes and Cancer. 23:10-15
A case of acute myeloid leukemia (AML) M1 with bone marrow eosinophilia was characterized by cytogenetics and fluorescence in situ hybridization (FISH). A complex karyotype including a der(12)t(12;17)(p12-13;q11) and a der(16)t(16;20)(p13;p11) was fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5845d4db848f09ff333690cee3fe5544
https://doi.org/10.1002/(sici)1098-2264(199809)23:1<10::aid-gcc2>3.0.co
https://doi.org/10.1002/(sici)1098-2264(199809)23:1<10::aid-gcc2>3.0.co
Autor:
B. Crescenzi, Ana Aventin, H. Van den Berghe, Iwona Wlodarska, Christina Mecucci, M.F. Martelli, D. Falzetti, R La Starza
Publikováno v:
Blood. 91:231-237
Fluorescent in situ hybridization (FISH) analysis with a panel of DNA probes for 13q13.1-q14.3 was performed on 20 cases of myeloid malignancies, of which 17 showed a del(13)(q) and three had translocations affecting 13q. By chromosome morphology, de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a362ac9c412d6f7030d2a5402b68b62
https://doi.org/10.1182/blood.v91.1.231.231_231_237
https://doi.org/10.1182/blood.v91.1.231.231_231_237
Publikováno v:
Cytogenetic and Genome Research. 81:68-72
Broken chromosomes are highly unstable and are subject to chromosome fusion or loss. As an exception, healing of human chromosomes occurs which can lead to constitutional or acquired terminal chromosome deletion disorders. Both de novo telomere addit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::008446a543d8fd0abf8d494afc08b34c
https://doi.org/10.1159/000014991
https://doi.org/10.1159/000014991
Autor:
Anna Aventin, D Falzetti, Arnold Criel, Júlia Inglés-Esteve, Jean-Jacques Cassiman, Iwona Wlodarska, Peter Marynen, Herman Van den Berghe, Cristina Mecucci
Publikováno v:
Blood. 89:1716-1722
Translocation t(5; 12)(q33; p13), resulting in an ETV6/PDGFRB gene fusion, is a recurrent chromosomal abnormality associated with chronic myelomonocytic leukemia (CMML). An analogous translocation was also found in four cell lines with features of pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dab10ca0faf754a1cfa9cf8fa90e6a1
https://doi.org/10.1182/blood.v89.5.1716
https://doi.org/10.1182/blood.v89.5.1716
Autor:
Roberta La Starza, Cristina Mecucci, D Falzetti, Michel Stul, Massimo F. Martelli, Brunangelo Falini, Ana Aventin
Publikováno v:
The Journal of Pathology. 178:227-231
Cytogenetic, in situ hybridization, and molecular studies were performed in a case of T-cell-rich B-cell lymphoma. Demonstration of Ig gene rearrangements for both heavy and light chains confirmed the B-lineage restriction of the neoplastic cell popu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::779b0d918206996df456c7b8c8848782
https://doi.org/10.1002/(sici)1096-9896(199602)178:2<227::aid-path437>3.0.co
https://doi.org/10.1002/(sici)1096-9896(199602)178:2<227::aid-path437>3.0.co
Autor:
Stefania Ciolli, J J Gonzalez-Aguilera, M F Martelli, D Falzetti, A M Fernandez Peralta, Christina Mecucci, Anna Aventin, Iwona Wlodarska, R La Starza
Publikováno v:
Leukemia. 15:861-863
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae41d1e8e8302f43f71bff53c5e1c20f
https://doi.org/10.1038/sj.leu.2402100
https://doi.org/10.1038/sj.leu.2402100
Autor:
Massimo F. Martelli, Carla Emiliani, Roberta La Starza, Cristina Mecucci, Aldo Orlacchio, Barbara Crescenzi, Caterina Matteucci, Silvia Romoli, Peter Marynen, D Falzetti
Publikováno v:
Cancer genetics and cytogenetics. 135(1)
Molecular cytogenetics is helpful to identify complex and cryptic genomic changes in malignancy. Human leukemic cell lines are an important tool for advancements of biological research on malignant cells, one critical step being characterization of g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49239097a53114b1663678e3e80511f5
https://pubmed.ncbi.nlm.nih.gov/12072200
https://pubmed.ncbi.nlm.nih.gov/12072200
Autor:
G Del Poeta, Alessandro Isidori, Giovanni Fernando Torelli, Stefania Ciolli, Franco Mandelli, Marco Gobbi, Marino Clavio, Christina Mecucci, Giorgina Specchia, Mario Sessarego, Sante Tura, Maria Concetta Petti, Domenico Russo, Antonio Cuneo, Giovanni Martinelli, Gian Luigi Castoldi, Vincenzo Liso, Maria Christina Cox, Nicoletta Testoni, Michele Malagola, Roberto Rondelli, Paolo Bernasconi, Giuseppe Visani, Pier Paolo Piccaluga, Franco Leoni, D Dini, D Falzetti, Renato Fanin, Marina Boni
We studied the impact of cytogenetics and kind of induction/consolidation therapy on 848 adult acute myeloid leukemia (AML) patients (age 15-83). The patients received three types of induction/consolidation regimen: standard (daunorubicin and cytosin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f6a2f9cfca4b91daac313d76f54783e
http://hdl.handle.net/11392/1199421
http://hdl.handle.net/11392/1199421
Autor:
D Falzetti, Caterina Carnovale-Scalzo, Francesco Nardi, Yan Aalto, Sakari Knuutila, Cristina Mecucci, Valeria Ascoli
Malignant mesothelioma (MM) is predominantly a sporadic malignancy linked to exposure to asbestos. Clustering of MM in families suggests genetic susceptibility as a contributing factor. We performed comparative genomic hybridization (CGH) analysis on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c43fd4a73389796c035a230df145e068
http://hdl.handle.net/11391/154058
http://hdl.handle.net/11391/154058