Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Silvia Bungaro"'
Integrated Genomic, Functional, and Prognostic Characterization of Atypical Chronic Myeloid Leukemia
Autor:
Diletta Fontana, Daniele Ramazzotti, Andrea Aroldi, Sara Redaelli, Vera Magistroni, Alessandra Pirola, Antonio Niro, Luca Massimino, Cristina Mastini, Virginia Brambilla, Silvia Bombelli, Silvia Bungaro, Alessandro Morotti, Delphine Rea, Fabio Stagno, Bruno Martino, Leonardo Campiotti, Giovanni Caocci, Emilio Usala, Michele Merli, Francesco Onida, Marco Bregni, Elena Maria Elli, Monica Fumagalli, Fabio Ciceri, Roberto A. Perego, Fabio Pagni, Luca Mologni, Rocco Piazza, Carlo Gambacorti-Passerini
Publikováno v:
HemaSphere, Vol 4, Iss 6, p e497 (2020)
Abstract. Atypical chronic myeloid leukemia (aCML) is a BCR-ABL1-negative clonal disorder, which belongs to the myelodysplastic/myeloproliferative group. This disease is characterized by recurrent somatic mutations in SETBP1, ASXL1 and ETNK1 genes, a
Externí odkaz:
https://doaj.org/article/3319347f08c04865829698754ec8c474
Autor:
Silvia Salmoiraghi, Marie Lorena Guinea Montalvo, Greta Ubiali, Manuela Tosi, Barbara Peruta, Pamela Zanghi, Elena Oldani, Cristina Boschini, Alexander Kohlmann, Silvia Bungaro, Tamara Intermesoli, Elisabetta Terruzzi, Emanuele Angelucci, Irene Cavattoni, Fabio Ciceri, Renato Bassan, Alessandro Rambaldi, Orietta Spinelli
Publikováno v:
Haematologica, Vol 101, Iss 6 (2016)
Externí odkaz:
https://doaj.org/article/4a2229056a3646a8b400c57bafdd4f51
Autor:
Alessia Casolaro, Josee Golay, Clara Albanese, Roberta Ceruti, Veronica Patton, Sabrina Cribioli, Alice Pezzoni, Marco Losa, Gemma Texido, Ursula Giussani, Francesco Marchesi, Nadia Amboldi, Barbara Valsasina, Silvia Bungaro, Gianni Cazzaniga, Alessandro Rambaldi, Martino Introna, Enrico Pesenti, Rachele Alzani
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e58424 (2013)
CD56 is expressed in 15-20% of acute myeloid leukaemias (AML) and is associated with extramedullary diffusion, multidrug resistance and poor prognosis. We describe the establishment and characterisation of a novel disseminated model of AML (AML-NS8),
Externí odkaz:
https://doaj.org/article/9ff701b67ac14375b7e6e3ca8f819c84
Autor:
Marco Severgnini, Mariella D’Angiò, Silvia Bungaro, Giovanni Cazzaniga, Ingrid Cifola, Grazia Fazio
Acute lymphoblastic leukemia (ALL) is the most frequent childhood cancer. For the last three decades, conventional cytogenetic and molecular approaches allowed the identification of genetic abnormalities having prognostic and therapeutic relevance. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e991cf2104e414ff4081a83be60b462
http://hdl.handle.net/10281/389765
http://hdl.handle.net/10281/389765
Integrated Genomic, Functional, and Prognostic Characterization of Atypical Chronic Myeloid Leukemia
Autor:
Emilio Usala, Giovanni Caocci, Daniele Ramazzotti, Alessandra Pirola, Leonardo Campiotti, Alessandro Morotti, Fabio Stagno, Roberto A. Perego, Silvia Bungaro, Cristina Mastini, Fabio Pagni, Silvia Bombelli, Fabio Ciceri, Vera Magistroni, Bruno Martino, Michele Merli, Antonio Niro, Sara Redaelli, Delphine Rea, Luca Mologni, Rocco Piazza, Diletta Fontana, Virginia Brambilla, Elena Maria Elli, Andrea Aroldi, Carlo Gambacorti-Passerini, Marco Bregni, Luca Massimino, Monica Fumagalli, Francesco Onida
Publikováno v:
HemaSphere
HemaSphere, Vol 4, Iss 6, p e497 (2020)
HemaSphere, Vol 4, Iss 6, p e497 (2020)
Supplemental Digital Content is available for this article.
Atypical chronic myeloid leukemia (aCML) is a BCR-ABL1-negative clonal disorder, which belongs to the myelodysplastic/myeloproliferative group. This disease is characterized by recurren
Atypical chronic myeloid leukemia (aCML) is a BCR-ABL1-negative clonal disorder, which belongs to the myelodysplastic/myeloproliferative group. This disease is characterized by recurren
Autor:
Barbara Peruta, Tamara Intermesoli, Emanuele Angelucci, Elisabetta Terruzzi, Orietta Spinelli, Silvia Salmoiraghi, Alessandro Rambaldi, Manuela Tosi, Pamela Zanghì, Greta Ubiali, Elena Oldani, Irene Cavattoni, Cristina Boschini, Fabio Ciceri, Alexander Kohlmann, Silvia Bungaro, Renato Bassan, Marie Lorena Guinea Montalvo
Publikováno v:
Haematologica. 101:e245-e248
In adult acute lymphoblastic leukemia (ALL) the evaluation of clinical and biological conventional risk criteria at diagnosis is important but not sufficient to predict clinical outcome. The impact of TP53 mutations has been investigated in a limited
Autor:
Silvia Bungaro, Marco Giordan, Grazia Fazio, G. De Rossi, Cristina Battaglia, L Corral, Giovanni Cazzaniga, R. Spinelli, Michela Bardini, Eleonora Mangano, Giuseppe Basso, Andrea Biondi, Ingrid Cifola
Publikováno v:
Leukemia 24 (2010): 169–176. doi:10.1038/leu.2009.203
info:cnr-pdr/source/autori:Bardini, M.; Spinelli, R.; Bungaro, S.; Mangano, E.; Corral, L.; Cifola, I.; Fazio, G.; Giordan, M.; Basso, G.; De Rossi, G.; Biondi, A.; Battaglia, C.; Cazzaniga, G./titolo:DNA copy-number abnormalities do not occur in infant ALL with t(4;11)%2FMLL-AF4/doi:10.1038%2Fleu.2009.203/rivista:Leukemia/anno:2010/pagina_da:169/pagina_a:176/intervallo_pagine:169–176/volume:24
info:cnr-pdr/source/autori:Bardini, M.; Spinelli, R.; Bungaro, S.; Mangano, E.; Corral, L.; Cifola, I.; Fazio, G.; Giordan, M.; Basso, G.; De Rossi, G.; Biondi, A.; Battaglia, C.; Cazzaniga, G./titolo:DNA copy-number abnormalities do not occur in infant ALL with t(4;11)%2FMLL-AF4/doi:10.1038%2Fleu.2009.203/rivista:Leukemia/anno:2010/pagina_da:169/pagina_a:176/intervallo_pagine:169–176/volume:24
The pathogenesis of infant acute lymphoblastic leukemia (ALL) is still not well defined. Short latency to leukemia and very high concordance rate for ALL in Mixed-Lineage Leukemia (MLL)-positive infant twins suggest that the MLL rearrangement itself
Autor:
Andrea Zangrando, Bryan D. Young, Tatiana Gorletta, Luca Lo Nigro, Andrea Biondi, Giovanni Cazzaniga, Dario Basso, Gertruy te Kronnie, Silvio Bicciato, Giuseppe Basso, Silvia Bungaro, Marta Campo Dell'Orto, Anna Leszl
Publikováno v:
Genes, Chromosomes and Cancer. 48:22-38
Pediatric acute lymphoblastic leukemia (ALL) comprises genetically distinct subtypes. However, 25% of cases still lack defined genetic hallmarks. To identify genomic aberrancies in childhood ALL patients nonclassifiable by conventional methods, we pe
Autor:
Grazia Fazio, Ingrid Cifola, Andrea Biondi, Gianluca De Bellis, Marco Severgnini, Giovanni Cazzaniga, Silvia Bungaro
Publikováno v:
Blood 124 (2014).
info:cnr-pdr/source/autori:Fazio, Grazia; Severgnini, Marco; Cifola, Ingrid; Bungaro, Silvia; Biondi, Andrea; De Bellis, Gianluca; Cazzaniga, Giovanni/titolo:Structural Variations Identified By Whole Transcriptome Sequencing (RNA-Seq) in Childhood ALL with Different Response to Therapy/doi:/rivista:Blood/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume:124
info:cnr-pdr/source/autori:Fazio, Grazia; Severgnini, Marco; Cifola, Ingrid; Bungaro, Silvia; Biondi, Andrea; De Bellis, Gianluca; Cazzaniga, Giovanni/titolo:Structural Variations Identified By Whole Transcriptome Sequencing (RNA-Seq) in Childhood ALL with Different Response to Therapy/doi:/rivista:Blood/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume:124
Introduction. Acute Lymphoblastic Leukemia (ALL) is the most frequent type of childhood leukemia. It is a multi-step process, characterized by the expansion of a pre-leukemic clone, accumulating cooperative genetic events required for the full transf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0a0a261b9cadca9021ddae40ea3259d
http://www.cnr.it/prodotto/i/348041
http://www.cnr.it/prodotto/i/348041
Autor:
Ilaria Iacobucci, Grazia Fazio, Valeria Cazzaniga, Marta Galbiati, Gianluca De Bellis, Clelia Tiziana Storlazzi, Marco Severgnini, Ingrid Cifola, Andrea Biondi, Giovanni Cazzaniga, Giuseppe Basso, Giovanni Martinelli, Giulia Daniele, Silvia Bungaro, Anna Leszl, Luciana Impera
Publikováno v:
Blood 122 (2013).
info:cnr-pdr/source/autori:Fazio, Grazia; Storlazzi, Clelia Tiziana; Severgnini, Marco; Cazzaniga, Valeria; Impera, Luciana; Daniele, Giulia; Iacobucci, Ilaria; Galbiati, Marta; Leszl, Anna; Bungaro, Silvia; Cifola, Ingrid; De Bellis, Gianluca; Martinelli, Giovanni; Basso, Giuseppe; Biondi, Andrea; Cazzaniga, Giovanni/titolo:Novel Chimeric Transcripts Involving PAX5 in B-Cell Precursor ALL/doi:/rivista:Blood/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume:122
info:cnr-pdr/source/autori:Fazio, Grazia; Storlazzi, Clelia Tiziana; Severgnini, Marco; Cazzaniga, Valeria; Impera, Luciana; Daniele, Giulia; Iacobucci, Ilaria; Galbiati, Marta; Leszl, Anna; Bungaro, Silvia; Cifola, Ingrid; De Bellis, Gianluca; Martinelli, Giovanni; Basso, Giuseppe; Biondi, Andrea; Cazzaniga, Giovanni/titolo:Novel Chimeric Transcripts Involving PAX5 in B-Cell Precursor ALL/doi:/rivista:Blood/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume:122
PAX5, located on 9p13, belongs to the PAX gene family and encodes for a transcription factor essential for B lymphoid cell commitment. It functions both as a transcriptional activator and repressor of different target genes involved in lineages devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1838ad8666aab403ef3827736598f9d
http://hdl.handle.net/10281/74642
http://hdl.handle.net/10281/74642