Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Luciana Impera"'
Autor:
Crescenzio Francesco Minervini, Cosimo Cumbo, Immacolata Redavid, Maria Rosa Conserva, Paola Orsini, Antonella Zagaria, Luisa Anelli, Nicoletta Coccaro, Giuseppina Tota, Luciana Impera, Elisa Parciante, Francesco Tarantini, Annamaria Giordano, Giorgina Specchia, Pellegrino Musto, Francesco Albano
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)
Abstract The evaluation of the somatic hypermutation of the clonotypic immunoglobulin heavy variable gene has become essential in the therapeutic management in chronic lymphocytic leukemia patients. European Research Initiative on Chronic Lymphocytic
Externí odkaz:
https://doaj.org/article/9fb8cdff84594f8c80b607a419cdaf59
Autor:
Cosimo Cumbo, Francesco Tarantini, Antonella Zagaria, Luisa Anelli, Crescenzio Francesco Minervini, Nicoletta Coccaro, Giuseppina Tota, Luciana Impera, Elisa Parciante, Maria Rosa Conserva, Immacolata Redavid, Paola Carluccio, Mario Delia, Annamaria Giordano, Maria Chiara Longo, Tommasina Perrone, Antonella Russo Rossi, Giorgina Specchia, Pellegrino Musto, Francesco Albano
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Inflammatory bowel diseases (IBDs) are a group of chronic conditions of the gastrointestinal tract in which nationwide studies have revealed a higher risk of hematological malignancies (HMs). Clonal hematopoiesis (CH) is a premalignant condition defi
Externí odkaz:
https://doaj.org/article/f839630c27d04da8aaad77d31af5a75d
Autor:
Paola Orsini, Luciana Impera, Elisa Parciante, Cosimo Cumbo, Crescenzio F. Minervini, Angela Minervini, Antonella Zagaria, Luisa Anelli, Nicoletta Coccaro, Paola Casieri, Giuseppina Tota, Claudia Brunetti, Alessandra Ricco, Paola Carluccio, Giorgina Specchia, Francesco Albano
Publikováno v:
Diagnostic Pathology, Vol 13, Iss 1, Pp 1-11 (2018)
Abstract Background Alu repeats, belonging to the Short Interspersed Repetitive Elements (SINEs) class, contain about 25% of CpG sites in the human genome. Alu sequences lie in gene-rich regions, so their methylation is an important transcriptional r
Externí odkaz:
https://doaj.org/article/b9879e1c3f604f248f794c96694e870b
Autor:
Antonella Zagaria, Luisa Anelli, Nicoletta Coccaro, Giuseppina Tota, Claudia Brunetti, Angela Minervini, Paola Casieri, Luciana Impera, Crescenzio Francesco Minervini, Annamaria Giordano, Paola Orsini, Cosimo Cumbo, Giorgina Specchia, Francesco Albano
Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 3, Pp 276-277 (2017)
Externí odkaz:
https://doaj.org/article/d76705f4256d4d7abb422eaba452c161
Autor:
Grazia Fazio, Giulia Daniele, Valeria Cazzaniga, Luciana Impera, Marco Severgnini, Ilaria Iacobucci, Marta Galbiati, Anna Leszl, Ingrid Cifola, Gianluca De Bellis, Paola Bresciani, Giovanni Martinelli, Giuseppe Basso, Andrea Biondi, Clelia Tiziana Storlazzi, Giovanni Cazzaniga
Publikováno v:
Haematologica, Vol 100, Iss 1 (2015)
Externí odkaz:
https://doaj.org/article/30fbd6049a2d40c986b3b542678e0c4b
Autor:
Luciana Impera, Giulia Daniele, Luisa Marra, Carmen Baldazzi, Ilaria Iacobucci, Giovanni Martinelli, Nicoletta Testoni, Clelia Tiziana Storlazzi
Publikováno v:
Hematology Reports, Vol 4, Iss 4, Pp e27-e27 (2012)
We describe a case of acute myeloid leukemia M5 showing a balanced t(2;10)(q31;p12) translocation. This has never been described before as the sole cytogenetic abnormality in a bone marrow cell clone at onset. Using fluorescence in situ hybridization
Externí odkaz:
https://doaj.org/article/b599a662ebf04af18abdfc244bfef666
Autor:
Giovanni Martinelli, Michele Baccarani, Robin Foà, Mario Luppi, Fabrizio Pane, Simona Soverini, Stefania Paolini, Leonardo Potenza, Antonella Vitale, Marco Vignetti, Maria Chiara Abbenante, Luciana Impera, Federica Cattina, Emanuela Ottaviani, Clelia Tiziana Storlazzi, Stefania Trino, Francesca Paoloni, Cristina Papayannidis, Annalisa Lonetti, Anna Ferrari, Ilaria Iacobucci
PDF file - 1.2MB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7613f2df28af5bab46c005940b8995e3
https://doi.org/10.1158/1078-0432.22443570
https://doi.org/10.1158/1078-0432.22443570
Autor:
Giovanni Martinelli, Michele Baccarani, Robin Foà, Mario Luppi, Fabrizio Pane, Simona Soverini, Stefania Paolini, Leonardo Potenza, Antonella Vitale, Marco Vignetti, Maria Chiara Abbenante, Luciana Impera, Federica Cattina, Emanuela Ottaviani, Clelia Tiziana Storlazzi, Stefania Trino, Francesca Paoloni, Cristina Papayannidis, Annalisa Lonetti, Anna Ferrari, Ilaria Iacobucci
Purpose: The 9p21 locus, encoding three important tumor suppressors (p16/CDKN2A, p14/ARF, and p15/CDKN2B), is a major target of inactivation in the pathogenesis of many human tumors.Patients and Methods: To explore, at high resolution, the frequency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::762df62ae7a2844abe17c70473cfa4fb
https://doi.org/10.1158/1078-0432.c.6519873
https://doi.org/10.1158/1078-0432.c.6519873
Autor:
Francesco Albano, Antonella Zagaria, Nicoletta Coccaro, Crescenzio Francesco Minervini, Pellegrino Musto, Ciro Leonardo Pierri, Cosimo Cumbo, Anna De Grassi, Immacolata Redavid, Maria Rosa Conserva, Immacolata Attolico, Luciana Impera, Giuseppina Tota, Luisa Anelli, Elisa Parciante, Anna Mestice, Francesco Tarantini
Publikováno v:
Leukemia & Lymphoma. 64:717-721
Germline mutations in the RUNX1 gene define a familial platelet disorder with a predisposition to myeloid malignancy (FPDMM). This autosomal dominant disorder is characterized by variable penetranc...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb36d823fa0296af340146c3ed3faef7
https://doi.org/10.1080/10428194.2021.1929960
https://doi.org/10.1080/10428194.2021.1929960
Autor:
Crescenzio Francesco Minervini, Maria Rosa Conserva, Nicoletta Coccaro, Pellegrino Musto, Cosimo Cumbo, Paola Orsini, Paola Carluccio, Immacolata Redavid, Elisa Parciante, Giuseppina Tota, Luisa Anelli, Antonella Zagaria, Francesco Tarantini, Giorgina Specchia, Francesco Albano, Luciana Impera
Publikováno v:
Leukemia & Lymphoma. 62:1219-1225
Acute promyelocytic leukemia (APL) patients carry in 27% of cases an activating mutation of the fms-like tyrosine kinase-3 (FLT3) gene: internal tandem duplication (ITD) or tyrosine kinase domain (TKD) point mutation. The simultaneous presence of bot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3820380860e7a214af8bac743ffeaab6
https://doi.org/10.1080/10428194.2020.1856838
https://doi.org/10.1080/10428194.2020.1856838