Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Adriana Agnese Amaro"'
Autor:
Ennio Nano, Francesco Reggiani, Adriana Agnese Amaro, Paola Monti, Monica Colombo, Nadia Bertola, Fabiana Ferrero, Franco Fais, Antonella Bruzzese, Enrica Antonia Martino, Ernesto Vigna, Noemi Puccio, Mariaelena Pistoni, Federica Torricelli, Graziella D’Arrigo, Gianluigi Greco, Giovanni Tripepi, Carlo Adornetto, Massimo Gentile, Manlio Ferrarini, Massimo Negrini, Fortunato Morabito, Antonino Neri, Giovanna Cutrona
Publikováno v:
Non-Coding RNA, Vol 10, Iss 5, p 46 (2024)
A “watch and wait” strategy, delaying treatment until active disease manifests, is adopted for most CLL cases; however, prognostic models incorporating biomarkers have shown to be useful to predict treatment requirement. In our prospective O-CLL1
Externí odkaz:
https://doaj.org/article/12018c25e2ae401a8ecc80790c15d969
Autor:
Francesco Reggiani, Marianna Ambrosio, Michela Croce, Enrica Teresa Tanda, Francesco Spagnolo, Edoardo Raposio, Mariangela Petito, Zeinab El Rashed, Alessandra Forlani, Ulrich Pfeffer, Adriana Agnese Amaro
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 21, p 15602 (2023)
The metastatic risk of uveal melanoma (UM) is defined by a limited number of molecular lesions, somatic mutations (SF3B1 and BAP1), and copy number alterations (CNA): monosomy of chromosome 3 (M3), chr8q gain (8q), chr6p gain (6p), yet the sequence o
Externí odkaz:
https://doaj.org/article/697f392df4c946f6ac065dccd4a5a09e
Autor:
Valentina Agnusdei, Sonia Minuzzo, Marica Pinazza, Alessandra Gasparini, Laura Pezzè, Adriana Agnese Amaro, Lorenza Pasqualini, Paola Del Bianco, Martina Tognon, Chiara Frasson, Pietro Palumbo, Yari Ciribilli, Ulrich Pfeffer, Massimo Carella, Alberto Amadori, Stefano Indraccolo
Publikováno v:
Haematologica, Vol 105, Iss 5 (2020)
Despite substantial progress in treatment of T-cell acute lymphoblastic leukemia (T-ALL), mortality remains relatively high, mainly due to primary or acquired resistance to chemotherapy. Further improvements in survival demand better understanding of
Externí odkaz:
https://doaj.org/article/9da59cf5276c4fad8340659c500323c4
Autor:
Nicoletta Ferrari, Ilaria Granata, Matteo Capaia, Marina Piccirillo, Mario Rosario Guarracino, Roberta Venè, Antonella Brizzolara, Andrea Petretto, Elvira Inglese, Martina Morini, Simonetta Astigiano, Adriana Agnese Amaro, Francesco Boccardo, Cecilia Balbi, Paola Barboro
Publikováno v:
Cell Communication and Signaling, Vol 15, Iss 1, Pp 1-14 (2017)
Abstract Background Prostate cancer (PCa), the second most common cancer affecting men worldwide, shows a broad spectrum of biological and clinical behaviour representing the epiphenomenon of an extreme heterogeneity. Androgen deprivation therapy is
Externí odkaz:
https://doaj.org/article/152055dcfe94475ebcb72884d12d5188
Autor:
Adriana Agnese Amaro, Rosaria Gangemi, Laura Emionite, Patrizio Castagnola, Gilberto Filaci, Martine J. Jager, Enrica Teresa Tanda, Francesco Spagnolo, Matteo Mascherini, Ulrich Pfeffer, Michela Croce
Publikováno v:
Cancers
Volume 15
Issue 3
Pages: 886
Volume 15
Issue 3
Pages: 886
Background: Metastatic uveal melanoma (MUM) is a highly aggressive, therapy-resistant disease. Driver mutations in Gα-proteins GNAQ and GNA11 activate MAP-kinase and YAP/TAZ pathways of oncogenic signalling. MAP-kinase and MEK-inhibitors do not sign
Publikováno v:
Biomedicines; Volume 10; Issue 12; Pages: 3240
There is a growing number of multi-domain genomic datasets for human tumors. Multi-domain data are usually interpreted after separately analyzing single-domain data and integrating the results post hoc. Data fusion techniques allow for the real integ
Autor:
Silvia, Borghini, Denise, Ferrera, Ignazia, Prigione, Michele, Fiore, Chiara, Ferraris, Valentina, Mirisola, Adriana Agnese, Amaro, Ilaria, Gueli, Luca, Zammataro, Marco, Gattorno, Ulrich, Pfeffer, Isabella, Ceccherini
Publikováno v:
Clinical and experimental rheumatology. 34(6 Suppl 102)
Tumour necrosis factor (TNF) receptor-associated periodic syndrome (TRAPS) is a multisystemic autoinflammatory condition associated with heterozygous TNFRSF1A mutations, presenting with a variety of clinical symptoms, many of which yet unexplained. I
Autor:
Salani, B., Marini, C., Del Rio, A., Ravera, S., Massollo, M., Orengo, A., Adriana Agnese Amaro, Passalacqua, M., Maffioli, S., Pfeffer, U., Sambuceti, G., Cordera, R., Maggi, D.
Publikováno v:
Publons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cdae4cccf8eaed413d0478ac2ec9472d
https://publons.com/publon/18691041/
https://publons.com/publon/18691041/