Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Ettore Rizzo"'
Autor:
Sarah L. Stenton, Melanie C. O’Leary, Gabrielle Lemire, Grace E. VanNoy, Stephanie DiTroia, Vijay S. Ganesh, Emily Groopman, Emily O’Heir, Brian Mangilog, Ikeoluwa Osei-Owusu, Lynn S. Pais, Jillian Serrano, Moriel Singer-Berk, Ben Weisburd, Michael W. Wilson, Christina Austin-Tse, Marwa Abdelhakim, Azza Althagafi, Giulia Babbi, Riccardo Bellazzi, Samuele Bovo, Maria Giulia Carta, Rita Casadio, Pieter-Jan Coenen, Federica De Paoli, Matteo Floris, Manavalan Gajapathy, Robert Hoehndorf, Julius O. B. Jacobsen, Thomas Joseph, Akash Kamandula, Panagiotis Katsonis, Cyrielle Kint, Olivier Lichtarge, Ivan Limongelli, Yulan Lu, Paolo Magni, Tarun Karthik Kumar Mamidi, Pier Luigi Martelli, Marta Mulargia, Giovanna Nicora, Keith Nykamp, Vikas Pejaver, Yisu Peng, Thi Hong Cam Pham, Maurizio S. Podda, Aditya Rao, Ettore Rizzo, Vangala G. Saipradeep, Castrense Savojardo, Peter Schols, Yang Shen, Naveen Sivadasan, Damian Smedley, Dorian Soru, Rajgopal Srinivasan, Yuanfei Sun, Uma Sunderam, Wuwei Tan, Naina Tiwari, Xiao Wang, Yaqiong Wang, Amanda Williams, Elizabeth A. Worthey, Rujie Yin, Yuning You, Daniel Zeiberg, Susanna Zucca, Constantina Bakolitsa, Steven E. Brenner, Stephanie M. Fullerton, Predrag Radivojac, Heidi L. Rehm, Anne O’Donnell-Luria
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-25 (2024)
Abstract Background A major obstacle faced by families with rare diseases is obtaining a genetic diagnosis. The average "diagnostic odyssey" lasts over five years and causal variants are identified in under 50%, even when capturing variants genome-wi
Externí odkaz:
https://doaj.org/article/29fbe7d26d88463789f004c8908aa4a7
Autor:
Gabriele Merati, Marianna Rossi, Anna Gallì, Elisa Roncoroni, Silvia Zibellini, Ettore Rizzo, Daniela Pietra, Cristina Picone, Barbara Rocca, Claudia Patricia Tobar Cabrera, Eleonora Gelli, Eugenio Santacroce, Luca Arcaini, Patrizia Zappasodi
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
Acute leukemia of ambiguous lineage (ALAL) is a rare type of leukemia and represents an unmet clinical need. In fact, due to heterogeneity, substantial rarity and absence of clinical trials, there are no therapeutic guidelines available. We investiga
Externí odkaz:
https://doaj.org/article/eab51768fab14e468d4f14307f1fa62d
Autor:
Giovanni Carapezza, Carlo Cusi, Ettore Rizzo, Laura Raddrizzani, Sebastiano Di Bella, Alessio Somaschini, Antonella Leone, Rosita Lupi, Margherita Mutarelli, Vincenzo Nigro, Diego di Bernardo, Paolo Magni, Antonella Isacchi, Roberta Bosotti
Publikováno v:
BMC Genomics, Vol 20, Iss 1, Pp 1-12 (2019)
Abstract Background Protein kinases are enzymes controlling different cellular functions. Genetic alterations often result in kinase dysregulation, making kinases a very attractive class of druggable targets in several human diseases. Existing approv
Externí odkaz:
https://doaj.org/article/a92baa76a04346bf8b7c7872513455a7
Autor:
Umberto Palatini, Pascal Miesen, Rebeca Carballar-Lejarazu, Lino Ometto, Ettore Rizzo, Zhijian Tu, Ronald P. van Rij, Mariangela Bonizzoni
Publikováno v:
BMC Genomics, Vol 18, Iss 1, Pp 1-15 (2017)
Abstract Background Arthropod-borne viruses (arboviruses) transmitted by mosquito vectors cause many important emerging or resurging infectious diseases in humans including dengue, chikungunya and Zika. Understanding the co-evolutionary processes amo
Externí odkaz:
https://doaj.org/article/030a2558b6b34a7e85753b5df20a6e6f
Autor:
Marzia Varettoni, Silvia Zibellini, Irene Defrancesco, Virginia Valeria Ferretti, Ettore Rizzo, Luca Malcovati, Anna Gallì, Matteo Giovanni Della Porta, Emanuela Boveri, Luca Arcaini, Chiara Candido, Marco Paulli, Mario Cazzola
Publikováno v:
Haematologica, Vol 102, Iss 12 (2017)
We analyzed MYD88 and CXCR4 mutation status of 260 patients with Waldenström macroglobulinemia or IgM monoclonal gammopathy of undetermined significance using allele-specific real time quantitative polymerase chain reaction and Sanger sequencing, re
Externí odkaz:
https://doaj.org/article/167287e719e040a3a76b1cdb3c418f3e
Autor:
Simone Marini, Ivan Limongelli, Ettore Rizzo, Alberto Malovini, Edoardo Errichiello, Annalisa Vetro, Tan Da, Orsetta Zuffardi, Riccardo Bellazzi
Publikováno v:
PLoS ONE, Vol 11, Iss 12, p e0164940 (2016)
Among the scientific challenges posed by complex diseases with a strong genetic component, two stand out. One is unveiling the role of rare and common genetic variants; the other is the design of classification models to improve clinical diagnosis an
Externí odkaz:
https://doaj.org/article/6fc982d8ffae484685729f65500bd04f
Autor:
Gabriele Todisco, Irene Fragiadaki, Stavros Papadakis, Helen A. Papadaki, Chiara Elena, Anastasios Batas, Anna Gallì, Elisabetta Molteni, Elisa Bono, Grigorios Tsaknakis, Luca Malcovati, Peggy Kanellou, Irene Mavroudi, Charalampos Pontikoglou, Stella Maxouri, Emmanouela Linardaki, Ettore Rizzo, Nektarios Tavernarakis
Publikováno v:
Blood. 138:1249-1257
The incidence and prognosis of clonal hematopoiesis in patients with isolated neutropenia among patients with idiopathic cytopenia of undetermined significance (ICUS), known as ICUS-N or chronic idiopathic neutropenia (CIN) patients, is poorly define
Autor:
Maria Creignou, Anna Gallì, Paola Guglielmelli, Mario Cazzola, Johanna Ungerstedt, Seishi Ogawa, Silvia Catricalà, Ettore Rizzo, Marios Dimitriou, Eva Hellström-Lindberg, Elisa Bono, Alessandro M. Vannucchi, Martina Sarchi, Elisa Rumi, Luca Malcovati, Vittorio Rosti, Yasuhito Nannya, Marco Roncador, Daniela Pietra, Chiara Elena, Elisabetta Molteni, Gabriele Todisco
Publikováno v:
Leukemia. 35:2371-2381
Somatic mutations in splicing factor genes frequently occur in myeloid neoplasms. While SF3B1 mutations are associated with myelodysplastic syndromes (MDS) with ring sideroblasts, SRSF2P95 mutations are found in different disease categories, includin
Autor:
Marianna Rossi, Maria Elena Nizzoli, Anna Gallì, Elisa Roncoroni, Silvia Zibellini, Gabriele Merati, Ettore Rizzo, Barbara Rocca, Daniela Pietra, Cristina Picone, Marco Brociner, Claudia Patricia Tobar Cabrera, Eleonora Gelli, Eugenio Santacroce, Luca Arcaini, Patrizia Zappasodi
Publikováno v:
American Journal of Hematology. 97
Autor:
Chiara Cavalloni, Massimo Gentile, Fabio Bergamini, Silvia Zibellini, Matteo G. Della Porta, Anna Gallì, Luca Arcaini, Marzia Varettoni, Sara Rattotti, Ettore Rizzo, Elena Flospergher, Ester Orlandi, Caterina Cristinelli, Nicole Fabbri, Marianna Rossi, Virginia Valeria Ferretti
Publikováno v:
Web of Science