Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Paolo Di Bartolomeo"'
Autor:
Giovanni Pagano, Luca Tiano, Federico V. Pallardó, Alex Lyakhovich, Sudit S. Mukhopadhyay, Paolo Di Bartolomeo, Adriana Zatterale, Marco Trifuoggi
Publikováno v:
Redox Biology, Vol 40, Iss , Pp 101860- (2021)
Fanconi anemia (FA) has been investigated since early studies based on two definitions, namely defective DNA repair and proinflammatory condition. The former definition has built up the grounds for FA diagnosis as excess sensitivity of patients’ ce
Externí odkaz:
https://doaj.org/article/55d50f4637334980a22a44acdc76487c
Autor:
Mauro Di Ianni, Beatrice Del Papa, Stefano Baldoni, Ambra Di Tommaso, Bianca Fabi, Emanuela Rosati, Annalisa Natale, Stella Santarone, Paola Olioso, Gabriele Papalinetti, Raffaella Giancola, Patrizia Accorsi, Paolo Di Bartolomeo, Paolo Sportoletti, Franca Falzetti
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
In allogeneic hematopoietic stem cell transplantation, which is the major curative therapy for hematological malignancies, T cells play a key role in the development of graft-versus-host disease (GvHD). NOTCH pathway is a conserved signal transductio
Externí odkaz:
https://doaj.org/article/8f236388b87f4c4591b90c05041343c9
Autor:
Mauro Di Ianni, Stefano Baldoni, Beatrice Del Papa, Patrizia Aureli, Erica Dorillo, Filomena De Falco, Elisa Albi, Emanuela Varasano, Ambra Di Tommaso, Raffaella Giancola, Patrizia Accorsi, Gianluca Rotta, Chiara Rompietti, Estevão Carlos Silva Barcelos, Antonio Francesco Campese, Paolo Di Bartolomeo, Isabella Screpanti, Emanuela Rosati, Franca Falzetti, Paolo Sportoletti
Publikováno v:
Frontiers in Oncology, Vol 8 (2018)
To investigate chronic lymphocytic leukemia (CLL)-initiating cells, we assessed NOTCH1 mutation/expression in hematopoietic stem cells (HSCs). In NOTCH1-mutated CLL, we detected subclonal mutations in 57% CD34+/CD38− HSCs. NOTCH1 mutation was prese
Externí odkaz:
https://doaj.org/article/22cb5b5b90a04145889dadc04b8f6e35
Autor:
Milton Percy Plasencia Linares, Damiano Pesaresi, Paolo Di Bartolomeo, Pier Luigi Bragato, Angela Saraò
Publikováno v:
Annals of Geophysics, Vol 54, Iss 1, Pp 67-75 (2011)
After the 1976 Friuli earthquake (Ms = 6.5) in north-eastern Italy that caused about 1,000 casualties and widespread destruction in the Friuli area, the Italian government established the Centro di Ricerche Sismologiche (CRS). This is now a departmen
Externí odkaz:
https://doaj.org/article/817f7da4542f4384b442d936d1ba6379
Autor:
Emanuele Angelucci, Susanne Matthes-Martin, Donatella Baronciani, Françoise Bernaudin, Sonia Bonanomi, Maria Domenica Cappellini, Jean-Hugues Dalle, Paolo Di Bartolomeo, Cristina Díaz de Heredia, Roswitha Dickerhoff, Claudio Giardini, Eliane Gluckman, Ayad Achmed Hussein, Naynesh Kamani, Milen Minkov, Franco Locatelli, Vanderson Rocha, Petr Sedlacek, Frans Smiers, Isabelle Thuret, Isaac Yaniv, Marina Cavazzana, Christina Peters
Publikováno v:
Haematologica, Vol 99, Iss 5 (2014)
Thalassemia major and sickle cell disease are the two most widely disseminated hereditary hemoglobinopathies in the world. The outlook for affected individuals has improved in recent years due to advances in medical management in the prevention and t
Externí odkaz:
https://doaj.org/article/c21749282e2947dcbf34c9d3354bbde9
Autor:
Enrico Priolo, Marco Romanelli, Carla Barnaba, Marco Mucciarelli, Giovanna Laurenzano, Lorella Dall'Olio, Nasser Abu Zeid, Riccardo Caputo, Giovanni Santarato, Luigi Vignola, Carmine Lizza, Paolo Di Bartolomeo
Publikováno v:
Annals of Geophysics, Vol 55, Iss 4 (2012)
Following the Ml 5.9 earthquake that struck the Emilia area in northern Italy on May 20, 2012, at 02:03:53 UTC, and in co-operation with the personnel of the Municipality of Ferrara and the University of Ferrara, a team of seismologists of the Istitu
Externí odkaz:
https://doaj.org/article/f177fb4aba334aa3ab3e628d5af0f98d
Autor:
Stella Santarone, Andrea Bacigalupo, Antonio M. Risitano, Elena Tagliaferri, Erminia Di Bartolomeo, Anna Paola Iori, Alessandro Rambaldi, Emanuele Angelucci, Alessandra Spagnoli, Federico Papineschi, Stefania Tamiazzo, Marta Di Nicola, Paolo Di Bartolomeo
Publikováno v:
Haematologica, Vol 95, Iss 6 (2010)
Background Paroxysmal nocturnal hemoglobinuria is an acquired clonal disorder of the hemopoietic stem cells for which the only curative treatment is allogeneic hematopoietic stem cell transplantation.Design and Methods The aim of this retrospective s
Externí odkaz:
https://doaj.org/article/2ca0c5deb17b454786f7b717506215fd
Autor:
Francesca Patriarca, Andrea Bacigalupo, Alessandra Sperotto, Miriam Isola, Maria Teresa Van Lint, Anna Paola Iori, Paolo Di Bartolomeo, Maurizio Musso, Pietro Pioltelli, Giuseppe Visani, Pasquale Iacopino, Renato Fanin, Alberto Bosi
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 2, Iss 2, Pp e2010010-e2010010 (2010)
Background Allogeneic stem cell transplantation (SCT) is a potentially curative treatment for myelofibrosis (MI), though limited by a high rate of transplant-related mortality (TRM). . In the present study we evaluate the outcome of MI patients under
Externí odkaz:
https://doaj.org/article/aa493e1019264092bd50d0e60037a37c
Autor:
Miriam Isola, Alessandra Sperotto, Andrea Bacigalupo, Francesca Patriarca, Maria Teresa Van Lint, Anna Paola Iori, Paolo Di Bartolomeo, Maurizio Musso, Pietro Pioltelli, Giuseppe Visani, Pasquale Iacopino, Renato Fanin, Alberto Bosi
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 2, Iss 2, Pp e2010010-e2010010 (2010)
BackgroundAllogeneic stem cell transplantation (SCT) is a potentially curative treatment for myelofibrosis (MI), though limited by a high rate of transplant-related mortality (TRM). . In the present study we evaluate the outcome of MI patients underg
Externí odkaz:
https://doaj.org/article/8fc56ffc41c84e439de6e835117630c5
Autor:
Franco Locatelli, Marco Zecca, Andrea Pession, Giuseppe Morreale, Daniela Longoni, Paolo Di Bartolomeo, Fulvio Porta, Franca Fagioli, Bruno Nobili, Maria Ester Bernardo, Chiara Messina
Publikováno v:
Haematologica, Vol 92, Iss 10 (2007)
Background and Objectives Hematopoietic stem cell transplantation (HSCT) still represents the only treatment potentially able to prevent/rescue the development of marrow failure and myeloid malignancies in patients with Fanconi anemia (FA). While in
Externí odkaz:
https://doaj.org/article/c5c6fb392f8e460bad74e6c6f4974876