Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Anna Marfia"'
Autor:
Elena Baiamonte, Rita Barone, Flavia Contino, Rosalia Di Stefano, Anna Marfia, Aldo Filosa, Emanuela D'Angelo, Salvatore Feo, Santina Acuto, Aurelio Maggio
Publikováno v:
Thalassemia Reports, Vol 7, Iss 1 (2017)
Successful gene therapy for β-thalassemia requires optimal numbers of autologous gene-transduced hematopoietic stem and progenitor cells (HSPCs) with high repopulating capacity. Previous studies suggested superior mobilization in these patients by t
Externí odkaz:
https://doaj.org/article/df256ac03d3c49c08c37b081b1b91404
Autor:
Cecilia Agueli, Rosaria Basiricò, Francesco Fabbiano, Valentina Rizzo, Lucia Cascio, Giuseppe Cammarata, Anna Marfia, Maria La Rosa, Salvo Mirto, Alessandra Santoro
Publikováno v:
Haematologica, Vol 92, Iss 5 (2007)
Although chromosomal abnormalities are detected by conventional cytogenetic analysis (CCA) in 40–60% of patients with acute myeloid leukemia (AML), cryptic chromosomal deletions may only be detected by molecular analysis. To determine their frequen
Externí odkaz:
https://doaj.org/article/54e7430b13a9463e8083122880a7e756
Autor:
Luisa Ferrari, Laura Vanelli, Anna Triolo, Antonio Regazzoli, Francesco Buccisano, Paola Omedè, Maria Matilde Ciriello, M Arras, Feliciano Visconte, Cinzia Armentano Conte, Rachele Amodeo, Giovanni Poletti, Francesco Lanza, Maria Cristina Pavanelli, Chiara Bartocci, Donatella Tanca, F. Rubba, Clorinda De Rosa, Anna Marfia, Elisa Boscaro, Anna Mestice, Virginia Catinella, Arianna Gatti, Bianca Maria Oliva, Massimo Geuna, Elisabetta Tedone, Elisa Cannizzo, Maria Stefania De Propris, Fiorella D'Auria, Maddalena Raia, Simone Cesaro, Anna Maria Santonocito, Angela Michelutti, Barbara Scarpati, Teodora Statuto, Francesca Ulbar, Catia Lo Pardo, Graziano Pianezze, Bruno Brando, Roberto Caporale, Pellegrino Musto, Laura Del Pup, Luigi Del Vecchio, Virginia Ottaviano, Giorgia Pantano, Alessandra Stacchini
Publikováno v:
Annals of Hematology. 98:1083-1093
In this study, we aimed at disclosing the main features of paroxysmal nocturnal hemoglobinuria (PNH) clones, their association with presentation syndromes, and their changes during follow-up. A large-scale, cooperative collection (583 clones from 529
Autor:
Alessandra Santoro, Maria Grazia Bica, Lea Dagnino, Anna Marfia, Francesco Fabbiano, Maria Pagano, Maria La Rosa, Giuseppe Cammarata, Roberta Nicoletti, Domenico Salemi, Cecilia Agueli, Maria Luisa Coniglio, Francesca Messana
Publikováno v:
American Journal of Hematology. 85:575-578
This study evaluated the loss and expression level of miRNAs 14q32 clusters in acute lymphoblastic leukemia (ALL) patients with cryptic deletions at 14q32 chromosomal band to investigate their involvement in this disease. We demonstrate that a subset
Autor:
Salvatore Mirto, Valentina Rizzo, Diamante Turri, Lea Dagnino, A Mineo, Luigi Augugliaro, Rosario Giustolisi, Maria La Rosa, Giuseppe Cammarata, Cecilia Agueli, Anna Marfia, Alessandra Santoro
Publikováno v:
Clinical Leukemia. 1:234-242
Background. Most chronic myeloid leukemia patients who receive imatinib as first line-terapy will obtain, after 12 months treatment, complete cytogenetic and molecular response . However several cases will not achieve molecular response, but their in
Autor:
Lucia Cascio, Rosaria Basiricò, Giuseppe Cammarata, Anna Marfia, Maria La Rosa, Alessandra Santoro, Valentina Rizzo, Cecilia Agueli, Francesco Fabbiano, Salvo Mirto
Publikováno v:
Haematologica. 92:678-681
Although chromosomal abnormalities are detected by conventional cytogenetic analysis (CCA) in 40-60% of patients with acute myeloid leukemia (AML), cryptic chromosomal deletions may only be detected by molecular analysis. To determine their frequency
Autor:
Luigi Augugliaro, Maria Grazia Bica, Cecilia Agueli, Riccardo Alessandro, Francesco Fabbiano, Stefania Raimondo, Domenico Salemi, Francesco Di Raimondo, Paola Dragotto, Anna Marfia, Valentina Randazzo, Chiara Corrado, Giuseppe Cammarata, Alessandra Santoro
Background Acute myeloid leukemia (AML) represents a heterogeneous disorder with recurrent chromosomal alterations and molecular abnormalities. Among AML with normal karyotype (NK-AML) FLT3 activating mutation, internal tandem duplication (FLT3-ITD),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df3725866bbb43118bdcb0ed15b1b3aa
http://hdl.handle.net/10447/145096
http://hdl.handle.net/10447/145096
Autor:
Salvatore Feo, Flavia Contino, Anna Marfia, Rita Barone, Aldo Filosa, Emanuela D'Angelo, Aurelio Maggio, Rosalia Di Stefano, Santina Acuto, Elena Baiamonte
Publikováno v:
Thalassemia Reports, Vol 7, Iss 1 (2017)
Thalassemia Reports; Volume 7; Issue 1; Pages: 6392
Thalassemia Reports; Volume 7; Issue 1; Pages: 6392
Successful gene therapy for β-thalassemia requires optimal numbers of autologous gene-transduced hematopoietic stem and progenitor cells (HSPCs) with high repopulating capacity. Previous studies suggested superior mobilization in these patients by t
Autor:
Flora Iovino, Giorgio Stassi, Riccardo Alessandro, Stefania Raimondo, Chiara Corrado, Alessandra Santoro, Giacomo De Leo, Ralph B. Arlinghaus, Simona Fontana, Elise C. Kohn, A. Flugy, Anna Marfia
Mutation of the Bcr–Abl oncoprotein is one of most frequent mechanisms by which chronic myelogenous leukemia (CML) cells become resistant to imatinib. Here, we show that treat- ment of cell lines harbouring wild type or mutant BCR–ABL with carbox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acbe9f03a0f77fa943cde1f8c9ab9063
http://hdl.handle.net/10447/56094
http://hdl.handle.net/10447/56094
Autor:
Luigi Augugliaro, Gabriele Civiletto, Domenico Salemi, Anna Marfia, Cecilia Agueli, Pietro Michele Floridia, Maria La Rosa, Giuseppe Cammarata, Angelo Mineo, Mario Russo, Francesco Fabbiano, Francesca Messana, Alessandra Santoro, Maria Grazia Bica, Lea Dagnino, Lucia Cascio
Acute myeloid leukemia (AML) the most common acute leukemia in adults is characterized by various cytogenetic and molecular abnormalities. However, the genetic etiology of the disease is not yet fully understood. MicroRNAs (miRNA) are small noncoding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25a54286dff62cd791defc272bfceb44
http://hdl.handle.net/10447/50291
http://hdl.handle.net/10447/50291