Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Emanuela Maserati"'
Autor:
Abdul Waheed Khan, Antonella Minelli, Annalisa Frattini, Giuseppe Montalbano, Alessia Bogni, Marco Fabbri, Giovanni Porta, Francesco Acquati, Rita Maria Pinto, Elena Bergami, Rossella Mura, Anna Pegoraro, Simone Cesaro, Marco Cipolli, Marco Zecca, Cesare Danesino, Franco Locatelli, Emanuela Maserati, Francesco Pasquali, Roberto Valli
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-9 (2020)
Abstract Background Clonal chromosome changes are often found in the bone marrow (BM) of patients with Shwachman-Diamond syndrome (SDS). The most frequent ones include an isochromosome of the long arm of chromosome 7, i (7)(q10), and an interstitial
Externí odkaz:
https://doaj.org/article/f3bc050564244f20b7a6bcde606e1c8f
Autor:
Elizabeth Nacheva, Katya Mokretar, Aynur Soenmez, Alan M Pittman, Colin Grace, Roberto Valli, Ayesha Ejaz, Selina Vattathil, Emanuela Maserati, Henry Houlden, Jan-Willem Taanman, Anthony H Schapira, Christos Proukakis
Publikováno v:
PLoS ONE, Vol 12, Iss 7, p e0180467 (2017)
Potential bias introduced during DNA isolation is inadequately explored, although it could have significant impact on downstream analysis. To investigate this in human brain, we isolated DNA from cerebellum and frontal cortex using spin columns under
Externí odkaz:
https://doaj.org/article/85a2ca19810844f4bdb02cb93582722d
Autor:
Maria Clara Bonaglia, Roberto Giorda, Silvana Beri, Cristina De Agostini, Francesca Novara, Marco Fichera, Lucia Grillo, Ornella Galesi, Annalisa Vetro, Roberto Ciccone, Maria Teresa Bonati, Sabrina Giglio, Renzo Guerrini, Sara Osimani, Susan Marelli, Claudio Zucca, Rita Grasso, Renato Borgatti, Elisa Mani, Cristina Motta, Massimo Molteni, Corrado Romano, Donatella Greco, Santina Reitano, Anna Baroncini, Elisabetta Lapi, Antonella Cecconi, Giulia Arrigo, Maria Grazia Patricelli, Chiara Pantaleoni, Stefano D'Arrigo, Daria Riva, Francesca Sciacca, Bernardo Dalla Bernardina, Leonardo Zoccante, Francesca Darra, Cristiano Termine, Emanuela Maserati, Stefania Bigoni, Emanuela Priolo, Armand Bottani, Stefania Gimelli, Frederique Bena, Alfredo Brusco, Eleonora di Gregorio, Irene Bagnasco, Ursula Giussani, Lucio Nitsch, Pierluigi Politi, Maria Luisa Martinez-Frias, Maria Luisa Martínez-Fernández, Nieves Martínez Guardia, Anna Bremer, Britt-Marie Anderlid, Orsetta Zuffardi
Publikováno v:
PLoS Genetics, Vol 7, Iss 7, p e1002173 (2011)
In this study, we used deletions at 22q13, which represent a substantial source of human pathology (Phelan/McDermid syndrome), as a model for investigating the molecular mechanisms of terminal deletions that are currently poorly understood. We charac
Externí odkaz:
https://doaj.org/article/5c43355a53914e768e4abdfa928036cf
Autor:
Emanuela Maserati, Claudio Panarello, Cristina Morerio, Roberto Valli, Barbara Pressato, Francesco Patitucci, Elisa Tassano, Alessandra Di Cesare-Merlone, Chiara Cugno, Carlo L. Balduini, Francesco Lo Curto, Carlo Dufour, Franco Locatelli, Francesco Pasquali
Publikováno v:
Haematologica, Vol 93, Iss 8 (2008)
Externí odkaz:
https://doaj.org/article/60d389601a264c8a8f9b4a9bc1cd4c82
Autor:
Giovanni Porta, Marco Fabbri, Emanuela Maserati, Marco Zecca, Giuseppe Montalbano, Marco Cipolli, Antonella Minelli, Roberto Valli, Cesare Danesino, Rita Maria Pinto, Abdul Waheed Khan, Francesco Pasquali, Alessia Bogni, Simone Cesaro, Annalisa Frattini, Elena Bergami, Franco Locatelli, Anna Pegoraro, R. Mura, Francesco Acquati
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-9 (2020)
Molecular Cytogenetics
Molecular Cytogenetics
Background Clonal chromosome changes are often found in the bone marrow (BM) of patients with Shwachman-Diamond syndrome (SDS). The most frequent ones include an isochromosome of the long arm of chromosome 7, i (7)(q10), and an interstitial deletion
Autor:
Lucia Nacci, Cesare Danesino, Marco Cipolli, Roberto Valli, Elena Nicolis, Jacopo Morini, Gabriele Babini, Emily Pintani, Emanuela Maserati, Claudia Scotti, Antonella Minelli, Andrea Ottolenghi, Simone Cesaro
Publikováno v:
British Journal of Haematology. 185:627-630
Autor:
Andrea Conti, Anna Michelato, Cristina Barlassina, Giovanni Micheloni, Alessia Rainero, Giorgia Millefanti, Matteo Barcella, Francesca D'Avila, Eleonora Piscitelli, Ksenija Buklijas, Silvia M. Sirchia, Cristina Pirrone, Orietta Spinelli, Emanuela Maserati, Fabrizio Angaroni, R. Casalone, Giovanni Porta, Lucia Tararà, Massimo Caccia, Roberto Valli
Publikováno v:
Cell Death and Disease, Vol 9, Iss 3, Pp 1-8 (2018)
Cell Death & Disease
Cell Death & Disease
Chronic Myeloid Leukemia (CML) is a stem cell cancer that arises when t(9;22) translocation occurs in a hematopoietic stem cells. This event results in the expression of the BCR-ABL1 fusion gene, which codes for a constitutively active tyrosine kinas
Autor:
Francesco Pasquali, Antonella Minelli, Giovanni Porta, Annalisa Frattini, Abdul Waheed Khan, Giovanna D'Amico, Simone Cesaro, Cesare Danesino, Giorgia Millefanti, Marco Cipolli, Roberto Valli, Giuseppe Montalbano, Marta Galbiati, Gianni Cazzaniga, Emanuela Maserati, Carla Olivieri
In Shwachman-Diamond syndrome (SDS), deletion of the long arm of chromosome 20, del(20)(q), often acquired in bone marrow (BM), may imply a lower risk of developing myelodysplastic syndrome/acute myeloid leukaemia (MDS/AML), due to the loss of the EI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f1ffa6b0444e483a93d868d951ea304
http://hdl.handle.net/10281/272263
http://hdl.handle.net/10281/272263
Autor:
Luciana Vinti, Francesco Pasquali, Antonella Minelli, Emanuela Maserati, Francesco Locatelli, Marco Fabbri, Giuseppe Montalbano, Annalisa Frattini, Roberto Valli, Carla Olivieri
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-9 (2018)
Background The majority of the cases of bone marrow failure syndromes/aplastic anaemias (BMFS/AA) are non-hereditary and considered idiopathic (80–85%). The peripheral blood picture is variable, with anaemia, neutropenia and/or thrombocytopenia, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::646ee570962adaf6b7863688d2eff6ee
https://hdl.handle.net/10807/229970
https://hdl.handle.net/10807/229970
Autor:
Emanuela Maserati, Francesca De Bernardi, Paolo Castelnuovo, Luca Volpi, Fabio Facchetti, Roberto Valli, Francesco Pasquali, Maurizio Bignami, A. Frattini
Publikováno v:
Genes, Chromosomes and Cancer. 54:771-775
Olfactory neuroblastoma is a rare tumor arising from the basal layer of the olfactory epithelium in the superior recesses of the nasal cavity. The rarity of this tumor, and the difficulties in culturing tumor cells has limited the generation of conve