Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Lucia Nacci"'
Autor:
Pierluigi Di Chiaro, Lucia Nacci, Stefania Brandini, Sara Polletti, Benedetta Donati, Francesco Gualdrini, Gianmaria Frige, Luca Mazzarella, Alessia Ciarrocchi, Alessandro Zerbi, Paola Spaggiari, Iros Barozzi, Giuseppe R. Diaferia, Gioacchino Natoli
Intratumor morphological heterogeneity predicts clinical outcomes of pancreatic ductal adenocarcinoma (PDAC). However, it is only partially understood at the molecular level and devoid of clinical actionability. In this study we set out to determine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e2dbeeb5d12696ffa0664ddde67061c
https://doi.org/10.1101/2022.12.12.520054
https://doi.org/10.1101/2022.12.12.520054
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:
Lucia Nacci
Publikováno v:
British journal of haematology. 184(5)
Autor:
Elena Nicolis, Lucia Nacci, Cesare Danesino, Giampiero Pietrocola, Antonella Minelli, Marco Cipolli, Roberto Valli, Letizia Pomponia Brescia, Ugo Ramenghi, Franco Locatelli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8a7910b8b1a23038cb72f4ce57545b8
http://hdl.handle.net/2318/1593283
http://hdl.handle.net/2318/1593283
Autor:
Monica Savio, Cristina Maccario, Maria Gomolka, Andrea Ottolenghi, Luca Mariotti, Lucia Nacci, Gabriele Babini, Antonella Minelli, Ulrike Kulka, Cesare Danesino, Jacopo Morini, U. Rößler, Giorgio Baiocco
Publikováno v:
Europe PubMed Central
Shwachman-Diamond syndrome is an autosomal-recessive disorder characterised by bone marrow failure and a cumulative risk of progression to acute myeloid leukaemia. The Shwachman-Bodian-Diamond syndrome (SBDS) gene, the only gene known to be causative
Autor:
Francesco Pasquali, A. Frattini, Lucia Nacci, Elena De Paoli, Emanuela Maserati, Roberto Valli
Publikováno v:
Pediatric Blood & Cancer. 64:e26454
Background Two chromosome anomalies are frequent in the bone marrow (BM) of patients with Shwachman–Diamond syndrome (SDS): an isochromosome of the long arm of chromosome 7, i(7)(q10), and an interstitial deletion of the long arm of chromosome 20,
Autor:
Zemira Cannioto, Antonella Minelli, F. Poli, Jacopo Morini, Cesare Danesino, Sandra Perobelli, Lucia Nacci, Elena Nicolis, Laura Sainati, Daniela Longoni, Marco Cipolli, Roberto Valli, Francesco Pasquali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebabcbcd986e75613a7c34b71094f5c0
http://hdl.handle.net/11562/945492
http://hdl.handle.net/11562/945492