Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Matilde De Luca"'
Autor:
Paolo Antonio Ascierto, Eliana Rulli, Anna Cecilia Bettini, Maria Grazia Vitale, Carlo Alberto Tondini, Matilde De Luca, Barbara Merelli, Mario Mandala, Sharon Nahm, Paul Lorigan, Andrea Bianchetti, Lucia Bonomi, Giorgia Negrini, Andrea Di Croce
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 9, Iss 2 (2021)
Background In ambulatory patients with cancer with asymptomatic or pauci-symptomatic SARS-CoV-2 infection, the safety of targeted therapies (TTs), chemotherapy (CT) or immune checkpoint inhibitors (ICIs) therapy is still unknown.Material and methods
Externí odkaz:
https://doaj.org/article/5d142b23383c4287b8f38875db6c9331
Autor:
Iwona Lugowska, Matilde De Luca, Barbara Merelli, Anna Mariuk-Jarema, Pawel Teterycz, Pawel Rogala, Bożena Cybulska-Stopa, Alice Labianca, Lorenza Di Guardo, Giovanni Randon
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 8, Iss 2 (2020)
Background Obesity is a risk factor for malignancy; however, its prognostic role in patients with metastatic melanoma is controversial. We aim to investigate the prognostic role of body mass index (BMI) in patients with metastatic melanoma receiving
Externí odkaz:
https://doaj.org/article/8bfef22853f647bdaee885bd165056af
Autor:
Riccardo Masetti, Salvatore Nicola Bertuccio, Annalisa Astolfi, Francesca Chiarini, Annalisa Lonetti, Valentina Indio, Matilde De Luca, Jessica Bandini, Salvatore Serravalle, Monica Franzoni, Martina Pigazzi, Alberto Maria Martelli, Giuseppe Basso, Franco Locatelli, Andrea Pession
Publikováno v:
Journal of Hematology & Oncology, Vol 10, Iss 1, Pp 1-5 (2017)
Abstract Background CBFA2T3-GLIS2 is a fusion gene found in 17% of non-Down syndrome acute megakaryoblastic leukemia (non-DS AMKL, FAB M7) and in 8% of pediatric cytogenetically normal acute myeloid leukemia (CN-AML, in association with several Frenc
Externí odkaz:
https://doaj.org/article/704b3991b6064a82b86ddf57edc38f55
Autor:
Annalisa Astolfi, Francesca Cipriani, Daria Messelodi, Matilde De Luca, Valentina Indio, Costanza Di Chiara, Arianna Giannetti, Lorenza Ricci, Iria Neri, Annalisa Patrizi, Giampaolo Ricci, Andrea Pession
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 2, p 233 (2021)
Atopic dermatitis is frequently associated with the onset of other allergic conditions, such as asthma, rhino-conjunctivitis and food allergy. The etiology of atopic dermatitis is marginally understood in spite of the number of predisposing factors,
Externí odkaz:
https://doaj.org/article/46648fc951db4f568305d41590b7d2bd
Autor:
Milena Urbini, Margherita Nannini, Annalisa Astolfi, Valentina Indio, Valentina Vicennati, Matilde De Luca, Giuseppe Tarantino, Federica Corso, Maristella Saponara, Lidia Gatto, Donatella Santini, Guido Di Dalmazi, Uberto Pagotto, Renato Pasquali, Andrea Pession, Guido Biasco, Maria A. Pantaleo
Publikováno v:
International Journal of Genomics, Vol 2018 (2018)
Background. Pheochromocytomas (PCCs) show the highest degree of heritability in human neoplasms. However, despite the wide number of alterations until now reported in PCCs, it is likely that other susceptibility genes remain still unknown, especially
Externí odkaz:
https://doaj.org/article/266029af3d70419fbb97fab551f8a5a1
Autor:
Guido Biasco, Annalisa Astolfi, Antonio D. Pinna, Paolo G. Casali, Giovanni Brandi, Silvia Stacchiotti, Paola Collini, Salvatore L. Renne, Elisa Gruppioni, Annalisa Altimari, Claudio Ceccarelli, M. Giulia Pirini, Donatella Santini, Paola Paterini, Manuela Ianni, Maristella Saponara, Lidia Gatto, Elena Fumagalli, Chiara Colombo, Giovanni Grignani, Bruno Vincenzi, Alessandro Gronchi, Sabrina Angelini, Giuseppe Tarantino, Matilde De Luca, Margherita Nannini, Gloria Ravegnini, Valentina Indio, Milena Urbini, Maria A. Pantaleo
Supplementary Table 2. The most important miRNA predicted as potential regulators of Neuroactive ligand-receptor interaction signature genes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::289b96d1630330abbef7acaff20ca232
https://doi.org/10.1158/1541-7786.22515766
https://doi.org/10.1158/1541-7786.22515766
Autor:
Guido Biasco, Annalisa Astolfi, Antonio D. Pinna, Paolo G. Casali, Giovanni Brandi, Silvia Stacchiotti, Paola Collini, Salvatore L. Renne, Elisa Gruppioni, Annalisa Altimari, Claudio Ceccarelli, M. Giulia Pirini, Donatella Santini, Paola Paterini, Manuela Ianni, Maristella Saponara, Lidia Gatto, Elena Fumagalli, Chiara Colombo, Giovanni Grignani, Bruno Vincenzi, Alessandro Gronchi, Sabrina Angelini, Giuseppe Tarantino, Matilde De Luca, Margherita Nannini, Gloria Ravegnini, Valentina Indio, Milena Urbini, Maria A. Pantaleo
Copy number alterations on chromosome 1, 14 and 22 with the related genes of Cancer Gene Census
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52efa9f7759ed3032214dd43819774a6
https://doi.org/10.1158/1541-7786.22515763.v1
https://doi.org/10.1158/1541-7786.22515763.v1
Autor:
Guido Biasco, Annalisa Astolfi, Antonio D. Pinna, Paolo G. Casali, Giovanni Brandi, Silvia Stacchiotti, Paola Collini, Salvatore L. Renne, Elisa Gruppioni, Annalisa Altimari, Claudio Ceccarelli, M. Giulia Pirini, Donatella Santini, Paola Paterini, Manuela Ianni, Maristella Saponara, Lidia Gatto, Elena Fumagalli, Chiara Colombo, Giovanni Grignani, Bruno Vincenzi, Alessandro Gronchi, Sabrina Angelini, Giuseppe Tarantino, Matilde De Luca, Margherita Nannini, Gloria Ravegnini, Valentina Indio, Milena Urbini, Maria A. Pantaleo
Supplementary Table 1. Significative pathways found by functional enrichment analysis with WEB-based GEne SeT AnaLysis Toolkit.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15db842dd6ca450bc7fa7449936ac9c1
https://doi.org/10.1158/1541-7786.22515769
https://doi.org/10.1158/1541-7786.22515769
Autor:
Guido Biasco, Annalisa Astolfi, Antonio D. Pinna, Paolo G. Casali, Giovanni Brandi, Silvia Stacchiotti, Paola Collini, Salvatore L. Renne, Elisa Gruppioni, Annalisa Altimari, Claudio Ceccarelli, M. Giulia Pirini, Donatella Santini, Paola Paterini, Manuela Ianni, Maristella Saponara, Lidia Gatto, Elena Fumagalli, Chiara Colombo, Giovanni Grignani, Bruno Vincenzi, Alessandro Gronchi, Sabrina Angelini, Giuseppe Tarantino, Matilde De Luca, Margherita Nannini, Gloria Ravegnini, Valentina Indio, Milena Urbini, Maria A. Pantaleo
Graphical view of copy number analysis. Copy number alterations detected on the chromosomes most frequently deleted in GIST (chr1, chr14 and chr22). For each patient a green bar indicates an heterozygously deleted region and a red bar indicates a gai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bda8853e3ee3b45b9ba1d2bb22129aec
https://doi.org/10.1158/1541-7786.22515775.v1
https://doi.org/10.1158/1541-7786.22515775.v1
Autor:
Guido Biasco, Annalisa Astolfi, Antonio D. Pinna, Paolo G. Casali, Giovanni Brandi, Silvia Stacchiotti, Paola Collini, Salvatore L. Renne, Elisa Gruppioni, Annalisa Altimari, Claudio Ceccarelli, M. Giulia Pirini, Donatella Santini, Paola Paterini, Manuela Ianni, Maristella Saponara, Lidia Gatto, Elena Fumagalli, Chiara Colombo, Giovanni Grignani, Bruno Vincenzi, Alessandro Gronchi, Sabrina Angelini, Giuseppe Tarantino, Matilde De Luca, Margherita Nannini, Gloria Ravegnini, Valentina Indio, Milena Urbini, Maria A. Pantaleo
Quadruple wild-type (WT) gastrointestinal stromal tumor (GIST) is a genomic subgroup lacking KIT/PDGFRA/RAS pathway mutations, with an intact succinate dehydrogenase (SDH) complex. The aim of this work is to perform a wide comprehensive genomic study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffbc7611f4312baac3a577eaecd88077
https://doi.org/10.1158/1541-7786.c.6541177
https://doi.org/10.1158/1541-7786.c.6541177