Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Annamaria Lavecchia"'
Autor:
Natalia Malara, Maria Laura Coluccio, Fabiana Grillo, Teresa Ferrazzo, Nastassia C. Garo, Giuseppe Donato, Annamaria Lavecchia, Franco Fulciniti, Anna Sapino, Eliano Cascardi, Antonella Pellegrini, Prassede Foxi, Cesare Furlanello, Giovanni Negri, Guido Fadda, Arrigo Capitanio, Salvatore Pullano, Virginia M. Garo, Francesca Ferrazzo, Alarice Lowe, Angela Torsello, Patrizio Candeloro, Francesco Gentile
Publikováno v:
Molecular Cancer, Vol 23, Iss 1, Pp 1-5 (2024)
Abstract Background the problem in early diagnosis of sporadic cancer is understanding the individual’s risk to develop disease. In response to this need, global scientific research is focusing on developing predictive models based on non-invasive
Externí odkaz:
https://doaj.org/article/3afe383205ca4c4bb4fbd6e1c3d0d554
Autor:
Nadia Innaro, Rita Gervasi, Teresa Ferrazzo, Nastassia C. Garo, Lucia S. Curto, Annamaria Lavecchia, Isabella Aquila, Giuseppe Donato, Natalia Malara
Publikováno v:
Cancer Medicine, Vol 11, Iss 24, Pp 4830-4837 (2022)
Abstract The overall estimated risk of recurrence after an apparently complete thyroid cancer resection ranges from 5% CTCs (p = 0.09) and with >30% S‐phase cells at baseline (p = 0.0015), predicting ≤1 year relapsing lesion event. These results
Externí odkaz:
https://doaj.org/article/bf3ca19cec924028adaf963ec1f4b769
Publikováno v:
Oral diseases.
Publikováno v:
Dermatologic therapy. 35(11)
Autor:
Chiara Mignogna, Patrizio Candeloro, Ivan Presta, Virginia Garo, Federica Figuccia, Maria Laura Coluccio, Nicola Coppedè, Annamaria Lavecchia, Giuseppe Donato, Natalia Malara, Francesco Gentile, Immanuel Valprapuram, Giuseppe Viglietto, Enzo Di Fabrizio
Publikováno v:
Cancers
Cancers (Basel) 12 (2020): 1362-1. doi:10.3390/cancers12061362
info:cnr-pdr/source/autori:Coluccio M.L.; Gentile F.; Presta I.; Donato G.; Coppede N.; Valprapuram I.; Mignogna C.; Lavecchia A.; Figuccia F.; Garo V.M.; Di Fabrizio E.; Candeloro P.; Viglietto G.; Malara N./titolo:Tailoring chemometric models on blood-derived cultures secretome to assess personalized cancer risk score/doi:10.3390%2Fcancers12061362/rivista:Cancers (Basel)/anno:2020/pagina_da:1362-1/pagina_a:/intervallo_pagine:1362-1/volume:12
Cancers, Vol 12, Iss 1362, p 1362 (2020)
Volume 12
Issue 6
Cancers (Basel) 12 (2020): 1362-1. doi:10.3390/cancers12061362
info:cnr-pdr/source/autori:Coluccio M.L.; Gentile F.; Presta I.; Donato G.; Coppede N.; Valprapuram I.; Mignogna C.; Lavecchia A.; Figuccia F.; Garo V.M.; Di Fabrizio E.; Candeloro P.; Viglietto G.; Malara N./titolo:Tailoring chemometric models on blood-derived cultures secretome to assess personalized cancer risk score/doi:10.3390%2Fcancers12061362/rivista:Cancers (Basel)/anno:2020/pagina_da:1362-1/pagina_a:/intervallo_pagine:1362-1/volume:12
Cancers, Vol 12, Iss 1362, p 1362 (2020)
Volume 12
Issue 6
The molecular protonation profiles obtained by means of an organic electrochemical transistor, which is used for analysis of molecular products released by blood-derived cultures, contain a large amount of information The transistor is based on the c
Autor:
Carlo M. Croce, Francesco Baudi, Francesco Trapasso, Eugenio Gaudio, Cristian Taccioli, Francesco Costanzo, Maddalena Di Sanzo, Chang Gong Liu, Barbara Quaresima, Maria Concetta Faniello, Annamaria Lavecchia, Giovanni Cuda, Francesco Romeo
Publikováno v:
Clinical Cancer Research. 14:6797-6803
Purpose: The aim of this study was to explore the gene expression pattern produced by the cancer-associated BRCA1 5083del19 founder mutation by using a microarray analysis. Such a mutation, identified in a subset of familial breast cancer patients, i
A novel missense germline mutation in exon 2 of the hMSH2 gene in a HNPCC family from Southern Italy
Autor:
Salvatore Venuta, Francesco Baudi, Francarlo Leone, Francesco Costanzo, Annamaria Lavecchia, Patrizia Doldo, Rosa Terracciano, Maria Concetta Faniello, Giuseppina Fersini, Giovanni Cuda, Barbara Quaresima, Loredana De Paola
Publikováno v:
Cancer Letters. 223:285-291
Germline mutations within the mismatch repair (MMR) genes are generally found in colorectal cancer (CRC) patients with a positive family history for the presence of the neoplasia. Clinical standard criteria have been established to define hereditary-
Autor:
F Fabiani, Annamaria Lavecchia, Francesco Costanzo, W D'Amico, Maria Concetta Faniello, Salvatore Venuta, Barbara Quaresima, Giovanni Cuda, L De Paola, Francesco Baudi
Publikováno v:
Breast Cancer Research : BCR