Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Wanda D'Amico"'
Publikováno v:
Journal of Information Privacy and Security. 11:262-273
Nowadays, the increasing number of unconventional biological attacks around the world, as well as innovative technologies and a larger availability of tools and materials, contribute to a wider expertise on dealing with devices and agents due to thei
Autor:
Bruno Scanu, Angela Tuzi, Marco Masi, Wanda D'Amico, Alessio Cimmino, Benedetto Teodoro Linaldeddu, Antonio Evidente, Lucia Maddau, Marco Evidente
Three new lactones and a new fatty acid ester, named sapinofuranones C and D, diplopyrone B, and diplobifuranylone C, respectively, were isolated from Diplodia corticola, together with sphaeropsidins A and C, diplopyrone, diplobifuranylones A and B,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0263785e01e3768fd9e18ac9c936b3fe
http://hdl.handle.net/11588/632098
http://hdl.handle.net/11588/632098
Autor:
A Martini, Luca Rubino, Nicoletta Vonesch, Paolo Visca, Wanda D'Amico, P. Tomao, Silvia Capanna, Fabio Tomei, Simona Di Renzi
Publikováno v:
American Journal of Infection Control. 40:459-461
The prevalence of tuberculosis (TB) among homeless shelter staff was assessed using the tuberculin skin test (TST) and the Quantiferon TB-Gold in tube interferon-γ release assay (QFT-TB). Investigation of 51 participants for whom both QFT-TB and TST
Autor:
Roberto Mugavero, Wanda D‘amico
Publikováno v:
Biosafety.
Autor:
Véronique Mathieu, Patrizia Scafato, Stefano Superchi, Wanda D'Amico, Lucia Maddau, Laura Pisani, Alessio Cimmino, Antonio Evidente, Aude Ingels, Robert Kiss
Publikováno v:
Scopus-Elsevier
This paper describes the enantioselective synthesis of analogues of sapinofuranones A and B, namely 5-substitutes dihydro- and 5 H-furan-ones, and their in vitro growth inhibitory activity against six cancer cell lines in comparison with fungal furan
Autor:
Alfredo Fusco, Wanda D'Amico, Barbara Tavernise, Luigi Insabato, Filippo Schepis, Guido Pettinato, Dolores Di Vizio, Maria Letizia Motti, Paolo Chieffi, Fernanda Fabiani, Letizia Cito, Salvatore Venuta, Angelo Boccia, Giuseppe Viglietto
Publikováno v:
Oncogene (Basingstoke) 24 (2005): 1882–1894.
info:cnr-pdr/source/autori:Di Vizio D, Cito L, Boccia A, Chieffi P, Insabato L, Pettinato G, Motti ML, Schepis F, D'Amico W, Fabiani F, Tavernise B, Venuta S, Fusco A, Viglietto G./titolo:Loss of the tumor suppressor gene PTEN marks the transition from intratubular germ cell neoplasias (ITGCN) to invasive germ cell tumors./doi:/rivista:Oncogene (Basingstoke)/anno:2005/pagina_da:1882/pagina_a:1894/intervallo_pagine:1882–1894/volume:24
info:cnr-pdr/source/autori:Di Vizio D, Cito L, Boccia A, Chieffi P, Insabato L, Pettinato G, Motti ML, Schepis F, D'Amico W, Fabiani F, Tavernise B, Venuta S, Fusco A, Viglietto G./titolo:Loss of the tumor suppressor gene PTEN marks the transition from intratubular germ cell neoplasias (ITGCN) to invasive germ cell tumors./doi:/rivista:Oncogene (Basingstoke)/anno:2005/pagina_da:1882/pagina_a:1894/intervallo_pagine:1882–1894/volume:24
PTEN/MMAC1/TEP1: (hereafter PTEN) is a tumor suppressor gene (located at 10q23) that is frequently mutated or deleted in sporadic human tumors. PTEN encodes a multifunctional phosphatase, which negatively regulates cell growth, migration and survival