Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Elisabetta Merli"'
Autor:
Luca Chiaraviglio, Chiara Lodovisi, Daniele Franci, Settimio Pavoncello, Elisabetta Merli, Tommaso Aureli, Nicola Blefari-Melazzi, Marco Donald Migliore, Mohamed-Slim Alouini
Publikováno v:
IEEE Open Journal of the Communications Society, Vol 3, Pp 1445-1465 (2022)
The rolling-out of 5G networks is recently including 5G Base Stations (BSs) operating on millimeter-Wave (mm-Wave) frequencies. The goal of this work is to shed light on the exposure assessment from commercial 5G mm-Wave 5G BSs, by focusing on the im
Externí odkaz:
https://doaj.org/article/993ab04ea0254e2f87f17f2cdb31d586
Autor:
Marco Donald Migliore, Daniele Franci, Settimio Pavoncello, Tommaso Aureli, Elisabetta Merli, Chiara Lodovisi, Luca Chiaraviglio, Fulvio Schettino
Publikováno v:
IEEE Access, Vol 10, Pp 103438-103446 (2022)
This paper describes an investigation on the application of the Maximum Power Extrapolation (MPE) technique on a fully operational Fixed Wireless Access (FWA) FR2-band 5G gNB. The data was acquired in [27.1-27.3] GHz band using a network scanner over
Externí odkaz:
https://doaj.org/article/c45cf977bd2f46b5b4c87a918334ac1a
Autor:
Fernando Formaggio, Antonio Toffoletti, Claudio Toniolo, Elisabetta Merli, Marina Gobbo, Simona Oancea, Barbara Biondi
Publikováno v:
Journal of Peptide Science. 18:37-44
A set of analogues of the 14-residue peptaibol tylopeptin B, containing the stable free-radical 4-amino-1-oxyl-2,2,6,6,-tetramethylpiperidine-4-carboxylic acid (TOAC) at one or two selected positions, was synthesized by the solid-phase methodology. A
Autor:
Marina Gobbo, Elisabetta Merli, Barbara Biondi, Simona Oancea, Antonio Toffoletti, Fernando Formaggio, Claudio Toniolo
Publikováno v:
Journal of peptide science (Online) 18 (2012): 37–44. doi:10.1002/psc.1413
info:cnr-pdr/source/autori:Marina Gobbo; Elisabetta Merli; Barbara Biondi; Simona Oancea; Antonio Toffoletti; Fernando Formaggio; Claudio Toniolo/titolo:Synthesis and preliminary conformational analysis of TOAC spin-labeled analogues of the medium-length peptaibiotic tylopeptin B/doi:10.1002%2Fpsc.1413/rivista:Journal of peptide science (Online)/anno:2012/pagina_da:37/pagina_a:44/intervallo_pagine:37–44/volume:18
info:cnr-pdr/source/autori:Marina Gobbo; Elisabetta Merli; Barbara Biondi; Simona Oancea; Antonio Toffoletti; Fernando Formaggio; Claudio Toniolo/titolo:Synthesis and preliminary conformational analysis of TOAC spin-labeled analogues of the medium-length peptaibiotic tylopeptin B/doi:10.1002%2Fpsc.1413/rivista:Journal of peptide science (Online)/anno:2012/pagina_da:37/pagina_a:44/intervallo_pagine:37–44/volume:18
A set of analogues of the 14-residue peptaibol tylopeptin B, containing the stable free-radical 4-amino-1-oxyl-2,2,6,6,-tetramethylpiperidine-4-carboxylic acid (TOAC) at one or two selected positions, was synthesized by the solid-phase methodology. A