Zobrazeno 1 - 10
of 12 966
pro vyhledávání: '"Bonanni"'
Autor:
Benedetti D, Olcese U, Bruno S, Barsotti M, Maestri Tassoni M, Bonanni E, Siciliano G, Faraguna U
Publikováno v:
Nature and Science of Sleep, Vol Volume 14, Pp 941-956 (2022)
Davide Benedetti,1 Umberto Olcese,2 Simone Bruno,1 Marta Barsotti,3 Michelangelo Maestri Tassoni,3,4 Enrica Bonanni,3,4 Gabriele Siciliano,3,4 Ugo Faraguna1,5 1Department of Translational Research and of New Surgical and Medical Technologies, Univers
Externí odkaz:
https://doaj.org/article/85b2391b1d174c55895026709c73781b
The emergence of negative longitudinal magnetoresistance in the topologically non-trivial transition-metal dichalcogenide PtSe$_2$ is studied. Low $T$/high $\mu_0 H$ transport is performed for arbitrary field directions, and an analytical framework i
Externí odkaz:
http://arxiv.org/abs/2407.16469
Autor:
Bonanni, Paolo, Cantón, Rafael, Gill, Dipender, Halfon, Philippe, Liebert, Uwe G., Nogales Crespo, Katya A., Pérez Martín, Jaime J., Trombetta, Claudia M.
This review explores and positions the value of serology testing to support current immunization policies and the broader policy response to the coronavirus disease 2019 (COVID-19) crisis in Europe. We applied an exploratory approach to analysing exi
Externí odkaz:
https://ul.qucosa.de/id/qucosa%3A88717
https://ul.qucosa.de/api/qucosa%3A88717/attachment/ATT-0/
https://ul.qucosa.de/api/qucosa%3A88717/attachment/ATT-0/
Autor:
Dominguez-Valentin, Mev, Plazzer, John-Paul, Sampson, Julian R., Engel, Christoph, Aretz, Stefan, Jenkins, Mark A., Sunde, Lone, Bernstein, Inge, Capella, Gabriel, Balaguer, Francesc, Macrae, Finlay, Winship, Ingrid M., Thomas, Huw, Evans, Dafydd Gareth, Burn, John, Greenblatt, Marc, de Vos tot Nederveen Cappel, Wouter H., Sijmons, Rolf H., Nielsen, Maartje, Bertario, Lucio, Bonanni, Bernardo, Tibiletti, Maria Grazia, Cavestro, Giulia Martina, Lindblom, Annika, Valle, Adriana Della, Lopez-Kostner, Francisco, Alvarez, Karin, Gluck, Nathan, Katz, Lior, Heinimann, Karl, Vaccaro, Carlos A., Nakken, Sigve, Hovig, Eivind, Green, Kate, Lalloo, Fiona, Hill, James, Vasen, Hans F. A., Perne, Claudia, Büttner, Reinhard, Görgens, Heike, Holinski-Feder, Elke, Morak, Monika, Holzapfel, Stefanie, Hüneburg, Robert, von Knebel Doeberitz, Magnus, Loeffler, Markus, Rahner, Nils, Weitz, Jürgen, Steinke-Lange, Verena, Schmiegel, Wolff, Vangala, Deepak, Crosbie, Emma J., Pineda, Marta, Navarro, Matilde, Brunet, Joan, Moreira, Leticia, Sánchez, Ariadna, Serra-Burriel, Miquel, Mints, Miriam, Kariv, Revital, Rosner, Guy, Alejandra Piñero, Tamara, Pavicic, Walter Hernán, Kalfayan, Pablo, ten Broeke, Sanne W., Mecklin, Jukka-Pekka, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepistö, Anna, Peltomäki, Päivi, Hopper, John L., Win, Aung Ko, Buchanan, Daniel D., Lindor, Noralane M., Gallinger, Steven, Le Marchand, Loïc, Newcomb, Polly A., Figueiredo, Jane C., Thibodeau, Stephen N., Therkildsen, Christina, Hansen, Thomas V. O., Lindberg, Lars, Rødland, Einar Andreas, Neffa, Florencia, Esperon, Patricia, Tjandra, Douglas, Möslein, Gabriela, Seppälä, Toni T., Møller, Pål
Background. Lynch syndrome is the most common genetic predisposition for hereditary cancer. Carriers of pathogenic changes in mismatch repair (MMR) genes have an increased risk of developing colorectal (CRC), endometrial, ovarian, urinary tract, pros
Externí odkaz:
https://ul.qucosa.de/id/qucosa%3A85197
https://ul.qucosa.de/api/qucosa%3A85197/attachment/ATT-0/
https://ul.qucosa.de/api/qucosa%3A85197/attachment/ATT-0/
Autor:
Triuzzi, Emanuele, Mengoni, Riccardo, Bonanni, Domenico, Ottaviani, Daniele, Beccari, Andrea, Palermo, Gianluca
Molecular docking is an essential step in the drug discovery process involving the detection of three-dimensional poses of a ligand inside the active site of the protein. In this paper, we address the Molecular Docking search phase by formulating the
Externí odkaz:
http://arxiv.org/abs/2405.06657
Autor:
Hajisharifi, Arash, Halder, Rahul, Girfoglio, Michele, Beccari, Andrea, Bonanni, Domenico, Rozza, Gianluigi
The numerical treatment of fluid-particle systems is a very challenging problem because of the complex coupling phenomena occurring between the two phases. Although accurate mathematical modelling is available to address this kind of application, the
Externí odkaz:
http://arxiv.org/abs/2403.14283
Autor:
Balan, Aravind Puthirath, Kumar, Aditya, Reiser, Patrick, Vas, Joseph, Denneulin, Thibaud, Lee, Khoa Dang, Saunderson, Tom G, Tschudin, Märta, Pellet-Mary, Clement, Dutta, Debarghya, Schrader, Carolin, Scholz, Tanja, Geuchies, Jaco, Fu, Shuai, Wang, Hai, Bonanni, Alberta, Lotsch, Bettina V., Nowak, Ulrich, Jakob, Gerhard, Gayles, Jacob, Kovacs, Andras, Dunin-Borkowski, Rafal E., Maletinsky, Patrick, Kläui, Mathias
The exchange bias phenomenon, inherent in exchange-coupled ferromagnetic and antiferromagnetic systems, has intrigued researchers for decades. Van der Waals materials, with their layered structure, provide an optimal platform for probing such physica
Externí odkaz:
http://arxiv.org/abs/2403.05383
Autor:
Santos, Ana R.N., Sheldrake, Helen M., Ibrahim, Ali I.M., Danta, Chhanda C., Bonanni, D., Daga, M., Oliaro-Bosso, s., Boschi, D., Lolli, M.L., Pors, Klaus
Yes
Tetrahydroisoquinoline (THIQ) is a key structural component in many biologically active molecules including natural products and synthetic pharmaceuticals. Here, we report on the use of transition-metal mediated [2 + 2 + 2] cyclotrimerisatio
Tetrahydroisoquinoline (THIQ) is a key structural component in many biologically active molecules including natural products and synthetic pharmaceuticals. Here, we report on the use of transition-metal mediated [2 + 2 + 2] cyclotrimerisatio
Externí odkaz:
http://hdl.handle.net/10454/17252
Autor:
Pippione, A.C., Carnovale, I.M., Bonanni, D., Sini, Marcella, Goyal, P., Marini, E., Pors, Klaus, Adinolfi, S., Zonari, D., Festuccia, C., Wahlgren, W.Y., Friemann, R., Bagnati, R., Boschi, D., Oliaro-Bosso, S., Lolli, M.L.
Yes
The aldo-keto reductase 1C3 (AKR1C3) isoform plays a vital role in the biosynthesis of androgens and is considered an attractive target in prostate cancer (PCa). No AKR1C3-targeted agent has to date been approved for clinical use. Flufenamic
The aldo-keto reductase 1C3 (AKR1C3) isoform plays a vital role in the biosynthesis of androgens and is considered an attractive target in prostate cancer (PCa). No AKR1C3-targeted agent has to date been approved for clinical use. Flufenamic
Externí odkaz:
http://hdl.handle.net/10454/16082
Autor:
Onofrj M, Carrozzino D, D'Amico A, Di Giacomo R, Delli Pizzi S, Thomas A, Onofrj V, Taylor JP, Bonanni L
Publikováno v:
Neuropsychiatric Disease and Treatment, Vol Volume 13, Pp 1313-1330 (2017)
Marco Onofrj,1,2 Danilo Carrozzino,3,4 Aurelio D’Amico,1,2 Roberta Di Giacomo,1,2 Stefano Delli Pizzi,1 Astrid Thomas,1,2 Valeria Onofrj,5 John-Paul Taylor,6 Laura Bonanni1,2 1Department of Neuroscience Imaging and Clinical Sciences, University “
Externí odkaz:
https://doaj.org/article/dd821bb9c8664f9d8c24f0681a5fa2c7