IRIS

TERRINONI, ALESSANDRO

TERRINONI, ALESSANDRO  

Dipartimento di Medicina Sperimentale  

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Risultati 1 - 20 di 118 (tempo di esecuzione: 0.036 secondi).
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-2000 A glutamine insertion in the 1A alpha helical domain of the keratin 4 gene in a familial case of white sponge nevus Terrinoni, A; Candi, E; Oddi, S; Gobello, T; Camaione, Db; Mazzanti, C; Zambruno, G; Knight, R; Melino, G Articolo su rivista
1-dic-2005 A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome Cassidy, A; van Steensel, M; Steijlen, P; van Geel, M; van der Velden, J; Morley, S; Terrinoni, A; Melino, G; Candi, E; Mclean, W Articolo su rivista
1-gen-2000 A mutation in the V1 domain of K16 is responsible for unilateral palmoplantar verrucous nevus Terrinoni, A; Puddu, P; Didona, B; De Laurenzi, V; Candi, E; Smith, Fjd; Mclean, Whi; Melino, G Articolo su rivista
1-gen-2001 A novel mutation in the keratin 13 gene causing oral white sponge nevus Terrinoni, A; Rugg, El; Lane, Eb; Melino, G; Felix, Dh; Munro, Cs; Mclean, Whi Articolo su rivista
1-gen-2004 A novel recessive connexin 31 (GJB3) mutation in a case of erythrokeratodermia variabilis [2] Terrinoni, A; Leta, A; Pedicelli, C; Candi, E; Ranalli, M; Puddu, P; Paradisi, M; Angelo, C; Baggetta, G; Melino, G Articolo su rivista
1-gen-2014 Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis Terrinoni, A; Giardina, E; Pertusi, G; Cascella, R; Serra, V; Bornacina, C; Palombo, R; Tiberio, R; Gattoni, M; Novelli, G; Annicchiarico Petruzzelli, M; Melino, G; Colombo, E Articolo su rivista
1-gen-1998 Accumulation of transposable elements in the heterochromatin and on the Y chromosome of Drosophila simulans and Drosophila melanogaster Junakovic, N; Terrinoni, A; Di Franco, C; Vieira, C; Loevenbruck, C Articolo su rivista
1-gen-1999 Additional complexity in p73: induction by mitogens in lymphoid cells and identification of two new splicing variants  and  De Laurenzi, V; Catani, Mv; Terrinoni, A; Corazzari, M; Melino, G; Costanzo, A; Levrero, M; Knight, R Articolo su rivista
1-gen-2000 An SRY-negative XX male with Huriez syndrome Vernole, P; Terrinoni, A; Didona, B; De Laurenzi, V; Rossi, P; Melino, G; Grimaldi, P Articolo su rivista
9-mar-2022 Anti-Inflammatory and Active Biological Properties of the Plant-Derived Bioactive Compounds Luteolin and Luteolin 7-Glucoside Caporali, S; De Stefano, A; Calabrese, C; Giovannelli, A; Pieri, M; Savini, I; Tesauro, M; Bernardini, S; Minieri, M; Terrinoni, A Articolo su rivista
1-feb-2021 Anti-inflammatory and proliferative properties of luteolin-7-O-glucoside De Stefano, A; Caporali, S; Di Daniele, N; Rovella, V; Cardillo, C; Schinzari, F; Minieri, M; Pieri, M; Candi, E; Bernardini, S; Tesauro, M; Terrinoni, A Articolo su rivista
1-gen-2023 Assessment of the Stability of Midregional Proadrenomedullin in Different Biological Matrices Angeletti, S; Legramante, Jm; Lia, Ms; D’Amico, L; Fogolari, M; Cella, E; De Cesaris, M; De Angelis, F; Pieri, M; Terrinoni, A; Bernardini, S; Minieri, M Articolo su rivista
1-gen-2004 Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene Terron-Kwiatkowski, A; Terrinoni, A; Didona, B; Melino, G; Atherton, Dj; Irvine, Ad; Mclean, Whi Articolo su rivista
1-apr-2020 Birt–Hogg–Dubé syndrome, from non-invasive dermatologic assessment to gene testing, molecular and ultrastructural histologic analysis Diluvio, L; Caporali, S; Lozzi, F; Campione, E; Mazzilli, S; Lanna, C; Bianchi, L; Bernardini, S; Minieri, M; Mauriello, A; Ferlosio, A; Candi, E; Terrinoni, A Articolo su rivista
1-set-2007 Cerebral cavernomas in a family with multiple cutaneous and uterine leiomyomas associated with a new mutation in the fumarate hydratase gene J Invest Dermatol. 2007 Sep;127(9):2271-3. Campione, E; Terrinoni, A; Orlandi, A; Codispoti, A; Melino, G; Bianchi, L; Mazzotta, A; Garaci, F; Ludovici, A; Chimenti, S Articolo su rivista
1-giu-2024 Characterization and Clinical Assessment of a Peculiar Case of Hemolytic Anemia Castelgrande, F; Viola, G; Calabrese, C; Iozzo, M; Massoud, R; Pieri, M; Minieri, M; Adorno, G; Bernardini, S; Terrinoni, A Articolo su rivista
1-gen-2017 Characterization of TG2 and TG1–TG2 double knock-out mouse epidermis Pitolli, C; Pietroni, V; Marekov, L; Terrinoni, A; Yamanishi, K; Mazzanti, C; Melino, G; Candi, E Articolo su rivista
5-mag-2011 Common fragile sites in colon cancer cell lines: role of mismatch repair, RAD51 and poly(ADP-ribose) polymerase-1 Vernole, P; Muzi, A; Volpi, A; Terrinoni, A; Dorio, As; Tentori, L; Shah, G; Graziani, G Articolo su rivista
23-apr-2010 Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss Terrinoni, A; Codispoti, A; Serra, V; Bruno, E; Didona, B; Paradisi, M; Nisticò, S; Campione, E; Napolitano, B; Diluvio, L; Melino, G Articolo su rivista
16-apr-2010 Connexin 26 (GJB2) mutations, causing KID Syndrome, are associated with cell death due to calcium gating deregulation Terrinoni, A; Codispoti, A; Serra, V; Didona, B; Bruno, E; Nistico', Rg; Giustizieri, M; Alessandrini, M; Campione, E; Melino, G Articolo su rivista