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Mostrati risultati da 143 a 162 di 1.511
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-2012 Association between OLR1 K167N SNP and Intima Media Thickness of the Common Carotid Artery in the General Population. Predazzi, I; Norata, G; Vecchione, L; Garlaschelli, K; Amati, F; Grigore, L; Cutuli, L; Pirillo, A; Tramontana, S; Romeo, F; Novelli, G; Catapano, Al Articolo su rivista
1-gen-2000 Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22 De Luca, A; Pasini, A; Amati, F; Botta, A; Spalletta, G; Alimenti, S; Caccamo, F; Conti, E; Trakalo, J; Macciardi, F; Macciardi, B; Novelli, G Intervento a convegno
1-set-1988 Association of cytogenetic abnormalities in a neuroblastoma and fragile sites expression Vernole, P; Concato, C; Pianca, C; Nicoletti, B; Melino, G Articolo su rivista
1-gen-1988 Association of cytogenetic abnormalities in a neuroblastoma and fragile sites expression Vernole, P; Concato, C; Pianca, C; Nicoletti, B; Melino, G Articolo su rivista
1-gen-2006 Association of genetic markers within the KIT and KITLG genes with human male infertility Galan, J; DE FELICI, M; Buch, B; Rivero, M; Segura, A; Royo, J; Cruz, N; Real, L; Ruiz, A Articolo su rivista
1-set-2007 Association of Trp53 polymorphic variants at codon 72 with nonsyndromic mental retardation Saccucci, P; Galasso, C; Rizzo, R; Gagliano, A; Refice, F; Lalli, C; Verrotti, A; Gloria, F; Curatolo, P Articolo su rivista
1-gen-2003 Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia De Luca, A; Conti, E; Grifone, N; Amati, F; Spalletta, G; Caltagirone, C; Bonaviri, G; Pasini, A; Gennarelli, M; Stefano, B; Berti, L; Mittler, G; Meisterernst, M; Dallapiccola, B; Novelli, G Articolo su rivista
1-gen-2001 Association study of a promoter polymorphism of UFD1L gene with schizophrenia De Luca, A; Pasini, A; Amati, F; Botta, A; Spalletta, G; Alimenti, S; Caccamo, F; Conti, E; Trakalo, J; Macciardi, F; DALLA PICCOLA, B; Novelli, G Articolo su rivista
1-gen-2008 ATG16L1 Ala197Thr Is Not Associated With Susceptibility to Crohn's Disease or With Phenotype in an Italian Population Perricone, C; Borgiani, P; Romano, S; Ciccacci, C; Fusco, G; Novelli, G; Biancone, L; Calabrese, E; Pallone, F Articolo su rivista
1-nov-2010 ATM kinase activity modulates cFLIP protein levels: potential interplay between DNA damage signalling and TRAIL-induced apoptosis Stagni, V; Mingardi, M; Santini, S; Giaccari, D; Barila', D Articolo su rivista
15-gen-2008 ATM Kinase activity modulates Fas sensitivity through the regulation of FLIP in lymphoid cells Stagni, V; di Bari, M; Cursi, S; Condo', I; Cencioni, M; Testi, R; Lerenthal, Y; Cundari, E; Barila', D Articolo su rivista
27-feb-2014 ATM kinase activity modulates ITCH E3-ubiquitin ligase activity Santini, S; Stagni, V; Giambruno, R; Fianco, G; Di Benedetto, A; Mottolese, M; Pellegrini, M; Barila', D Articolo su rivista
4-giu-2019 Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations. Strafella, C; Caputo, V; Minozzi, G; Milano, F; Arcangeli, M; Sobhy, N; Abdelmaksood, R; Hashad, D; Vakirlis, E; Novelli, G; Cascella, R; Giardina, E Articolo su rivista
1-gen-2012 ATP regulation of the ligand-binding properties in temperate and cold-adapted haemoglobins. X-ray structure and ligand-binding kinetics in the sub-Antarctic fish Eleginops maclovinus Coppola, D; Abbruzzetti, S; Nicoletti, F; Merlino, A; Gambacurta, A; Giordano, D; Howes, B; De Sanctis, G; Vitagliano, L; Bruno, S; Di Prisco, G; Mazzarella, L; Smulevich, G; Coletta, M; Viappiani, C; Vergara, A; Verde, C Articolo su rivista
1-dic-1999 Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome Amati, F; Conti, E; Novelli, A; Bengala, M; Diglio, M; Marino, B; Giannotti, A; Gabrielli, O; Novelli, G; Dallapiccola, B 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-mar-2001 Autism: evidence of association with adenosine deaminase genetic polymorphism Bottini, N; De Luca, D; Saccucci, P; Fiumara, A; Elia, M; Porfirio, M; Lucarelli, P; Curatolo, P Articolo su rivista
7-nov-2022 Autoantibodies against type I IFNs in patients with critical influenza pneumonia Zhang, Q; Pizzorno, A; Miorin, L; Bastard, P; Gervais, A; Le Voyer, T; Bizien, L; Manry, J; Rosain, J; Philippot, Q; Goavec, K; Padey, B; Cupic, A; Laurent, E; Saker, K; Vanker, M; Särekannu, K; García-Salum, T; Ferres, M; Le Corre, N; Sánchez-Céspedes, J; Balsera-Manzanero, M; Carratala, J; Retamar-Gentil, P; Abelenda-Alonso, G; Valiente, A; Tiberghien, P; Zins, M; Debette, S; Meyts, I; Haerynck, F; Castagnoli, R; Notarangelo, Ld; Gonzalez-Granado, Li; Dominguez-Pinilla, N; Andreakos, E; Triantafyllia, V; Rodríguez-Gallego, C; Solé-Violán, J; Ruiz-Hernandez, Jj; Rodríguez de Castro, F; Ferreres, J; Briones, M; Wauters, J; Vanderbeke, L; Feys, S; Kuo, C; Lei, W; Ku, C; Tal, G; Etzioni, A; Hanna, S; Fournet, T; Casalegno, J; Queromes, G; Argaud, L; Javouhey, E; Rosa-Calatrava, M; Cordero, E; Aydillo, T; Medina, Ra; Kisand, K; Puel, A; Jouanguy, E; Abel, L; Cobat, A; Trouillet-Assant, S; García-Sastre, A; Casanova, J; Novelli, G Articolo su rivista
20-ago-2010 Autoimmune-associated PTPN22 R620W variation reduces phosphorylation of lymphoid phosphatase on an inhibitory tyrosine residue Fiorillo, E; Orrú, V; Stanford, S; Liu, Y; Salek, M; Rapini, N; Schenone, A; Saccucci, P; Delogu, L; Angelini, F; MANCA BITTI, Ml; Schmedt, C; Chan, A; Acuto, O; Bottini, N Articolo su rivista
1-gen-1992 Autosomal dominant pure cerebellar ataxia. Neurological and genetic study. Frontali, M; Spadaro, M; Giunti, P; Bianco, F; Iodice, C; Persichetti, F; Colazza, G; Lulli, P; Terrenato, L; Morocutti, C Articolo su rivista
Mostrati risultati da 143 a 162 di 1.511
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