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Mostrati risultati da 221 a 240 di 1.506
Data di pubblicazione Titolo Autore(i) Tipo File
1-apr-2003 Caspase-dependent cleavage of c-Abl contributes to apoptosis Barila', D; Rufini, A; Condo', I; Ventura, N; Dorey, K; Superti Furga, G; Testi, R Articolo su rivista
1-gen-2019 CausalTAB: The PSI-MITAB 2.8 updated format for signalling data representation and dissemination Perfetto, L; Acencio, Ml; Bradley, G; Cesareni, G; Del Toro, N; Fazekas, D; Hermjakob, H; Korcsmaros, T; Kuiper, M; Laegreid, A; Lo Surdo, P; Lovering, Rc; Orchard, S; Porras, P; Thomas, Pd; Toure, V; Zobolas, J; Licata, L Articolo su rivista
1-gen-2001 Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models Botta, A; Amati, F; Novelli, G Articolo su rivista
23-lug-2009 CC chemokine ligand 2 down-modulation by selected Toll-like receptor agonist combinations contributes to T helper 1 polarization in human dendritic cells Del Cornò, M; Michienzi, A; Masotti, A; Da Sacco, L; Bottazzo, G; Belardelli, F; Gessani, S Articolo su rivista
1-gen-2011 CD4 intragenic SNPs associate with HIV-2 plasma viral load and CD4 count in a community-based study from Guinea-Bissau, West Africa Hennig, B; Velez Edwards, D; Schim van der Loeff, M; Bisseye, C; Edwards, T; Tacconelli, A; Novelli, G; Aaby, P; Kaye, S; Scott, W; Jaye, A; Whittle, H; Williams, S; Hill, A; Sirugo, G Articolo su rivista
1-lug-1996 cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene Pizzuti, A; Amati, F; Calabrese, G; Mari, A; Colosimo, A; Silani, V; Giardino, L; Ratti, A; Penso, D; Calzà, L; Palka, G; Scarlato, G; Novelli, G; Dallapiccola, B Articolo su rivista
1-gen-2019 Cell-free DNA analysis in healthy individuals by next-generation sequencing: a proof of concept and technical validation study Alborelli, I; Generali, D; Jermann, P; Cappelletti, Mr; Ferrero, G; Scaggiante, B; Bortul, M; Zanconati, F; Nicolet, S; Haegele, J; Bubendorf, L; Aceto, N; Scaltriti, M; Mucci, G; Quagliata, L; Novelli, G Articolo su rivista
1-gen-2016 Central Italy: History of ancient and current migrations Messina, F; Rolfo, Mf; Rickards, O Contributo in libro
1-gen-2008 The central proline rich region of POB1/REPS2 plays a regulatory role in epidermal growth factor receptor endocytosis by binding to 14-3-3 and SH3 domain-containing proteins Tomassi, L; Costantini, A; Corallino, S; Santonico, E; Carducci, M; Cesareni, G; Castagnoli, L Articolo su rivista
1-gen-2008 Cftr gene targeting in mouse embryonic stem cells mediated by Small Fragment Homologous Replacement (SFHR) Sangiuolo, Fc; Scaldaferri, M; Filareto, A; Spitalieri, P; Guerra, L; Favia, M; Caroppo, R; Mango, R; Bruscia, E; Gruenert, D; Casavola, V; DE FELICI, M; Novelli, G Articolo su rivista
1-gen-1992 Characterisation of a human glioblastoma cell line (LI) expressing hypothalamic and pituitary hormones Savarese, A; Annicchiarico Petruzzelli, M; Citro, G; Zupi, G; Spagnoli, Lg; Colantoni, A; Vernole, P; Stephanou, A; Knight, Ra; Guerrieri, P; Melino, G Articolo su rivista
1-gen-2016 Characterisation of genetic structure of the Mayan population in Guatemala by autosomal STR analysis Martinez Gonzalez, L; Alvarez Cubero, M; Saiz, M; Alvarez, J; MARTINEZ-LABARGA, Mc; Lorente, J Articolo su rivista
1-ago-2021 Characterization of a natural variant of human NDP52 and its functional consequences on mitophagy Di Rita, A; Angelini, D; Maiorino, T; Caputo, V; Cascella, R; Kumar, M; Tiberti, M; Lambrughi, M; Wesch, N; Löhr, F; Dötsch, V; Carinci, M; D'Acunzo, P; Chiurchiù, V; Papaleo, E; Rogov, V; Giardina, E; Battistini, L; Strappazzon, F Articolo su rivista
1-gen-2011 Characterization of a novel CYP2C9 gene mutation and structural bioinformatic protein analysis in a warfarin hypersensitive patient Ciccacci, C; Falconi, M; Paolillo, N; Oteri, F; Forte, V; Novelli, G; Desideri, A; Borgiani, P Articolo su rivista
1-gen-1983 Characterization of a rare allele of the phosphoglucomutase locus 1 (PGM81) in an Italian family by isoelectric focusing Rickards, O; Santolamazza, P; De Stefano, G Articolo su rivista
1-feb-2005 Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population Vallo, L; Bonifazi, E; Borgiani, P; Novelli, G; Botta, A Articolo su rivista
1-gen-1997 Characterization of a small family (CAIII) of microsatellite-containing sequences with X-Y homology Malaspina, P; Ciminelli, Bm; Viggiano, L; Iodice, C; Cruciani, F; Santolamazza, P; Sellitto, D; Scozzari, R; Terrenato, L; Rocchi, M; Novelletto, A Articolo su rivista
1-gen-2015 Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome Walz, K; Cohen, D; Neilsen, Pm; Foster, J; Brancati, F; Demir, K; Fisher, R; Moffat, M; Verbeek, Ne; Bjorgo, K; Lo Castro, A; Curatolo, P; Novelli, G; Abad, C; Lei, C; Zhang, L; Diaz-Horta, O; Young, Ji; Callen, Df; Tekin, M Articolo su rivista
1-gen-2024 Characterization of caffeine response regulatory variants in vascular endothelial cells Boye, C; A Kalita, C; S Findley, A; Alazizi, A; Wei, J; Wen, X; Pique-Regi, R; Luca, F Articolo su rivista
1-set-2021 Characterization of FMR1 Repeat Expansion and Intragenic Variants by Indirect Sequence Capture Grosso, V; Marcolungo, L; Maestri, S; Alfano, M; Lavezzari, D; Iadarola, B; Salviati, A; Mariotti, B; Botta, A; D'Apice, Mr; Novelli, G; Delledonne, M; Rossato, M Articolo su rivista
Mostrati risultati da 221 a 240 di 1.506
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