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Mostrati risultati da 1.423 a 1.442 di 1.506
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-1997 Translational control of terminal oligopyrimidine mRNAs requires a specific regulator Loreni, F; Amaldi, F Articolo su rivista
1-gen-1992 Translational regulation of ribosomal protein synthesis in Xenopus cultured cells: mRNA relocation between polysomes and RNP during nutritional shifts Loreni, F; Amaldi, F Articolo su rivista
1-gen-2004 Translational regulation of terminal oligopyrimidine mRNAs induced by serum and amino acids involves distinct signaling events Caldarola, S; Amaldi, F; Proud, C; Loreni, F Articolo su rivista
1-gen-1990 Translational regulation of the expression of ribosomal protein genes in Xenopus laevis Amaldi, F; Pierandrei Amaldi, P Articolo su rivista
1-gen-2005 Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests Botta, A; Tacconelli, A; Bagni, I; Giardina, E; Bonifazi, E; Pietropolli, A; Clementi, M; Novelli, G Articolo su rivista
1-dic-2014 TRAP1-dependent regulation of p70S6K is involved in the attenuation of protein synthesis and cell migration: Relevance in human colorectal tumors Matassa, D; Agliarulo, I; Amoroso, M; Maddalena, F; Sepe, L; Ferrari, M; Sagar, V; D'Amico, S; Loreni, F; Paolella, G; Landriscina, M; Esposito, F Articolo su rivista
1-mar-2014 Tug of war between survival and death: exploring ATM function in cancer. Stagni, V; Oropallo, V; Fianco, G; Antonelli, M; Cinà, I; Barila', D Articolo su rivista
1-gen-2011 Tumor necrosis factor promoter polymorphism TNF*-857 is a risk allele for psoriatic arthritis independent of the PSORS1 locus. Giardina, E; Hüffmeier, U; Ravindran, J; Behrens, F; Lepre, T; Mchugh, N; Korendowych, E; Burkhardt, H; Novelli, G; Reis, A Articolo su rivista
1-gen-2020 Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy Passarelli, C; Selvatici, R; Carrieri, A; Di Raimo, Fr; Falzarano, Ms; Fortunato, F; Rossi, R; Straub, V; Bushby, K; Reza, M; Zharaieva, I; D'Amico, A; Bertini, E; Merlini, L; Sabatelli, P; Borgiani, P; Novelli, G; Messina, S; Pane, M; Mercuri, E; Claustres, M; Tuffery-Giraud, S; Aartsma-Rus, A; Spitali, P; T'Hoen, Pac; Lochmüller, H; Strandberg, K; Al-Khalili, C; Kotelnikova, E; Lebowitz, M; Schwartz, E; Muntoni, F; Scapoli, C; Ferlini, A Articolo su rivista
14-ago-2009 Tumor suppressor density-enhanced phosphatase-1 (DEP-1) inhibits the RAS pathway by direct dephosphorylation of ERK1/2 kinases Sacco, F; Tinti, M; Palma, A; Ferrari, E; Nardozza, A; Hooft van Huijsduijnen, R; Takahashi, T; Castagnoli, L; Cesareni, G Articolo su rivista
25-dic-1993 Two different snoRNAs are encoded in introns of amphibian and human L1 ribosomal protein genes Prislei, S; Michienzi, A; Presutti, C; Fragapane, P; Bozzoni, I Articolo su rivista
5-apr-2022 Two Different Therapeutic Approaches for SARS-CoV-2 in hiPSCs-Derived Lung Organoids Spitalieri, P; Centofanti, F; Murdocca, M; Scioli, Mg; Latini, A; Di Cesare, S; Citro, G; Rossi, A; Orlandi, A; Miersch, S; Sidhu, Ss; Pandolfi, Pp; Botta, A; Sangiuolo, F; Novelli, G Articolo su rivista
1-gen-1998 Two ethnic-specific polymorphisms in the human beta pseudogene of hemoglobin Pompei, F; Ciminelli, Bm; Modiano, G Articolo su rivista
1-gen-1998 Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria) Chambliss, K; Hinson, D; Trettel, F; Malaspina, P; Novelletto, A; Jakobs, C; Gibson, K Articolo su rivista
1-gen-1995 Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): Exclusion from the critical region on 8p Amati, F; Mari, A; Mingarelli, R; Gennarelli, M; Digilio, Mc; Giannotti, A; Marino, B; Novelli, G; Dallapiccola, B Articolo su rivista
1-gen-2021 Two reck splice variants (Long and short) are differentially expressed in patients with stable and unstable coronary artery disease: A pilot study Vancheri, C; Morini, E; Prandi, Fr; Alkhoury, E; Celotto, R; Romeo, F; Novelli, G; Amati, F Articolo su rivista
1-gen-1990 Two unrelated patients with familial hyperproinsulinemia due to a mutation substituting histidine for arginine at position 65 in the proinsulin molecule: Identification of the mutation by direct sequencing of genomic deoxyribonucleic acid amplified by polymerase chain reaction Barbetti, F; Raben, N; Kadowaki, T; Cama, A; Accili, D; Gabbay, Kh; Merenich, Ja; Taylor, Si; Roth, J Articolo su rivista
1-apr-2002 Two-loci ADA haplotypes in autistic disorder Lucarelli, P; Saccucci, P; Bottini, N; De Luca, D; Fiumara, A; Elia, M; Bottini, N; Porfirio, M; Curatolo, P Articolo su rivista
1-ago-2004 Type 2 diabetes and the genetics of signal transduction: a study of interaction between adenosine deaminase and acid phosphatase locus 1 polymorphisms Bottini, N; Gloria Bottini, F; Borgiani, P; Antonacci, E; Lucarelli, P; Bottini, E Articolo su rivista
1-gen-2022 Type I IFNs promote cancer cell stemness by triggering the epigenetic regulator KDM1B Musella, M; Guarracino, A; Manduca, N; Galassi, C; Ruggiero, E; Potenza, A; Maccafeo, E; Manic, G; Mattiello, L; Soliman Abdel Rehim, S; Signore, M; Pietrosanto, M; Helmer-Citterich, M; Pallocca, M; Fanciulli, M; Bruno, T; De Nicola, F; Corleone, G; Di Benedetto, A; Ercolani, C; Pescarmona, E; Pizzuti, L; Guidi, F; Sperati, F; Vitale, S; Macchia, D; Spada, M; Schiavoni, G; Mattei, F; De Ninno, A; Businaro, L; Lucarini, V; Bracci, L; Aricò, E; Ziccheddu, G; Facchiano, F; Rossi, S; Sanchez, M; Boe, A; Biffoni, M; De Maria, R; Vitale, I; Sistigu, A Articolo su rivista
Mostrati risultati da 1.423 a 1.442 di 1.506
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