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Mostrati risultati da 959 a 978 di 1.519
Data di pubblicazione Titolo Autore(i) Tipo File
15-gen-2009 Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia Veneziano, L; Guida, S; Mantuano, E; Bernard, P; Tarantino, P; Boccone, L; Hisama, F; Carrera, P; Iodice, C; Frontali, M Articolo su rivista
1-gen-2017 Next Generation Sequencing and ALS: known genes, different phenotyphes. Campopiano, R; Ryskalin, L; Giardina, E; Zampatti, S; Busceti, C; Biagioni, F; Ferese, R; Storto, M; Gambardella, S; Fornai, F Articolo su rivista
19-ott-2010 NF-kappaB inhibits T-cell activation-induced, p73-dependent cell death by induction of MDM2 Busuttil, V; Droin, N; Mccormick, L; Bernassola, F; Candi, E; Melino, G; Green, D Articolo su rivista
1-ott-2019 Ngs analysis for molecular diagnosis of Retinitis Pigmentosa (RP): Detection of a novel variant in PRPH2 gene Strafella, C; Caputo, V; Pagliaroli, G; Iozzo, N; Campoli, G; Carboni, S; Peconi, C; Galota, Rm; Zampatti, S; Minozzi, G; Novelli, G; Giardina, E; Cascella, R Articolo su rivista
1-gen-2006 NMR structure of the p63 SAM domain and dynamical properties of G534V and T537P pathological mutants, identified in the AEC syndrome Cicero, Do; Falconi, V; Candi, E; Mele, S; Cadot, B; DI VENERE, A; Rufini, S; Melino, G; Desideri, A Intervento a convegno
1-gen-2020 No evidence for allelic association between Covid-19 and ACE2 genetic variants by direct exome sequencing in 99 SARS-CoV-2 positive patients Novelli, A; Biancolella, M; Borgiani, P; Cocciadiferro, D; Colona, Vl; D’Apice, Mr; Rogliani, P; Zaffina, S; Leonardis, F; Campana, A; Raponi, M; Andreoni, M; Grelli, S; Novelli, G Altro
1-gen-2006 No evidence of association between BDNF gene variants and age-at-onset of Huntington's disease Di Maria, E; Marasco, A; Tartari, M; Ciotti, P; Abbruzzese, G; Novelli, G; Bellone, E; Cattaneo, E; Mandich, P Articolo su rivista
1-gen-2022 No Time to Die: How Kidney Cancer Evades Cell Death Ganini, C; Montanaro, M; Scimeca, M; Palmieri, G; Anemona, L; Concetti, L; Melino, G; Bove, P; Amelio, I; Candi, E; Mauriello, A Articolo su rivista
1-gen-2006 Non disjunction rates of mouse chromosomes involved in heterozygous Rb rearrangements measured by chromosome painting of spermatocytes. II. The effects of trivalent combinations and genetic background Scascitelli, M; Gustavino, B; Pacchierotti, F; Spirito, F; Rizzoni, M Articolo su rivista
1-gen-2004 Nondisjunction rates of mouse specific chromosomes involved in heterozygous Rb rearrangements measured by chromosome painting of spermatocytes II. I. The effects of the number of trivalents Scascitelli, M; Gustavino, B; Pacchierotti, F; Spirito, F; Rizzoni, M Articolo su rivista
1-gen-2004 Nonsense-mediated and nonstop decay of ribosomal protein S19 mRNA in Diamond-Blackfan anemia Chatr Aryamontri, A; Angelini, M; Garelli, E; Tchernia, G; Ramenghi, U; Dianzani, I; Loreni, F Articolo su rivista
1-gen-1991 Normal coding sequence of insulin gene in Pima Indians and Nauruans, two groups with highest prevalence of type II diabetes Raben, N; Barbetti, F; Cama, A; Lesniak, Ma; Lillioja, S; Zimmet, P; Serjeantson, Sw; Taylor, Si; Roth, J Articolo su rivista
30-apr-2010 Normal myogenesis and increased apoptosis in myotonic dystrophy type 1 muscle cells Loro, E; Rinaldi, F; Malena, A; Masiero, E; Novelli, G; Angelini, C; Romeo, V; Sandri, M; Botta, A; Vergani, L Articolo su rivista
1-gen-2007 Novel and recurrent ALDH3A2 mutations in Italian patients with Sjogren-Larsson syndrome Didona, B; Codispoti, A; Bertini, E; Rizzo, Wb; Carney, G; Zambruno, G; Dionisi Vici, C; Paradisi, M; Pedicelli, C; Melino, G; Terrinoni, A Articolo su rivista
1-gen-2001 Novel and recurrent mutations in the genes encoding keratins k6a, k16 and k17 in 13 cases of pachyonychia congenita Terrinoni, A; Smith, Fjd; Didona, B; Canzona, F; Paradisi, M; Huber, M; Hohl, D; David, A; Verloes, A; Leigh, Im; Munro, Cs; Melino, G; Mclean, Whi Articolo su rivista
1-gen-2014 A novel approach to represent and compare RNA secondary structures Mattei, E; Ausiello, G; Ferrè, F; HELMER CITTERICH, M Articolo su rivista
1-mag-2010 Novel CLCN1 mutation in carbamazepine-responsive myotonia congenita Lyons, M; Duron, R; Molinero, I; Sangiuolo, Fc; Holden, K Articolo su rivista
9-nov-2011 Novel HBsAg markers tightly correlate with occult HBV infection and strongly affect HBsAg detection Svicher, V; Cento, V; Bernassola, M; Neumann Fraune, M; Hemert, F; Chen, M; Salpini, R; Liu, C; Longo, R; Visca, M; Romano, S; Micheli, V; Bertoli, A; Gori, C; CECCHERINI SILBERSTEIN, F; Sarrecchia, C; Andreoni, M; Angelico, M; Ursitti, A; Spanò, A; Zhang, J; Verheyen, J; Cappiello, G; Perno, Cf Articolo su rivista
31-ago-2016 A novel method for the identification of conserved structural patterns in RNA: From small scale to high-throughput applications Pietrosanto, M; Mattei, E; HELMER CITTERICH, M; Ferrè, F Articolo su rivista
1-gen-2001 Novel mutations of the transglutaminase 1 gene in lamellar ichthyosis Yang, J; Ahn, K; Cho, M; Yoneda, K; Lee, C; Lee, J; Lee, E; Candi, E; Melino, G; Ahvazi, B; Steinert, P Articolo su rivista
Mostrati risultati da 959 a 978 di 1.519
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