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Mostrati risultati da 967 a 986 di 1.517
Data di pubblicazione Titolo Autore(i) Tipo File
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
1-gen-1999 Novel RNA-binding motif: The KH module Adinolfi, S; Bagni, C; Morelli, Mac; Fraternali, F; Musco, G; Pastore, A Articolo su rivista
1-ott-2010 A novel syndrome of mandibular hypoplasia, deafness, and progeroid features associated with lipodystrophy, undescended testes, and male hypogonadism Shastry, S; Simha, V; Godbole, K; Sbraccia, P; Melancon, S; Yajnik, C; Novelli, G; Kroiss, M; Garg, A Articolo su rivista
1-apr-2009 Now you can! Reality & Future Applications of array CGH in prenatal diagnosis Postorivo, D; Nardone, A; Biancolella, M; Mesoraca, A; Novelli, G Articolo su rivista
1-gen-2021 NUAK2 and RCan2 participate in the p53 mutant pro-tumorigenic network Mammarella, E; Zampieri, C; Panatta, E; Melino, G; Amelio, I Articolo su rivista
15-ott-2000 Nuclear tyrosine phosphorylation: the beginning of a map Cans, C; Mangano, R; Barila', D; Neubauer, G; Superti_furga, G Articolo su rivista
1-gen-1989 Nucleolin from Xenopus laevis: cDNA cloning and expression during development Caizergues Ferrer, M; Mariottini, P; Curie, C; Lapeyre, B; Gas, N; Amalric, F; Amaldi, F Articolo su rivista
22-mag-2013 Nucleos: a web server for the identification of nucleotide-binding sites in protein structures Parca, L; Ferré, F; Ausiello, G; HELMER CITTERICH, M Articolo su rivista
5-set-1983 Nucleotide sequence and intron structure of the apocytochrome b gene of Neurospora crassa mitochondria HELMER CITTERICH, M; Morelli, G; Macino, G Articolo su rivista
1-gen-1985 Nucleotide sequence of the L1 ribosomal protein gene of Xenopus laevis: remarkable sequence homology among introns Loreni, F; Ruberti, I; Bozzoni, I; Pierandrei Amaldi, P; Amaldi, F Articolo su rivista
1-gen-2005 nuevos polimorfismos genéticos (PG) Rickards, O; MARTINEZ-LABARGA, Mc; Biondi, G Contributo in libro
Mostrati risultati da 967 a 986 di 1.517
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