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Sfoglia per ???browse.type.metadata.subjectIsicrui???  Biologia Molecolare e Genetica

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Mostrati risultati da 933 a 952 di 1.506
Data di pubblicazione Titolo Autore(i) Tipo File
27-feb-2014 Nectin-4 mutations causing ectodermal dysplasia with syndactyly perturb the Rac1 pathway and the kinetics of adherens junction formation Fortugno, P; Josselin, E; Tsiakas, K; Agolini, E; Cestra, G; Teson, M; Santer, R; Castiglia, D; Novelli, G; Dallapiccola, B; Kurth, I; Lopez, M; Zambruno, G; Brancati, F Articolo su rivista
1-gen-2017 Neonatal Diabetes: permanent neonatal diabetes and transient neonatal diabetes Barbetti, F; Mammì, C; Liu, M; Grasso, V; Arvan, P; Remedi, M; Nichols, C Contributo in libro
1-gen-2005 Neonatal screening, clinical features and genetic testing for galactosemia [3] Zaffanello, M; Zamboni, G; Schadewaldt, P; Borgiani, P; Novelli, G Articolo su rivista
1-gen-1998 Network analyses of Y-chromosomal types in Europe, Northern Africa, and Western Asia reveal specific patterns of geographic distribution Malaspina, P; Cruciani, F; Ciminelli, Bm; Terrenato, L; Santolamazza, P; Alonso, A; Banyko, J; Brdicka, R; Garcia, O; Gaudiano, C; Guanti, G; Kidd, K; Lavinha, J; Avila, M; Mandich, P; Moral, P; Qamar, R; Mehdi, S; Ragusa, A; Stefanescu, G; Caraghin, M; Tyler Smith, C; Scozzari, R; Novelletto, A Articolo su rivista
1-gen-2013 Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutations Lo Castro, A; Brancati, F; Digilio, M; Garaci, F; Bollero, P; Alfieri, P; Curatolo, P Articolo su rivista
27-dic-2011 Neuronal differentiation by TAp73 is mediated by microRNA-34a regulation of synaptic protein targets Agostini, M; Tucci, P; Killick, R; Candi, E; Sayan, B; Rivetti di Val Cervo, P; Nicotera, P; Mckeon, F; Knight, R; Mak, T; Melino, G Articolo su rivista
1-gen-2005 Neuroprotection by the caspase-1 inhibitor Ac-YVAD-(acyloxy)mk in experimental neuroAIDS is independent from IL-1β generation Corasaniti, Mt; Russo, R; Amantea, D; Gliozzi, M; Siviglia, E; Stringaro, Ar; Malorni, W; Melino, G; Bagetta, G Articolo su rivista
1-gen-2009 A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form Concolino, P; Mello, E; Minucci, A; Giardina, E; Zuppi, C; Toscano, V; Capoluongo, E Articolo su rivista
1-gen-2003 New data on the world distribution of paraoxonase (PON1 Gln 192 -> Arg) gene frequencies Scacchi, R; Corbo, R; Rickards, O; De Stefano, G Articolo su rivista
1-gen-2005 New hints on the pH-driven tautomeric equilibria of the topotecan anticancer drug in aqueous solutions from an integrated spectroscopic and quantum-mechanical approach Sanna, N; Chillemi, G; Grandi, A; Castelli, S; Desideri, A; Barone, V Articolo su rivista
1-gen-2016 A New Homozygous Frameshift Mutation in the HSD3B2 Gene in an Apparently Nonconsanguineous Italian Family Bizzarri, C; Massimi, A; Federici, L; Cualbu, A; Loche, S; Bellincampi, L; Bernardini, S; Cappa, M; Porzio, O Articolo su rivista
1-gen-2007 New insights in atherosclerosis research: LOX-1, leading actor of cardiovascular diseases [Nuovi approfondimenti nella ricerca su l'ateroslerosi: LOX-1, un primo attore nelle malattie cardiovascolari] Novelli, G; Mango, R; Vecchione, L; Mariotti, E; Borgiani, P; Mehta, J; Romeo, F Articolo su rivista
1-gen-2021 New insights into the evolution of human y chromosome palindromes through mutation and gene conversion Bonito, M; D'Atanasio, E; Ravasini, F; Cariati, S; Finocchio, A; Novelletto, A; Trombetta, B; Cruciani, F Articolo su rivista
1-gen-2006 New p63 targets in keratinocytes identified by a genome-wide approach Vigano, M; Lamartine, J; Testoni, B; Merico, D; Alotto, D; Castagnoli, C; Robert, A; Candi, E; Melino, G; Gidrol, X; Mantovani, R Articolo su rivista
1-gen-2010 New PRSS1 and common CFTR mutations in a child with acute recurrent pancreatitis, could be considered an "Hereditary" form of pancreatitis ? Corleto, V; Gambardella, S; Gullotta, F; D'Apice, M; Piciucchi, M; Galli, E; Lucidi, V; Novelli, G; Delle Fave, G Articolo su rivista
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
Mostrati risultati da 933 a 952 di 1.506
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