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Nano-strategies targeting the integrin αvβ3 network for cancer therapy
2021-01-01 Cheng, T; Chang, W; Chu, H; De Luca, R; Pedersen, J; Incerpi, S; Li, Z; Shih, Y; Lin, H; Wang, K; Whang-Peng, J
Nectin-4 mutations causing ectodermal dysplasia with syndactyly perturb the Rac1 pathway and the kinetics of adherens junction formation
2014-02-27 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
Neonatal Diabetes: permanent neonatal diabetes and transient neonatal diabetes
2017-01-01 Barbetti, F; Mammì, C; Liu, M; Grasso, V; Arvan, P; Remedi, M; Nichols, C
Neonatal screening, clinical features and genetic testing for galactosemia [3]
2005-01-01 Zaffanello, M; Zamboni, G; Schadewaldt, P; Borgiani, P; Novelli, G
Network analyses of Y-chromosomal types in Europe, Northern Africa, and Western Asia reveal specific patterns of geographic distribution
1998-01-01 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
Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutations
2013-01-01 Lo Castro, A; Brancati, F; Digilio, M; Garaci, F; Bollero, P; Alfieri, P; Curatolo, P
Neuronal differentiation by TAp73 is mediated by microRNA-34a regulation of synaptic protein targets
2011-12-27 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
Neuroprotection by the caspase-1 inhibitor Ac-YVAD-(acyloxy)mk in experimental neuroAIDS is independent from IL-1β generation
2005-01-01 Corasaniti, Mt; Russo, R; Amantea, D; Gliozzi, M; Siviglia, E; Stringaro, Ar; Malorni, W; Melino, G; Bagetta, G
A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form
2009-01-01 Concolino, P; Mello, E; Minucci, A; Giardina, E; Zuppi, C; Toscano, V; Capoluongo, E
New data on the world distribution of paraoxonase (PON1 Gln 192 -> Arg) gene frequencies
2003-01-01 Scacchi, R; Corbo, R; Rickards, O; De Stefano, G
New hints on the pH-driven tautomeric equilibria of the topotecan anticancer drug in aqueous solutions from an integrated spectroscopic and quantum-mechanical approach
2005-01-01 Sanna, N; Chillemi, G; Grandi, A; Castelli, S; Desideri, A; Barone, V
A New Homozygous Frameshift Mutation in the HSD3B2 Gene in an Apparently Nonconsanguineous Italian Family
2016-01-01 Bizzarri, C; Massimi, A; Federici, L; Cualbu, A; Loche, S; Bellincampi, L; Bernardini, S; Cappa, M; Porzio, O
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]
2007-01-01 Novelli, G; Mango, R; Vecchione, L; Mariotti, E; Borgiani, P; Mehta, J; Romeo, F
New insights into the evolution of human y chromosome palindromes through mutation and gene conversion
2021-01-01 Bonito, M; D'Atanasio, E; Ravasini, F; Cariati, S; Finocchio, A; Novelletto, A; Trombetta, B; Cruciani, F
New p63 targets in keratinocytes identified by a genome-wide approach
2006-01-01 Vigano, M; Lamartine, J; Testoni, B; Merico, D; Alotto, D; Castagnoli, C; Robert, A; Candi, E; Melino, G; Gidrol, X; Mantovani, R
New PRSS1 and common CFTR mutations in a child with acute recurrent pancreatitis, could be considered an "Hereditary" form of pancreatitis ?
2010-01-01 Corleto, V; Gambardella, S; Gullotta, F; D'Apice, M; Piciucchi, M; Galli, E; Lucidi, V; Novelli, G; Delle Fave, G
Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia
2009-01-15 Veneziano, L; Guida, S; Mantuano, E; Bernard, P; Tarantino, P; Boccone, L; Hisama, F; Carrera, P; Iodice, C; Frontali, M
Next Generation Sequencing and ALS: known genes, different phenotyphes.
2017-01-01 Campopiano, R; Ryskalin, L; Giardina, E; Zampatti, S; Busceti, C; Biagioni, F; Ferese, R; Storto, M; Gambardella, S; Fornai, F
NF-kappaB inhibits T-cell activation-induced, p73-dependent cell death by induction of MDM2
2010-10-19 Busuttil, V; Droin, N; Mccormick, L; Bernassola, F; Candi, E; Melino, G; Green, D
Ngs analysis for molecular diagnosis of Retinitis Pigmentosa (RP): Detection of a novel variant in PRPH2 gene
2019-10-01 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
Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
---|---|---|---|---|
1-gen-2021 | Nano-strategies targeting the integrin αvβ3 network for cancer therapy | Cheng, T; Chang, W; Chu, H; De Luca, R; Pedersen, J; Incerpi, S; Li, Z; Shih, Y; Lin, H; Wang, K; Whang-Peng, J | Articolo su rivista | |
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 |
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