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1.1 Articolo su rivista: [23921] Home page tipologia

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Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 9.181 a 9.200 di 23.921
Titolo Data di pubblicazione Autore(i) File
Le disfunzioni dell’organizzazione del lavoro: mobbing e dintorni 1-gen-2018 Lazzari, C.
It's always a women's problem! Micro-entrepreneurs, work-family balance and economic crisis 1-gen-2018 Cesaroni, Francesca Maria; Pediconi, Maria Gabriella; Sentuti, Annalisa
Gene expression analysis in myotonic dystrophy: Indications for a common molecular pathogenic pathway in DM1 and DM2 1-gen-2007 Botta, A; Vallo, L; Rinaldi, F; Bonifazi, E; Amati, F; Biancolella, M; Gambardella, S; Mancinelli, E; Angelini, C; Meola, G; Novelli, G
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 1-gen-2015 Cascella, R; Strafella, C; Ragazzo, M; Zampatti, S; Borgiani, P; Gambardella, S; Pirazzoli, A; Novelli, G; Giardina, E
Methamphetamine increases Prion Protein and induces dopamine-dependent expression of protease resistant PrPsc 1-gen-2017 Ferrucci, M; Ryskalin, L; Biagioni, F; Gambardella, S; Busceti, Cl; Falleni, A; Lazzeri, G; Fornai, F
Gene expression profiling of fibroblasts from a human progeroid disease (Mandibuloacral dysplasia, MAD #248370) through cDNA microarrays 1-gen-2004 Amati, F; Biancolella, M; D'Apice, Mr; Gambardella, S; Mango, R; Sbraccia, P; D'Adamo, M; Margiotti, K; Nardone, A; Lewis, M; Novelli, G
Gene symbol: ED1. Disease: Ectodermal dysplasia 1-gen-2008 Gambardella, S
Neurons other than motor neurons in motor neuron disease 1-gen-2017 Ruffoli, R; Biagioni, F; Busceti, Cl; Gaglione, A; Ryskalin, L; Gambardella, S; Frati, A; Fornai, F
Gene symbol: ED1. Disease: Ectodermal dysplasia 1-gen-2008 Gambardella, S
The Autophagoproteasome a Novel Cell Clearing Organelle in Baseline and Stimulated Conditions 1-gen-2016 Lenzi, P; Lazzeri, G; Biagioni, F; Busceti, Cl; Gambardella, S; Salvetti, A; Fornai, F
Design, Construction and Validation of Targeted BAC Array-Based CGH Test for Detecting the Most Commons Chromosomal Abnormalities 1-gen-2010 Gambardella, S; Ciabattoni, E; Motta, F; Stoico, G; Gullotta, F; Biancolella, M; Nardone, Am; Novelli, A; Brunetti, E; Bernardini, L; Novelli, G
Toward the pharmacogenomics of cystic fibrosis - an update 1-gen-2004 Sangiuolo, F; D'Apice, Mr; Gambardella, S; Di Daniele, N; Novelli, G
Gene expression profile study in CFTR mutated bronchial cell lines 1-gen-2006 Gambardella, S; Biancolella, M; D'Apice, Mr; Amati, F; Sangiuolo, F; Farcomeni, A; Chillemi, G; Bueno, S; Desideri, A; Novelli, G
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing 1-gen-2017 Cascella, R; Strafella, C; Longo, G; Manzo, L; Ragazzo, M; De Felici, C; Gambardella, S; Marsella, L T; Novelli, G; Borgiani, P; Sangiuolo, F; Cusumano, A; Ricci, F; Giardina, E
Segregation analysis in cystic fibrosis at-risk family demonstrates that the M348K CFTR mutation is a rare innocuous polymorphism 1-gen-2004 D'Apice, Mr; Gambardella, S; Russo, S; Lucidi, V; Nardone, Am; Pietropolli, A; Novelli, G
The Monoamine Brainstem Reticular Formation as a Paradigm for Re-Defining Various Phenotypes of Parkinson's Disease Owing Genetic and Anatomical Specificity 1-gen-2017 Gambardella, S; Ferese, R; Biagioni, F; Busceti, Cl; Campopiano, R; Griguoli, Amp; Limanaqi, F; Novelli, G; Storto, M; Fornai, F
Bone marrow and umbilical cord blood human mesenchymal stem cells: state of the art 1-gen-2010 Malgieri, A; Kantzari, E; Patrizi, Mp; Gambardella, S
A fluorescence-based sequence-specific primer PCR for the screening of HLA-B*57:01 1-gen-2010 Giardina, E; Stocchi, L; Cuzzola, Vf; Zampatti, S; Gambardella, S; Patrizi, Mp; Bramanti, P; Pirazzoli, A; Novelli, G
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS) 1-gen-2016 Ferese, R; Zampatti, S; Griguoli, Amp; Fornai, F; Giardina, E; Barrano, G; Albano, V; Campopiano, R; Scala, S; Novelli, G; Gambardella, S
New PRSS1 and common CFTR mutations in a child with acute recurrent pancreatitis, could be considered an "Hereditary" form of pancreatitis? 1-gen-2010 Corleto, Vd; Gambardella, S; Gullotta, F; D'Apice, Mr; Piciucchi, M; Galli, E; Lucidi, V; Novelli, G; Delle Fave, G
Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 9.181 a 9.200 di 23.921
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Tipologia
  • 1 Contributo su rivista23919
  • 4 Contributo Atto di Convegno (ex...2
  • 2 Contributo in Volume(ex Articol...1
Autore
  • VELTRI, MICHELE834
  • MAGNANI, MAURO671
  • MARTELLI, FILIPPO393
  • VETRANO, FLAVIO384
  • VICERE', ANDREA361
  • STOCCHI, VILBERTO359
  • GUIDI, GIANLUCA MARIA347
  • ROCCHI, MARCO BRUNO LUIGI328
  • PIERGIOVANNI, FRANCESCO309
  • GHEZZI, PIETRO295
Data di pubblicazione
  • In corso di stampa46
  • 2020 - 20265788
  • 2010 - 20198106
  • 2000 - 20095471
  • 1990 - 19992897
  • 1980 - 19891294
  • 1970 - 1979283
  • 1962 - 196936
Editore
  • Verona : Euroconference48
  • Societa Editrice il Mulino Spa:St...34
  • Elsevier BV:PO Box 211, 1000 AE A...29
  • Edizioni Quattroventi di Anna Ver...23
  • Editrice Scuola Spa:via L Cadorna...20
  • -Milano : Franco Angeli -Genova...15
  • Katlenburg-Lindau : European Geop...15
  • Franco Angeli Riviste SRL:viale M...14
  • G. Giappichelli Editore, Torino13
  • Il Mulino, Bologna13
Rivista
  • JOURNAL OF HIGH ENERGY PHYSICS255
  • PHYSICAL REVIEW LETTERS213
  • STUDI URBINATI DI SCIENZE GIURIDI...154
  • PHYSICAL REVIEW D145
  • PHYSICS LETTERS. SECTION B144
  • STUDI URBINATI B, SCIENZE UMANE E...136
  • CLASSICAL AND QUANTUM GRAVITY134
  • PICCOLA IMPRESA113
  • SOCIOLOGIA DELLA COMUNICAZIONE108
  • PLOS ONE92
Serie
  • WORKING PAPERS OLYMPUS1
Keyword
  • Humans178
  • Animals127
  • COVID-19104
  • Italy76
  • Male73
  • Gravitational Waves59
  • Female57
  • LIGO53
  • Mice52
  • inflammation49
Lingua
  • eng11826
  • ita6691
  • fre220
  • spa151
  • ger104
  • lat40
  • por30
  • rus28
  • grc11
  • ara6
Accesso al fulltext
  • no fulltext20990
  • open1970
  • restricted576
  • partially open337
  • reserved40
  • embargoed7
  • mixed1