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Population genetics and structure of the Blacks from Rio Cayapa, North-Western Ecuador.
1995-01-01 DE STEFANO, G; MARTINEZ-LABARGA, Mc; Rickards, O
The population history of the Croatian linguistic minority of Molise (southern Italy): a maternal view
2005-01-01 Babalini, C; Martinez-Labarga, C; Tolk, H; Kivisild, T; Giampaolo, R; Tarsi, T; Contini, I; Barac, L; Janicijevic, B; Klaric, I; Pericic, M; Sujoldzic, A; Villems, R; Biondi, G; Rudan, P; Rickards, O
Population structure in the Mediterranean basin: A Y chromosome perspective
2006-01-01 Capelli, C; Redhead, N; Romano, V; Cali, F; Lefranc, G; Delague, V; Megarbane, A; Novelletto, A; Malaspina, P; Terrenato, L; Ii,
Population studies on human phosphoglucomutase-1 thermostability polymorphism.
1984-01-01 Scozzari, R; Iodice, C; Sellitto, D; Brdicka, R; Mura, G; SANTA¬CHIARA BENERECETTI, S
Population variation analysis at nine loci containing expressed trinucleotide repeats
1997-01-01 Jodice, C; Giovannone, B; Calabresi, V; Bellocchi, M; Terrenato, L; Novelletto, A
Population variation analysis at nine loci containing expressed trinucleotide repeats
1997-09-01 Iodice, C; Giovannone, B; Calabresi, V; Bellocchi, M; Terrenato, L; Novelletto, A
Position and sequence conservation in Amniota of polymorphic enhancer HS1.2 within the palindrome of IgH 3'Regulatory Region.
2011-01-01 D'Addabbo, P; Scascitelli, M; Giambra, V; Rocchi, M; Frezza, D
Potentially active copies of the gypsy retroelement are confined to the Y chromosome of some strains of Drosophila melanogaster possibly as the result of the female-specific effect of the flamenco gene
1998-01-01 Chalvet, F; Di Franco, C; Terrinoni, A; Pelisson, A; Junakovic, N; Bucheton, A
Practical guidelines for managing patients with 22q11.2 deletion syndrome.
2011-01-01 Bassett, A; McDonald McGinn, D; Devriendt, K; Digilio, M; Goldenberg, P; Habel, A; Marino, B; Oskarsdottir, S; Philip, N; Sullivan, K; Swillen, A; Vorstman, J; Abadie, V; Allgrove, J; Amati, F; Baker, K; Baylis, A; Beaujard, M; Beemer, F; Boers, M; Bolton, P; Boot, E; Brigstocke, S; Burtey, S; Campbell, L; Chabloz, M; Chow, E; Clayton Smith, J; Cubells, J; Debbané, M; Delrue, M; De Smedt, B; Duijff, S; Eicher, P; Emanuel, B; Evers, L; Flahault, A; Forsythe, A; Frebourg, T; Gennery, A; Goldmuntz, E; Gosling, A; Handler, S; Heine Suñer, D; Hilmarsson, A; Hogan, A; Hordijk, R; Howley, S; Illingworth, E; Jackson, O; Joyce, H; Kawame, H; Kelly, R; Kemp, A; Kempf, L; Kimpen, J; Kirschner, R; Klaassen, P; Kumararatne, D; Lambert, M; Lima, K; Lindsay, E; Macerola, S; Malki, M; Marlin, S; Mascarenhas, M; Monks, S; Moran, V; Morrow, B; Moss, E; Murphy, C; Naqvi, N; Nielsen, B; Niklasson, L; Nordgarden, H; Oenema Mostert, C; Ottet, M; Pasca, C; Pasquariello, P; Persson, C; Portnoi, M; Prasad, S; Rockers, K; Saitta, S; Scambler, P; Schaer, M; Schneider, M; Sell, D; Solot, C; Sommerlad, B; Unanue, N; Sundram, F; Van Aken, K; van Amelsvoort, T; van der Molen, A; Widdershoven, J; Zackai, E
pRb2/p130 promotes radiation-induced cell death in the glioblastoma cell line HJC12 by p73 upregulation and Bcl-2 downregulation
2002-01-01 Pucci, B; Claudio, Pp; Masciullo, V; Bellincampi, L; Terrinoni, A; Khalili, K; Melino, G; Giordano, A
Precision Medicine in Non-Communicable Diseases
2020-02-07 Novelli, G; Biancolella, M; Latini, A; Spallone, A; Borgiani, P; Papaluca, M
Predictive parameters after molecular absorbent recirculating system treatment integrated with model for end stage liver disease model in patients with acute-on-chronic liver failure
2010-05-01 Novelli, G; Rossi, M; Ferretti, G; Pugliese, F; Travaglia, D; Guidi, S; Novelli, S; Lai, Q; Morabito, V; Berloco, P
Preface: BITS2014, the annual meeting of the Italian Society of Bioinformatics
2015-01-01 Facchiano, A; Angelini, C; Bosotti, R; Guffanti, A; Marabotti, A; Marangoni, R; Pascarella, S; Romano, P; Zanzoni, A; HELMER CITTERICH, M
Preferential central nucleation of type 2 myofibers is an invariable feature of myotonic dystrophy type 2
2008-01-01 Pisani, V; Panico, M; Terracciano, C; Bonifazi, E; Meola, G; Novelli, G; Bernardi, G; Angelini, C; Massa, R
A preliminary analysis of volatile metabolites of human induced pluripotent stem cells along the in vitro differentiation
2017-01-01 Capuano, R; Spitalieri, P; Talarico, R; Domakoski, Ac; Catini, A; Paolesse, R; Martinelli, E; Novelli, G; Sangiuolo, Fc; DI NATALE, C
Prenatal diagnosis of Cockayne syndrome type A based on the identification of two novel mutations in the ERCC8 gene
2009-02-01 Conte, C; D'Apice, M; Botta, A; Sangiuolo, Fc; Novelli, G
Prenatal diagnosis of genomic disorders and chromosome abnormalities using array-based comparative genomic hybridization
2007-01-01 Gullotta, F; Biancolella, M; Costa, E; Colapietro, I; Nardone, A; Molinaro, P; Pietropolli, A; Narcisi, M; Di Rosa, C; Novelli, G
Preservation of ancient DNA in thermally damaged archaeological bone
2009-01-01 Ottoni, C; Koon, H; Collins, M; Penkman, K; Rickards, O; Craig, O
Prevalence of Fabry disease and GLA variants in young patients with acute stroke: The challenge to widen the screening. The Fabry-Stroke Italian Registry
2024-01-01 Romani, I; Sarti, C; Nencini, P; Pracucci, G; Zedde, M; Cianci, V; Nucera, A; Moller, J; Orsucci, D; Toni, D; Palumbo, P; Casella, C; Pinto, V; Barbarini, L; Bella, R; Scoditti, U; Ragno, M; Mezzapesa, Dm; Tassi, R; Volpi, G; Diomedi, M; Bigliardi, G; Cavallini, Am; Chiti, A; Ricci, S; Cecconi, E; Linoli, G; Sacco, S; Rasura, M; Giordano, A; Bonetti, B; Melis, M; Cariddi, Lp; Dossi, Rc; Grisendi, I; Aguglia, U; Di Ruzza, Mr; Melis, M; Sbardella, E; Vista, M; Valenti, R; Musolino, Rf; Passarella, B; Direnzo, V; Pennisi, G; Genovese, A; Di Marzio, F; Sgobio, R; Acampa, M; Nannucci, S; Dagostino, F; Dell'Acqua, Ml; Cuzzoni, Mg; Picchioni, A; Calchetti, B; Notturno, F; Di Lisi, F; Forlivesi, S; Delodovici, Ml; Buechner, Sc; Biagini, S; Accavone, D; Manna, R; Morrone, A; Inzitari, D
Prevalence of factor V Leiden mutation in non-European populations
1997-01-01 Pepe, G; Rickards, O; Vanegas, O; Brunelli, T; Gori, A; Giusti, B; Attanasio, M; Prisco, D; Gensini, G; Abbate, R
Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
---|---|---|---|---|
1-gen-1995 | Population genetics and structure of the Blacks from Rio Cayapa, North-Western Ecuador. | DE STEFANO, G; MARTINEZ-LABARGA, Mc; Rickards, O | Intervento a convegno | |
1-gen-2005 | The population history of the Croatian linguistic minority of Molise (southern Italy): a maternal view | Babalini, C; Martinez-Labarga, C; Tolk, H; Kivisild, T; Giampaolo, R; Tarsi, T; Contini, I; Barac, L; Janicijevic, B; Klaric, I; Pericic, M; Sujoldzic, A; Villems, R; Biondi, G; Rudan, P; Rickards, O | Articolo su rivista | |
1-gen-2006 | Population structure in the Mediterranean basin: A Y chromosome perspective | Capelli, C; Redhead, N; Romano, V; Cali, F; Lefranc, G; Delague, V; Megarbane, A; Novelletto, A; Malaspina, P; Terrenato, L; Ii, | Articolo su rivista | |
1-gen-1984 | Population studies on human phosphoglucomutase-1 thermostability polymorphism. | Scozzari, R; Iodice, C; Sellitto, D; Brdicka, R; Mura, G; SANTA¬CHIARA BENERECETTI, S | Articolo su rivista | |
1-gen-1997 | Population variation analysis at nine loci containing expressed trinucleotide repeats | Jodice, C; Giovannone, B; Calabresi, V; Bellocchi, M; Terrenato, L; Novelletto, A | Articolo su rivista | |
1-set-1997 | Population variation analysis at nine loci containing expressed trinucleotide repeats | Iodice, C; Giovannone, B; Calabresi, V; Bellocchi, M; Terrenato, L; Novelletto, A | Articolo su rivista | |
1-gen-2011 | Position and sequence conservation in Amniota of polymorphic enhancer HS1.2 within the palindrome of IgH 3'Regulatory Region. | D'Addabbo, P; Scascitelli, M; Giambra, V; Rocchi, M; Frezza, D | Articolo su rivista | |
1-gen-1998 | Potentially active copies of the gypsy retroelement are confined to the Y chromosome of some strains of Drosophila melanogaster possibly as the result of the female-specific effect of the flamenco gene | Chalvet, F; Di Franco, C; Terrinoni, A; Pelisson, A; Junakovic, N; Bucheton, A | Articolo su rivista | |
1-gen-2011 | Practical guidelines for managing patients with 22q11.2 deletion syndrome. | Bassett, A; McDonald McGinn, D; Devriendt, K; Digilio, M; Goldenberg, P; Habel, A; Marino, B; Oskarsdottir, S; Philip, N; Sullivan, K; Swillen, A; Vorstman, J; Abadie, V; Allgrove, J; Amati, F; Baker, K; Baylis, A; Beaujard, M; Beemer, F; Boers, M; Bolton, P; Boot, E; Brigstocke, S; Burtey, S; Campbell, L; Chabloz, M; Chow, E; Clayton Smith, J; Cubells, J; Debbané, M; Delrue, M; De Smedt, B; Duijff, S; Eicher, P; Emanuel, B; Evers, L; Flahault, A; Forsythe, A; Frebourg, T; Gennery, A; Goldmuntz, E; Gosling, A; Handler, S; Heine Suñer, D; Hilmarsson, A; Hogan, A; Hordijk, R; Howley, S; Illingworth, E; Jackson, O; Joyce, H; Kawame, H; Kelly, R; Kemp, A; Kempf, L; Kimpen, J; Kirschner, R; Klaassen, P; Kumararatne, D; Lambert, M; Lima, K; Lindsay, E; Macerola, S; Malki, M; Marlin, S; Mascarenhas, M; Monks, S; Moran, V; Morrow, B; Moss, E; Murphy, C; Naqvi, N; Nielsen, B; Niklasson, L; Nordgarden, H; Oenema Mostert, C; Ottet, M; Pasca, C; Pasquariello, P; Persson, C; Portnoi, M; Prasad, S; Rockers, K; Saitta, S; Scambler, P; Schaer, M; Schneider, M; Sell, D; Solot, C; Sommerlad, B; Unanue, N; Sundram, F; Van Aken, K; van Amelsvoort, T; van der Molen, A; Widdershoven, J; Zackai, E | Articolo su rivista | |
1-gen-2002 | pRb2/p130 promotes radiation-induced cell death in the glioblastoma cell line HJC12 by p73 upregulation and Bcl-2 downregulation | Pucci, B; Claudio, Pp; Masciullo, V; Bellincampi, L; Terrinoni, A; Khalili, K; Melino, G; Giordano, A | Articolo su rivista | |
7-feb-2020 | Precision Medicine in Non-Communicable Diseases | Novelli, G; Biancolella, M; Latini, A; Spallone, A; Borgiani, P; Papaluca, M | Articolo su rivista | |
1-mag-2010 | Predictive parameters after molecular absorbent recirculating system treatment integrated with model for end stage liver disease model in patients with acute-on-chronic liver failure | Novelli, G; Rossi, M; Ferretti, G; Pugliese, F; Travaglia, D; Guidi, S; Novelli, S; Lai, Q; Morabito, V; Berloco, P | Articolo su rivista | |
1-gen-2015 | Preface: BITS2014, the annual meeting of the Italian Society of Bioinformatics | Facchiano, A; Angelini, C; Bosotti, R; Guffanti, A; Marabotti, A; Marangoni, R; Pascarella, S; Romano, P; Zanzoni, A; HELMER CITTERICH, M | Articolo su rivista | |
1-gen-2008 | Preferential central nucleation of type 2 myofibers is an invariable feature of myotonic dystrophy type 2 | Pisani, V; Panico, M; Terracciano, C; Bonifazi, E; Meola, G; Novelli, G; Bernardi, G; Angelini, C; Massa, R | Articolo su rivista | |
1-gen-2017 | A preliminary analysis of volatile metabolites of human induced pluripotent stem cells along the in vitro differentiation | Capuano, R; Spitalieri, P; Talarico, R; Domakoski, Ac; Catini, A; Paolesse, R; Martinelli, E; Novelli, G; Sangiuolo, Fc; DI NATALE, C | Articolo su rivista | |
1-feb-2009 | Prenatal diagnosis of Cockayne syndrome type A based on the identification of two novel mutations in the ERCC8 gene | Conte, C; D'Apice, M; Botta, A; Sangiuolo, Fc; Novelli, G | Articolo su rivista | |
1-gen-2007 | Prenatal diagnosis of genomic disorders and chromosome abnormalities using array-based comparative genomic hybridization | Gullotta, F; Biancolella, M; Costa, E; Colapietro, I; Nardone, A; Molinaro, P; Pietropolli, A; Narcisi, M; Di Rosa, C; Novelli, G | Articolo su rivista | |
1-gen-2009 | Preservation of ancient DNA in thermally damaged archaeological bone | Ottoni, C; Koon, H; Collins, M; Penkman, K; Rickards, O; Craig, O | Articolo su rivista | |
1-gen-2024 | Prevalence of Fabry disease and GLA variants in young patients with acute stroke: The challenge to widen the screening. The Fabry-Stroke Italian Registry | Romani, I; Sarti, C; Nencini, P; Pracucci, G; Zedde, M; Cianci, V; Nucera, A; Moller, J; Orsucci, D; Toni, D; Palumbo, P; Casella, C; Pinto, V; Barbarini, L; Bella, R; Scoditti, U; Ragno, M; Mezzapesa, Dm; Tassi, R; Volpi, G; Diomedi, M; Bigliardi, G; Cavallini, Am; Chiti, A; Ricci, S; Cecconi, E; Linoli, G; Sacco, S; Rasura, M; Giordano, A; Bonetti, B; Melis, M; Cariddi, Lp; Dossi, Rc; Grisendi, I; Aguglia, U; Di Ruzza, Mr; Melis, M; Sbardella, E; Vista, M; Valenti, R; Musolino, Rf; Passarella, B; Direnzo, V; Pennisi, G; Genovese, A; Di Marzio, F; Sgobio, R; Acampa, M; Nannucci, S; Dagostino, F; Dell'Acqua, Ml; Cuzzoni, Mg; Picchioni, A; Calchetti, B; Notturno, F; Di Lisi, F; Forlivesi, S; Delodovici, Ml; Buechner, Sc; Biagini, S; Accavone, D; Manna, R; Morrone, A; Inzitari, D | Articolo su rivista | |
1-gen-1997 | Prevalence of factor V Leiden mutation in non-European populations | Pepe, G; Rickards, O; Vanegas, O; Brunelli, T; Gori, A; Giusti, B; Attanasio, M; Prisco, D; Gensini, G; Abbate, R | Articolo su rivista |
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