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Formoterol-induced downregulation of the beta2-adrenoceptor in asthmatics with homozygous glycine-16 polymorphism
2013 Fuso, Leonello; Di Perna, Alessandra; Longobardi, Anna; Trove', Andrea; Bisceglia, Michela; Bibi, Benedetta; Angelozzi, Carla; Tiziano, Francesco Danilo; Antonelli Incalzi, Raffaele
Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder
2009 Gurrieri, Fiorella; Neri, Giovanni; Boccuto, Luigi
Gene expression profiling of pancreas neuroendocrine tumors with different ki67‐based grades
2021 Simbolo, M.; Bilotta, M.; Mafficini, A.; Luchini, C.; Furlan, D.; Inzani, F.; Petrone, G.; Bonvissuto, D.; Rosa, S. L.; Schinzari, G.; Bianchi, A.; Rossi, E.; Menghi, R.; Giuliante, F.; Boccia, S.; Scarpa, A.; Rindi, G.
-Genetic analysis of the dystroglycan gene in brochopulmnary dysplasia affected premature newbors
2007 Concolino, P.; Capoluongo, E.; Santonocito, E.; Vento, Giovanni; Tana, Milena; Romagnoli, Costantino; Zuppi, Cecilia; Ameglio, F.; Brancaccio, A.; Sciandra, F.
Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges
2014 Marangi, Giuseppe; Traynor, Bj
Genetic counselling in ALS: facts, uncertainties and clinical suggestions
2013 Chiò, A; Battistini, S; Calvo, A; Caponnetto, C; Conforti, Fl; Corbo, M; Giannini, F; Mandrioli, J; Mora, G; Sabatelli, Mario; Ajmone, C; Mastro, E; Pain, D; Mandich, P; Penco, S; Restagno, G; Zollino, Marcella; Surbone, A.
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
2010 Pola, Roberto; Gaetani, Eleonora
A Genome-wide Association Study of Myasthenia Gravis
2015 Renton, Ae; Pliner, Ha; Provenzano, Carlo; Evoli, Amelia; Ricciardi, R; Nalls, Ma; Marangi, Giuseppe; Abramzon, Y; Arepalli, S; Chong, S; Hernandez, Dg; Johnson, Jo; Bartoccioni, Emanuela; Scuderi, Flavia; Maestri, M; Gibbs, Jr; Errichiello, E; Chiò, A; Restagno, G; Sabatelli, Mario; Macek, M; Scholz, Sw; Corse, A; Chaudhry, V; Benatar, M; Barohn, Rj; Mcvey, A; Pasnoor, M; Dimachkie, Mm; Rowin, J; Kissel, J; Freimer, M; Kaminski, Hj; Sanders, Db; Lipscomb, B; Massey, Jm; Chopra, M; Howard, Jf; Koopman, Wj; Nicolle, Mw; Pascuzzi, Rm; Pestronk, A; Wulf, C; Florence, J; Blackmore, D; Soloway, A; Siddiqi, Z; Muppidi, S; Wolfe, G; Richman, D; Mezei, Mm; Jiwa, T; Oger, J; Drachman, Db; Traynor, Bj
A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium.
2011 Boccia, Stefania; Inhance, Consortium
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome.
2009 Neri, Giovanni
Geographic heterogeneity in the prevalence of human papillomavirus in head and neck cancer
2017 Anantharaman, Devasena; Abedi Ardekani, Behnoush; Beachler, Daniel C; Gheit, Tarik; Olshan, Andrew F; Wisniewski, Kathy; Wunsch Filho, Victor; Toporcov, Tatiana N; Tajara, Eloiza H; Levi, José Eduardo; Moyses, Raquel A; Boccia, Stefania; Cadoni, Gabriella; Rindi, Guido; Ahrens, Wolfgang; Merletti, Franco; Conway, David I; Wright, Sylvia; Carreira, Christine; Renard, Helene; Chopard, Priscilia; McKay Chopin, Sandrine; Scelo, Ghislaine; Tommasino, Massimo; Brennan, Paul; D'Souza, Gypsyamber
Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin.
2008 Hennies, Hc; Kornak, U; Zhang, H; Egerer, J; Zhang, X; Seifert, W; Kuhnisch, J; Budde, B; Natebus, M; Brancati, F; Wilcox, Wr; Muller, D; Kaplan, Pb; Rajab, A; Zampino, Giuseppe; Fodale, V; Dallapiccola, B; Newman, W; Metcalfe, K; Clayton Smith, J; Tassabehji, M; Steinmann, B; Barr, Fa; Nurnberg, P; Wieacker, P; Mundlos, S.
Glucokinase regulatory protein gene polymorphism affects liver fibrosis in non-alcoholic fatty liver disease
2014 Petta, S; Miele, Luca; Bugianesi, E; Cammà, C; Rosso, C; Boccia, Stefania; Cabibi, D; Di Marco, V; Grimaudo, S; Grieco, Antonio; Pipitone, Rm; Marchesini, G; Craxì, A.
Glucokinase Regulatory Protein Gene Polymorphism Affects Liver Fibrosis in Non-Alcoholic Fatty Liver Disease
2014 Petta, S; Miele, Luca; Bugianesi, E; Cammà, C; Rosso, C; Boccia, Stefania; Cabibi, D; Di Marco, V; Grimaudo, S; Grieco, Antonio; Pipitone, Rm; Marchesini, G; Craxì, A.
Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype.
2010 Martinelli, S; De Luca, A; Cavaliere, M. L; Zampino, Giuseppe; Gelb, Bd; Tartaglia, Marco
HLA class II allele analysis in MuSK-positive myasthenia gravis suggests a role for DQ5.
2009 Bartoccioni, Emanuela; Scuderi, Flavia; Augugliaro, A.; Chiatamonte Ranieri, Sofia; Sauchielli, Donato; Alboini, Paolo; Marino, Mariapaola; Evoli, Amelia
Homocysteinemia is inversely correlated with platelet count and inversely correlated with sE-and sP-selectin levels in females homozygous for C677T methylenetetrahydrofolate reductase
2005 Rongioletti, Mauro; Baldassini, Mauro; Papa, Fabrizio; Capoluongo, Ettore Domenico; Rocca, Bianca; De Cristofaro, Raimondo; Salvati, Giuseppina; Larciprete, Giovanni; Stroppolo, Annalisa; Angelucci, Piero Antonio; Cirese, Elio; Ameglio, Franco
Hypoxia-inducible factor-1α(Pro-582-Ser) polymorphism prevents iron deprivation in healthy blood donors
2013 Torti, Lorenza; Teofili, Luciana; Capodimonti, Sara; Nuzzolo, Eugenia Rosa; Iachininoto, Maria Grazia; Massini, Giuseppina; Coluzzi, S; Tafuri, A; Fiorin, F; Girelli, G; Zini Tanzi, Gina; Larocca, Luigi Maria
Identification of a potential proinflammatory genetic profile influencing carotid plaque vulnerability.
2014 Biscetti, Federico; Straface, Giuseppe; Bertoletti, Giovanni; Vincenzoni, Claudio; Snider, Francesco; Arena, Vincenzo; Landolfi, Raffaele; Flex, Andrea
Impairment of different protein domains causes variable clinical presentation within Pitt-Hopkins syndrome and suggests intragenic molecular syndromology of TCF4
2017 Bedeschi, Maria Francesca; Marangi, Giuseppe; Calvello, Maria Rosaria; Ricciardi, Stefania; Leone, Francesca Pia Chiara; Baccarin, Marco; Guerneri, Silvana; Orteschi, Daniela; Murdolo, Marina; Lattante, Serena; Frangella, Silvia; Keena, Beth; Harr, Margaret H.; Zackai, Elaine; Zollino, Marcella
Data di pubblicazione | Titolo | Autore(i) | File |
---|---|---|---|
1-gen-2013 | Formoterol-induced downregulation of the beta2-adrenoceptor in asthmatics with homozygous glycine-16 polymorphism | Fuso, Leonello; Di Perna, Alessandra; Longobardi, Anna; Trove', Andrea; Bisceglia, Michela; Bibi, Benedetta; Angelozzi, Carla; Tiziano, Francesco Danilo; Antonelli Incalzi, Raffaele | |
1-gen-2009 | Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder | Gurrieri, Fiorella; Neri, Giovanni; Boccuto, Luigi | |
1-gen-2021 | Gene expression profiling of pancreas neuroendocrine tumors with different ki67‐based grades | Simbolo, M.; Bilotta, M.; Mafficini, A.; Luchini, C.; Furlan, D.; Inzani, F.; Petrone, G.; Bonvissuto, D.; Rosa, S. L.; Schinzari, G.; Bianchi, A.; Rossi, E.; Menghi, R.; Giuliante, F.; Boccia, S.; Scarpa, A.; Rindi, G. | |
1-gen-2007 | -Genetic analysis of the dystroglycan gene in brochopulmnary dysplasia affected premature newbors | Concolino, P.; Capoluongo, E.; Santonocito, E.; Vento, Giovanni; Tana, Milena; Romagnoli, Costantino; Zuppi, Cecilia; Ameglio, F.; Brancaccio, A.; Sciandra, F. | |
1-gen-2014 | Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges | Marangi, Giuseppe; Traynor, Bj | |
1-gen-2013 | Genetic counselling in ALS: facts, uncertainties and clinical suggestions | Chiò, A; Battistini, S; Calvo, A; Caponnetto, C; Conforti, Fl; Corbo, M; Giannini, F; Mandrioli, J; Mora, G; Sabatelli, Mario; Ajmone, C; Mastro, E; Pain, D; Mandich, P; Penco, S; Restagno, G; Zollino, Marcella; Surbone, A. | |
1-gen-2010 | Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm | Pola, Roberto; Gaetani, Eleonora | |
1-gen-2015 | A Genome-wide Association Study of Myasthenia Gravis | Renton, Ae; Pliner, Ha; Provenzano, Carlo; Evoli, Amelia; Ricciardi, R; Nalls, Ma; Marangi, Giuseppe; Abramzon, Y; Arepalli, S; Chong, S; Hernandez, Dg; Johnson, Jo; Bartoccioni, Emanuela; Scuderi, Flavia; Maestri, M; Gibbs, Jr; Errichiello, E; Chiò, A; Restagno, G; Sabatelli, Mario; Macek, M; Scholz, Sw; Corse, A; Chaudhry, V; Benatar, M; Barohn, Rj; Mcvey, A; Pasnoor, M; Dimachkie, Mm; Rowin, J; Kissel, J; Freimer, M; Kaminski, Hj; Sanders, Db; Lipscomb, B; Massey, Jm; Chopra, M; Howard, Jf; Koopman, Wj; Nicolle, Mw; Pascuzzi, Rm; Pestronk, A; Wulf, C; Florence, J; Blackmore, D; Soloway, A; Siddiqi, Z; Muppidi, S; Wolfe, G; Richman, D; Mezei, Mm; Jiwa, T; Oger, J; Drachman, Db; Traynor, Bj | |
1-gen-2011 | A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. | Boccia, Stefania; Inhance, Consortium | |
1-gen-2009 | Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome. | Neri, Giovanni | |
1-gen-2017 | Geographic heterogeneity in the prevalence of human papillomavirus in head and neck cancer | Anantharaman, Devasena; Abedi Ardekani, Behnoush; Beachler, Daniel C; Gheit, Tarik; Olshan, Andrew F; Wisniewski, Kathy; Wunsch Filho, Victor; Toporcov, Tatiana N; Tajara, Eloiza H; Levi, José Eduardo; Moyses, Raquel A; Boccia, Stefania; Cadoni, Gabriella; Rindi, Guido; Ahrens, Wolfgang; Merletti, Franco; Conway, David I; Wright, Sylvia; Carreira, Christine; Renard, Helene; Chopard, Priscilia; McKay Chopin, Sandrine; Scelo, Ghislaine; Tommasino, Massimo; Brennan, Paul; D'Souza, Gypsyamber | |
1-gen-2008 | Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin. | Hennies, Hc; Kornak, U; Zhang, H; Egerer, J; Zhang, X; Seifert, W; Kuhnisch, J; Budde, B; Natebus, M; Brancati, F; Wilcox, Wr; Muller, D; Kaplan, Pb; Rajab, A; Zampino, Giuseppe; Fodale, V; Dallapiccola, B; Newman, W; Metcalfe, K; Clayton Smith, J; Tassabehji, M; Steinmann, B; Barr, Fa; Nurnberg, P; Wieacker, P; Mundlos, S. | |
1-gen-2014 | Glucokinase regulatory protein gene polymorphism affects liver fibrosis in non-alcoholic fatty liver disease | Petta, S; Miele, Luca; Bugianesi, E; Cammà, C; Rosso, C; Boccia, Stefania; Cabibi, D; Di Marco, V; Grimaudo, S; Grieco, Antonio; Pipitone, Rm; Marchesini, G; Craxì, A. | |
1-gen-2014 | Glucokinase Regulatory Protein Gene Polymorphism Affects Liver Fibrosis in Non-Alcoholic Fatty Liver Disease | Petta, S; Miele, Luca; Bugianesi, E; Cammà, C; Rosso, C; Boccia, Stefania; Cabibi, D; Di Marco, V; Grimaudo, S; Grieco, Antonio; Pipitone, Rm; Marchesini, G; Craxì, A. | |
1-gen-2010 | Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype. | Martinelli, S; De Luca, A; Cavaliere, M. L; Zampino, Giuseppe; Gelb, Bd; Tartaglia, Marco | |
1-gen-2009 | HLA class II allele analysis in MuSK-positive myasthenia gravis suggests a role for DQ5. | Bartoccioni, Emanuela; Scuderi, Flavia; Augugliaro, A.; Chiatamonte Ranieri, Sofia; Sauchielli, Donato; Alboini, Paolo; Marino, Mariapaola; Evoli, Amelia | |
1-gen-2005 | Homocysteinemia is inversely correlated with platelet count and inversely correlated with sE-and sP-selectin levels in females homozygous for C677T methylenetetrahydrofolate reductase | Rongioletti, Mauro; Baldassini, Mauro; Papa, Fabrizio; Capoluongo, Ettore Domenico; Rocca, Bianca; De Cristofaro, Raimondo; Salvati, Giuseppina; Larciprete, Giovanni; Stroppolo, Annalisa; Angelucci, Piero Antonio; Cirese, Elio; Ameglio, Franco | |
1-gen-2013 | Hypoxia-inducible factor-1α(Pro-582-Ser) polymorphism prevents iron deprivation in healthy blood donors | Torti, Lorenza; Teofili, Luciana; Capodimonti, Sara; Nuzzolo, Eugenia Rosa; Iachininoto, Maria Grazia; Massini, Giuseppina; Coluzzi, S; Tafuri, A; Fiorin, F; Girelli, G; Zini Tanzi, Gina; Larocca, Luigi Maria | |
1-gen-2014 | Identification of a potential proinflammatory genetic profile influencing carotid plaque vulnerability. | Biscetti, Federico; Straface, Giuseppe; Bertoletti, Giovanni; Vincenzoni, Claudio; Snider, Francesco; Arena, Vincenzo; Landolfi, Raffaele; Flex, Andrea | |
1-gen-2017 | Impairment of different protein domains causes variable clinical presentation within Pitt-Hopkins syndrome and suggests intragenic molecular syndromology of TCF4 | Bedeschi, Maria Francesca; Marangi, Giuseppe; Calvello, Maria Rosaria; Ricciardi, Stefania; Leone, Francesca Pia Chiara; Baccarin, Marco; Guerneri, Silvana; Orteschi, Daniela; Murdolo, Marina; Lattante, Serena; Frangella, Silvia; Keena, Beth; Harr, Margaret H.; Zackai, Elaine; Zollino, Marcella |
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