Sfoglia per ???browse.type.metadata.subjectErc2011??? LS2 - Genetics, Genomics, Bioinformatics and Systems Biology: genetics, population genetics, molecular genetics, genomics, transcriptomics, proteomics, metabolomics, bioinformatics, computational biology, biostatistics, biological modelling and simulation, systems biology, genetic epidemiology
Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis
2020 Cuellar, Araceli; Bala, Krithi; Di Pietro, Lorena; Barba, Marta; Yagnik, Garima; Liu, Jia Lie; Stevens, Christina; Hur, David J; Ingersoll, Roxann G; Justice, Cristina M; Drissi, Hicham; Kim, Jinoh; Lattanzi, Wanda; Boyadjiev, Simeon A
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.
Generation of an induced pluripotent stem cell line (CSS012-A (7672)) carrying the p.G376D heterozygous mutation in the TARDBP protein
2021 D'Anzi, A.; Altieri, F.; Perciballi, E.; Ferrari, D.; Torres, B.; Bernardini, L.; Lattante, Serena; Sabatelli, Mario; Vescovi, A. L.; Rosati, J.
Genetic advances in craniosynostosis
2017 Lattanzi, Wanda; Barba, Marta; Di Pietro, Lorena; Boyadjiev, Simeon A.
Genetic and epigenetic alterations of RB2/p130 tumor suppressor gene in human sporadic retinoblastoma: Implications for pathogenesis and therapeutic approach
2005 Tosi, Gian Marco; Trimarchi, Carmela; Macaluso, Marcella; La Sala, Dario; Ciccodicola, Alfredo; Lazzi, Stefano; Massaro-Giordano, Mina; Caporossi, Aldo; Giordano, Antonio; Cinti, Caterina
Genetic and physiological bases of healthy attributes of grapes and wine
2015 Bavaresco, Luigi; Morreale, G.; Flamini, R.
Genetic causes of amyotrophic lateral sclerosis: New genetic analysis methodologies entailing new opportunities and challenges
2015 Marangi, Giuseppe; Traynor, Bryan J.
Genetic characterization and implications for conservation of the last autochthonous Mouflon population in Europe
2021 Satta, V.; Mereu, P.; Barbato, Mario; Pirastru, M.; Bassu, G.; Manca, L.; Naitana, S.; Leoni, G. G.
Genetic counseling in hereditary non-polyposis colorectal cancer
1996 Heouaine, A; Mareni, C; Varesco, L; Genuardi, Maurizio; Neri, G
A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability
2006 Marroni, F; Pastrello, C; Benatti, P; Torrini, M; Barana, D; Cordisco, E; Viel, A; Mareni, C; Oliani, C; Genuardi, Maurizio; Bailey-Wilson, J; de Leon, M; Presciuttini, S
Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths
2019 Martinez-Matilla, M.; Blanco-Verea, A.; Santori, M.; Ansede-Bermejo, J.; Ramos-Luis, E.; Gil, R.; Bermejo, A. M.; Lotufo-Neto, F.; Hirata, M. H.; Brisighelli, Francesca; Paramo, M.; Carracedo, A.; Brion, M.
Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer
2004 de Leon, M; Benatti, P; Di Gregorio, C; Pedroni, M; Losi, L; Genuardi, M; Viel, A; Fornasarig, M; Lucci-Cordisco, E; Anti, M; Ponti, G; Borghi, F; Lamberti, I; Roncucci, L
Genetic testing of cancer predisposition
2000 Genuardi, M; Caluseriu, O; Cordisco, E; Rovella, V; Neri, G
A genetically unique Chinese cattle population shows evidence of common ancestry with wild species when analysed with a reduced ascertainment bias SNP panel
2020 Barbato, Mario; Reichel, M. P.; Passamonti, Matilde Maria; Low, W. Y.; Colli, Licia; Tearle, R.; Williams, John Lewis; Ajmone Marsan, Paolo
A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis
2020 Justice, Cm; Cuellar, A; Bala, K; Sabourin, Ja; Cunningham, Ml; Crawford, K; Phipps, Jm; Zhou, Y; Cilliers, D; Byren, Jc; Johnson, D; Wall, Sa; Morton, Jev; Noons, P; Sweeney, E; Weber, Bertram; Rees, Kem; Wilson, Lc; Simeonov, E; Kaneva, R; Yaneva, N; Georgiev, K; Bussarsky, A; Senders, C; Zwienenberg, M; Boggan, J; Roscioli, T; Tamburrini, Gianpiero; Barba, Marta; Conway, K; Sheffield, Vc; Brody, L; Mills, Jl; Kay, D; Sicko, Rj; Langlois, Ph; Tittle, Rk; Botto, Ld; Jenkins, Mm; Lasalle, Jm; Lattanzi, Wanda; Wilkie, Aom; Wilson, Af; Romitti, Pa; Boyadjiev, Sa
Genome-wide association study of sporadic brain arteriovenous malformations
2016 Weinsheimer, Shantel; Bendjilali, Nasrine; Nelson, Jeffrey; Guo, Diana E; Zaroff, Jonathan G; Sidney, Stephen; Mcculloch, Charles E; Al Shahi Salman, Rustam; Berg, Jonathan N; Koeleman, Bobby P. C; Simon, Matthias; Bostroem, Azize; Fontanella, Marco; Sturiale, Carmelo Lucio; Pola, Roberto; Puca, Alfredo; Lawton, Michael T; Young, William L; Pawlikowska, Ludmila; Klijn, Catharina J. M; Kim, Helen
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells
2016 Tabolacci, Elisabetta; Mancano, Giorgia; Lanni, Stella; Palumbo, Federica; Goracci, Martina; Ferrè, Fabrizio; Helmer Citterich, Manuela; Neri, Giovanni
Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts
2000 Percesepe, A; Pedroni, M; Sala, E; Menigatti, M; Borghi, F; Losi, L; Viel, A; Genuardi, Maurizio; Benatti, P; Roncucci, L; Peltomaki, P; de Leon, M
Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations
2008 Vignoli, M; Scaini, M; Ghiorzo, P; Sestini, R; Bruno, W; Menin, C; Gensini, F; Piazzini, M; Testori, A; Manoukian, S; Orlando, C; D'Andrea, E; Bianchi-Scarra, G; Genuardi, Maurizio
Genomic signatures of adaptive introgression from European mouflon into domestic sheep
2017 Barbato, Mario; Hailer, Frank; Orozco-Terwengel, Pablo; Kijas, James; Mereu, Paolo; Cabras, Pierangela; Mazza, Raffaele; Pirastru, Monica; Bruford, Michael W.
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-2020 | Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis | Cuellar, Araceli; Bala, Krithi; Di Pietro, Lorena; Barba, Marta; Yagnik, Garima; Liu, Jia Lie; Stevens, Christina; Hur, David J; Ingersoll, Roxann G; Justice, Cristina M; Drissi, Hicham; Kim, Jinoh; Lattanzi, Wanda; Boyadjiev, Simeon A | |
| 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-2021 | Generation of an induced pluripotent stem cell line (CSS012-A (7672)) carrying the p.G376D heterozygous mutation in the TARDBP protein | D'Anzi, A.; Altieri, F.; Perciballi, E.; Ferrari, D.; Torres, B.; Bernardini, L.; Lattante, Serena; Sabatelli, Mario; Vescovi, A. L.; Rosati, J. | |
| 1-gen-2017 | Genetic advances in craniosynostosis | Lattanzi, Wanda; Barba, Marta; Di Pietro, Lorena; Boyadjiev, Simeon A. | |
| 1-gen-2005 | Genetic and epigenetic alterations of RB2/p130 tumor suppressor gene in human sporadic retinoblastoma: Implications for pathogenesis and therapeutic approach | Tosi, Gian Marco; Trimarchi, Carmela; Macaluso, Marcella; La Sala, Dario; Ciccodicola, Alfredo; Lazzi, Stefano; Massaro-Giordano, Mina; Caporossi, Aldo; Giordano, Antonio; Cinti, Caterina | |
| 1-gen-2015 | Genetic and physiological bases of healthy attributes of grapes and wine | Bavaresco, Luigi; Morreale, G.; Flamini, R. | |
| 1-gen-2015 | Genetic causes of amyotrophic lateral sclerosis: New genetic analysis methodologies entailing new opportunities and challenges | Marangi, Giuseppe; Traynor, Bryan J. | |
| 1-gen-2021 | Genetic characterization and implications for conservation of the last autochthonous Mouflon population in Europe | Satta, V.; Mereu, P.; Barbato, Mario; Pirastru, M.; Bassu, G.; Manca, L.; Naitana, S.; Leoni, G. G. | |
| 1-gen-1996 | Genetic counseling in hereditary non-polyposis colorectal cancer | Heouaine, A; Mareni, C; Varesco, L; Genuardi, Maurizio; Neri, G | |
| 1-gen-2006 | A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability | Marroni, F; Pastrello, C; Benatti, P; Torrini, M; Barana, D; Cordisco, E; Viel, A; Mareni, C; Oliani, C; Genuardi, Maurizio; Bailey-Wilson, J; de Leon, M; Presciuttini, S | |
| 1-gen-2019 | Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths | Martinez-Matilla, M.; Blanco-Verea, A.; Santori, M.; Ansede-Bermejo, J.; Ramos-Luis, E.; Gil, R.; Bermejo, A. M.; Lotufo-Neto, F.; Hirata, M. H.; Brisighelli, Francesca; Paramo, M.; Carracedo, A.; Brion, M. | |
| 1-gen-2004 | Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer | de Leon, M; Benatti, P; Di Gregorio, C; Pedroni, M; Losi, L; Genuardi, M; Viel, A; Fornasarig, M; Lucci-Cordisco, E; Anti, M; Ponti, G; Borghi, F; Lamberti, I; Roncucci, L | |
| 1-gen-2000 | Genetic testing of cancer predisposition | Genuardi, M; Caluseriu, O; Cordisco, E; Rovella, V; Neri, G | |
| 1-gen-2020 | A genetically unique Chinese cattle population shows evidence of common ancestry with wild species when analysed with a reduced ascertainment bias SNP panel | Barbato, Mario; Reichel, M. P.; Passamonti, Matilde Maria; Low, W. Y.; Colli, Licia; Tearle, R.; Williams, John Lewis; Ajmone Marsan, Paolo | |
| 1-gen-2020 | A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis | Justice, Cm; Cuellar, A; Bala, K; Sabourin, Ja; Cunningham, Ml; Crawford, K; Phipps, Jm; Zhou, Y; Cilliers, D; Byren, Jc; Johnson, D; Wall, Sa; Morton, Jev; Noons, P; Sweeney, E; Weber, Bertram; Rees, Kem; Wilson, Lc; Simeonov, E; Kaneva, R; Yaneva, N; Georgiev, K; Bussarsky, A; Senders, C; Zwienenberg, M; Boggan, J; Roscioli, T; Tamburrini, Gianpiero; Barba, Marta; Conway, K; Sheffield, Vc; Brody, L; Mills, Jl; Kay, D; Sicko, Rj; Langlois, Ph; Tittle, Rk; Botto, Ld; Jenkins, Mm; Lasalle, Jm; Lattanzi, Wanda; Wilkie, Aom; Wilson, Af; Romitti, Pa; Boyadjiev, Sa | |
| 1-gen-2016 | Genome-wide association study of sporadic brain arteriovenous malformations | Weinsheimer, Shantel; Bendjilali, Nasrine; Nelson, Jeffrey; Guo, Diana E; Zaroff, Jonathan G; Sidney, Stephen; Mcculloch, Charles E; Al Shahi Salman, Rustam; Berg, Jonathan N; Koeleman, Bobby P. C; Simon, Matthias; Bostroem, Azize; Fontanella, Marco; Sturiale, Carmelo Lucio; Pola, Roberto; Puca, Alfredo; Lawton, Michael T; Young, William L; Pawlikowska, Ludmila; Klijn, Catharina J. M; Kim, Helen | |
| 1-gen-2016 | Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells | Tabolacci, Elisabetta; Mancano, Giorgia; Lanni, Stella; Palumbo, Federica; Goracci, Martina; Ferrè, Fabrizio; Helmer Citterich, Manuela; Neri, Giovanni | |
| 1-gen-2000 | Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts | Percesepe, A; Pedroni, M; Sala, E; Menigatti, M; Borghi, F; Losi, L; Viel, A; Genuardi, Maurizio; Benatti, P; Roncucci, L; Peltomaki, P; de Leon, M | |
| 1-gen-2008 | Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations | Vignoli, M; Scaini, M; Ghiorzo, P; Sestini, R; Bruno, W; Menin, C; Gensini, F; Piazzini, M; Testori, A; Manoukian, S; Orlando, C; D'Andrea, E; Bianchi-Scarra, G; Genuardi, Maurizio | |
| 1-gen-2017 | Genomic signatures of adaptive introgression from European mouflon into domestic sheep | Barbato, Mario; Hailer, Frank; Orozco-Terwengel, Pablo; Kijas, James; Mereu, Paolo; Cabras, Pierangela; Mazza, Raffaele; Pirastru, Monica; Bruford, Michael W. |
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