Sfoglia per ???browse.type.metadata.typeResearch??? AREA05 - SCIENZE BIOLOGICHE
Genetic basis of single-suture synostoses: genes, chromosomes and clinical implications
2012 Lattanzi, Wanda; Bukvic, N; Barba, Marta; Tamburrini, Gianpiero; Bernardini, Camilla; Michetti, Fabrizio; Di Rocco, Concezio
Genetic causes of amyotrophic lateral sclerosis: New genetic analysis methodologies entailing new opportunities and challenges
2015 Marangi, Giuseppe; Traynor, Bryan J.
Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges
2014 Marangi, Giuseppe; Traynor, Bj
Genetic Characterization of a Cohort of Italian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
2023 Concolinopaola, ; Perrucci, Alessia; Carrozza, Cinzia; Urbani, Andrea
Genetic counselling in ALS: facts, uncertainties and clinical suggestions
2014 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; Conte, Amelia; Luigetti, Marco; Lattante, Serena; Marangi, Giuseppe
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.
Genetic deletion of α7 nicotinic acetylcholine receptors induces an age-dependent Alzheimer's disease-like pathology
2021 Tropea, M. R.; Li Puma, Domenica Donatella; Melone, M.; Gulisano, W.; Arancio, O.; Grassi, Claudio; Conti, F.; Puzzo, D.
Genetic Diversity of Mycobacterium tuberculosis Isolates in the Metropolitan Area of Rome
2018 Cannas, A.; Camassa, Maria Serena; Sali, Michela; Butera, O.; Mazzarelli, A.; Sanguinetti, Maurizio; Di Caro, A.; Delogu, Giovanni; Girardi, E.
Genetic Diversity of Mycobacterium tuberculosis Isolates in the Metropolitan Area of Rome
2018 Cannas, Angela; Camassa, Maria Serena; Sali, Michela; Butera, Ornella; Mazzarelli, Antonio; Sanguinetti, Maurizio; Di Caro, Antonino; Delogu, Giovanni; Girardi, Enrico
Genetic Engineering of Dystroglycan in Animal Models of Muscular Dystrophy
2015 Sciandra, Francesca; Bigotti, Maria Giulia; Giardina, Bruno; Bozzi, Manuela; Brancaccio, Andrea
Genetic imprinting:the paradigm of Prader Willi and Angelman syndromes
2009 Gurrieri, Fiorella; Accadia, Maria Rosaria
Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing
2016 Coll, Monica; Allegue, Catarina; Partemi, Sara; Mates, Jesus; Del Olmo, Bernat; Campuzano, Oscar; Pascali, Vincenzo Lorenzo; Iglesias, Anna; Striano, Pasquale; Oliva, Antonio; Brugada, Ramon
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.
Genistein affects adipose tissue deposition in a dose-dependent and gender-specific manner
2006 Penza, M; Montani, C; Romani, A; Vignolini, P; Pampaloni, B; Tanini, A; Brandi, M. L; Alonso Magdalena, P; Nadal, A; Ottobrini, L; Parolini, Ornella; Bignotti, E; Calza, S; Maggi, Aldo Marco; Grigolato, P. G; Di Lorenzo, Andrea Alessandro Daniele
Genome-wide analyses of platinum-induced ototoxicity in childhood cancer patients: Results of GO-CAT and United Kingdom MAGIC consortia
2023 Hurkmans, E. G. E.; Klumpers, M. J.; Dello Russo, Cinzia; De Witte, W.; Guchelaar, H. -J.; Gelderblom, H.; Cleton-Jansen, A. -M.; Vermeulen, S. H.; Kaal, S.; van der Graaf, W. T. A.; Flucke, U.; Gidding, C. E. M.; Schreuder, H. W. B.; de Bont, E. S. J. M.; Caron, H. N.; Gattuso, G.; Schiavello, E.; Terenziani, M.; Massimino, M.; Mccowage, G.; Nagabushan, S.; Limaye, A.; Rose, V.; Catchpoole, D.; Jorgensen, A. L.; Barton, C.; Delaney, L.; Hawcutt, D. B.; Pirmohamed, M.; Pizer, B.; Coenen, M. J. H.; te Loo, D. M. W. M.
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
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
Genome-wide expression profiling of the response to short-term exposure to fluconazole in Cryptococcus neoformans serotype A
2011 Florio, Ar; Ferrari, S; De Carolis, Elena; Torelli, Riccardo; Fadda, Giovanni; Sanguinetti, Maurizio; Sanglard, D; Posteraro, Brunella
Genome-Wide Gene Expression Profiling of Human Narcolepsy
2012 Bernardini, Camilla; Lattanzi, Wanda; Bosco, P; Franceschini, C; Plazzi, G; Michetti, Fabrizio; Ferri, R.
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome.
2009 Neri, Giovanni
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-2012 | Genetic basis of single-suture synostoses: genes, chromosomes and clinical implications | Lattanzi, Wanda; Bukvic, N; Barba, Marta; Tamburrini, Gianpiero; Bernardini, Camilla; Michetti, Fabrizio; Di Rocco, Concezio | |
| 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-2014 | Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges | Marangi, Giuseppe; Traynor, Bj | |
| 1-gen-2023 | Genetic Characterization of a Cohort of Italian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency | Concolinopaola, ; Perrucci, Alessia; Carrozza, Cinzia; Urbani, Andrea | |
| 1-gen-2014 | 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; Conte, Amelia; Luigetti, Marco; Lattante, Serena; Marangi, Giuseppe | |
| 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-2021 | Genetic deletion of α7 nicotinic acetylcholine receptors induces an age-dependent Alzheimer's disease-like pathology | Tropea, M. R.; Li Puma, Domenica Donatella; Melone, M.; Gulisano, W.; Arancio, O.; Grassi, Claudio; Conti, F.; Puzzo, D. | |
| 1-gen-2018 | Genetic Diversity of Mycobacterium tuberculosis Isolates in the Metropolitan Area of Rome | Cannas, A.; Camassa, Maria Serena; Sali, Michela; Butera, O.; Mazzarelli, A.; Sanguinetti, Maurizio; Di Caro, A.; Delogu, Giovanni; Girardi, E. | |
| 1-gen-2018 | Genetic Diversity of Mycobacterium tuberculosis Isolates in the Metropolitan Area of Rome | Cannas, Angela; Camassa, Maria Serena; Sali, Michela; Butera, Ornella; Mazzarelli, Antonio; Sanguinetti, Maurizio; Di Caro, Antonino; Delogu, Giovanni; Girardi, Enrico | |
| 1-gen-2015 | Genetic Engineering of Dystroglycan in Animal Models of Muscular Dystrophy | Sciandra, Francesca; Bigotti, Maria Giulia; Giardina, Bruno; Bozzi, Manuela; Brancaccio, Andrea | |
| 1-gen-2009 | Genetic imprinting:the paradigm of Prader Willi and Angelman syndromes | Gurrieri, Fiorella; Accadia, Maria Rosaria | |
| 1-gen-2016 | Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing | Coll, Monica; Allegue, Catarina; Partemi, Sara; Mates, Jesus; Del Olmo, Bernat; Campuzano, Oscar; Pascali, Vincenzo Lorenzo; Iglesias, Anna; Striano, Pasquale; Oliva, Antonio; Brugada, Ramon | |
| 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-2006 | Genistein affects adipose tissue deposition in a dose-dependent and gender-specific manner | Penza, M; Montani, C; Romani, A; Vignolini, P; Pampaloni, B; Tanini, A; Brandi, M. L; Alonso Magdalena, P; Nadal, A; Ottobrini, L; Parolini, Ornella; Bignotti, E; Calza, S; Maggi, Aldo Marco; Grigolato, P. G; Di Lorenzo, Andrea Alessandro Daniele | |
| 1-gen-2023 | Genome-wide analyses of platinum-induced ototoxicity in childhood cancer patients: Results of GO-CAT and United Kingdom MAGIC consortia | Hurkmans, E. G. E.; Klumpers, M. J.; Dello Russo, Cinzia; De Witte, W.; Guchelaar, H. -J.; Gelderblom, H.; Cleton-Jansen, A. -M.; Vermeulen, S. H.; Kaal, S.; van der Graaf, W. T. A.; Flucke, U.; Gidding, C. E. M.; Schreuder, H. W. B.; de Bont, E. S. J. M.; Caron, H. N.; Gattuso, G.; Schiavello, E.; Terenziani, M.; Massimino, M.; Mccowage, G.; Nagabushan, S.; Limaye, A.; Rose, V.; Catchpoole, D.; Jorgensen, A. L.; Barton, C.; Delaney, L.; Hawcutt, D. B.; Pirmohamed, M.; Pizer, B.; Coenen, M. J. H.; te Loo, D. M. W. M. | |
| 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-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 | Genome-wide expression profiling of the response to short-term exposure to fluconazole in Cryptococcus neoformans serotype A | Florio, Ar; Ferrari, S; De Carolis, Elena; Torelli, Riccardo; Fadda, Giovanni; Sanguinetti, Maurizio; Sanglard, D; Posteraro, Brunella | |
| 1-gen-2012 | Genome-Wide Gene Expression Profiling of Human Narcolepsy | Bernardini, Camilla; Lattanzi, Wanda; Bosco, P; Franceschini, C; Plazzi, G; Michetti, Fabrizio; Ferri, R. | |
| 1-gen-2009 | Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome. | Neri, Giovanni |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile