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Mostrati risultati da 1.798 a 1.817 di 4.416
Data di pubblicazione Titolo Autore(i) File
1-gen-2013 Genes, pseudogenes and like genes: The case of 21-hydroxylase in Italian population Concolino, Paola; Mello Dottoressa, Enrica; Minucci, Angelo; Giardina, Bruno; Capoluongo, Ettore Domenico
1-gen-2017 Genetic advances in craniosynostosis Lattanzi, Wanda; Barba, Marta; Di Pietro, Lorena; Boyadjiev, Simeon A.
1-gen-2018 Genetic and pharmacological regulation of the endocannabinoid CB1 receptor in Duchenne muscular dystrophy Iannotti, F. A.; Pagano, E.; Guardiola, O.; Adinolfi, S.; Saccone, V.; Consalvi, S.; Piscitelli, F.; Gazzerro, E.; Busetto, G.; Carrella, D.; Capasso, R.; Puri, P. L.; Minchiotti, G.; Di Marzo, V.
1-gen-2021 Genetic and phenotypic characterization of in-host developed azole-resistant aspergillus flavus isolates Buil, J. B.; Houbraken, J.; Reijers, M. H.; Zoll, J.; Sanguinetti, Maurizio; Meis, J. F.; Verweij, P. E.; Melchers, W. J. G.
1-gen-2015 Genetic and toxicologic investigation of Sudden Cardiac Death in a patient with Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) under cocaine and alcohol effects Cittadini, Francesca; De Giovanni, N; Alcalde, M; Partemi, S; Carbone, A; Campuzano, O; Brugada, R; Oliva, Antonio
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-2014 Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges Marangi, Giuseppe; Traynor, Bj
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-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, Angela; Camassa, Maria Serena; Sali, Michela; Butera, Ornella; Mazzarelli, Antonio; Sanguinetti, Maurizio; Di Caro, Antonino; Delogu, Giovanni; Girardi, Enrico
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-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.
Mostrati risultati da 1.798 a 1.817 di 4.416
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