Sfoglia per ???browse.type.metadata.typeResearch??? AREA05 - SCIENZE BIOLOGICHE
A gene toolbox for monitoring autophagy transcription
2021 Bordi, Matteo; De Cegli, Rossella; Testa, Beatrice; Nixon Ralph, A.; Ballabio, Andrea; Cecconi, Francesco
Generalized EPID calibration for in vivo transit dosimetry
2011 Fidanzio, Andrea; Cilla, Savino; Azario, Luigi; Piermattei, Angelo
Generalized EPID calibration for in-vivo transit dosimetry
2009 Piermattei, Angelo; Fidanzio, Andrea; Azario, Luigi; Cilla, Savino
Generalized EPID calibration for in-vivo transit dosimetry A. Fidanzio, S. Cilla, F. Greco, L. Azario, A. Piermattei
2011 Piermattei, Angelo; Fidanzio, Andrea; Cilla, Savino; Greco, Francesca; Azario, Luigi
Generation and characterization of a human iPSC line from an ALS patient carrying the Q66K-MATR3 mutation
2018 Pollini, Daniele; Loffredo, Rosa; Cardano, Marina; Conti, Luciano; Lattante, Serena; Notarangelo, Angelantonio; Sabatelli, Mario; Provenzani, Alessandro
Generation and Release of Mitochondrial-Derived Vesicles in Health, Aging and Disease
2020 Picca, Anna; Guerra, Flora; Calvani, Riccardo; Coelho-Junior, Hélio José; Bossola, Maurizio; Landi, Francesco; Bernabei, Roberto; Bucci, Cecilia; Marzetti, Emanuele
Generation in human plasma of misfolded, aggregation-prone electronegative LDL
2009 De Spirito, Marco
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.
Generation of an induced pluripotent stem cell line (UCSCi001-A) from a patient with early-onset amyotrophic lateral sclerosis carrying a FUS variant
2021 Martello, F.; Lattante, S.; Doronzio, P. N.; Conte, A.; Bisogni, G.; Orteschi, D.; Pirozzi, F.; Sabatelli, M.; Zollino, M.; Marangi, G.
Generation of an induced pluripotent stem cell line (UCSCi002-A) from a patient with a variant in TARDBP gene associated with familial amyotrophic lateral sclerosis and frontotemporal dementia
2022 Martello, Francesco; Lattante, Serena; Doronzio, Paolo Niccolo'; Conte, A.; Bisogni, G.; Orteschi, D.; Luigetti, Marco; Marrucci, M. A.; Zollino, Marcella; Sabatelli, Mario; Marangi, Giuseppe
Genes and molecular pathways of the osteogenic process
2011 Lattanzi, Wanda; Bernardini, Camilla
Genes, pseudogenes and like genes: The case of 21-hydroxylase in Italian population
2013 Concolino, Paola; Mello Dottoressa, Enrica; Minucci, Angelo; Giardina, Bruno; Capoluongo, Ettore Domenico
Genetic advances in craniosynostosis
2017 Lattanzi, Wanda; Barba, Marta; Di Pietro, Lorena; Boyadjiev, Simeon A.
Genetic and pharmacological regulation of the endocannabinoid CB1 receptor in Duchenne muscular dystrophy
2018 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.
Genetic and phenotypic characterization of in-host developed azole-resistant aspergillus flavus isolates
2021 Buil, J. B.; Houbraken, J.; Reijers, M. H.; Zoll, J.; Sanguinetti, Maurizio; Meis, J. F.; Verweij, P. E.; Melchers, W. J. G.
Genetic and toxicologic investigation of Sudden Cardiac Death in a patient with Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) under cocaine and alcohol effects
2015 Cittadini, Francesca; De Giovanni, N; Alcalde, M; Partemi, S; Carbone, A; Campuzano, O; Brugada, R; Oliva, Antonio
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
2014 Marangi, Giuseppe; Traynor, Bj
Genetic causes of amyotrophic lateral sclerosis: New genetic analysis methodologies entailing new opportunities and challenges
2015 Marangi, Giuseppe; Traynor, Bryan J.
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
Data di pubblicazione | Titolo | Autore(i) | File |
---|---|---|---|
1-gen-2021 | A gene toolbox for monitoring autophagy transcription | Bordi, Matteo; De Cegli, Rossella; Testa, Beatrice; Nixon Ralph, A.; Ballabio, Andrea; Cecconi, Francesco | |
1-gen-2011 | Generalized EPID calibration for in vivo transit dosimetry | Fidanzio, Andrea; Cilla, Savino; Azario, Luigi; Piermattei, Angelo | |
1-gen-2009 | Generalized EPID calibration for in-vivo transit dosimetry | Piermattei, Angelo; Fidanzio, Andrea; Azario, Luigi; Cilla, Savino | |
1-gen-2011 | Generalized EPID calibration for in-vivo transit dosimetry A. Fidanzio, S. Cilla, F. Greco, L. Azario, A. Piermattei | Piermattei, Angelo; Fidanzio, Andrea; Cilla, Savino; Greco, Francesca; Azario, Luigi | |
1-gen-2018 | Generation and characterization of a human iPSC line from an ALS patient carrying the Q66K-MATR3 mutation | Pollini, Daniele; Loffredo, Rosa; Cardano, Marina; Conti, Luciano; Lattante, Serena; Notarangelo, Angelantonio; Sabatelli, Mario; Provenzani, Alessandro | |
1-gen-2020 | Generation and Release of Mitochondrial-Derived Vesicles in Health, Aging and Disease | Picca, Anna; Guerra, Flora; Calvani, Riccardo; Coelho-Junior, Hélio José; Bossola, Maurizio; Landi, Francesco; Bernabei, Roberto; Bucci, Cecilia; Marzetti, Emanuele | |
1-gen-2009 | Generation in human plasma of misfolded, aggregation-prone electronegative LDL | De Spirito, Marco | |
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-2021 | Generation of an induced pluripotent stem cell line (UCSCi001-A) from a patient with early-onset amyotrophic lateral sclerosis carrying a FUS variant | Martello, F.; Lattante, S.; Doronzio, P. N.; Conte, A.; Bisogni, G.; Orteschi, D.; Pirozzi, F.; Sabatelli, M.; Zollino, M.; Marangi, G. | |
1-gen-2022 | Generation of an induced pluripotent stem cell line (UCSCi002-A) from a patient with a variant in TARDBP gene associated with familial amyotrophic lateral sclerosis and frontotemporal dementia | Martello, Francesco; Lattante, Serena; Doronzio, Paolo Niccolo'; Conte, A.; Bisogni, G.; Orteschi, D.; Luigetti, Marco; Marrucci, M. A.; Zollino, Marcella; Sabatelli, Mario; Marangi, Giuseppe | |
1-gen-2011 | Genes and molecular pathways of the osteogenic process | Lattanzi, Wanda; Bernardini, Camilla | |
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 |
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