Sfoglia per Autore
Histone deacetylase inhibitors control the transcription and alternative splicing of prohibitin in thyroid tumor cells
2011-01-01 Puppin, Cinzia; Passon, Nadia; Franzoni, Alessandra; Russo, Diego; Damante, Giuseppe
Histone post-translational modifications associated to BAALC expression in leukemic cells.
2012-01-01 Franzoni, Alessandra; Passon, Nadia; Fabbro, Dora; Tiribelli, Mario; Damiani, Daniela; Damante, Giuseppe
ANALISI DI CARCINOMI PAPILLIFERI TIROIDEI MEDIANTE CGH-ARRAY
2013-06-05 Passon, Nadia
Somatic amplifications and deletions in genome of papillary thyroid carcinomas
2015-01-01 Passon, Nadia; Bregant, Elisa; Sponziello, Marialuisa; Dima, BIANCA ANA MARIA; Rosignolo, Francesca; Durante, Cosimo; Celano, Marilena; Russo, Diego; Filetti, Sebastiano; Damante, Giuseppe
Microdeletion 15q26.2qter and Microduplication 18q23 in a patient with prader-willi-like syndrome: Clinical findings
2016-01-01 Dello Russo, Patrizia; Demori, Eliana; Sechi, Annalisa; Passon, Nadia; Romagno, Daniela; Gnan, Chiara; Zoratti, Raffaele; Damante, Giuseppe
Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approaches
2018-01-01 Baldan, Federica; Mio, Catia; Allegri, Lorenzo; Passon, Nadia; Lepore, Saverio M.; Russo, Diego; Damante, Giuseppe
Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder
2018-01-01 Baldan, Federica; Gnan, Chiara; Franzoni, Alessandra; Ferino, Lucia; Allegri, Lorenzo; Passon, Nadia; Damante, Giuseppe
Quantitative PCR evaluation of deletions/duplications identified by array CGH
2019-01-01 Baldan, F.; Passon, N.; Burra, S.; Demori, E.; Dello Russo, P.; Damante, G.
CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers
2020-01-01 Mio, C.; Passon, N.; Baldan, F.; Bregant, E.; Monaco, E.; Mancini, L.; Demori, E.; Damante, G.
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype
2020-01-01 Mio, C.; Allegri, L.; Passon, N.; Bregant, E.; Demori, E.; Franzoni, A.; Driul, D.; Riccio, A.; Damante, G.; Baldan, F.
A case of familial brain-lung-thyroid syndrome due to a NKX2.1 run-on mutation
2022-01-01 Baldan, F; Cavaliere, E; Gortan, Aj; Passon, N; Fabbro, D; Marin, D; Carecchio, M; Credendino, Sc; Gallo, R; Cogo, P; Damante, G; De Vita, G
A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases
2024-01-01 Zucco, J.; Baldan, F.; Allegri, L.; Bregant, E.; Passon, N.; Franzoni, A.; D'Elia, A. V.; Faletra, F.; Damante, G.; Mio, C.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Histone deacetylase inhibitors control the transcription and alternative splicing of prohibitin in thyroid tumor cells | 1-gen-2011 | Puppin, Cinzia; Passon, Nadia; Franzoni, Alessandra; Russo, Diego; Damante, Giuseppe | |
| Histone post-translational modifications associated to BAALC expression in leukemic cells. | 1-gen-2012 | Franzoni, Alessandra; Passon, Nadia; Fabbro, Dora; Tiribelli, Mario; Damiani, Daniela; Damante, Giuseppe | |
| ANALISI DI CARCINOMI PAPILLIFERI TIROIDEI MEDIANTE CGH-ARRAY | 5-giu-2013 | Passon, Nadia | |
| Somatic amplifications and deletions in genome of papillary thyroid carcinomas | 1-gen-2015 | Passon, Nadia; Bregant, Elisa; Sponziello, Marialuisa; Dima, BIANCA ANA MARIA; Rosignolo, Francesca; Durante, Cosimo; Celano, Marilena; Russo, Diego; Filetti, Sebastiano; Damante, Giuseppe | |
| Microdeletion 15q26.2qter and Microduplication 18q23 in a patient with prader-willi-like syndrome: Clinical findings | 1-gen-2016 | Dello Russo, Patrizia; Demori, Eliana; Sechi, Annalisa; Passon, Nadia; Romagno, Daniela; Gnan, Chiara; Zoratti, Raffaele; Damante, Giuseppe | |
| Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approaches | 1-gen-2018 | Baldan, Federica; Mio, Catia; Allegri, Lorenzo; Passon, Nadia; Lepore, Saverio M.; Russo, Diego; Damante, Giuseppe | |
| Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder | 1-gen-2018 | Baldan, Federica; Gnan, Chiara; Franzoni, Alessandra; Ferino, Lucia; Allegri, Lorenzo; Passon, Nadia; Damante, Giuseppe | |
| Quantitative PCR evaluation of deletions/duplications identified by array CGH | 1-gen-2019 | Baldan, F.; Passon, N.; Burra, S.; Demori, E.; Dello Russo, P.; Damante, G. | |
| CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers | 1-gen-2020 | Mio, C.; Passon, N.; Baldan, F.; Bregant, E.; Monaco, E.; Mancini, L.; Demori, E.; Damante, G. | |
| A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype | 1-gen-2020 | Mio, C.; Allegri, L.; Passon, N.; Bregant, E.; Demori, E.; Franzoni, A.; Driul, D.; Riccio, A.; Damante, G.; Baldan, F. | |
| A case of familial brain-lung-thyroid syndrome due to a NKX2.1 run-on mutation | 1-gen-2022 | Baldan, F; Cavaliere, E; Gortan, Aj; Passon, N; Fabbro, D; Marin, D; Carecchio, M; Credendino, Sc; Gallo, R; Cogo, P; Damante, G; De Vita, G | |
| A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases | 1-gen-2024 | Zucco, J.; Baldan, F.; Allegri, L.; Bregant, E.; Passon, N.; Franzoni, A.; D'Elia, A. V.; Faletra, F.; Damante, G.; Mio, C. |
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