FABBRO, Dora
FABBRO, Dora
DSMB - DIPARTIMENTO DI SCIENZE MEDICHE E BIOLOGICHE (attivo dal 01/01/2011 al 31/12/2016)
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 deletion 3' to the PAX6 gene in familial aniridia cases
2007-01-01 D'Elia, Av; Pellizzari, Lucia; Fabbro, Dora; Pianta, Annalisa; Divizia, Mt; Rinaldi, R; Grammatico, B; Grammatico, P; Arduino, C; Damante, Giuseppe
BAALC overexpression retains its negative prognostic role across all cytogenetic risk groups in acute myeloid leukemia patients
2013-01-01 Damiani, Daniela; Tiribelli, Mario; Franzoni, A; Michelutti, A; Fabbro, Dora; Cavallin, M; Toffoletti, Eleonora; Simeone, Erica; Fanin, Renato; Damante, Giuseppe
EGFR expression is linked to osteopontin and Nf-κB signaling in clear cell renal cell carcinoma.
2013-01-01 Matušan Ilijaš, K; Damante, Giuseppe; Fabbro, Dora; Dorđević, G; Hadžisejdić, I; Grahovac, M; Avirović, M; Grahovac, B; Jonjić, N; Lučin, K.
FREQUENCY OF FACTOR V, PROTHROMBIN AND METHYLENETETRAHYDROFOLATE REDUCTASE GENE VARIANTS IN PREECLAMPSIA
2002-01-01 D'Elia, Angela Valentina; Driul, Lorenza; Giacomello, Roberta; Colaone, Roberta; Fabbro, Dora; DI LEONARDO, Cristina; Florio, Pietro; Petraglia, F.; Marchesoni, Diego; Damante, Giuseppe
Functional analysis of a novel RUNX2 missense mutation found in a family with cleidocranial dysplasia
2005-01-01 Puppin, C; Pellizzari, L; Fabbro, D; Fogolari, F; Tell, G; Tessa, A; Santorelli, F. M.; Damante, G
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
Immunoglobulin K light chain deficiency: A rare, but probably underestimated, humoral immune defect
2016-01-01 Sala, Pierguido; Colatutto, Antonio; Fabbro, Dora; Mariuzzi, Laura; Marzinotto, Stefania; Toffoletto, Barbara; Perosa, Anna R.; Damante, Giuseppe
Investigation of endothelin-1 type A receptor gene polymorphism (-231 G>A) in preeclampsia susceptibility
2007-01-01 Clementi, M; Damante, Giuseppe; Fabbro, Dora; Fantinato, S.; Leon, A; Lisi, V; Micciche', F; Paternoster, D. M.; Stecca, A.
Mutations R67X and W303X of the protein Z-dependent protease inhibitor gene and venous thromboembolic disease: a case-control study in Italian subjects
2007-01-01 Fabbro, Dora; Barillari, G; Damante, Giuseppe
Osteopontin expression is an independent factor for poor survival in oral squamous cell carcinoma: a computer-assisted analysis on TMA sections.
2013-01-01 Avirović, M; Matušan Ilijaš, K; Damante, Giuseppe; Fabbro, Dora; Cerović, R; Juretić, M; Grahovac, B; Jonjić, N; Lučin, K.
Using the AlphaFold system to the interpretation of variants of uncertain significance
2023-01-01 Franzoni, A; Driul, D; Passon, N; Fabbro, D; Baldan, F; Cogo, P; Fogolari, F; Damante, G
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 deletion 3' to the PAX6 gene in familial aniridia cases | 1-gen-2007 | D'Elia, Av; Pellizzari, Lucia; Fabbro, Dora; Pianta, Annalisa; Divizia, Mt; Rinaldi, R; Grammatico, B; Grammatico, P; Arduino, C; Damante, Giuseppe | |
| BAALC overexpression retains its negative prognostic role across all cytogenetic risk groups in acute myeloid leukemia patients | 1-gen-2013 | Damiani, Daniela; Tiribelli, Mario; Franzoni, A; Michelutti, A; Fabbro, Dora; Cavallin, M; Toffoletti, Eleonora; Simeone, Erica; Fanin, Renato; Damante, Giuseppe | |
| EGFR expression is linked to osteopontin and Nf-κB signaling in clear cell renal cell carcinoma. | 1-gen-2013 | Matušan Ilijaš, K; Damante, Giuseppe; Fabbro, Dora; Dorđević, G; Hadžisejdić, I; Grahovac, M; Avirović, M; Grahovac, B; Jonjić, N; Lučin, K. | |
| FREQUENCY OF FACTOR V, PROTHROMBIN AND METHYLENETETRAHYDROFOLATE REDUCTASE GENE VARIANTS IN PREECLAMPSIA | 1-gen-2002 | D'Elia, Angela Valentina; Driul, Lorenza; Giacomello, Roberta; Colaone, Roberta; Fabbro, Dora; DI LEONARDO, Cristina; Florio, Pietro; Petraglia, F.; Marchesoni, Diego; Damante, Giuseppe | |
| Functional analysis of a novel RUNX2 missense mutation found in a family with cleidocranial dysplasia | 1-gen-2005 | Puppin, C; Pellizzari, L; Fabbro, D; Fogolari, F; Tell, G; Tessa, A; Santorelli, F. M.; Damante, G | |
| 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 | |
| Immunoglobulin K light chain deficiency: A rare, but probably underestimated, humoral immune defect | 1-gen-2016 | Sala, Pierguido; Colatutto, Antonio; Fabbro, Dora; Mariuzzi, Laura; Marzinotto, Stefania; Toffoletto, Barbara; Perosa, Anna R.; Damante, Giuseppe | |
| Investigation of endothelin-1 type A receptor gene polymorphism (-231 G>A) in preeclampsia susceptibility | 1-gen-2007 | Clementi, M; Damante, Giuseppe; Fabbro, Dora; Fantinato, S.; Leon, A; Lisi, V; Micciche', F; Paternoster, D. M.; Stecca, A. | |
| Mutations R67X and W303X of the protein Z-dependent protease inhibitor gene and venous thromboembolic disease: a case-control study in Italian subjects | 1-gen-2007 | Fabbro, Dora; Barillari, G; Damante, Giuseppe | |
| Osteopontin expression is an independent factor for poor survival in oral squamous cell carcinoma: a computer-assisted analysis on TMA sections. | 1-gen-2013 | Avirović, M; Matušan Ilijaš, K; Damante, Giuseppe; Fabbro, Dora; Cerović, R; Juretić, M; Grahovac, B; Jonjić, N; Lučin, K. | |
| Using the AlphaFold system to the interpretation of variants of uncertain significance | 1-gen-2023 | Franzoni, A; Driul, D; Passon, N; Fabbro, D; Baldan, F; Cogo, P; Fogolari, F; Damante, G |