BIONE, SILVIA
BIONE, SILVIA
Istituto di Genetica Molecolare "Luigi Luca Cavalli Sforza"
A comparative transcriptional map of a region of 250 kb on the human and mouse X chromosome between the G6PD and the FLN1 genes.
1995 Rivella S; Tamanini F; Bione S; Mancini M; Herman G; Chatterjee A; Maestrini E; Toniolo D.
A family of transmembrane proteins with homology to the MET-hepatocyte growth factor receptor.
1996 Maestrini E; Tamagnone L; Longati P; Cremona O; Gulisano M; Bione S; Tamanini F; Neel BG; Toniolo D; Comoglio PM.
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility.
1998 Bione S; Sala C; Manzini C; Arrigo G; Zuffardi O; Banfi S; Borsani G; Jonveaux P; Philippe C; Zuccotti M; Ballabio A; Toniolo D.
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure.
2009 Corre, T; Schuettler, J; Bione, S; Marozzi, A; Persani, L; Rossetti, R; Torricelli, F; Giotti, I; Vogt, P; Toniolo, D; on behalf of the Italian Network for the study of Ovarian, Dysfunctions
A mutation in the X-linked Emery-Dreifuss muscular dystrophy gene in a patient affected with conduction cardiomyopathy
2001 Vohanka, S; Vytopil, M; Bednarik, J; Lukas, Z; Kadanka, Z; Schildberger, J; Ricotti, R; Bione, S; Toniolo, D
A new system biology approach to mine expression data from gene functional analysis.
2013 Cremaschi, P; Rovida, S; Colì, C; Carriero, R; Sacchi, L; Lisa, A; Sacchi, G; Bione, S
A novel X-linked gene, G4.5. is responsible for Barth syndrome.
1996 Bione S; D'Adamo P; Maestrini E; Gedeon AK; Bolhuis PA; Toniolo D.
A susceptibility gene for premature ovarian failure (POF) maps to proximal Xq28.
2004 Rossetti F; Rizzolio F; Pramparo T; Sala C; Bione S; Bernardi F; Goegan M; Zuffardi O; Toniolo D.
Alterations in the expression, structure and function of Progesterone Receptor Membrane Component-1 (PGRMC1) in premature ovarian failure.
2008 Mansouri MR; Schuster J; Badhai J; Stattin EL; Losel R; Wehling M; Carlsson B; Hovatta O; Karlstrom PO; Golovleva I; Toniolo D; Bione S; Peluso J; Dahl N.
Alternative Splicing Changes Promoted by NOVA2 Upregulation in Endothelial Cells and Relevance for Gastric Cancer
2023 Di Matteo, A; Belloni, E; Pradella, D; Chiaravalli, Am; Pini, Gm; Bugatti, M; Alfieri, R; Barzan, C; Franganillo Tena, E; Bione, S; Terenzani, E; Sessa, F; Wyatt, Cdr; Vermi, W; Ghigna, C
An Association Rule Mining Approach to Discover lncRNAs Expression Patterns in Cancer Datasets.
2015 Cremaschi, P; Carriero, R; Astrologo, S; Colì, C; Lisa, A; Parolo, S; Bione, S
An X chromosome-linked gene encoding a protein with characteristics of a rhoGAP predominantly expressed in hematopoietic cells.
1996 Tribioli, C; Droetto, S; Bione, S; Cesareni, G; Torrisi, Mr; Lotti, Lv; Lanfrancone, L; Toniolo, D; Pelicci, P
Analysis of intergenic conserved sequences in the POF critical region on X chromosome
2003 C. Sala; F. Rizzolio; P. Magni; C. Larizza; R. Sozzi; A. Nuzzo; S. Bione; F. Rossetti; R. Bellazzi; D. Toniolo
Are myocardial infarction-associated single nucleotide polymorphisms associated with ischemic stroke?
2012 Cheng, Yc; Anderson, Cd; Bione, S; Keene, K; Maguire, Jm; Nalls, M; Rasheed, A; Zeginigg, M; Attia, J; Baker, R; Barlera, S; Biffi, A; Bookman, E; Brott, Tg; Brown RD, Jr; Chen, F; Chen, Wm; Ciusani, E; Cole, Jw; Cortellini, L; Danesh, J; Doheny, K; Ferrucci, L; Grazia Franzosi, M; Frossard, P; Furie, Kl; Golledge, J; Hankey, Gj; Hernandez, D; Holliday, Eg; Hsu, Fc; Jannes, J; Kamal, A; Khan, Ms; Kittner, Sj; Koblar, Sa; Lewis, M; Lincz, L; Lisa, A; Matarin, M; Moscato, P; Mychaleckyj, Jc; Parati, Ea; Parolo, S; Pugh, E; Rost, Ns; Schallert, M; Schmidt, H; Scott, Rj; Sturm, Jw; Yadav, S; Zaidi, M; Boncoraglio, Gb; Levi, Cr; Meschia, Jf; Rosand, J; Sale, M; Saleheen, D; Schmidt, R; Sharma, P; Worrall, B; Mitchell, Bd; GARNET Collaborative Research, Group; Geneva, Consortium; on behalf of the International Stroke Genetics, Consortium
Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population.
2011 Sorice, R; Bione, S; Sansanelli, S; Ulivi, S; Athanasakis, E; Lanzara, C; Nutile, T; Sala, C; Camaschella, C; D'Adamo, P; Gasparini, P; Ciullo, M; Toniolo, D
Association studies of candidate genes for Premature Ovarian Failure (POF)
2007 Bione, S; Rizzolio, F; Corre, T; Sala, C; Testa, M; Ricotti, R; Marozzi, A; Persani, L; Zuffardi, O; Toniolo, D
Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype
2019 Theil, Af; Botta, E; Raams, A; Smith, Dec; Mendes, Mi; Caligiuri, G; Giachetti, S; Bione, S; Carriero, R; Liberi, G; Zardoni, L; Swagemakers, Sma; Salomons, Gs; Sarasin, A; Lehmann, A; van der Spek, Pj; Ogi, T; Hoeijmakers, Jhj; Vermeulen, W; Orioli, D
BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein.
2009 Rossetti, R; Di Pasquale, E; Marozzi, A; Bione, S; Toniolo, D; Grammatico, P; Nelson, Lm; Beckpeccoz, P; Persani, L
CABGen: new bioinformatic resources at IGM-CNR.
2011 Bione, S; Sacchi, G; Cavallisforza, Ll; Fiorani, O; Zei, G; Parolo, S; Biamonti, G; Lisa, A
Cell migration and cell cycle genes are highly modulated during neoplastic transformation of human fibroblasts
2011 Ostano, P; Bione, S; Belgiovine, C; Chiodi, I; Chiorino, G; Mondello, C
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A comparative transcriptional map of a region of 250 kb on the human and mouse X chromosome between the G6PD and the FLN1 genes. | 1-gen-1995 | Rivella S; Tamanini F; Bione S; Mancini M; Herman G; Chatterjee A; Maestrini E; Toniolo D. | |
| A family of transmembrane proteins with homology to the MET-hepatocyte growth factor receptor. | 1-gen-1996 | Maestrini E; Tamagnone L; Longati P; Cremona O; Gulisano M; Bione S; Tamanini F; Neel BG; Toniolo D; Comoglio PM. | |
| A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility. | 1-gen-1998 | Bione S; Sala C; Manzini C; Arrigo G; Zuffardi O; Banfi S; Borsani G; Jonveaux P; Philippe C; Zuccotti M; Ballabio A; Toniolo D. | |
| A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure. | 1-gen-2009 | Corre, T; Schuettler, J; Bione, S; Marozzi, A; Persani, L; Rossetti, R; Torricelli, F; Giotti, I; Vogt, P; Toniolo, D; on behalf of the Italian Network for the study of Ovarian, Dysfunctions | |
| A mutation in the X-linked Emery-Dreifuss muscular dystrophy gene in a patient affected with conduction cardiomyopathy | 1-gen-2001 | Vohanka, S; Vytopil, M; Bednarik, J; Lukas, Z; Kadanka, Z; Schildberger, J; Ricotti, R; Bione, S; Toniolo, D | |
| A new system biology approach to mine expression data from gene functional analysis. | 1-gen-2013 | Cremaschi, P; Rovida, S; Colì, C; Carriero, R; Sacchi, L; Lisa, A; Sacchi, G; Bione, S | |
| A novel X-linked gene, G4.5. is responsible for Barth syndrome. | 1-gen-1996 | Bione S; D'Adamo P; Maestrini E; Gedeon AK; Bolhuis PA; Toniolo D. | |
| A susceptibility gene for premature ovarian failure (POF) maps to proximal Xq28. | 1-gen-2004 | Rossetti F; Rizzolio F; Pramparo T; Sala C; Bione S; Bernardi F; Goegan M; Zuffardi O; Toniolo D. | |
| Alterations in the expression, structure and function of Progesterone Receptor Membrane Component-1 (PGRMC1) in premature ovarian failure. | 1-gen-2008 | Mansouri MR; Schuster J; Badhai J; Stattin EL; Losel R; Wehling M; Carlsson B; Hovatta O; Karlstrom PO; Golovleva I; Toniolo D; Bione S; Peluso J; Dahl N. | |
| Alternative Splicing Changes Promoted by NOVA2 Upregulation in Endothelial Cells and Relevance for Gastric Cancer | 1-gen-2023 | Di Matteo, A; Belloni, E; Pradella, D; Chiaravalli, Am; Pini, Gm; Bugatti, M; Alfieri, R; Barzan, C; Franganillo Tena, E; Bione, S; Terenzani, E; Sessa, F; Wyatt, Cdr; Vermi, W; Ghigna, C | |
| An Association Rule Mining Approach to Discover lncRNAs Expression Patterns in Cancer Datasets. | 1-gen-2015 | Cremaschi, P; Carriero, R; Astrologo, S; Colì, C; Lisa, A; Parolo, S; Bione, S | |
| An X chromosome-linked gene encoding a protein with characteristics of a rhoGAP predominantly expressed in hematopoietic cells. | 1-gen-1996 | Tribioli, C; Droetto, S; Bione, S; Cesareni, G; Torrisi, Mr; Lotti, Lv; Lanfrancone, L; Toniolo, D; Pelicci, P | |
| Analysis of intergenic conserved sequences in the POF critical region on X chromosome | 1-gen-2003 | C. Sala; F. Rizzolio; P. Magni; C. Larizza; R. Sozzi; A. Nuzzo; S. Bione; F. Rossetti; R. Bellazzi; D. Toniolo | |
| Are myocardial infarction-associated single nucleotide polymorphisms associated with ischemic stroke? | 1-gen-2012 | Cheng, Yc; Anderson, Cd; Bione, S; Keene, K; Maguire, Jm; Nalls, M; Rasheed, A; Zeginigg, M; Attia, J; Baker, R; Barlera, S; Biffi, A; Bookman, E; Brott, Tg; Brown RD, Jr; Chen, F; Chen, Wm; Ciusani, E; Cole, Jw; Cortellini, L; Danesh, J; Doheny, K; Ferrucci, L; Grazia Franzosi, M; Frossard, P; Furie, Kl; Golledge, J; Hankey, Gj; Hernandez, D; Holliday, Eg; Hsu, Fc; Jannes, J; Kamal, A; Khan, Ms; Kittner, Sj; Koblar, Sa; Lewis, M; Lincz, L; Lisa, A; Matarin, M; Moscato, P; Mychaleckyj, Jc; Parati, Ea; Parolo, S; Pugh, E; Rost, Ns; Schallert, M; Schmidt, H; Scott, Rj; Sturm, Jw; Yadav, S; Zaidi, M; Boncoraglio, Gb; Levi, Cr; Meschia, Jf; Rosand, J; Sale, M; Saleheen, D; Schmidt, R; Sharma, P; Worrall, B; Mitchell, Bd; GARNET Collaborative Research, Group; Geneva, Consortium; on behalf of the International Stroke Genetics, Consortium | |
| Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population. | 1-gen-2011 | Sorice, R; Bione, S; Sansanelli, S; Ulivi, S; Athanasakis, E; Lanzara, C; Nutile, T; Sala, C; Camaschella, C; D'Adamo, P; Gasparini, P; Ciullo, M; Toniolo, D | |
| Association studies of candidate genes for Premature Ovarian Failure (POF) | 1-gen-2007 | Bione, S; Rizzolio, F; Corre, T; Sala, C; Testa, M; Ricotti, R; Marozzi, A; Persani, L; Zuffardi, O; Toniolo, D | |
| Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype | 1-gen-2019 | Theil, Af; Botta, E; Raams, A; Smith, Dec; Mendes, Mi; Caligiuri, G; Giachetti, S; Bione, S; Carriero, R; Liberi, G; Zardoni, L; Swagemakers, Sma; Salomons, Gs; Sarasin, A; Lehmann, A; van der Spek, Pj; Ogi, T; Hoeijmakers, Jhj; Vermeulen, W; Orioli, D | |
| BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein. | 1-gen-2009 | Rossetti, R; Di Pasquale, E; Marozzi, A; Bione, S; Toniolo, D; Grammatico, P; Nelson, Lm; Beckpeccoz, P; Persani, L | |
| CABGen: new bioinformatic resources at IGM-CNR. | 1-gen-2011 | Bione, S; Sacchi, G; Cavallisforza, Ll; Fiorani, O; Zei, G; Parolo, S; Biamonti, G; Lisa, A | |
| Cell migration and cell cycle genes are highly modulated during neoplastic transformation of human fibroblasts | 1-gen-2011 | Ostano, P; Bione, S; Belgiovine, C; Chiodi, I; Chiorino, G; Mondello, C |