EnglishFANTINI, Sebastian
Risultati 1 - 8 di 8 (tempo di esecuzione: 0.001 secondi).
| Titolo | Data di pubblicazione | Autore(i) | |
|---|---|---|---|
| 1 | Scapula development is governed by genetic interactions of Pbx1 with its family members and with Emx2 via their cooperative control of Alx1 | 2010 | Capellini, T. D.; Vaccari, G.; Ferretti, E.; Fantini, Sebastian; He, M.; Pellegrini, Massimo; Quintana, L.; Di Giacomo, G.; Sharpe, J.; Selleri, L.; Zappavigna, Vincenzo |
| 2 | NUP98 fusion oncoproteins interact with the APC/CCdc20 as a pseudosubstrate and prevent mitotic checkpoint complex binding | 2016 | Salsi, Valentina; Fantini, Sebastian; Zappavigna, Vincenzo |
| 3 | An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning. | 2012 | Brison N;Debeer P;Fantini S;Oley C;Zappavigna V;Luyten FP;Tylzanowski P |
| 4 | The miR-196b miRNA inhibits the GATA6 intestinal transcription factor and is upregulated in colon cancer patients | 2017 | Fantini, Sebastian; Salsi, Valentina; Reggiani, Luca; Maiorana, Antonino; Zappavigna, Vincenzo |
| 5 | MicroRNA-196b is transcribed from an autonomous promoter and is directly regulated by Cdx2 and by posterior Hox proteins during embryogenesis | 2015 | Fantini, Sebastian; Salsi, Valentina; Vitobello, Antonio; Rijli, Filippo M.; Zappavigna, Vincenzo |
| 6 | KLF4 mediates the effect of 5-ASA on the b-catenin pathway in colon cancer cells | 2018 | Parenti, Sandra; Montorsi, Lucia; Fantini, Sebastian; Mammoli, Fabiana; Gemelli, Claudia; Atene, Claudio Giacinto; Losi, Lorena; Frassineti, Chiara; Calabretta, Bruno; Tagliafico, Enrico; Ferrari, Sergio; Zanocco-Marani, Tommaso; Grande, Alexis |
| 7 | Control of pelvic girdle development by genes of the Pbx family and Emx2. | 2011 | Capellini TD;Handschuh K;Quintana L;Ferretti E;Di Giacomo G;Fantini S;Vaccari G;Clarke SL;Wenger AM;Bejerano G;Sharpe J;Zappavigna V;Selleri L |
| 8 | A G220V substitution within the N-terminal transcription regulating domain of HOXD13 causes a variant synpolydactyly phenotype. | 2009 | Fantini S; Vaccari G; Brison N; Debeer P; Tylzanowski P; Zappavigna V. |
Nome completo:
FANTINI, Sebastian
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