FANTINI, Sebastian

FANTINI, Sebastian  

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A G220V substitution within the N-terminal transcription regulating domain of HOXD13 causes a variant synpolydactyly phenotype. 1-gen-2009 Fantini, Sebastian; Vaccari, Giulia; Brison, N; Debeer, P; Tylzanowski, P; Zappavigna, Vincenzo
Control of pelvic girdle development by genes of the Pbx family and Emx2. 1-gen-2011 Capellini, Td; Handschuh, K; Quintana, L; Ferretti, E; Di Giacomo, G; Fantini, Sebastian; Vaccari, G; Clarke, Sl; Wenger, Am; Bejerano, G; Sharpe, J; Zappavigna, Vincenzo; Selleri, L.
Depletion of Trichoplein (TpMs) Causes Chromosome Mis-Segregation, DNA Damage and Chromosome Instability in Cancer Cells 1-gen-2020 Lauriola, Angela; Martello, Andrea; Fantini, Sebastian; Marverti, Gaetano; Zanocco-Marani, Tommaso; Davalli, Pierpaola; Guardavaccaro, Daniele; Mai, Sabine; Caporali, Andrea; D’Arca, Domenico
Gene expression profile correlates with molecular and clinical features in patients with myelofibrosis 1-gen-2021 Rontauroli, S.; Castellano, S.; Guglielmelli, P.; Zini, R.; Bianchi, E.; Genovese, E.; Carretta, C.; Parenti, S.; Fantini, S.; Mallia, S.; Tavernari, L.; Sartini, S.; Mirabile, M.; Mannarelli, C.; Gesullo, F.; Pacilli, A.; Pietra, D.; Rumi, E.; Salmoiraghi, S.; Mora, B.; Villani, L.; Grilli, A.; Rosti, V.; Barosi, G.; Passamonti, F.; Rambaldi, A.; Malcovati, L.; Cazzola, M.; Bicciato, S.; Tagliafico, E.; Vannucchi, A. M.; Manfredini, R.
Genomic analysis of hematopoietic stem cell at the single-cell level: Optimization of cell fixation and whole genome amplification (WGA) protocol 1-gen-2020 Carretta, C.; Mallia, S.; Genovese, E.; Parenti, S.; Rontauroli, S.; Bianchi, E.; Fantini, S.; Sartini, S.; Tavernari, L.; Tagliafico, E.; Manfredini, R.
HOX cluster-embedded micro-RNAs and cancer 1-gen-2018 Fantini, S.; Salsi, V.; Zappavigna, V.
KLF4 mediates the effect of 5-ASA on the b-catenin pathway in colon cancer cells 1-gen-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
MicroRNA-196b is transcribed from an autonomous promoter and is directly regulated by Cdx2 and by posterior Hox proteins during embryogenesis 1-gen-2015 Fantini, Sebastian; Salsi, Valentina; Vitobello, Antonio; Rijli, Filippo M.; Zappavigna, Vincenzo
The miR-196b miRNA inhibits the GATA6 intestinal transcription factor and is upregulated in colon cancer patients 1-gen-2017 Fantini, Sebastian; Salsi, Valentina; Reggiani, Luca; Maiorana, Antonino; Zappavigna, Vincenzo
Mutated clones driving leukemic transformation are already detectable at the single-cell level in CD34-positive cells in the chronic phase of primary myelofibrosis 1-gen-2021 Parenti, Sandra; Rontauroli, Sebastiano; Carretta, Chiara; Mallia, Selene; Genovese, Elena; Chiereghin, Chiara; Peano, Clelia; Tavernari, Lara; Bianchi, Elisa; Fantini, Sebastian; Sartini, Stefano; Romano, Oriana; Bicciato, Silvio; Tagliafico, Enrico; Della Porta, Matteo; Manfredini, Rossella
An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning. 1-gen-2012 Brison, N; Debeer, P; Fantini, Sebastian; Oley, C; Zappavigna, Vincenzo; Luyten, Fp; Tylzanowski, P.
NUP98 fusion oncoproteins interact with the APC/CCdc20 as a pseudosubstrate and prevent mitotic checkpoint complex binding 1-gen-2016 Salsi, Valentina; Fantini, Sebastian; Zappavigna, Vincenzo
NUP98 fusion oncoproteins promote aneuploidy by attenuating the mitotic spindle checkpoint 1-gen-2014 Salsi, Valentina; Ferrari, Silvia; Gorello, Paolo; Fantini, Sebastian; Chiavolelli, Francesca; Mecucci, Cristina; Zappavigna, Vincenzo
Physiological expression of miR-130a during differentiation of CD34+ human hematopoietic stem cells results in the inhibition of monocyte differentiation 1-gen-2019 Mammoli, F.; Parenti, S.; Lomiento, M.; Gemelli, C.; Atene, C. G.; Grande, A.; Corradini, R.; Manicardi, Agnese; Fantini, S.; Zanocco-Marani, T.; Ferrari, S.
Promoter Methylation Leads to Decreased ZFP36 Expression and Deregulated NLRP3 Inflammasome Activation in Psoriatic Fibroblasts 1-gen-2021 Bertesi, M.; Fantini, S.; Alecci, C.; Lotti, R.; Martello, A.; Parenti, S.; Carretta, C.; Marconi, A.; Grande, A.; Pincelli, C.; Zanocco Marani, T.
Scapula development is governed by genetic interactions of Pbx1 with its family members and with Emx2 via their cooperative control of Alx1 1-gen-2010 T. D., Capellini; G., Vaccari; E., Ferretti; Fantini, Sebastian; M., He; Pellegrini, Massimo; L., Quintana; G., Di Giacomo; J., Sharpe; L., Selleri; Zappavigna, Vincenzo
Wnt/CTNNB1 signal transduction pathway inhibits the expression of ZFP36 in squamous cell carcinoma, by inducing transcriptional repressors SNAI1, SLUG and TWIST 1-gen-2020 Zanfi, E. D.; Fantini, S.; Lotti, R.; Bertesi, M.; Marconi, A.; Grande, A.; Manfredini, R.; Pincelli, C.; Zanocco-Marani, T.