ZAPPAVIGNA, Vincenzo
ZAPPAVIGNA, Vincenzo
Dipartimento di Scienze della Vita
A cup full of functions
2005 Piccioni, F.; Zappavigna, Vincenzo; Verrotti, A.
A G220V substitution within the N-terminal transcription regulating domain of HOXD13 causes a variant synpolydactyly phenotype.
2009 Fantini, Sebastian; Vaccari, Giulia; Brison, N; Debeer, P; Tylzanowski, P; Zappavigna, Vincenzo
A novel homeo-domain protein, prep 1, forms a regulatory complex with pbx proteins in vivo
1997 Berthelsen, J.; Zappavigna, V.; Mavilio, F.; Blasi, F.
An 147L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of function
2003 G., Caronia; F. R., Goodman; C. M. E., Mckeown; P. J., Scambler; Zappavigna, Vincenzo
An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning.
2012 Brison, N; Debeer, P; Fantini, Sebastian; Oley, C; Zappavigna, Vincenzo; Luyten, Fp; Tylzanowski, P.
Cellule e segnali
2012 Marigo, Valeria; Zappavigna, Vincenzo
Characterization of PREP2, a paralog of PREP1, which defines a novel sub-family of the MEINOX TALE homeodomain transcription factors
2002 Fognani, C; KILSTRUP NIELSEN, C; Berthelsen, J; Ferretti, E; Zappavigna, Vincenzo; Blasi, F.
Comparison of mouse and human HOX-4 complexes defines conserved sequences involved in the regulation of Hox-4.4
1992 Renucci, A.; Zappavigna, V.; Zakany, J.; Izpisua-Belmonte, J. -C.; Burki, K.; Duboule, D.
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, Sebastian; Vaccari, G; Clarke, Sl; Wenger, Am; Bejerano, G; Sharpe, J; Zappavigna, Vincenzo; Selleri, L.
Control of vertebrate limb outgrowth by the proximal factor Meis2 and distal antagonism of BMPs by Gremlin
1999 Capdevila, J.; Tsukui, T.; Esteban, C. R.; Zappavigna, V.; Belmonte, J. C. I.
Corrigendum: ‘Building a perfect body’: Control of vertebrate organogenesis by PBX-dependent regulatory networks (Genes & Development 33: 258–275 (2019)
2019 Selleri, L.; Zappavigna, V.; Ferretti, E.
Cup is a nucleocytoplasmic shuttling protein that interacts with the eukaryotic translation initiation factor 4E to modulate Drosophila ovary development
2004 Zappavigna, Vincenzo; F., Piccioni; Jc, Villaescusa; Ac, Verrotti
Definition of the transcriptional activation domains of three human HOX proteins depends on the DNA-Binding context
1998 Ma, Vigano'; G., DI ROCCO; Zappavigna, Vincenzo; Mavilio, Fulvio
Developed to cull: How a master control gene of development turned into a regulator of innate immune homeostasis
2008 Zappavigna, V.
Differential and stage-related expression in embryonic tissues of a new human homoeobox gene
1986 Mavilio, F.; Simeone, A.; Giampaolo, A.; Faiella, A.; Zappavigna, V.; Acampora, D.; Poiana, G.; Russo, G.; Peschle, C.; Boncinelli, E.
Differential expression of human HOX-2 genes along the anterior-posterior axis in embryonic central nervous system
1989 Giampaolo, A.; Acampora, D.; Zappavigna, V.; Pannese, M.; D'Esposito, M.; Care, A.; Feiella, A.; Stornaiuolo, A.; Russo, G.; Simeone, A.; Boncinelli, E.; Peschle, C.
Dysregulation of NF–Y splicing drives metabolic rewiring and aggressiveness in colon cancer
2023 Belluti, S.; Mularoni, V.; Campani, Virginia; Rigillo, G.; Cuoghi, L.; Ronzio, M.; Miserocchi, G.; Dolfini, D.; Righi, Valeria; Alessandrini, A.; Zappavigna, V.; Imbriano, C.
Emx2 is a dose-dependent negative regulator of Sox2 telencephalic enhancers.
2012 Mariani, J; Favaro, R; Lancini, C; Vaccari, G; Ferri, Al; Bertolini, J; Tonoli, D; Latorre, E; Caccia, R; Ronchi, A; Ottolenghi, S; Miyagi, S; Okuda, A; Zappavigna, Vincenzo; Nicolis, Sk
Erratum: An I47L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of function (Development (2003) vol. 130 (1701-1712))
2003 Caronia, G.; Goodman, F. R.; Mckeown, C. M. E.; Scambler, P. J.; Zappavigna, V.
Functional dissection of a transcriptionally active, target specific Hox/Pbx complex.
1997 G., DI ROCCO; Mavilio, Fulvio; Zappavigna, Vincenzo
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
A cup full of functions | 1-gen-2005 | Piccioni, F.; Zappavigna, Vincenzo; Verrotti, A. | |
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 | |
A novel homeo-domain protein, prep 1, forms a regulatory complex with pbx proteins in vivo | 1-gen-1997 | Berthelsen, J.; Zappavigna, V.; Mavilio, F.; Blasi, F. | |
An 147L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of function | 1-gen-2003 | G., Caronia; F. R., Goodman; C. M. E., Mckeown; P. J., Scambler; Zappavigna, Vincenzo | |
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. | |
Cellule e segnali | 1-gen-2012 | Marigo, Valeria; Zappavigna, Vincenzo | |
Characterization of PREP2, a paralog of PREP1, which defines a novel sub-family of the MEINOX TALE homeodomain transcription factors | 1-gen-2002 | Fognani, C; KILSTRUP NIELSEN, C; Berthelsen, J; Ferretti, E; Zappavigna, Vincenzo; Blasi, F. | |
Comparison of mouse and human HOX-4 complexes defines conserved sequences involved in the regulation of Hox-4.4 | 1-gen-1992 | Renucci, A.; Zappavigna, V.; Zakany, J.; Izpisua-Belmonte, J. -C.; Burki, K.; Duboule, D. | |
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. | |
Control of vertebrate limb outgrowth by the proximal factor Meis2 and distal antagonism of BMPs by Gremlin | 1-gen-1999 | Capdevila, J.; Tsukui, T.; Esteban, C. R.; Zappavigna, V.; Belmonte, J. C. I. | |
Corrigendum: ‘Building a perfect body’: Control of vertebrate organogenesis by PBX-dependent regulatory networks (Genes & Development 33: 258–275 (2019) | 1-gen-2019 | Selleri, L.; Zappavigna, V.; Ferretti, E. | |
Cup is a nucleocytoplasmic shuttling protein that interacts with the eukaryotic translation initiation factor 4E to modulate Drosophila ovary development | 1-gen-2004 | Zappavigna, Vincenzo; F., Piccioni; Jc, Villaescusa; Ac, Verrotti | |
Definition of the transcriptional activation domains of three human HOX proteins depends on the DNA-Binding context | 1-gen-1998 | Ma, Vigano'; G., DI ROCCO; Zappavigna, Vincenzo; Mavilio, Fulvio | |
Developed to cull: How a master control gene of development turned into a regulator of innate immune homeostasis | 1-gen-2008 | Zappavigna, V. | |
Differential and stage-related expression in embryonic tissues of a new human homoeobox gene | 1-gen-1986 | Mavilio, F.; Simeone, A.; Giampaolo, A.; Faiella, A.; Zappavigna, V.; Acampora, D.; Poiana, G.; Russo, G.; Peschle, C.; Boncinelli, E. | |
Differential expression of human HOX-2 genes along the anterior-posterior axis in embryonic central nervous system | 1-gen-1989 | Giampaolo, A.; Acampora, D.; Zappavigna, V.; Pannese, M.; D'Esposito, M.; Care, A.; Feiella, A.; Stornaiuolo, A.; Russo, G.; Simeone, A.; Boncinelli, E.; Peschle, C. | |
Dysregulation of NF–Y splicing drives metabolic rewiring and aggressiveness in colon cancer | 1-gen-2023 | Belluti, S.; Mularoni, V.; Campani, Virginia; Rigillo, G.; Cuoghi, L.; Ronzio, M.; Miserocchi, G.; Dolfini, D.; Righi, Valeria; Alessandrini, A.; Zappavigna, V.; Imbriano, C. | |
Emx2 is a dose-dependent negative regulator of Sox2 telencephalic enhancers. | 1-gen-2012 | Mariani, J; Favaro, R; Lancini, C; Vaccari, G; Ferri, Al; Bertolini, J; Tonoli, D; Latorre, E; Caccia, R; Ronchi, A; Ottolenghi, S; Miyagi, S; Okuda, A; Zappavigna, Vincenzo; Nicolis, Sk | |
Erratum: An I47L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of function (Development (2003) vol. 130 (1701-1712)) | 1-gen-2003 | Caronia, G.; Goodman, F. R.; Mckeown, C. M. E.; Scambler, P. J.; Zappavigna, V. | |
Functional dissection of a transcriptionally active, target specific Hox/Pbx complex. | 1-gen-1997 | G., DI ROCCO; Mavilio, Fulvio; Zappavigna, Vincenzo |