BALDINI, ANTONIO
BALDINI, ANTONIO
DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE
Tbx1 deletion in Islet1-fated cells recapitulates the cardiovascular Tbx1 mutant phenotype
2005 Pavone, LUIGI MICHELE; Evans, S; Baldini, Antonio
Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome.
2007 Xu, H; Baldini, Antonio
Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants.
2006 Vitelli, F; Zhang, Z; Huynh, T; Sobotka, A; Mupo, A; Baldini, Antonio
In vivo response to high-resolution variation of Tbx1 mRNA dosage.
2008 Zhang, Z; Baldini, Antonio
Mapping on human and mouse chromosomes of the gene for the beta-galactoside-binding protein, an autocrine-negative growth factor.
1993 Baldini, Antonio; Gress, T; Patel, K; Muresu, R; Chiariotti, Lorenzo; Williamson, P; Boyd, Y; Casciano, I; Wells, V; Bruni, CARMELO BRUNO; Mallucci, L; Siniscalco, M.
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization.
1994 Lindsay, E. A.; Grillo, A; Ferrero, G. B.; Roth, E. J.; Magenis, E; Grompe, M; Hultn, M; Gould, C; Baldini, Antonio; Zoghbi, H. Y.; Ballabio, Andrea
Recovery from arterial growth delay reduces the penetrance of cardiovascular defects in mice deleted for the DiGeorge Syndrome region
2001 Lindsay, E. A.; Baldini, Antonio
Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8.
1996 Mills, K. A.; Mathews, K. D.; Scherpbierheddema, T; Buetow, K. H.; Baldini, Antonio; Ballabio, Andrea; Borsani, G.
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice
2001 Lindsay, E. A.; Vitelli, F.; Su, H.; Morishima, M.; Huynh, T.; Pramparo, T.; Jurecic, V.; Ogunrinu, G.; Sutherland, H.; Scambler, P.; Bradley, A.; Baldini, Antonio
Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis.
2003 Morishima, M; Yanagisawa, H; Yanagisawa, M; Baldini, Antonio
Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway?
2003 Vitelli, F; Baldini, Antonio
Congenital Heart Disease in Mice Deficient for the DiGeorge Syndrome Region.
1999 Lindsay, E. A.; Botta, A.; Jurecic, V.; Cheah, Y. C.; Rivera, S.; Rosenblatt, H.; Bradley, A.; Baldini, Antonio
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract.
2004 Xu, H; Morishima, M; Wylie, Jn; Schwartz, Rj; Bruneau, Bg; Lindsay, Ea; Baldini, Antonio
Microarray analysis of the Df1 mouse model of the 22q11 Deletion Syndrome.
2005 Prescott, K; Ivins, S; Hubank, M; Lindsay, Ea; Baldini, Antonio; Scambler, P.
Genetic analysis of Down syndrome-associated heart defects in mice
2011 Liu, C.; Morishima, M.; Yu, T.; Matsui, S.; Zhang, L.; Fu, D.; Pao, A.; Costa, A.; Gardiner, K.; Cowell, J.; Nowak, N. J.; Parmacek, M. S.; Liang, P.; Baldini, Antonio; Yu, Y. E.
Manipulation of endogenous regulatory elements and transgenic analyses of the Tbx1 gene
2010 Zhang, Z.; Baldini, Antonio
The Transcriptional Activity of Individual Ribosomal Dna Gene Clusters Is Modulated By Serum Concentration
1985 A., Decapoa; P., Marlekaj; Baldini, Antonio; N., Archidiacono; M., Rocchi
Timed mutation and cell-fate mapping reveal reiterated roles of Tbx1 during embryogenesis, and a crucial function during segmentation of the pharyngeal system via regulation of endoderm expansion
2005 H. S., Xu; F., Cerrato; Baldini, Antonio
22q11 deletions and cardiac disease
1996 M. B., Lewin; E. A., Lindsay; Baldini, Antonio
Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome
1996 H. F., Sutherland; R., Wadey; J. M., Mckie; C., Taylor; U., Atif; K. A., Johnstone; S., Halford; U. J., Kim; J., Goodship; Baldini, Antonio; P. J., Scambler
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| Tbx1 deletion in Islet1-fated cells recapitulates the cardiovascular Tbx1 mutant phenotype | 4.1 Articoli in Atti di convegno | 2005 | Pavone, LUIGI MICHELE; Evans, S; Baldini, Antonio | |
| Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome. | 1.1 Articolo in rivista | 2007 | Xu, H; Baldini, Antonio | |
| Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants. | 1.1 Articolo in rivista | 2006 | Vitelli, F; Zhang, Z; Huynh, T; Sobotka, A; Mupo, A; Baldini, Antonio | |
| In vivo response to high-resolution variation of Tbx1 mRNA dosage. | 1.1 Articolo in rivista | 2008 | Zhang, Z; Baldini, Antonio | |
| Mapping on human and mouse chromosomes of the gene for the beta-galactoside-binding protein, an autocrine-negative growth factor. | 1.1 Articolo in rivista | 1993 | Baldini, Antonio; Gress, T; Patel, K; Muresu, R; Chiariotti, Lorenzo; Williamson, P; Boyd, Y; Casciano, I; Wells, V; Bruni, CARMELO BRUNO; Mallucci, L; Siniscalco, M. | |
| Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization. | 1.1 Articolo in rivista | 1994 | Lindsay, E. A.; Grillo, A; Ferrero, G. B.; Roth, E. J.; Magenis, E; Grompe, M; Hultn, M; Gould, C; Baldini, Antonio; Zoghbi, H. Y.; Ballabio, Andrea | |
| Recovery from arterial growth delay reduces the penetrance of cardiovascular defects in mice deleted for the DiGeorge Syndrome region | 1.1 Articolo in rivista | 2001 | Lindsay, E. A.; Baldini, Antonio | |
| Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8. | 1.1 Articolo in rivista | 1996 | Mills, K. A.; Mathews, K. D.; Scherpbierheddema, T; Buetow, K. H.; Baldini, Antonio; Ballabio, Andrea; Borsani, G. | |
| Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice | 1.1 Articolo in rivista | 2001 | Lindsay, E. A.; Vitelli, F.; Su, H.; Morishima, M.; Huynh, T.; Pramparo, T.; Jurecic, V.; Ogunrinu, G.; Sutherland, H.; Scambler, P.; Bradley, A.; Baldini, Antonio | |
| Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis. | 1.1 Articolo in rivista | 2003 | Morishima, M; Yanagisawa, H; Yanagisawa, M; Baldini, Antonio | |
| Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway? | 1.1 Articolo in rivista | 2003 | Vitelli, F; Baldini, Antonio | |
| Congenital Heart Disease in Mice Deficient for the DiGeorge Syndrome Region. | 1.1 Articolo in rivista | 1999 | Lindsay, E. A.; Botta, A.; Jurecic, V.; Cheah, Y. C.; Rivera, S.; Rosenblatt, H.; Bradley, A.; Baldini, Antonio | |
| Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. | 1.1 Articolo in rivista | 2004 | Xu, H; Morishima, M; Wylie, Jn; Schwartz, Rj; Bruneau, Bg; Lindsay, Ea; Baldini, Antonio | |
| Microarray analysis of the Df1 mouse model of the 22q11 Deletion Syndrome. | 1.1 Articolo in rivista | 2005 | Prescott, K; Ivins, S; Hubank, M; Lindsay, Ea; Baldini, Antonio; Scambler, P. | |
| Genetic analysis of Down syndrome-associated heart defects in mice | 1.1 Articolo in rivista | 2011 | Liu, C.; Morishima, M.; Yu, T.; Matsui, S.; Zhang, L.; Fu, D.; Pao, A.; Costa, A.; Gardiner, K.; Cowell, J.; Nowak, N. J.; Parmacek, M. S.; Liang, P.; Baldini, Antonio; Yu, Y. E. | |
| Manipulation of endogenous regulatory elements and transgenic analyses of the Tbx1 gene | 1.1 Articolo in rivista | 2010 | Zhang, Z.; Baldini, Antonio | |
| The Transcriptional Activity of Individual Ribosomal Dna Gene Clusters Is Modulated By Serum Concentration | 1.1 Articolo in rivista | 1985 | A., Decapoa; P., Marlekaj; Baldini, Antonio; N., Archidiacono; M., Rocchi | |
| Timed mutation and cell-fate mapping reveal reiterated roles of Tbx1 during embryogenesis, and a crucial function during segmentation of the pharyngeal system via regulation of endoderm expansion | 1.1 Articolo in rivista | 2005 | H. S., Xu; F., Cerrato; Baldini, Antonio | |
| 22q11 deletions and cardiac disease | 1.1 Articolo in rivista | 1996 | M. B., Lewin; E. A., Lindsay; Baldini, Antonio | |
| Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome | 1.1 Articolo in rivista | 1996 | H. F., Sutherland; R., Wadey; J. M., Mckie; C., Taylor; U., Atif; K. A., Johnstone; S., Halford; U. J., Kim; J., Goodship; Baldini, Antonio; P. J., Scambler |