BALDINI, ANTONIO
BALDINI, ANTONIO
DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE
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
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.
PPARδ up-regulates 14-3-3ε in human endothelial cells via C/Ebpβ.
2007 Brunelli, L; Cieslik, Ak; Alcorn, Jl; Vatta, M; Baldini, Antonio
Diagnosis of Genetic and Malignant Diseases Using Chromosome Specific DNA Probes, Multiple Fluorochromes and Optical Imaging Systems
1992 Baldini, Antonio; Ward, D. C.; P., Lichter; L., Manuelidis
Cloning and Comparative Mapping of A Chromosome-20-specific Alphoid Dna-sequence
1991 Baldini, Antonio; N., Archidiacono; R., Carbone; A., Bolino; V., Shridhar; O., Miller; D. A., Miller; D. C., Ward; M., Rocchi
p53 suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome.
2014 Caprio, C; 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.
Genetic dissection of the DiGeorge syndrome phenotype
2002 F., Vitelli; E. A., Lindsay; Baldini, Antonio
14-3-3? plays a role in cardiac ventricular compaction by regulating the cardiomyocyte cell cycle.
2012 Kosaka, Y; Cieslik, Ka; L, Li; Lezin, G; Maguire, Ct; Saijoh, Y; Toyo oka, K; Gambello, Mj; Vatta, M; Wynshaw Boris, A; Baldini, Antonio; Yost, Hj; Brunelli, L.
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
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
In vivo response to high-resolution variation of Tbx1 mRNA dosage.
2008 Zhang, Z; Baldini, Antonio
A genetic link between Tbx1 and Fibroblast Growth Factor Signaling
2002 Vitelli, F.; Taddei, I.; Morishima, M.; Meyers, E. N.; Lindsay, E. A.; Baldini, Antonio
Structure and chromosomal locations of mouse steroid receptor coactivator gene family
1999 G., Ning; V., Jurecic; Baldini, Antonio; J. M., Xu
Are primary cilia involved in Embryonic Stem Cells differentiation and/or the maintenance of the undifferentiated state?
2009 M., Morleo; A., Vitale; Baldini, Antonio; Franco, Brunella
Tbx1 deletion in Islet1-fated cells recapitulates the cardiovascular Tbx1 mutant phenotype
2005 Pavone, LUIGI MICHELE; Evans, S; Baldini, Antonio
TBX1 is required for inner ear morphogenesis
2003 F., Vitelli; A., Viola; M., Morishima; T., Pramparo; Baldini, Antonio; E., Lindsay
Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome.
2007 Xu, H; Baldini, Antonio
A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field
2007 T., Huynh; L., Chen; P., Terrell; Baldini, Antonio
Identification and molecular characterization of de novo translocation t(8;14)(q22.3;q13) associated with a vascular and tissue overgrowth syndrome
2001 Q., Wang; A. A., Timur; P., Szafranski; A., Sadgephour; V., Jurecic; J., Cowell; Baldini, Antonio; D. J., Driscoll
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| 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 | |
| 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. | |
| PPARδ up-regulates 14-3-3ε in human endothelial cells via C/Ebpβ. | 1.1 Articolo in rivista | 2007 | Brunelli, L; Cieslik, Ak; Alcorn, Jl; Vatta, M; Baldini, Antonio | |
| Diagnosis of Genetic and Malignant Diseases Using Chromosome Specific DNA Probes, Multiple Fluorochromes and Optical Imaging Systems | 6.1 Brevetto | 1992 | Baldini, Antonio; Ward, D. C.; P., Lichter; L., Manuelidis | |
| Cloning and Comparative Mapping of A Chromosome-20-specific Alphoid Dna-sequence | 1.1 Articolo in rivista | 1991 | Baldini, Antonio; N., Archidiacono; R., Carbone; A., Bolino; V., Shridhar; O., Miller; D. A., Miller; D. C., Ward; M., Rocchi | |
| p53 suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome. | 1.1 Articolo in rivista | 2014 | Caprio, C; 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. | |
| Genetic dissection of the DiGeorge syndrome phenotype | 1.1 Articolo in rivista | 2002 | F., Vitelli; E. A., Lindsay; Baldini, Antonio | |
| 14-3-3? plays a role in cardiac ventricular compaction by regulating the cardiomyocyte cell cycle. | 1.1 Articolo in rivista | 2012 | Kosaka, Y; Cieslik, Ka; L, Li; Lezin, G; Maguire, Ct; Saijoh, Y; Toyo oka, K; Gambello, Mj; Vatta, M; Wynshaw Boris, A; Baldini, Antonio; Yost, Hj; Brunelli, L. | |
| 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 | |
| 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 | |
| In vivo response to high-resolution variation of Tbx1 mRNA dosage. | 1.1 Articolo in rivista | 2008 | Zhang, Z; Baldini, Antonio | |
| A genetic link between Tbx1 and Fibroblast Growth Factor Signaling | 1.1 Articolo in rivista | 2002 | Vitelli, F.; Taddei, I.; Morishima, M.; Meyers, E. N.; Lindsay, E. A.; Baldini, Antonio | |
| Structure and chromosomal locations of mouse steroid receptor coactivator gene family | 1.1 Articolo in rivista | 1999 | G., Ning; V., Jurecic; Baldini, Antonio; J. M., Xu | |
| Are primary cilia involved in Embryonic Stem Cells differentiation and/or the maintenance of the undifferentiated state? | 4.1 Articoli in Atti di convegno | 2009 | M., Morleo; A., Vitale; Baldini, Antonio; Franco, Brunella | |
| 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 | |
| TBX1 is required for inner ear morphogenesis | 1.1 Articolo in rivista | 2003 | F., Vitelli; A., Viola; M., Morishima; T., Pramparo; Baldini, Antonio; E., Lindsay | |
| Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome. | 1.1 Articolo in rivista | 2007 | Xu, H; Baldini, Antonio | |
| A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field | 1.1 Articolo in rivista | 2007 | T., Huynh; L., Chen; P., Terrell; Baldini, Antonio | |
| Identification and molecular characterization of de novo translocation t(8;14)(q22.3;q13) associated with a vascular and tissue overgrowth syndrome | 1.1 Articolo in rivista | 2001 | Q., Wang; A. A., Timur; P., Szafranski; A., Sadgephour; V., Jurecic; J., Cowell; Baldini, Antonio; D. J., Driscoll |