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.
A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field
2007 T., Huynh; L., Chen; P., Terrell; Baldini, Antonio
Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway?
2003 Vitelli, F; Baldini, Antonio
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract
2004 H. S., Xu; M., Morishima; J. N., Wylie; R. J., Schwartz; B. G., Bruneau; E. A., Lindsay; Baldini, Antonio
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.
Tbx1 Mutation Causes Multiple Cardiovascular Defects and Disrupts Neural Crest and Cranial Nerve Migratory Pathways
2002 Vitelli, F.; Morishima, M.; Taddei, I.; Lindsay, E. A.; Baldini, Antonio
Congenital heart disease in mice deficient for the DiGeorge syndrome region
1999 E. A., Lindsay; A., Botta; V., Jurecic; S., Carattini Rivera; Y. C., Cheah; H. M., Rosenblatt; A., Bradley; Baldini, Antonio
Subepicardial endothelial cells invade the embryonic ventricle wall to form coronary arteries.
2013 Tian, X; Hu, T; Zhang, H; He, L; Huang, X; Liu, Q; Yu, W; He, L; Yang, Z; Zhang, Z; Zhong, Tp; Yang, X; Yang, Z; Yan, Y; Baldini, Antonio; Sun, Y; Lu, J; Schwartz, Rj; Evans, Sm; Gittenberger de Groot, Ac; Red Horse, K; Zhou, B.
PPARδ up-regulates 14-3-3ε in human endothelial cells via C/Ebpβ.
2007 Brunelli, L; Cieslik, Ak; Alcorn, Jl; Vatta, M; Baldini, Antonio
Genetic dissection of the DiGeorge syndrome phenotype
2002 F., Vitelli; E. A., Lindsay; Baldini, Antonio
Structure and chromosomal locations of mouse steroid receptor coactivator gene family
1999 G., Ning; V., Jurecic; Baldini, Antonio; J. M., Xu
The 22q11.2 deletion syndrome: a gene dosage perspective
2006 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.
Transcriptional Control in Cardiac Progenitors: Tbx1 Interacts with the BAF Chromatin Remodeling Complex and Regulates Wnt5a
2012 L., Chen; F. G., Fulcoli; R., Ferrentino; S., Martucciello; E. A., Illingworth; Baldini, Antonio
Tbx1 regulates progenitor cell proliferation in the dental epithelium by modulating Pitx2 activation of p21
2010 H. J., Cao; S., Florez; M., Amen; T., Huynh; Z., Skobe; Baldini, Antonio; B. A., Amendt
Tbx1 is required for inner ear morphogenesis.
2003 Vitelli, F; Viola, A; Pramparo, T; Baldini, Antonio; Lindsay, E. A.
Cloning and chromosome mapping of human and chicken Iroquois (IRX) genes
2001 K., Ogura; K., Matsumoto; A., Kuroiwa; T., Isobe; T., Otoguro; V., Jurecic; Baldini, Antonio; Y., Matsuda; T., Ogura
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
A Human Alpha-satellite Dna Subset Specific For Chromosome-12
1990 Baldini, Antonio; M., Rocchi; N., Archidiacono; O. J., Miller; D. A., Miller
| 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. | |
| 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 | |
| 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 | |
| Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract | 1.1 Articolo in rivista | 2004 | H. S., Xu; M., Morishima; J. N., Wylie; R. J., Schwartz; B. G., Bruneau; E. A., Lindsay; Baldini, Antonio | |
| 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. | |
| Tbx1 Mutation Causes Multiple Cardiovascular Defects and Disrupts Neural Crest and Cranial Nerve Migratory Pathways | 1.1 Articolo in rivista | 2002 | Vitelli, F.; Morishima, M.; Taddei, I.; Lindsay, E. A.; Baldini, Antonio | |
| Congenital heart disease in mice deficient for the DiGeorge syndrome region | 1.1 Articolo in rivista | 1999 | E. A., Lindsay; A., Botta; V., Jurecic; S., Carattini Rivera; Y. C., Cheah; H. M., Rosenblatt; A., Bradley; Baldini, Antonio | |
| Subepicardial endothelial cells invade the embryonic ventricle wall to form coronary arteries. | 1.1 Articolo in rivista | 2013 | Tian, X; Hu, T; Zhang, H; He, L; Huang, X; Liu, Q; Yu, W; He, L; Yang, Z; Zhang, Z; Zhong, Tp; Yang, X; Yang, Z; Yan, Y; Baldini, Antonio; Sun, Y; Lu, J; Schwartz, Rj; Evans, Sm; Gittenberger de Groot, Ac; Red Horse, K; Zhou, B. | |
| 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 | |
| Genetic dissection of the DiGeorge syndrome phenotype | 1.1 Articolo in rivista | 2002 | F., Vitelli; E. A., Lindsay; 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 | |
| The 22q11.2 deletion syndrome: a gene dosage perspective | 1.1 Articolo in rivista | 2006 | 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. | |
| Transcriptional Control in Cardiac Progenitors: Tbx1 Interacts with the BAF Chromatin Remodeling Complex and Regulates Wnt5a | 1.1 Articolo in rivista | 2012 | L., Chen; F. G., Fulcoli; R., Ferrentino; S., Martucciello; E. A., Illingworth; Baldini, Antonio | |
| Tbx1 regulates progenitor cell proliferation in the dental epithelium by modulating Pitx2 activation of p21 | 1.1 Articolo in rivista | 2010 | H. J., Cao; S., Florez; M., Amen; T., Huynh; Z., Skobe; Baldini, Antonio; B. A., Amendt | |
| Tbx1 is required for inner ear morphogenesis. | 1.1 Articolo in rivista | 2003 | Vitelli, F; Viola, A; Pramparo, T; Baldini, Antonio; Lindsay, E. A. | |
| Cloning and chromosome mapping of human and chicken Iroquois (IRX) genes | 1.1 Articolo in rivista | 2001 | K., Ogura; K., Matsumoto; A., Kuroiwa; T., Isobe; T., Otoguro; V., Jurecic; Baldini, Antonio; Y., Matsuda; T., Ogura | |
| 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 | |
| A Human Alpha-satellite Dna Subset Specific For Chromosome-12 | 1.1 Articolo in rivista | 1990 | Baldini, Antonio; M., Rocchi; N., Archidiacono; O. J., Miller; D. A., Miller |