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.
TBX1 is required for inner ear morphogenesis
2003 F., Vitelli; A., Viola; M., Morishima; T., Pramparo; Baldini, Antonio; E., Lindsay
Tbx1 deletion in Islet1-fated cells recapitulates the cardiovascular Tbx1 mutant phenotype
2005 Pavone, LUIGI MICHELE; Evans, S; Baldini, Antonio
PPARδ up-regulates 14-3-3ε in human endothelial cells via C/Ebpβ.
2007 Brunelli, L; Cieslik, Ak; Alcorn, Jl; Vatta, M; 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.
Localization of the Human Prostate Transglutaminase (Type IV) Gene (TGM4) to Chromosome 3p21.33-p22 by Fluorescence in Situ Hybridization
1995 V., Gentile; F. J., Grant; Porta, Raffaele; Baldini, Antonio
Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner
2009 F. G., Fulcoli; T., Huynh; P. J., Scambler; 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
Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway?
2003 Vitelli, F; Baldini, Antonio
A pivotal role for endogenous TGF-beta-activated kinase-1 in the LKB1/AMP-activated protein kinase energy-sensor pathway
2006 M., Xie; D., Zhang; J. R., B.; Y., Li; H., Zhang; M., Morishima; D. L., Mann; G. E., Taffet; Baldini, Antonio; D. S., Khoury; M. D., Schneider
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
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
Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice.
2013 Freyer, L; Nowotschin, S; Pirity, Mk; Baldini, Antonio; Morrow, Be
Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis.
2003 Morishima, M; Yanagisawa, H; Yanagisawa, M; 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
Selection of A Human Chromosome-21 Enriched Yac Sub-library Using A Chromosome-specific Composite Probe
1992 M. T., Ross; D., Nizetic; C., Nguyen; C., Knights; R., Vatcheva; N., Burden; C., Douglas; G., Zehetner; D. C., Ward; Baldini, Antonio; H., Lehrach
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments
2001 R., Paylor; K. L., Mcilwain; R., Mcaninch; A., Nellis; L. A., Yuva Paylor; Baldini, Antonio; E. A., Lindsay
Cyp26 genes a1, b1 and c1 are down-regulated in Tbx1 null mice and inhibition of Cyp26 enzyme function produces a phenocopy of DiGeorge Syndrome in the chick.
2006 Roberts, C; Ivins, S; Cook, Ac; Baldini, Antonio; Scambler, Pj
| 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. | |
| 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 | |
| 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 | |
| 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 | |
| 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. | |
| Localization of the Human Prostate Transglutaminase (Type IV) Gene (TGM4) to Chromosome 3p21.33-p22 by Fluorescence in Situ Hybridization | 1.1 Articolo in rivista | 1995 | V., Gentile; F. J., Grant; Porta, Raffaele; Baldini, Antonio | |
| Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner | 1.1 Articolo in rivista | 2009 | F. G., Fulcoli; T., Huynh; P. J., Scambler; 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 | |
| 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 | |
| A pivotal role for endogenous TGF-beta-activated kinase-1 in the LKB1/AMP-activated protein kinase energy-sensor pathway | 1.1 Articolo in rivista | 2006 | M., Xie; D., Zhang; J. R., B.; Y., Li; H., Zhang; M., Morishima; D. L., Mann; G. E., Taffet; Baldini, Antonio; D. S., Khoury; M. D., Schneider | |
| 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 | |
| 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 | |
| Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice. | 1.1 Articolo in rivista | 2013 | Freyer, L; Nowotschin, S; Pirity, Mk; Baldini, Antonio; Morrow, Be | |
| Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis. | 1.1 Articolo in rivista | 2003 | Morishima, M; Yanagisawa, H; Yanagisawa, M; 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 | |
| Selection of A Human Chromosome-21 Enriched Yac Sub-library Using A Chromosome-specific Composite Probe | 1.1 Articolo in rivista | 1992 | M. T., Ross; D., Nizetic; C., Nguyen; C., Knights; R., Vatcheva; N., Burden; C., Douglas; G., Zehetner; D. C., Ward; Baldini, Antonio; H., Lehrach | |
| Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments | 1.1 Articolo in rivista | 2001 | R., Paylor; K. L., Mcilwain; R., Mcaninch; A., Nellis; L. A., Yuva Paylor; Baldini, Antonio; E. A., Lindsay | |
| Cyp26 genes a1, b1 and c1 are down-regulated in Tbx1 null mice and inhibition of Cyp26 enzyme function produces a phenocopy of DiGeorge Syndrome in the chick. | 1.1 Articolo in rivista | 2006 | Roberts, C; Ivins, S; Cook, Ac; Baldini, Antonio; Scambler, Pj |