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 deletion in Islet1-fated cells recapitulates the cardiovascular Tbx1 mutant phenotype
2005 Pavone, LUIGI MICHELE; Evans, S; 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
Tbx1 is required for inner ear morphogenesis.
2003 Vitelli, F; Viola, A; Pramparo, T; Baldini, Antonio; Lindsay, E. A.
Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice.
2013 Freyer, L; Nowotschin, S; Pirity, Mk; Baldini, Antonio; Morrow, Be
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
Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice
2010 T., Yu; S. J., Clapcote; Z. Y., Li; C. H., Liu; A., Pao; A. R., Bechard; S., Carattini Rivera; S. I., Matsui; J. C., Roder; Baldini, Antonio; W. C., Mobley; A., Bradley; Y. E., Yu
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
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
Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis
2003 M., Morishima; H., Yanagisawa; M., Yanagisawa; Baldini, Antonio
Structure and chromosomal locations of mouse steroid receptor coactivator gene family
1999 G., Ning; V., Jurecic; Baldini, Antonio; J. M., Xu
Early thyroid development requires a Tbx1-Fgf8 pathway
2009 G., Lania; Z., Zhang; T., Huynh; C., Caprio; A. M., Moon; F., Vitelli; Baldini, Antonio
Fate map of serotonin transporter-expressing cells in developing mouse heart
2007 Pavone, LUIGI MICHELE; Mastellone, V.; Corona, M.; Maharajan, V.; Avallone, Luigi; Baldini, Antonio
Dissecting contiguous gene defects: TBX1.
2005 Baldini, Antonio
Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome.
2007 Xu, H; Baldini, Antonio
22q11 deletions and cardiac disease
1996 M. B., Lewin; E. A., Lindsay; Baldini, Antonio
In vivo genetic ablation of the periotic mesoderm affects cell proliferation survival and differentiation in the cochlea
2007 H. S., Xu; L., Chen; Baldini, Antonio
Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells
2007 H. S., Xu; A., Viola; Z., Zhang; C. P., Gerken; E. A., Lindsay Illingworth; Baldini, Antonio
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1.
2005 Ivins, S; LAMMERTS VAN BEUREN, K; Roberts, C; James, C; Lindsay, Ea; Baldini, Antonio; Ataliotis, P; 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 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 | |
| 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 | |
| Tbx1 is required for inner ear morphogenesis. | 1.1 Articolo in rivista | 2003 | Vitelli, F; Viola, A; Pramparo, T; Baldini, Antonio; Lindsay, E. A. | |
| 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 | |
| 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 | |
| Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice | 1.1 Articolo in rivista | 2010 | T., Yu; S. J., Clapcote; Z. Y., Li; C. H., Liu; A., Pao; A. R., Bechard; S., Carattini Rivera; S. I., Matsui; J. C., Roder; Baldini, Antonio; W. C., Mobley; A., Bradley; Y. E., Yu | |
| 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 | |
| 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 | |
| Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis | 1.1 Articolo in rivista | 2003 | M., Morishima; H., Yanagisawa; M., Yanagisawa; 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 | |
| Early thyroid development requires a Tbx1-Fgf8 pathway | 1.1 Articolo in rivista | 2009 | G., Lania; Z., Zhang; T., Huynh; C., Caprio; A. M., Moon; F., Vitelli; Baldini, Antonio | |
| Fate map of serotonin transporter-expressing cells in developing mouse heart | 4.1 Articoli in Atti di convegno | 2007 | Pavone, LUIGI MICHELE; Mastellone, V.; Corona, M.; Maharajan, V.; Avallone, Luigi; Baldini, Antonio | |
| Dissecting contiguous gene defects: TBX1. | 1.1 Articolo in rivista | 2005 | 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 | |
| 22q11 deletions and cardiac disease | 1.1 Articolo in rivista | 1996 | M. B., Lewin; E. A., Lindsay; Baldini, Antonio | |
| In vivo genetic ablation of the periotic mesoderm affects cell proliferation survival and differentiation in the cochlea | 1.1 Articolo in rivista | 2007 | H. S., Xu; L., Chen; Baldini, Antonio | |
| Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells | 1.1 Articolo in rivista | 2007 | H. S., Xu; A., Viola; Z., Zhang; C. P., Gerken; E. A., Lindsay Illingworth; Baldini, Antonio | |
| Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. | 1.1 Articolo in rivista | 2005 | Ivins, S; LAMMERTS VAN BEUREN, K; Roberts, C; James, C; Lindsay, Ea; Baldini, Antonio; Ataliotis, P; Scambler, Pj |