BALDINI, ANTONIO
BALDINI, ANTONIO
DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE
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.
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
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.
Tbx1 deletion in Islet1-fated cells recapitulates the cardiovascular Tbx1 mutant phenotype
2005 Pavone, LUIGI MICHELE; Evans, S; Baldini, Antonio
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
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
Manipulation of endogenous regulatory elements and transgenic analyses of the Tbx1 gene
2010 Zhang, Z.; 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
Schizophrenia and Chromosomal Deletions Within 22q11.2
1995 E. A., Lindsay; M. A., Morris; A., Gos; G., Nestadt; P. S., Wolyniec; V. K., Lasseter; R., Shprintzen; S. E., Antonarakis; Baldini, Antonio; A. E., Pulver
The 22q11.2 deletion syndrome: a gene dosage perspective
2006 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
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
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
Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis.
2003 Morishima, M; Yanagisawa, H; Yanagisawa, M; Baldini, Antonio
TBX1 is required for inner ear morphogenesis
2003 F., Vitelli; A., Viola; M., Morishima; T., Pramparo; Baldini, Antonio; E., Lindsay
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
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
Early thyroid development requires a Tbx1-Fgf8 pathway
2009 G., Lania; Z., Zhang; T., Huynh; C., Caprio; A. M., Moon; F., Vitelli; Baldini, Antonio
Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome.
2007 Xu, H; Baldini, Antonio
Structure and chromosomal locations of mouse steroid receptor coactivator gene family
1999 G., Ning; V., Jurecic; Baldini, Antonio; J. M., Xu
Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
---|---|---|---|---|
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. | |
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 | |
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. | |
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 | |
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 | |
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 | |
Manipulation of endogenous regulatory elements and transgenic analyses of the Tbx1 gene | 1.1 Articolo in rivista | 2010 | Zhang, Z.; 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 | |
Schizophrenia and Chromosomal Deletions Within 22q11.2 | 1.1 Articolo in rivista | 1995 | E. A., Lindsay; M. A., Morris; A., Gos; G., Nestadt; P. S., Wolyniec; V. K., Lasseter; R., Shprintzen; S. E., Antonarakis; Baldini, Antonio; A. E., Pulver | |
The 22q11.2 deletion syndrome: a gene dosage perspective | 1.1 Articolo in rivista | 2006 | 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 | |
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 | |
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 | |
Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis. | 1.1 Articolo in rivista | 2003 | Morishima, M; Yanagisawa, H; Yanagisawa, M; 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 | |
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 | |
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 | |
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 | |
Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome. | 1.1 Articolo in rivista | 2007 | Xu, H; 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 |