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 a negative modulator of Mef2c
2012 L. S., Pane; Z., Zhang; R., Ferrentino; T., Huynh; L., Cutillo; Baldini, Antonio
DiGeorge Syndrome: A gene at last.
2003 Baldini, Antonio
Microarray analysis of the Df1 mouse model of the 22q11 Deletion Syndrome.
2005 Prescott, K; Ivins, S; Hubank, M; Lindsay, Ea; Baldini, Antonio; Scambler, P.
DiGeorge syndrome: complex pathogenesis? Maybe, maybe not
2000 Baldini, Antonio
Recovery from arterial growth delay reduces the penetrance of cardiovascular defects in mice deleted for the DiGeorge Syndrome region
2001 Lindsay, E. A.; Baldini, Antonio
A Human Alphoid Dna Clone From the Ecori Dimeric Family - Genomic and Internal Organization and Chromosomal Assignment
1989 Baldini, Antonio; D. I., Smith; M., Rocchi; O. J., Miller; D. A., Miller
Chromosomal Assignment of Human Yac Clones By Fluorescence Insitu Hybridization - Use of Single-yeast-colony Pcr and Multiple Labeling
1992 Baldini, Antonio; M., Ross; D., Nizetic; R., Vatcheva; E. A., Lindsay; H., Lehrach; M., Siniscalco
A 12-Mb complete coverage BAC contig map in human chromosome 16p13.1-p11.2
1999 Y. C., Cao; H. L., Kang; X. Q., Xu; M., Wang; S. H., Dho; J. R., Huh; B. J., Lee; F., Kalush; D., Bocskai; Y., Ding; J. G., Tesmer; J., Lee; E., Moon; V., Jurecic; Baldini, Antonio; H. U., Weier; N. A., Doggett; M. I., Simon; M. D., Adams; U. J., Kim
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
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
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
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
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 deletion in Islet1-fated cells recapitulates the cardiovascular Tbx1 mutant phenotype
2005 Pavone, LUIGI MICHELE; Evans, S; Baldini, Antonio
22q11 deletions and cardiac disease
1996 M. B., Lewin; E. A., Lindsay; 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
Dissecting contiguous gene defects: TBX1.
2005 Baldini, Antonio
| 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 a negative modulator of Mef2c | 1.1 Articolo in rivista | 2012 | L. S., Pane; Z., Zhang; R., Ferrentino; T., Huynh; L., Cutillo; Baldini, Antonio | |
| DiGeorge Syndrome: A gene at last. | 1.1 Articolo in rivista | 2003 | Baldini, Antonio | |
| Microarray analysis of the Df1 mouse model of the 22q11 Deletion Syndrome. | 1.1 Articolo in rivista | 2005 | Prescott, K; Ivins, S; Hubank, M; Lindsay, Ea; Baldini, Antonio; Scambler, P. | |
| DiGeorge syndrome: complex pathogenesis? Maybe, maybe not | 1.1 Articolo in rivista | 2000 | Baldini, Antonio | |
| Recovery from arterial growth delay reduces the penetrance of cardiovascular defects in mice deleted for the DiGeorge Syndrome region | 1.1 Articolo in rivista | 2001 | Lindsay, E. A.; Baldini, Antonio | |
| A Human Alphoid Dna Clone From the Ecori Dimeric Family - Genomic and Internal Organization and Chromosomal Assignment | 1.1 Articolo in rivista | 1989 | Baldini, Antonio; D. I., Smith; M., Rocchi; O. J., Miller; D. A., Miller | |
| Chromosomal Assignment of Human Yac Clones By Fluorescence Insitu Hybridization - Use of Single-yeast-colony Pcr and Multiple Labeling | 1.1 Articolo in rivista | 1992 | Baldini, Antonio; M., Ross; D., Nizetic; R., Vatcheva; E. A., Lindsay; H., Lehrach; M., Siniscalco | |
| A 12-Mb complete coverage BAC contig map in human chromosome 16p13.1-p11.2 | 1.1 Articolo in rivista | 1999 | Y. C., Cao; H. L., Kang; X. Q., Xu; M., Wang; S. H., Dho; J. R., Huh; B. J., Lee; F., Kalush; D., Bocskai; Y., Ding; J. G., Tesmer; J., Lee; E., Moon; V., Jurecic; Baldini, Antonio; H. U., Weier; N. A., Doggett; M. I., Simon; M. D., Adams; U. J., Kim | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 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 | |
| 22q11 deletions and cardiac disease | 1.1 Articolo in rivista | 1996 | M. B., Lewin; E. A., Lindsay; 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 | |
| Dissecting contiguous gene defects: TBX1. | 1.1 Articolo in rivista | 2005 | Baldini, Antonio |