IRIS

BALDINI, ANTONIO

BALDINI, ANTONIO  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

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Titolo Tipologia Data di pubblicazione Autore(i) File
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.
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.
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
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
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
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
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
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
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.
DiGeorge Syndrome: A gene at last. 1.1 Articolo in rivista 2003 Baldini, Antonio
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 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 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
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
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
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
p53 suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome. 1.1 Articolo in rivista 2014 Caprio, C; Baldini, Antonio
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