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BALDINI, ANTONIO

BALDINI, ANTONIO  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

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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
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
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
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
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.
Manipulation of endogenous regulatory elements and transgenic analyses of the Tbx1 gene 1.1 Articolo in rivista 2010 Zhang, Z.; Baldini, Antonio
Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia. 1.1 Articolo in rivista 1997 Lee, B.; Thirunavukkarasu, K.; Zhou, L.; Pastore, Lucio; Baldini, Antonio; Hecht, J.; Geoffroy, V.; Ducy, P.; Karsenty, G.
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
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
The 22q11.2 deletion syndrome: a gene dosage perspective 1.1 Articolo in rivista 2006 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.