IRIS

BALDINI, ANTONIO

BALDINI, ANTONIO  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

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Risultati 1 - 20 di 120 (tempo di esecuzione: 0.053 secondi).
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 required for inner ear morphogenesis 1.1 Articolo in rivista 2003 F., Vitelli; A., Viola; M., Morishima; T., Pramparo; Baldini, Antonio; E., Lindsay
Pitx2 promotes development of splanchnic mesoderm-derived branchiomeric muscle 1.1 Articolo in rivista 2006 F. Y., Dong; X. X., Sun; W., Liu; D., Ai; E., Klysik; M. F., Lu; J., Hadley; L., Antoni; L., Chen; Baldini, Antonio; P., Francis West; J. F., Martin
Tbx1 regulates Vegfr3 and is required for lymphatic vessel development 1.1 Articolo in rivista 2010 L., Chen; A., Mupo; T., Huynh; S., Cioffi; M., Woods; C. L., Jin; W., Mckeehan; L., Thompson Snipes; Baldini, Antonio; E., Illingworth
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
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.
Localization of the Human Prostate Transglutaminase (Type IV) Gene (TGM4) to Chromosome 3p21.33-p22 by Fluorescence in Situ Hybridization 1.1 Articolo in rivista 1995 V., Gentile; F. J., Grant; Porta, Raffaele; 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
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. 1.1 Articolo in rivista 2004 Xu, H; Morishima, M; Wylie, Jn; Schwartz, Rj; Bruneau, Bg; Lindsay, Ea; Baldini, Antonio
14-3-3? plays a role in cardiac ventricular compaction by regulating the cardiomyocyte cell cycle. 1.1 Articolo in rivista 2012 Kosaka, Y; Cieslik, Ka; L, Li; Lezin, G; Maguire, Ct; Saijoh, Y; Toyo oka, K; Gambello, Mj; Vatta, M; Wynshaw Boris, A; Baldini, Antonio; Yost, Hj; Brunelli, L.
Mouse models for Down syndrome-associated developmental cognitive disabilities. 1.1 Articolo in rivista 2011 Liu, C; Belichenko, Pv; Zhang, L; Fu, D; Kleschevnikov, Am; Baldini, Antonio; Antonarakis, Se; Mobley, Wc; Yu, Ye
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
p53 suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome. 1.1 Articolo in rivista 2014 Caprio, C; Baldini, Antonio