BALDINI, ANTONIO

BALDINI, ANTONIO  

Dipartimento di Medicina molecolare e Biotecnologie mediche  

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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
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
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
Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development 1.1 Articolo in rivista 2006 Z., Zhang; T., Huynh; 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.
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
Tbx1 is required for inner ear morphogenesis. 1.1 Articolo in rivista 2003 Vitelli, F; Viola, A; Pramparo, T; Baldini, Antonio; Lindsay, E. A.
Simultaneous Visualization of 7 Different Dna Probes By Insitu Hybridization Using Combinatorial Fluorescence and Digital Imaging Microscopy 1.1 Articolo in rivista 1992 T., Ried; Baldini, Antonio; T. C., Rand; D. C., Ward
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
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
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
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
Genetic analysis of Down syndrome-associated heart defects in mice 1.1 Articolo in rivista 2011 Liu, C.; Morishima, M.; Yu, T.; Matsui, S.; Zhang, L.; Fu, D.; Pao, A.; Costa, A.; Gardiner, K.; Cowell, J.; Nowak, N. J.; Parmacek, M. S.; Liang, P.; Baldini, Antonio; Yu, Y. E.
Gain of Function of Tbx1 Affects Pharyngeal and Heart Development in the Mouse 1.1 Articolo in rivista 2009 F., Vitelli; T., Huynh; Baldini, Antonio
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
In vivo response to high-resolution variation of Tbx1 mRNA dosage. 1.1 Articolo in rivista 2008 Zhang, Z; Baldini, Antonio
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
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