IRIS

BALDINI, ANTONIO

BALDINI, ANTONIO  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

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Risultati 1 - 20 di 120 (tempo di esecuzione: 0.05 secondi).
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
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.
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
A Human Alpha-satellite Dna Subset Specific For Chromosome-12 1.1 Articolo in rivista 1990 Baldini, Antonio; M., Rocchi; N., Archidiacono; O. J., Miller; D. A., Miller
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.
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
DiGeorge Syndrome: an update 1.1 Articolo in rivista 2004 Baldini, Antonio
Cloning and chromosome mapping of human and chicken Iroquois (IRX) genes 1.1 Articolo in rivista 2001 K., Ogura; K., Matsumoto; A., Kuroiwa; T., Isobe; T., Otoguro; V., Jurecic; Baldini, Antonio; Y., Matsuda; T., Ogura
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.
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
Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: Genetic evidence of impaired tissue response to Fgf8 1.1 Articolo in rivista 2010 F., Vitelli; G., Lania; T., Huynh; Baldini, Antonio
DiGeorge syndrome: the use of model organisms to dissect complex genetics 1.1 Articolo in rivista 2002 Baldini, Antonio