p53 suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome von Caprio, Cinzia, Baldini, Antonio

Volltext

Subepicardial endothelial cells invade the embryonic ventricle wall to form coronary arteries von Tian, Xueying, Hu, Tianyuan, Zhang, Hui, He, Lingjuan, Huang, Xiuzhen, Liu, Qiaozhen, Yu, Wei, He, Liang, Yang, Zhongzhou, Zhang, Zhen, Zhong, Tao P, Yang, Xiao, Yang, Zhen, Yan, Yan, Baldini, Antonio, Sun, Yunfu, Lu, Jie, Schwartz, Robert J, Evans, Sylvia M, Gittenberger-de Groot, Adriana C, Red-Horse, Kristy, Zhou, Bin

Volltext

Cardiopharyngeal mesoderm origins of musculoskeletal and connective tissues in the mammalian pharynx von Adachi, Noritaka, Bilio, Marchesa, Baldini, Antonio, Kelly, Robert G.

Volltext

Rebalancing gene haploinsufficiency in vivo by targeting chromatin von Fulcoli, Filomena Gabriella, Franzese, Monica, Liu, Xiangyang, Zhang, Zhen, Angelini, Claudia, Baldini, Antonio

Volltext

Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development von Zhang, Zhen, Huynh, Tuong, Baldini, Antonio

Volltext

Tbx1 regulates extracellular matrix-cell interactions in the second heart field von Alfano, Daniela, Altomonte, Alessandra, Cortes, Claudio, Bilio, Marchesa, Kelly, Robert G, Baldini, Antonio

Volltext

A dual role forTbx1in cardiac lymphangiogenesis through genetic interaction withVegfr3 von Martucciello, Stefania, Turturo, Maria Giuseppina, Bilio, Marchesa, Cioffi, Sara, Chen, Li, Baldini, Antonio, Illingworth, Elizabeth

Volltext

Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm von Nomaru, Hiroko, Liu, Yang, De Bono, Christopher, Righelli, Dario, Cirino, Andrea, Wang, Wei, Song, Hansoo, Racedo, Silvia E., Dantas, Anelisa G., Zhang, Lu, Cai, Chen-Leng, Angelini, Claudia, Christiaen, Lionel, Kelly, Robert G., Baldini, Antonio, Zheng, Deyou, Morrow, Bernice E.

Volltext

Transcriptional and epigenetic characterization of a new in vitro platform to model the formation of human pharyngeal endoderm von Cipriano, Andrea, Colantoni, Alessio, Calicchio, Alessandro, Fiorentino, Jonathan, Gomes, Danielle, Moqri, Mahdi, Parker, Alexander, Rasouli, Sajede, Caldwell, Matthew, Briganti, Francesca, Roncarolo, Maria Grazia, Baldini, Antonio, Weinacht, Katja G, Tartaglia, Gian Gaetano, Sebastiano, Vittorio

Volltext

Transcriptional control in cardiac progenitors: Tbx1 interacts with the BAF chromatin remodeling complex and regulates Wnt5a von Chen, Li, Fulcoli, Filomena Gabriella, Ferrentino, Rosa, Martucciello, Stefania, Illingworth, Elizabeth A, Baldini, Antonio

Volltext

TBX1 Represses Vegfr2 Gene Expression and Enhances the Cardiac Fate of VEGFR2+ Cells von Lania, Gabriella, Ferrentino, Rosa, Baldini, Antonio

Volltext

EZH2 is required for parathyroid and thymic development through differentiation of the third pharyngeal pouch endoderm von Caprio, Cinzia, Lania, Gabriella, Bilio, Marchesa, Ferrentino, Rosa, Chen, Li, Baldini, Antonio

Volltext

Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome von Bhalla, Pratibha, Du, Qiumei, Kumar, Ashwani, Xing, Chao, Moses, Angela, Dozmorov, Igor, Wysocki, Christian A, Cleaver, Ondine B, Pirolli, Timothy J, Markert, Mary Louise, de la Morena, Maria Teresa, Baldini, Antonio, van Oers, Nicolai Sc

Volltext

Timed mutation and cell-fate mapping reveal reiterated roles of Tbx1 during embryogenesis, and a crucial function during segmentation of the pharyngeal system via regulation of end... von Xu, Huansheng, Cerrato, Fabiana, Baldini, Antonio

Volltext

A Pivotal Role for Endogenous TGF-β-Activated Kinase-1 in the LKB1/AMP-Activated Protein Kinase Energy-Sensor Pathway von Xie, Min, Zhang, Dou, Dyck, Jason R. B., Li, Yi, Zhang, Hui, Morishima, Masae, Mann, Douglas L., Taffet, George E., Baldini, Antonio, Khoury, Dirar S., Schneider, Michael D.

Volltext

Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice von Mastromoro, Gioia, Calcagni, Giulio, Versacci, Paolo, Putotto, Carolina, Chinali, Marcello, Lambiase, Caterina, Unolt, Marta, Pelliccione, Elena, Anaclerio, Silvia, Caprio, Cinzia, Cioffi, Sara, Bilio, Marchesa, Baban, Anwar, Drago, Fabrizio, Digilio, Maria Cristina, Marino, Bruno, Baldini, Antonio

Volltext

Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome von Favicchia, Ilaria, Flore, Gemma, Cioffi, Sara, Lania, Gabriella, Baldini, Antonio, Illingworth, Elizabeth

Volltext

A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field von Huynh, Tuong, Chen, Li, Terrell, Phillip, Baldini, Antonio

Volltext

TBX1 and Basal Cell Carcinoma: Expression and Interactions with Gli2 and Dvl2 Signaling von Caprio, Cinzia, Varricchio, Silvia, Bilio, Marchesa, Feo, Federica, Ferrentino, Rosa, Russo, Daniela, Staibano, Stefania, Alfano, Daniela, Missero, Caterina, Ilardi, Gennaro, Baldini, Antonio

Volltext

A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome von Lania, Gabriella, Franzese, Monica, Adachi, Noritaka, Bilio, Marchesa, Flore, Gemma, Russo, Annalaura, D'Agostino, Erika, Angelini, Claudia, Kelly, Robert G., Baldini, Antonio

Volltext