Search Results - "Bilio, Marchesa"

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

“…Cardiopharyngeal mesoderm (CPM) gives rise to muscles of the head and heart. Using genetic lineage analysis in mice, we show that CPM develops into a broad…”
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miRNeye: a microRNA expression atlas of the mouse eye by Karali, Marianthi, Peluso, Ivana, Gennarino, Vincenzo A, Bilio, Marchesa, Verde, Roberta, Lago, Giampiero, Dollé, Pascal, Banfi, Sandro

“…MicroRNAs (miRNAs) are key regulators of biological processes. To define miRNA function in the eye, it is essential to determine a high-resolution profile of…”
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Tbx1 regulates extracellular matrix-cell interactions in the second heart field by Alfano, Daniela, Altomonte, Alessandra, Cortes, Claudio, Bilio, Marchesa, Kelly, Robert G, Baldini, Antonio

“…Abstract Tbx1, the major candidate gene for DiGeorge or 22q11.2 deletion syndrome, is required for efficient incorporation of cardiac progenitors of the second…”
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EZH2 is required for parathyroid and thymic development through differentiation of the third pharyngeal pouch endoderm by Caprio, Cinzia, Lania, Gabriella, Bilio, Marchesa, Ferrentino, Rosa, Chen, Li, Baldini, Antonio

“…The Ezh2 gene encodes a histone methyltransferase of the polycomb repressive complex 2 that methylates histone H3 lysine 27. In this study, we investigated…”
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Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice by 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

“…Patients with 22q11 deletion syndrome (22q11.2DS) present, in about 75% of cases, typical patterns of cardiac defects, with a particular involvement on the…”
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TBX1 and Basal Cell Carcinoma: Expression and Interactions with Gli2 and Dvl2 Signaling by Caprio, Cinzia, Varricchio, Silvia, Bilio, Marchesa, Feo, Federica, Ferrentino, Rosa, Russo, Daniela, Staibano, Stefania, Alfano, Daniela, Missero, Caterina, Ilardi, Gennaro, Baldini, Antonio

“…Early events of basal cell carcinoma (BCC) tumorigenesis are triggered by inappropriate activation of SHH signaling, via the loss of ( ) or by activating…”
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A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome by Lania, Gabriella, Franzese, Monica, Adachi, Noritaka, Bilio, Marchesa, Flore, Gemma, Russo, Annalaura, D'Agostino, Erika, Angelini, Claudia, Kelly, Robert G., Baldini, Antonio

“…ABSTRACT TBX1 is a key regulator of pharyngeal apparatus (PhAp) development. Vitamin B12 (vB12) treatment partially rescues aortic arch patterning defects of…”
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VEGFR3 modulates brain microvessel branching in a mouse model of 22q11.2 deletion syndrome by Cioffi, Sara, Flore, Gemma, Martucciello, Stefania, Bilio, Marchesa, Turturo, Maria Giuseppina, Illingworth, Elizabeth

“…The loss of a single copy of TBX1 accounts for most of the clinical signs and symptoms of 22q11.2 deletion syndrome, a common genetic disorder that is…”
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Tbx1 represses Mef2c gene expression and is correlated with histone 3 deacetylation of the anterior heart field enhancer by Pane, Luna Simona, Fulcoli, Filomena Gabriella, Cirino, Andrea, Altomonte, Alessandra, Ferrentino, Rosa, Bilio, Marchesa, Baldini, Antonio

“…The gene is haploinsufficient in 22q11.2 deletion syndrome (22q11.2DS), and genetic evidence from human patients and mouse models points to a major role of…”
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A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 by Martucciello, Stefania, Turturo, Maria Giuseppina, Bilio, Marchesa, Cioffi, Sara, Chen, Li, Baldini, Antonio, Illingworth, Elizabeth

“…The transcription factor TBX1 is the major gene implicated in 22q11.2 deletion syndrome (22q11.2DS). The complex clinical phenotype includes vascular anomalies…”
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Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome by Flore, Gemma, Cioffi, Sara, Bilio, Marchesa, Illingworth, Elizabeth

“…In mammals, proper temporal control of neurogenesis and neural migration during embryonic development ensures correct formation of the cerebral cortex. Changes…”
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Tbx1 regulates brain vascularization by Cioffi, Sara, Martucciello, Stefania, Fulcoli, Filomena Gabriella, Bilio, Marchesa, Ferrentino, Rosa, Nusco, Edoardo, Illingworth, Elizabeth

“…The transcription factor TBX1 is the major gene involved in 22q11.2 deletion syndrome (22q11.2DS). Using mouse models of these diseases, we have previously…”
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