Pax9 is required for cardiovascular development and interacts with Tbx1 in the pharyngeal endoderm to control 4th pharyngeal arch artery morphogenesis

Developmental defects affecting the heart and aortic arch arteries are a significant phenotype observed in individuals with 22q11 deletion syndrome and are caused by a microdeletion on chromosome 22q11. TBX1, one of the deleted genes, is expressed throughout the pharyngeal arches and is considered a...

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Detalles Bibliográficos
Autores principales: Phillips, Helen M., Stothard, Catherine A., Shaikh Qureshi, Wasay M., Kousa, Anastasia I., Briones-Leon, J. Alberto, Khasawneh, Ramada R., O'Loughlin, Chloe, Sanders, Rachel, Mazzotta, Silvia, Dodds, Rebecca, Seidel, Kerstin, Bates, Timothy, Nakatomi, Mitsushiro, Cockell, Simon J., Schneider, Jürgen E., Mohun, Timothy J., Maehr, René, Kist, Ralf, Peters, Heiko, Bamforth, Simon D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765178/
https://www.ncbi.nlm.nih.gov/pubmed/31444215
http://dx.doi.org/10.1242/dev.177618

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765178/
https://www.ncbi.nlm.nih.gov/pubmed/31444215
http://dx.doi.org/10.1242/dev.177618

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