Endoderm-specific deletion ofTbx1reveals an FGF-independent role for Tbx1 in pharyngeal apparatus morphogenesis

Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling

(2012) Subreena Simrick et al.   DEVELOPMENTAL DYNAMICS

Sprouty genes are essential for the normal development of epibranchial ganglia in the mouse embryo

(2011) Subreena Simrick et al.   DEVELOPMENTAL BIOLOGY

Redundant and dosage sensitive requirements for Fgf3 and Fgf10 in cardiovascular development

(2011) Lisa D. Urness et al.   DEVELOPMENTAL BIOLOGY

Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: Genetic evidence of impaired tissue response to Fgf8

(2010) Francesca Vitelli et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

22q11 Deletion Syndrome: A Role for TBX1 in Pharyngeal and Cardiovascular Development

(2010) Peter J. Scambler   PEDIATRIC CARDIOLOGY

Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm

(2009) A. Calmont et al.   DEVELOPMENT

Fibroblast growth factor (FGF) gene expression in the developing cerebellum suggests multiple roles for FGF signaling during cerebellar morphogenesis and development

(2009) Yuichiro Yaguchi et al.   DEVELOPMENTAL DYNAMICS

FRS2αis required for the separation, migration, and survival of pharyngeal-endoderm derived organs including thyroid, ultimobranchial body, parathyroid, and thymus

(2009) Yoko Kameda et al.   DEVELOPMENTAL DYNAMICS

Sox17-2A-iCre: A knock-in mouse line expressing Cre recombinase in endoderm and vascular endothelial cells

(2009) Silvia Engert et al.   GENESIS