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

A Mechanism for Gene-Environment Interaction in the Etiology of Congenital Scoliosis

(2012) Duncan B. Sparrow et al.   CELL

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

(2011) Subreena Simrick et al.   DEVELOPMENTAL BIOLOGY

Sprouty2 controls proliferation of palate mesenchymal cells via fibroblast growth factor signaling

(2010) Kaori Matsumura et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Conditional expression of Spry1 in neural crest causes craniofacial and cardiac defects

(2010) Xuehui Yang et al.   BMC DEVELOPMENTAL BIOLOGY

BMPs and FGFs target Notch signalling via jagged 2 to regulate tooth morphogenesis and cytodifferentiation

(2010) T. A. Mitsiadis et al.   DEVELOPMENT

Tbx1 Regulates Proliferation and Differentiation of Multipotent Heart Progenitors

(2009) Li Chen et al.   CIRCULATION RESEARCH

Genetic Variation at the Proprotein Convertase Subtilisin/Kexin Type 5 Gene Modulates High-Density Lipoprotein Cholesterol Levels

(2009) Iulia Iatan et al.   Circulation-Cardiovascular Genetics

Gain of function ofTbx1affects pharyngeal and heart development in the mouse

(2009) Francesca Vitelli et al.   GENESIS

Combined modality treatment improves tumor control and overall survival in patients with early stage Hodgkin's lymphoma: a systematic review

(2009) C. Herbst et al.   HAEMATOLOGICA

Hodgkin's Lymphoma in Adolescents Treated With Adult Protocols: A Report From the German Hodgkin Study Group

(2009) Dennis A. Eichenauer et al.   JOURNAL OF CLINICAL ONCOLOGY

Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner

(2009) F. Gabriella Fulcoli et al.   PLoS One

Chordin Is a Modifier of Tbx1 for the Craniofacial Malformations of 22q11 Deletion Syndrome Phenotypes in Mouse

(2009) Murim Choi et al.   PLoS Genetics

Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome

(2008) Elizabeth Goldmuntz et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

An FGF autocrine loop initiated in second heart field mesoderm regulates morphogenesis at the arterial pole of the heart

(2008) E. J. Park et al.   DEVELOPMENT

Specific regions within the embryonic midbrain and cerebellum require different levels of FGF signaling during development

(2008) M. A. Basson et al.   DEVELOPMENT