Loss of Cited2 causes congenital heart disease by perturbing left–right patterning of the body axis

Conditional deletion of Cited2 results in defective corneal epithelial morphogenesis and maintenance

(2009) Yu Chen et al.   DEVELOPMENTAL BIOLOGY

The transcription co-factor CITED2 functions during sex determination and early gonad development

(2009) Frank William Buaas et al.   HUMAN MOLECULAR GENETICS

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly

(2009) Erich Roessler et al.   MOLECULAR GENETICS AND METABOLISM

Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency

(2008) Simon T. MacDonald et al.   CARDIOVASCULAR RESEARCH

Cited2 is required for the proper formation of the hyaloid vasculature and for lens morphogenesis

(2008) Y. Chen et al.   DEVELOPMENT

Cited2 is required for fetal lung maturation

(2008) Bing Xu et al.   DEVELOPMENTAL BIOLOGY

Broad mesodermal and endodermal deletion ofNodalat postgastrulation stages results solely in left/right axial defects

(2008) Amit Kumar et al.   DEVELOPMENTAL DYNAMICS

BMP/SMAD1 signaling sets a threshold for the left/right pathway in lateral plate mesoderm and limits availability of SMAD4

(2008) M. B. Furtado et al.   GENES & DEVELOPMENT

Mutation of HAIRY-AND-ENHANCER-OF-SPLIT-7 in humans causes spondylocostal dysostosis

(2008) D. B. Sparrow et al.   HUMAN MOLECULAR GENETICS