The relationship between variable SHH signaling and the severity of structural defects in the face and brain.
The FASEB Journal
Cellular dynamics of tissue fusion in craniofacial development and orofacial clefting.
The FASEB Journal
A craniosynostosis-syndrome related Fgfr2 mutation promotes early craniofacial defects in chick.
The FASEB Journal
Quantifying the Genotype to Phenotype Map in Developing Mice.
The FASEB Journal
Effects of Bone Morphogenetic Proteins on TGF-beta, Wnt and BMP Pathways During Tibial Fracture Repair.
The FASEB Journal
Understanding the development of variable craniofacial phenotypes caused by altered methylation affecting Wnt9b in A-strain mice.
The FASEB Journal
Identification and Validation of Gene Expression Profile in Facial Dysmorphology of Craniosynostosis Crouzon Syndrome.
The FASEB Journal
Untangling Sources of Phenotypic Variation Characterizing the Craniofacial Disease Holoprosencephaly.
The FASEB Journal
The cellular basis of hypoxia induced craniofacial malformations.
The FASEB Journal
Postnatal Organogenesis by Transdifferentiation.
The FASEB Journal