Research

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Cleft Lip/Palate

Woman in labThe role of cleft lip/palate genes in the regulation of orofacial ectoderm adhesion dynamics:

Cleft lip/palate (CL/P) is one of the most common human birth defects. Despite many genes having been identified to cause CL/P, the precise roles of these genes in craniofacial development and the contribution of not-genetic factors remain largely unknown. The Cox Lab pursues the function of multiple prominent cleft lip/palate genes in the facial ectoderm. More specifically, we are dissecting the role(s) of these genes and their protein products in regulating the endocytosis and recycling of adherens and tight junction complexes.

Craniofacial Microsomia

ScienceMolecular mechanisms underlying Craniofacial Microsomia

Craniofacial microsomia (CFM) is characterized by craniofacial asymmetry that can involve the maxillae, the mandible and external ear, among other tissues. Various hypotheses have been put forth to explain this sporadic and variable condition that include both genetic and environmental insults. Our work in this area capitalizes on whole genome sequencing technologies in patient cohorts and detailed investigation of the pathogenetic mechanisms in unique animal models of CFM.

Third Research Area

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Fourth Research Area

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Fifth Research Area

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Sixth Research Area

microscopeEnter a detailed description of this area of your research. Image size is 300 x 200

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Laboratory Collaborations

(Name of lab) current collaborators include: list names here. If you've added collaborators to your team page, link to their profiles. For example: Dr. Layla Cronin, Boston Children's Hospital.