Research output per year
Research output per year
Jill’s research group uses a functional genomics approach to explore the fundamental processes underlying craniofacial development, and in particular, centers on identifying and delineating the role of factors that underlie the human congenital anomaly, cleft palate. Cleft palate has an estimated incidence of 1 in 2500 live births and in approximately 50% of cases, it occurs as an isolated entity while the remainder of cases arise as part of syndromes where structures other than the palate are affected.
Recent advances in delineating the molecular mechanisms underlying cleft palate have been largely derived from analysis of syndromic forms of cleft palate; for example mutations in the genes encoding the transcription factors p63 and interferon regulatory factor 6, the cell adhesion molecule nectin 1 and the nucleolar phosphoprotein Tcof1 underlie congenital malformation syndromes that display cleft palate as part of the phenotype. Jill's laboratory is using a combination of approaches including developmental biology, gene targeting, mouse transgenics and biochemical techniques to investigate the role of these genes and to piece together the pathways in which they function during palate development.
Current Lab Members
Karen Mitchell, Post-doc
Ron Blance, RA
Rose Richardson, 2nd year PhD student
Robert Sullivan, 1st year PhD student
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review