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Novel strategies to understand and treat craniofacial malformations

Description 
The formation of the head and face is a tightly regulated process, with variations from the genetic program leading to craniofacial defects. We have established a mouse model of craniofacial malformation that shows cleft lip and cleft palate upon inhibition of the retinoic acid pathway. Strikingly, removing the Gdf11 gene in this context is able to rescue these craniofacial defects. We are investigating the mechanisms underlying this genetic interaction, with the aim of harnessing this observation for therapeutical purposes. In this research project, you will be using mouse genetics, state-of-the-art imaging techniques (micro computed tomography and light-sheet microscopy, 3D image analysis and virtual reality softwares), tissue culture techniques (embryonic stem cell and neural crest cell cultures), as well as genomic techniques (RNA sequencing, ATACseq, bioinformatics). This project is suitable for PhD students, but can be tailored for Honours or Master students to tackle parts of it.
Essential criteria: 
Minimum entry requirements can be found here: https://www.monash.edu/admissions/entry-requirements/minimum
Keywords 
Development, regenerative medicine, embryonic stem cells, neural crest cells, 3D image analysis, mouse genetics, genomics
School 
Australian Regenerative Medicine Institute (ARMI)
Available options 
PhD/Doctorate
Masters by research
Honours
BMedSc(Hons)
Time commitment 
Full-time
Top-up scholarship funding available 
No
Physical location 
Clayton Campus
Co-supervisors 
Dr 
Jan Manent
Assoc Prof 
Edwina McGlinn

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