Description
Differences of sex development include sex chromosome aneuploidies such as Turner syndrom (TS) and Klinefelter syndrome (KS). Women with TS lack one X chromosome leading to various health issues, including growth impairment and infertility. The X chromosome carries about 900 genes and while most of these genes on the second X chromosome is inactivated, about 15% remain active and are therefore candidate genes causing TS. Men with KS carry an additional X chromosome often leading to neurocognitive challenges and infertility. We have developed rat models for TS and KS and using transcriptomic approaches we will identify when expression of X and Y genes and downstream targets are first affected in various organs and tissues. We will intergrate our data with patients data obtained from international collaborators.
Essential criteria:
Minimum entry requirements can be found here: https://www.monash.edu/admissions/entry-requirements/minimum
Keywords
X chromosome, Y chromosome, infertility, cognition, intersex, genomics, human genetics
School
School of Clinical Sciences at Monash Health / Hudson Institute of Medical Research » Molecular and Translational Sciences
Available options
PhD/Doctorate
Masters by research
Honours
BMedSc(Hons)
Graduate Diploma
Time commitment
Full-time
Top-up scholarship funding available
No
Physical location
Monash Health Translation Precinct (Monash Medical Centre)
Co-supervisors
Dr
Shanie Landen