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Research
MEIS proteins as partners of the TLX1/HOX11 oncoproteinAberrant expression of the TLX1/HOX11 proto-oncogene is associated with a significant subset of T-cell acute lymphoblastic leukemias...
Research
The common BDNF polymorphism may be a modifier of disease severity in Rett syndromeRett syndrome (RTT) is caused by mutations in the transcriptional repressor methyl CpG-binding protein 2 (MECP2).
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Applications are invited for the Louisa Alessandri Memorial Fund Scholarship, valued at $10,000, which is intended to help students with physical disabilities to achieve their career aspirations.
Research
Genetics of Otitis MediaTo determine the genes that play a role in childhood susceptibility to severe OM we established the Western Australian Family Study of OM.
We are delighted to share that The Kids has successfully completed its Athena SWAN Bronze Action Plan.
At The Kids Research Institute Australia, we have a dedicated and diverse team of over 1,000 staff, students and honorary researchers.