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 Publications
  Regulation of NR4A nuclear receptor expression by oncogenic BRAF in melanoma cells
  The recycling endosome protein Rab17 regulates melanocytic filopodia formation and melanosome trafficking
  NFIA controls telencephalic progenitor cell differentiation through repression of the Notch effector Hes1
  Multiple genes and locus interactions in susceptibility to vitiligo
  PPAR³ agonists attenuate proliferation and modulate Wnt/²-catenin signalling in melanoma cells
  Analysis of Cultured Human Melanocytes Based on Polymorphisms within the SLC45A2/MATP, SLC24A5/NCKX5, and OCA2/P Loci
  Melanocortin-1 receptor signaling markedly induces the expression of the NR4A nuclear receptor subgroup in melanocytic cells
  Non-DNA binding, dominant-negative, human PPAR gamma mutations cause lipodystrophic insulin resistance
  Halofenate is a selective peroxisome proliferator-activated receptor gamma modulator with antidiabetic activity
  A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis
  Orphan nuclear receptors: therapeutic opportunities in skeletal muscle
  Co-expression of SOX9 and SOX10 during melanocytic differentiation in vitro
  Skeletal muscle and nuclear hormone receptors: Implications for cardiovascular and metabolic disease
  Anlaysis of complementary expression profiles following WT1 induction versus repression reveals the cholesterol/fatty acid synthetic pathways as a possible major target of WT1
  Tyrosine Agonists reverse the molecular defects associated with dominant-negative mutations in human peroxisome proliferator-activated receptor gamma
  Human melanoblasts in culture: Expression of BRN2 and synergistic regulation by fibroblast growth factor-2, stem cell factor, and endothelin-3
  Wnt-4 regulation by the Wilms' tumour suppressor gene, WT1
  A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate
  The human melanocortin-1 receptor locus: analysis of transcription unit, locus polymorphism and haplotype evolution
  Domains of Brn-2 that mediate homodimerization and interaction with general and melanocytic transcription factors
  Redox regulation of Brn-2/N-Oct-3 POU domain DNA binding activity and proteolytic formation of N-Oct-5 during melanoma cell nuclear extraction
  Chromosomal structure of the human TYRP1 and TYRP2 loci and comparison of the tyrosinase-related protein gene family
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