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Dr Rebecca BiltonBiography/ BackgroundResearch Positions and Experience:Post-doctoral Scientist (September 2005 - )/ Post-doctoral Fellow (July 2007-.
Characterisation of the oxygen-sensor, FIH-1.
Laboratory of Dr D. Peet, Molecular and Biomedical Sciences, The
University of Adelaide, Australia.
Funded by a Heart Foundation Grant, the ARC Special Research Centre for the Molecular Genetics of Development and a 3 year APDI Fellowship. Post-doctoral Fellow (September 2003-2005).
Expression and function of the acetyl-transferase ARD1, in angiogenesis
and cancer.
Laboratory of Dr J. Pouyssegur. Signalisation, Biologie du Developpement
et Cancer, CNRS-UMR 6543, Centre Antoine Lacassagne, Nice, France.
Funded by competitive fellowships from the World Health Organisation (1 year) and CNRS Poste Rouge -Foreign Research Associate Fellowship (1 year). Post-doctoral position (2003, 6 months).
Research into the biological function of the HIF-1a asparagine
hydroxylase, FIH1.
Laboratory of Assoc. Prof. M. Whitelaw, Molecular Biosciences, The
University of Adelaide, Australia.
PhD candidature (1999- 2003).
Studies into the Receptor-Mediated Induction of Hypoxia Inducible Factor
1a
Biochemistry discipline, The University of Adelaide, Australia.
Funded with an APA and a CRC/CSIRO Top-up Scholarship for 4 years. Research Assistant (1997-1999).
Research on the identification, localisation and function of the Battens
protein (CLN3p) and screening for putative Breast cancer tumour
suppressor genes.
Laboratory of Prof. G. Sutherland. Department of Cytogenetics and
Molecular Biology, WCH, Adelaide, Australia.
Funded as part of an NHMRC grant. Research Assistant (2 month placement, Feb-March 1998).
Large-scale reverse genetic screen for C.elegans mutants.
Nemapharm Biotech. Cambridge, Boston, USA.
QualificationsPhD in Science (Biochemistry). 2003.Studies into the Receptor-Mediated Induction of Hypoxia Inducible Factor 1a. Biochemistry, Molecular Biosciences, Adelaide University. Bachelor of Biotechnology (Honours). Research Interestshttp://www.adelaide.edu.au/mbs/research/peet/PublicationsWong YS, Farooq M, Bilton RL, Lee Y, Teo EW, Peet DJ, Ge R, Raghunath M. Prolyl/ asparaginyl hydroxylase inhibitors accelerate angiogenesis through HIF-1a: Novel applications of hydralazine, ciclopirox and pyridine-2, 4-dicarboxylate. Circ Res (submitted) Manuscript No: CIRCRESAHA/2007/157313. Impact Factor : 9.4Bilton RL, Trottier E, Pouyssegur J and Brahimi-Horn MC. ARDent about acetylation and deacetylation in hypoxia signalling. Trends Cell Biol. 2006 16(12):616-21. Impact Factor : 11.79 ; Citations (2) Bilton RL, Mazure NM, Trottier E, Hattab M, Dery MA, Richard DE, Pouyssegur J and Brahimi-Horn MC. Arrest-defective-1 protein, an acetyltransferase, does not alter stability of hypoxia-inducible factor (HIF)-1a and is not induced by hypoxia or HIF. J Biol Chem. 2005 280(35):31132-40. Impact Factor: 5.85; Citations (24) Mazure NM, Brahimi-Horn MC, Berta MA, Bilton RL, Dayan F, Ginouves A, Berra E and Pouyssegur J. HIF-1: master and commander of the hypoxic world. Biochem Pharmacol. 2004. 68(6):971-80. Impact Factor: 3.61; Citations (30) Bilton RL and Booker GW. The subtle side to Hypoxia Inducible Factor (HIF1a) regulation. Eur J Biochem. 2003. 270:1-8. Impact Factor: 3.16; Citations (42) Settasatian C, Whitmore SA, Crawford J, Bilton RL, Cleton-Jansen, AM, Sutherland GR, Callen DF. Genomic structure and expression analysis of the spastic paraplegia gene, SPG7. Hum Genet. 1999 Jul-Aug; 105(1-2):139-44. Impact Factor: 4.33; Citations (13) Kremmidiotis G, Lensink IL, Bilton RL, Woollatt E, Chataway TK, Sutherland GR, Callen DF.The Batten disease gene product (CLN3p) is a Golgi integral membrane protein. Hum Mol Genet. 1999 Mar; 8(3):523-31. Impact Factor: 7.76; Citations (31) Entry last updated: Friday, 3 Aug 2007 The information in this directory is provided to support the academic, administrative and business activities of the University of Adelaide. To facilitate these activities, entries in the University Phone Directory are not limited to University employees. The use of information provided here for any other purpose, including the sending of unsolicited commercial material via email or any other electronic format, is strictly prohibited. The University reserves the right to recover all costs incurred in the event of breach of this policy. |
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