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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Paul H. Anderson

Endocrine Research Laboratory

Hanson Institute

Frome Road

Adelaide 5000

Australia

[email]@imvs.sa.gov.au

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Endocrine Research Laboratory, Hanson Institute, Frome Road, Adelaide 5000, Australia. 2005 - 2008
  • Discipline of Medicine, Faculty of Health Science, University of Adelaide and The Hanson Institute, Adelaide, Australia. 2008
  • Hanson Institute, Institute of Medical and Veterinary Science, Adelaide, SA 5000, Australia. 2007

References

  1. Co-expression of CYP27B1 enzyme with the 1.5kb CYP27B1 promoter-luciferase transgene in the mouse. Anderson, P.H., Hendrix, I., Sawyer, R.K., Zarrinkalam, R., Manavis, J., Sarvestani, G.T., May, B.K., Morris, H.A. Mol. Cell. Endocrinol. (2008) [Pubmed]
  2. The skeleton as an intracrine organ for vitamin D metabolism. Anderson, P.H., Atkins, G.J. Mol. Aspects Med. (2008) [Pubmed]
  3. Vitamin D depletion induces RANKL-mediated osteoclastogenesis and bone loss in a rodent model. Anderson, P.H., Sawyer, R.K., Moore, A.J., May, B.K., O'Loughlin, P.D., Morris, H.A. J. Bone Miner. Res. (2008) [Pubmed]
  4. RNAi-mediated silencing of CYP27B1 abolishes 1,25(OH)2D3 synthesis and reduces osteocalcin and CYP24 mRNA expression in human osteosarcoma (HOS) cells. Anderson, P.H., Atkins, G.J., Findlay, D.M., Oloughlin, P.D., Welldon, K., Vincent, C., Morris, H.A. J. Steroid Biochem. Mol. Biol. (2007) [Pubmed]
  5. Modulation of CYP27B1 and CYP24 mRNA expression in bone is independent of circulating 1,25(OH)2D3 levels. Anderson, P.H., O'Loughlin, P.D., May, B.K., Morris, H.A. Bone (2005) [Pubmed]
 
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