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Jian-Hua Chen

University of Cambridge Metabolic Research Laboratories

Institute of Metabolic Science

University of Cambridge

Cambridge CB2 0QQ

U.K

[email]@cam.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0QQ, U.K. 2009 - 2010
  • Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0QQ, UK. 2004 - 2008

References

  1. Early-life nutrition influences thymic growth in male mice that may be related to the regulation of longevity. Chen, J.H., Tarry-Adkins, J.L., Heppolette, C.A., Palmer, D.B., Ozanne, S.E. Clin. Sci. (2010) [Pubmed]
  2. Maternal protein restriction affects gene expression profiles in the kidney at weaning with implications for the regulation of renal function and lifespan. Chen, J.H., Tarry-Adkins, J.L., Matharu, K., Yeo, G.S., Ozanne, S.E. Clin. Sci. (2010) [Pubmed]
  3. Maternal protein restriction affects postnatal growth and the expression of key proteins involved in lifespan regulation in mice. Chen, J.H., Martin-Gronert, M.S., Tarry-Adkins, J., Ozanne, S.E. PLoS. ONE (2009) [Pubmed]
  4. Adverse effects of reduced oxygen tension on the proliferative capacity of rat kidney and insulin-secreting cell lines involve DNA damage and stress responses. Chen, J.H., Jones, R.H., Tarry-Adkins, J., Smith, N.H., Ozanne, S.E. Exp. Cell Res. (2008) [Pubmed]
  5. DNA damage, cellular senescence and organismal ageing: causal or correlative?. Chen, J.H., Hales, C.N., Ozanne, S.E. Nucleic Acids Res. (2007) [Pubmed]
  6. Heterogeneity in premature senescence by oxidative stress correlates with differential DNA damage during the cell cycle. Chen, J.H., Ozanne, S.E., Hales, C.N. DNA Repair (Amst.) (2005) [Pubmed]
  7. Analysis of expression of growth factor receptors in replicatively and oxidatively senescent human fibroblasts. Chen, J.H., Ozanne, S.E., Hales, C.N. FEBS Lett. (2005) [Pubmed]
  8. Loss of proliferative capacity and induction of senescence in oxidatively stressed human fibroblasts. Chen, J.H., Stoeber, K., Kingsbury, S., Ozanne, S.E., Williams, G.H., Hales, C.N. J. Biol. Chem. (2004) [Pubmed]
 
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