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Alison H. Banham

LRF Haemato-oncology Group

Nuffield Department of Clinical Laboratory Sciences

University of Oxford

John Radcliffe Hospital

UK

[email]@ndcls.ox.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • LRF Haemato-oncology Group, Nuffield Department of Clinical Laboratory Sciences, University of Oxford, John Radcliffe Hospital, UK. 2006 - 2009
  • University of Oxford, John Radcliffe Hospital, Nuffield Department of Clinical Laboratory Sciences, Headington, UK. 2009
  • Leukemia Research Fund Immunodiagnostics Unit, Nuffield Department of Clinical Laboratory Sciences, John Radcliffe Hospital, University of Oxford, United Kingdom. 2005

References

  1. Monoclonal antibodies raised to the human FOXP3 protein can be used effectively for detecting Foxp3(+) T cells in other mammalian species. Banham, A.H., Lyne, L., Scase, T.J., Blacklaws, B.A. Vet. Immunol. Immunopathol. (2009) [Pubmed]
  2. Therapeutic targeting of FOXP3-positive regulatory T cells using a FOXP3 peptide vaccine WO2008081581. Banham, A.H., Pulford, K. Expert. Opin. Ther. Pat (2009) [Pubmed]
  3. Cell-surface IL-7 receptor expression facilitates the purification of FOXP3(+) regulatory T cells. Banham, A.H. Trends Immunol. (2006) [Pubmed]
  4. FOXP3+ regulatory T cells: Current controversies and future perspectives. Banham, A.H., Powrie, F.M., Suri-Payer, E. Eur. J. Immunol. (2006) [Pubmed]
  5. Expression of the FOXP1 transcription factor is strongly associated with inferior survival in patients with diffuse large B-cell lymphoma. Banham, A.H., Connors, J.M., Brown, P.J., Cordell, J.L., Ott, G., Sreenivasan, G., Farinha, P., Horsman, D.E., Gascoyne, R.D. Clin. Cancer Res. (2005) [Pubmed]
 
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