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Shiva Reddy

School of Biological Sciences

University of Auckland

Private Bag 92019

Auckland

New Zealand

[email]@auckland.ac.nz

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland, New Zealand. 2003 - 2008
  • Department of Paediatrics, University of Auckland School of Medicine, New Zealand. 2000 - 2003
  • Department of Paediatrics, The Research Centre for Developmental Medicine and Biology, Faculty of Medicine and Health Science, University of Auckland, New Zealand. 2001

References

  1. Presence of residual beta cells and co-existing islet autoimmunity in the NOD mouse during longstanding diabetes: a combined histochemical and immunohistochemical study. Reddy, S., Chai, R.C., Rodrigues, J.A., Hsu, T.H., Robinson, E. J. Mol. Histol. (2008) [Pubmed]
  2. Persistence of residual beta cells and islet autoimmunity during increasing duration of diabetes in NOD mice and experimental approaches toward reversing new-onset disease with bioactive peptides. Reddy, S., Cheung, C.C., Chai, R.C., Rodrigues, J.A. Ann. N. Y. Acad. Sci. (2008) [Pubmed]
  3. Immunolocalization of monocyte chemoattractant protein-1 in islets of NOD mice during cyclophosphamide administration. Reddy, S., Bai, Y., Robinson, E., Ross, J. Ann. N. Y. Acad. Sci. (2006) [Pubmed]
  4. Young NOD mice show increased diabetes sensitivity to low doses of streptozotocin. Reddy, S., Chang, M., Robinson, E. Ann. N. Y. Acad. Sci. (2006) [Pubmed]
  5. Histopathological changes in insulin, glucagon and somatostatin cells in the islets of NOD mice during cyclophosphamide-accelerated diabetes: a combined immunohistochemical and histochemical study. Reddy, S., Pathipati, P., Bai, Y., Robinson, E., Ross, J.M. J. Mol. Histol. (2005) [Pubmed]
  6. Immunohistochemical demonstration of nitrotyrosine, a biomarker of oxidative stress, in islet cells of the NOD mouse. Reddy, S., Bradley, J. Ann. N. Y. Acad. Sci. (2004) [Pubmed]
  7. Immunohistochemical study of caspase-3-expressing cells within the pancreas of non-obese diabetic mice during cyclophosphamide-accelerated diabetes. Reddy, S., Bradley, J., Ginn, S., Pathipati, P., Ross, J.M. Histochem. Cell Biol. (2003) [Pubmed]
  8. Immunolocalization of caspase-3 in pancreatic islets of NOD mice during cyclophosphamide-accelerated diabetes. Reddy, S., Bradley, J., Ross, J.M. Ann. N. Y. Acad. Sci. (2003) [Pubmed]
  9. IL-1beta expression in islet cells of the NOD mouse and its spatial relationship to beta cells and inducible nitric oxide synthase. Reddy, S., Young, M. Ann. N. Y. Acad. Sci. (2002) [Pubmed]
  10. Prevention of cyclophosphamide-induced accelerated diabetes in the NOD mouse by nicotinamide or a soy protein-based infant formula. Reddy, S., Karanam, M., Robinson, E. Int. J. Exp. Diabetes Res. (2001) [Pubmed]
  11. Prevention of autoimmune diabetes by oral administration of syngeneic pancreatic extract to young NOD mice. Reddy, S., Stefanovic, N., Karanam, M. Pancreas (2000) [Pubmed]
  12. Dual-label immunohistochemical study of interleukin-4-and interferon-gamma-expressing cells within the pancreas of the NOD mouse during disease acceleration with cyclophosphamide. Reddy, S., Karanam, M., Poole, C.A., Ross, J.M. Autoimmunity (2000) [Pubmed]
 
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