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

Alfred S. L. Cheng

Institute of Digestive Disease

The Chinese University of Hong Kong

Hong Kong SAR

China

[email]@cuhk.edu.hk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Institute of Digestive Disease, The Chinese University of Hong Kong, Hong Kong SAR, China. 2011
  • Department of Medicine and Therapeutics, Prince of Wales Hospital, Shatin, New Territories, China. 2003 - 2004

References

  1. EZH2-mediated concordant repression of Wnt antagonists promotes β-catenin-dependent hepatocarcinogenesis. Cheng, A.S., Lau, S.S., Chen, Y., Kondo, Y., Li, M.S., Feng, H., Ching, A.K., Cheung, K.F., Wong, H.K., Tong, J.H., Jin, H., Choy, K.W., Yu, J., To, K.F., Wong, N., Huang, T.H., Sung, J.J. Cancer Res. (2011) [Pubmed]
  2. Cyclooxygenase-2 pathway correlates with vascular endothelial growth factor expression and tumor angiogenesis in hepatitis B virus-associated hepatocellular carcinoma. Cheng, A.S., Chan, H.L., To, K.F., Leung, W.K., Chan, K.K., Liew, C.T., Sung, J.J. Int. J. Oncol. (2004) [Pubmed]
  3. Specific COX-2 inhibitor, NS-398, suppresses cellular proliferation and induces apoptosis in human hepatocellular carcinoma cells. Cheng, A.S., Chan, H.L., Leung, W.K., Wong, N., Johnson, P.J., Sung, J.J. Int. J. Oncol. (2003) [Pubmed]
 
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