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William G. Kaelin

Department of Medical Oncology

Dana-Farber Cancer Institute and Brigham and Women's Hospital

Harvard Medical School

Boston

USA

[email]@*.harvard.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Medical Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Harvard Medical School, Boston, USA. 1998 - 2013
  • Howard Hughes Medical Institute, Chevy Chase, Maryland 20815-6789, USA. 2005 - 2008
  • Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA. 1997 - 2003
  • Dana-Farber Cancer Institute and Brigham and Women's Hospital, Boston, MA 02115, USA. 1998

References

  1. Influence of metabolism on epigenetics and disease. Kaelin, W.G., McKnight, S.L. Cell (2013) [Pubmed]
  2. New cancer targets emerging from studies of the Von Hippel-Lindau tumor suppressor protein. Kaelin, W.G. Ann. N. Y. Acad. Sci. (2010) [Pubmed]
  3. Treatment of kidney cancer: insights provided by the VHL tumor-suppressor protein. Kaelin, W.G. Cancer (2009) [Pubmed]
  4. SDH5 mutations and familial paraganglioma: somewhere Warburg is smiling. Kaelin, W.G. Cancer. Cell (2009) [Pubmed]
  5. Synthetic lethality: a framework for the development of wiser cancer therapeutics. Kaelin, W.G. Genome. Med (2009) [Pubmed]
  6. The von Hippel-Lindau tumour suppressor protein: O2 sensing and cancer. Kaelin, W.G. Nat. Rev. Cancer (2008) [Pubmed]
  7. Oxygen sensing by metazoans: the central role of the HIF hydroxylase pathway. Kaelin, W.G., Ratcliffe, P.J. Mol. Cell (2008) [Pubmed]
  8. Kidney cancer: now available in a new flavor. Kaelin, W.G. Cancer. Cell (2008) [Pubmed]
  9. The von Hippel-Lindau tumor suppressor protein and clear cell renal carcinoma. Kaelin, W.G. Clin. Cancer Res. (2007) [Pubmed]
  10. Von Hippel-Lindau disease. Kaelin, W.G. Annual. Review. Pathology (2007) [Pubmed]
  11. Proline hydroxylation and gene expression. Kaelin, W.G. Annu. Rev. Biochem. (2005) [Pubmed]
  12. The concept of synthetic lethality in the context of anticancer therapy. Kaelin, W.G. Nat. Rev. Cancer (2005) [Pubmed]
  13. The von Hippel-Lindau protein, HIF hydroxylation, and oxygen sensing. Kaelin, W.G. Biochem. Biophys. Res. Commun. (2005) [Pubmed]
  14. The von Hippel-Lindau tumor suppressor gene and kidney cancer. Kaelin, W.G. Clin. Cancer Res. (2004) [Pubmed]
  15. E2F1 as a target: promoter-driven suicide and small molecule modulators. Kaelin, W.G. Cancer Biol. Ther. (2003) [Pubmed]
  16. The von Hippel-Lindau gene, kidney cancer, and oxygen sensing. Kaelin, W.G. J. Am. Soc. Nephrol. (2003) [Pubmed]
  17. How oxygen makes its presence felt. Kaelin, W.G. Genes Dev. (2002) [Pubmed]
  18. Molecular basis of the VHL hereditary cancer syndrome. Kaelin, W.G. Nat. Rev. Cancer (2002) [Pubmed]
  19. The emerging p53 gene family. Kaelin, W.G. J. Natl. Cancer Inst. (1999) [Pubmed]
  20. Functions of the retinoblastoma protein. Kaelin, W.G. Bioessays (1999) [Pubmed]
  21. Taking aim at novel molecular targets in cancer therapy. Kaelin, W.G. J. Clin. Invest. (1999) [Pubmed]
  22. Choosing anticancer drug targets in the postgenomic era. Kaelin, W.G. J. Clin. Invest. (1999) [Pubmed]
  23. The p53 gene family. Kaelin, W.G. Oncogene (1999) [Pubmed]
  24. Another p53 Doppelgänger?. Kaelin, W.G. Science (1998) [Pubmed]
  25. Functions of the von Hippel-Lindau tumour suppressor protein. Kaelin, W.G., Iliopoulos, O., Lonergan, K.M., Ohh, M. J. Intern. Med. (1998) [Pubmed]
  26. Alterations in G1/S cell-cycle control contributing to carcinogenesis. Kaelin, W.G. Ann. N. Y. Acad. Sci. (1997) [Pubmed]
 
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