von Hippel-Lindau disease.
By R. Lonser, G. Glenn, McClellan Walther, Emily Y. Chew, S. Libutti, W. Marston Linehan, E. Oldfield. The Lancet, 2003
2,062 citations recorded by the source corpus.
Subfields: Cancer Research, Pulmonary and Respiratory Medicine, Surgery
View Paper: https://www.semanticscholar.org/paper/e140f0179be12f6f84a2e212ac13484c16be38be
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In Cancer Research
In Pulmonary and Respiratory Medicine
Citations in the corpus
- The von Hippel–Lindau tumour suppressor protein: O2 sensing and cancer (2008, neutral): “Both HIF-dependent and HIF-independent VHL functions are likely to contribute to VHL-defective tumorigenesi”
- Angiogenesis as a therapeutic target (2005, positive): “Renal cell carcinomas have a particularly high level of VEGF-A expression, consistent with the notion that inactivating VHL mutations occur in about 50p of such tumour”
- Discovery and development of bevacizumab, an anti-VEGF antibody for treating cancer (2004, neutral): “The gene encoding VHL is inactivated in patients with von Hippel-Lindau disease, an autosomal dominant neoplasia syndrome characterized by capillary haemangioblastomas in retina and cerebellum, and in most sporadic clear-cell renal carcinoma”