| Mutation IN Von Hippel Lindau tumor suppressor is associated with polycythemia | None |
| Although no evidence for a classic tumor suppressor role for VHL in NB could be obtained, a strong correlation was observed between reduced levels of VHL mRNA and low patient survival probability. | None |
| These results suggest that the tumor suppressor pVHL has an unexpected function to upregulate the tumor suppressor p53. | None |
| Loss of the tumor suppressor Vhlh leads to upregulation of Cxcr4 and rapidly progressive glomerulonephritis in mice. | None |
| The von Hippel-Lindau tumor suppressor protein controls ciliogenesis by orienting microtubule growth. | None |
| VHL protein exerts its tumor suppressor action, at least partially, via inhibition of p22phox-based Nox4/Nox1 NADPH oxidase-dependent reactive oxygen species generation | None |
| Podocyte deletion of VHL, the gene encoding for von Hippel-Lindau tumor suppressor protein, leads to rapidly progressive glomerulonephritis. | None |
| HIF-1alpha stabilization correlates with down-regulation of the tumour suppressor von Hippel-Lindau protein (pVHL. | None |
| microtubule-dependent functions of von Hippel-Lindau tumour suppressor are influenced by kinesin-2 | None |
| Allele-specific regulation of primary cilia function by the von Hippel-Lindau tumor suppressor. | None |
| A yeast two-hybrid system reconstituting substrate recognition of the von Hippel-Lindau tumor suppressor protein. | None |
| The von hippel-lindau tumor suppressor protein: an update. | None |
| Clusterin shows possible important functions in tumor suppression by the von Hippel-Lindau disease (VHL) gene product. May provide better understanding of retinal hemangioblastoma associated with VHL disease. | None |
| The VHL tumor suppressor and HIF: insights from genetic studies in mice. | None |
| The von Hippel-Lindau tumor suppressor protein and Egl-9-Type proline hydroxylases regulate the large subunit of RNA polymerase II in response to oxidative stress. | None |
| VHL mutation alone is insufficient for tumor formation; study shows that epididymal cystadenomas from VHL patients frequently also lack expression of the PTEN tumor suppressor and display activation of phosphatidylinositol 3-kinase pathway signaling. | None |
| Endothelial function of von Hippel-Lindau tumor suppressor gene: control of fibroblast growth factor receptor signaling. | None |
| genetic variants of HIF1A (Hypoxia-inducible factor 1-alpha )and VHL(von Hippel-Lindau tumor suppressor protein) are not associated with acute mountain sickness symptoms that occur in Sherpas at extremely high altitudes | None |
| Key role for activin B in cellular transformation after loss of the von Hippel-Lindau tumor suppressor. | None |
| novel homeostatic control of keratinocyte proliferation and migration mediated via TAK1 regulation of von Hippel-Lindau tumor suppressor | None |