pVHL(19) is a biologically active product of the von Hippel–Lindau gene arising from internal translation initiation

Ítems similars

• Diverse Effects of Mutations in Exon II of the von Hippel-Lindau (VHL) Tumor Suppressor Gene on the Interaction of pVHL with the Cytosolic Chaperonin and pVHL-Dependent Ubiquitin Ligase Activity
  per: Hansen, William J., et al.
  Publicat: (2002)
• The von Hippel-Lindau Protein pVHL Inhibits Ribosome Biogenesis and Protein Synthesis
  per: Zhao, Wen-Ting, et al.
  Publicat: (2013)
• The von Hippel–Lindau tumour suppressor gene: uncovering the expression of the pVHL172 isoform
  per: Chesnel, F, et al.
  Publicat: (2015)
• The molecular basis of von Hippel-Lindau disease.
  per: Iliopoulos, O., et al.
  Publicat: (1997)
• VHL Mutations Linked to Type 2C von Hippel-Lindau Disease Cause Extensive Structural Perturbations in pVHL
  per: Knauth, Katja, et al.
  Publicat: (2009)