Review on VHL (von Hippel-Lindau tumor suppressor), with data on DNA, on the protein encoded, and where the gene is implicated
Mutations in the von Hippel-Lindau (VHL) tumour-suppressor gene result in several forms of cancer. I...
Abstract A germline mutation in the Von-Hippel Lindau (VHL) gene predisposes carriers to development...
Von Hippel-Lindau disease (VHL disease or VHL syndrome) is a familial multisystem neoplastic syndrom...
Von Hippel-Lindau (VHL) disease (OMIM 193300) is an tumor suppressor gene is located on the short ar...
Von Hippel-Lindau (VHL) disease is a hereditary tumor syndrome in which carriers are at an increased...
AbstractThe von Hippel-Lindau tumor suppressor gene (VHL) is best known as an E3 ubiquitin ligase th...
Von Hippel-Lindau (VHL) disease is a hereditary cancer syndrome, where the affected kindreds manifes...
VHLD is an autosomal-dominant disorder transmitted with incomplete penetrance. It results from a def...
Inheritance of one mutant von Hippel-Lindau (VHL) allele gives rise to the development of the autoso...
Mutations of the so-called cancer-susceptibility genes impair the biological function of key factors...
von Hippel-Lindau (vHL) disease is a heritable multisystem cancer syndrome that is associated with a...
AbstractLoss of von Hippel–Lindau protein (pVHL) is known to contribute to the initiation and progre...
Mutational inactivation of the VHL gene is the cause of von Hippel-Lindau (VHL) disease, an autosoma...
VHL is a tumor suppressor gene localized on chromo-some 3p25–26. Mutations of the VHL gene were desc...
The von Hippel-Lindau tumour suppressor gene (VHL) targets hypoxia inducible factor (HIF)-alpha subu...
Mutations in the von Hippel-Lindau (VHL) tumour-suppressor gene result in several forms of cancer. I...
Abstract A germline mutation in the Von-Hippel Lindau (VHL) gene predisposes carriers to development...
Von Hippel-Lindau disease (VHL disease or VHL syndrome) is a familial multisystem neoplastic syndrom...
Von Hippel-Lindau (VHL) disease (OMIM 193300) is an tumor suppressor gene is located on the short ar...
Von Hippel-Lindau (VHL) disease is a hereditary tumor syndrome in which carriers are at an increased...
AbstractThe von Hippel-Lindau tumor suppressor gene (VHL) is best known as an E3 ubiquitin ligase th...
Von Hippel-Lindau (VHL) disease is a hereditary cancer syndrome, where the affected kindreds manifes...
VHLD is an autosomal-dominant disorder transmitted with incomplete penetrance. It results from a def...
Inheritance of one mutant von Hippel-Lindau (VHL) allele gives rise to the development of the autoso...
Mutations of the so-called cancer-susceptibility genes impair the biological function of key factors...
von Hippel-Lindau (vHL) disease is a heritable multisystem cancer syndrome that is associated with a...
AbstractLoss of von Hippel–Lindau protein (pVHL) is known to contribute to the initiation and progre...
Mutational inactivation of the VHL gene is the cause of von Hippel-Lindau (VHL) disease, an autosoma...
VHL is a tumor suppressor gene localized on chromo-some 3p25–26. Mutations of the VHL gene were desc...
The von Hippel-Lindau tumour suppressor gene (VHL) targets hypoxia inducible factor (HIF)-alpha subu...
Mutations in the von Hippel-Lindau (VHL) tumour-suppressor gene result in several forms of cancer. I...
Abstract A germline mutation in the Von-Hippel Lindau (VHL) gene predisposes carriers to development...
Von Hippel-Lindau disease (VHL disease or VHL syndrome) is a familial multisystem neoplastic syndrom...
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