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コーパス検索結果 (1語後でソート)

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1 are initiated by somatic inactivation of the VHL tumor suppressor gene.
2 d by germ line mutations that inactivate the VHL tumor suppressor gene.
3 sease is caused by germline mutations of the VHL tumor suppressor gene.
4 ting of tumors caused by inactivation of the VHL tumor suppressor gene.
5  is caused by mutational inactivation of the VHL tumor suppressor gene.
6 or may not have a germline mutation in their VHL tumor-suppressor gene.
7 lelic inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene.
8 ation/inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene.
9 in ligase activity of the von Hippel-Lindau (VHL) tumor suppressor gene.
10 ated with mutation of the von Hippel-Lindau (VHL) tumor suppressor gene.
11 lelic inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene.
12 s due to mutations in the Von Hippel-Lindau (VHL) tumor suppressor gene.
13 ted by the product of the von Hippel-Lindau (VHL) tumor suppressor gene.
14 s from germline and somatic mutations in the VHL tumor suppressor gene and is characterized by highly
15 ease is caused by germ-line mutations in the VHL tumor suppressor gene and is the most common cause o
16     Patients with germ line mutations in the VHL tumor suppressor gene are predisposed to the develop
17 tivating mutations of the von Hippel-Lindau (VHL) tumor suppressor gene are associated with inherited
18 epigenetic changes in the von Hippel-Lindau (VHL) tumor suppressor gene are common in sporadic conven
19 erm line mutations in the Von Hippel-Lindau (VHL) tumor suppressor gene are predisposed to the develo
20          Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene cause tissue-specific tumors,
21       Inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene causes the familial cancer sy
22 mline inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene causes the von Hippel-Lindau
23               Loss of the von Hippel-Lindau (VHL) tumor suppressor gene contributes to proliferative
24 he E-cadherin (E-cad) and von Hippel-Lindau (VHL) tumor suppressor gene CpG island regions in normal
25 y explain why patients with mutations in the VHL tumor suppressor gene display cancerous lesions in s
26                      Thus, loss of Tsc-2 and VHL tumor suppressor gene function appears to have simil
27                   Loss of von Hippel-Lindau (VHL) tumor suppressor gene function occurs in familial a
28                                          The VHL tumor suppressor gene has previously been reported t
29                       The von Hippel-Lindau (VHL) tumor suppressor gene has a critical role in the pa
30 e mutations in one of the three exons of the VHL tumor suppressor gene have been found in the majorit
31      The discovery of a relationship for the VHL tumor suppressor gene, hypoxia inducible factor-1 al
32 ity of selectively targeting the loss of the VHL tumor suppressor gene in clear cell renal carcinoma
33 ghts into the role of the von-Hippel Lindau (VHL) tumor suppressor gene in hereditary and sporadic cl
34 c clear-cell RCC tumors are characterized by VHL tumor suppressor gene inactivation.
35                        Thus, the loss of the VHL tumor suppressor gene is central to changes that con
36                                          The VHL tumor suppressor gene is inactivated in patients wit
37   In VHL disease, a germline mutation of the VHL tumor suppressor gene is inherited, and loss of func
38                       The von Hippel-Lindau (VHL) tumor suppressor gene is inactivated in both sporad
39                       The von Hippel-Lindau (VHL) tumor suppressor gene is inactivated in the majorit
40       Inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene is linked to the hereditary V
41                       The von Hippel-Lindau (VHL) tumor suppressor gene is mutated as an early event
42                       The von Hippel-Lindau (VHL) tumor suppressor gene is mutated in most human kidn
43                       The von Hippel-Lindau (VHL) tumor suppressor gene is mutated in patients with V
44                       The von Hippel-Lindau (VHL) tumor suppressor gene is mutated in patients with V
45 r loss of function of the von Hippel-Lindau (VHL) tumor suppressor gene is regularly found in sporadi
46 he hereditary loss of the von Hippel-Lindau (VHL) tumor suppressor gene is the leading cause of death
47 The absence of functional von Hippel-Lindau (VHL) tumor suppressor gene leads to the development of n
48  to loss of chromosome 3p, which harbors the VHL tumor suppressor gene, loss of chromosome 14q, which
49   Loss of function in the von Hippel-Lindau (VHL) tumor suppressor gene occurs in familial and most s
50 ther allelic loss of the recently identified VHL tumor suppressor gene on chromosome 3p25-26 occurs i
51  is the result of a germline mutation of the VHL tumor suppressor gene on the short arm of chromosome
52  that mutations and allelic deletions of the VHL tumor suppressor gene play a role in the tumorigenes
53                             Mutations in the VHL tumor suppressor gene predispose individuals to high
54 ting mutations within the von Hippel-Lindau (VHL) tumor suppressor gene predispose patients to develo
55 Germline mutations in the von Hippel-Lindau (VHL) tumor suppressor gene predispose people to renal ca
56    Inheritance of an inactivated form of the VHL tumor suppressor gene predisposes patients to develo
57   The inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene predisposes affected individu
58                We have demonstrated that the VHL tumor suppressor gene product represses TGF-beta1 mR
59 nt on the presence of the von Hippel-Lindau (VHL) tumor suppressor gene product, pVHL.
60        The product of the von Hippel-Lindau (VHL) tumor suppressor gene, pVHL, functions as a ubiquit
61                             Mutations in the VHL tumor suppressor gene result in constitutive express
62 in which mutations in the von Hippel-Lindau (VHL) tumor suppressor gene result in accumulation of hyp
63  hemangioblastomas in the von Hippel-Lindau (VHL) tumor suppressor gene syndrome, VHL disease, are un
64        The product of the von Hippel-Lindau (VHL) tumor suppressor gene, the gene inactivated in VHL
65 ), cells deficient in the von Hippel-Lindau (VHL) tumor suppressor gene use glutamine to generate cit
66             Recently, the Von-Hippel Lindau (VHL) tumor suppressor gene was identified at chromosome
67 by an inactivation of the von Hippel-Lindau (VHL) tumor-suppressor gene with subsequent stabilization
68 sease is caused by germline mutations in the VHL tumor suppressor gene, with Type 2B missense VHL mut

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