BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 25563310)

  • 1. Clinical and genetic investigation of a multi-generational Chinese family afflicted with Von Hippel-Lindau disease.
    Zhang J; Ma J; Du X; Wu D; Ai H; Bai J; Dong S; Yang Q; Qu K; Lyu Y; Valenzuela RK; Liu C
    Chin Med J (Engl); 2015 Jan; 128(1):32-8. PubMed ID: 25563310
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Familial and genetic study in a large Chinese kindred with von Hippel-Lindau disease and gene mutation analysis].
    Zhang J; Huang YR; Wang JD; Fan XD
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):5-9. PubMed ID: 14767899
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic study of a large Chinese kindred with von Hippel-Lindau disease.
    Huang YR; Zhang J; Wang JD; Fan XD
    Chin Med J (Engl); 2004 Apr; 117(4):552-7. PubMed ID: 15109448
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Intronic mutation of the VHL gene associated with central nervous system hemangioblastomas in two Chinese families with Von Hippel-Lindau disease: case report.
    Liu Z; Zhou J; Li L; Yi Z; Lu R; Li C; Gong K
    BMC Med Genet; 2020 Oct; 21(1):191. PubMed ID: 33004005
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Family history of von Hippel-Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patients.
    Wu P; Zhang N; Wang X; Ning X; Li T; Bu D; Gong K
    J Hum Genet; 2012 Apr; 57(4):238-43. PubMed ID: 22357542
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel mutation links to von Hippel-Lindau syndrome in a Chinese family with hemangioblastoma.
    Fu XM; Zhao SL; Gui JC; Jiang YQ; Shen MN; Su DL; Gu BJ; Wang XQ; Ren QJ; Yin XD; Huang WB; Chen XG
    Genet Mol Res; 2015 May; 14(2):4513-20. PubMed ID: 25966224
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Germline mutations in the von Hippel-Lindau disease (VHL) gene in mainland Chinese families.
    Zhang J; Huang Y; Pan J; Liu D; Zhou L; Xue W; Chen Q; Dong B; Xuan H
    J Cancer Res Clin Oncol; 2008 Nov; 134(11):1211-8. PubMed ID: 18446368
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a novel duplication mutation in the VHL gene in a large Chinese family with Von Hippel-Lindau (VHL) syndrome.
    Cao LH; Kuang BH; Chen C; Hu C; Sun Z; Chen H; Wang SS; Luo Y
    Genet Mol Res; 2014 Dec; 13(4):10177-83. PubMed ID: 25501229
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Von Hippel-Lindau syndrome. A pleomorphic condition.
    Friedrich CA
    Cancer; 1999 Dec; 86(11 Suppl):2478-82. PubMed ID: 10630173
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel mutation in the VHL gene in a Chinese family with von Hippel-Lindau disease.
    Wu X; Chen L; Zhang Y; Xie H; Xue M; Wang Y; Huang H
    BMC Med Genet; 2018 Nov; 19(1):204. PubMed ID: 30477447
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genotype-phenotype correlations in Chinese von Hippel-Lindau disease patients.
    Peng S; Shepard MJ; Wang J; Li T; Ning X; Cai L; Zhuang Z; Gong K
    Oncotarget; 2017 Jun; 8(24):38456-38465. PubMed ID: 28388566
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Von Hippel-Lindau disease type 2 in a Chinese family with a VHL p.W88X truncation.
    Zhang M; Wang J; Jiang J; Zhan X; Ling Y; Lu Z; Guo J; Gao X
    Endocrine; 2015 Feb; 48(1):83-8. PubMed ID: 25069792
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Germline mutation of Glu70Lys is highly frequent in Korean patients with von Hippel-Lindau (VHL) disease.
    Hwang S; Ku CR; Lee JI; Hur KY; Lee MS; Lee CH; Koo KY; Lee JS; Rhee Y
    J Hum Genet; 2014 Sep; 59(9):488-93. PubMed ID: 25078357
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial and genetic researches on three Chinese families with von Hippel-Lindau disease.
    Mao XC; Su ZP; Yu WQ; Zheng WM; Zeng YJ
    Neurol Res; 2009 Sep; 31(7):743-7. PubMed ID: 19133167
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Germ line mutations in Chinese kindreds with von Hippel-Lindau syndrome].
    Zhang J; Huang YR; Pan JH; Liu DM; Zhou LX; Xue W; Chen Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Apr; 24(2):124-7. PubMed ID: 17407064
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular-genetic diagnostics of von Hippel-Lindau syndrome (VHL) in Bulgaria: first complex mutation event in the VHL gene.
    Glushkova M; Dimova P; Yordanova I; Todorov T; Tourtourikov I; Mitev V; Todorova A
    Int J Neurosci; 2018 Feb; 128(2):117-124. PubMed ID: 28849724
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Large germline deletion of the VHL gene in Chinese families with von Hippel-Lindau syndrome].
    Zhang J; Chen HG; Xue W; Zhou LX; Huang YR
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):539-41. PubMed ID: 19806577
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical and mutation analysis of four Chinese families with von Hippel-Lindau disease.
    Chen J; Geng W; Zhao Y; Zhao H; Wang G; Huang F; Liu F; Geng X
    Clin Transl Oncol; 2013 May; 15(5):391-7. PubMed ID: 23143947
    [TBL] [Abstract][Full Text] [Related]  

  • 19. VHL Germline Mutations in Argentinian Patients with Clinical Diagnoses or Single Typical Manifestations of Type 1 von Hippel-Lindau Disease.
    Mathó C; Sansó G; Diez B; Barontini M; Pennisi PA
    Genet Test Mol Biomarkers; 2016 Dec; 20(12):771-776. PubMed ID: 27617348
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A variety of phenotype with R161Q germline mutation of the von Hippel-Lindau tumor suppressor gene in Japanese kindred.
    Iida K; Okimura Y; Takahashi K; Inomata S; Iguchi G; Kaji H; Chihara K
    Int J Mol Med; 2004 Mar; 13(3):401-4. PubMed ID: 14767570
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.