BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

169 related articles for article (PubMed ID: 18474617)

  • 1. Combined VHLH and PTEN mutation causes genital tract cystadenoma and squamous metaplasia.
    Frew IJ; Minola A; Georgiev S; Hitz M; Moch H; Richard S; Vortmeyer AO; Krek W
    Mol Cell Biol; 2008 Jul; 28(14):4536-48. PubMed ID: 18474617
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inactivation of the tumor suppressor gene von Hippel-Lindau (VHL) in granulocytes contributes to development of liver hemangiomas in a mouse model.
    Bader HL; Hsu T
    BMC Cancer; 2016 Oct; 16(1):797. PubMed ID: 27733136
    [TBL] [Abstract][Full Text] [Related]  

  • 3. pVHL and PTEN tumour suppressor proteins cooperatively suppress kidney cyst formation.
    Frew IJ; Thoma CR; Georgiev S; Minola A; Hitz M; Montani M; Moch H; Krek W
    EMBO J; 2008 Jun; 27(12):1747-57. PubMed ID: 18497742
    [TBL] [Abstract][Full Text] [Related]  

  • 4. VHL and PTEN loss coordinate to promote mouse liver vascular lesions.
    Chen S; Sanford CA; Sun J; Choi V; Van Dyke T; Samulski RJ; Rathmell WK
    Angiogenesis; 2010 Mar; 13(1):59-69. PubMed ID: 20221685
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Von Hippel-Lindau mutations disrupt vascular patterning and maturation via Notch.
    Arreola A; Payne LB; Julian MH; de Cubas AA; Daniels AB; Taylor S; Zhao H; Darden J; Bautch VL; Rathmell WK; Chappell JC
    JCI Insight; 2018 Feb; 3(4):. PubMed ID: 29467323
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Epididymal Cystadenomas in von Hippel-Lindau Disease Showing Increased Activity on 68Ga DOTATATE PET/CT.
    Papadakis GZ; Millo C; Sadowski SM; Bagci U; Patronas NJ
    Clin Nucl Med; 2016 Oct; 41(10):781-2. PubMed ID: 27454594
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epididymal cystadenomas and epithelial tumourlets: effects of VHL deficiency on the human epididymis.
    Gläsker S; Tran MG; Shively SB; Ikejiri B; Lonser RR; Maxwell PH; Zhuang Z; Oldfield EH; Vortmeyer AO
    J Pathol; 2006 Sep; 210(1):32-41. PubMed ID: 16841375
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Germline mutation of von Hippel-Lindau (VHL) gene 695 G>A (R161Q) in a patient with a peculiar phenotype with type 2C VHL syndrome.
    Santarpia L; Lapa D; Benvenga S
    Ann N Y Acad Sci; 2006 Aug; 1073():198-202. PubMed ID: 17102087
    [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. Epididymal cystadenomas in von Hippel-Lindau disease.
    Choyke PL; Glenn GM; Wagner JP; Lubensky IA; Thakore K; Zbar B; Linehan WM; Walther MM
    Urology; 1997 Jun; 49(6):926-31. PubMed ID: 9187702
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Somatic von Hippel-Lindau mutation in clear cell papillary cystadenoma of the epididymis.
    Gilcrease MZ; Schmidt L; Zbar B; Truong L; Rutledge M; Wheeler TM
    Hum Pathol; 1995 Dec; 26(12):1341-6. PubMed ID: 8522307
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A role for von Hippel-Lindau protein in pancreatic beta-cell function.
    Puri S; Cano DA; Hebrok M
    Diabetes; 2009 Feb; 58(2):433-41. PubMed ID: 19033400
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of a new
    Lenglet M; Robriquet F; Schwarz K; Camps C; Couturier A; Hoogewijs D; Buffet A; Knight SJL; Gad S; Couvé S; Chesnel F; Pacault M; Lindenbaum P; Job S; Dumont S; Besnard T; Cornec M; Dreau H; Pentony M; Kvikstad E; Deveaux S; Burnichon N; Ferlicot S; Vilaine M; Mazzella JM; Airaud F; Garrec C; Heidet L; Irtan S; Mantadakis E; Bouchireb K; Debatin KM; Redon R; Bezieau S; Bressac-de Paillerets B; Teh BT; Girodon F; Randi ML; Putti MC; Bours V; Van Wijk R; Göthert JR; Kattamis A; Janin N; Bento C; Taylor JC; Arlot-Bonnemains Y; Richard S; Gimenez-Roqueplo AP; Cario H; Gardie B
    Blood; 2018 Aug; 132(5):469-483. PubMed ID: 29891534
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Von Hippel-Lindau (VHL) disease: an update on the clinico-pathologic and genetic aspects.
    Shehata BM; Stockwell CA; Castellano-Sanchez AA; Setzer S; Schmotzer CL; Robinson H
    Adv Anat Pathol; 2008 May; 15(3):165-71. PubMed ID: 18434768
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel gene mutation in von Hippel-Lindau disease - a report of two cases.
    Wang J; Cao W; Wang Z; Zhu H
    BMC Med Genet; 2019 Dec; 20(1):194. PubMed ID: 31823746
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Von Hippel-Lindau disease: a single gene, several hereditary tumors.
    Crespigio J; Berbel LCL; Dias MA; Berbel RF; Pereira SS; Pignatelli D; Mazzuco TL
    J Endocrinol Invest; 2018 Jan; 41(1):21-31. PubMed ID: 28589383
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype-phenotype analysis of von Hippel-Lindau syndrome in Korean families: HIF-α binding site missense mutations elevate age-specific risk for CNS hemangioblastoma.
    Lee JS; Lee JH; Lee KE; Kim JH; Hong JM; Ra EK; Seo SH; Lee SJ; Kim MJ; Park SS; Seong MW
    BMC Med Genet; 2016 Jul; 17(1):48. PubMed ID: 27439424
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Case of parotid mucoepidermoid carcinoma: Expanding the spectrum of von Hippel-Lindau-related neoplasms.
    Berger MH; Kerr DA; Rangel Filho AE; Sargi ZB
    Head Neck; 2017 Mar; 39(3):E51-E54. PubMed ID: 28006088
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Germline mutations in the new E1' cryptic exon of the
    Buffet A; Calsina B; Flores S; Giraud S; Lenglet M; Romanet P; Deflorenne E; Aller J; Bourdeau I; Bressac-de Paillerets B; Calatayud M; Dehais C; De Mones Del Pujol E; Elenkova A; Herman P; Kamenický P; Lejeune S; Sadoul JL; Barlier A; Richard S; Favier J; Burnichon N; Gardie B; Dahia PL; Robledo M; Gimenez-Roqueplo AP
    J Med Genet; 2020 Nov; 57(11):752-759. PubMed ID: 31996412
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.