229 related articles for article (PubMed ID: 15642664)
1. Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosis.
Cario H; Schwarz K; Jorch N; Kyank U; Petrides PE; Schneider DT; Uhle R; Debatin KM; Kohne E
Haematologica; 2005 Jan; 90(1):19-24. PubMed ID: 15642664
[TBL] [Abstract][Full Text] [Related]
2. Mutations of von Hippel-Lindau tumor-suppressor gene and congenital polycythemia.
Pastore Y; Jedlickova K; Guan Y; Liu E; Fahner J; Hasle H; Prchal JF; Prchal JT
Am J Hum Genet; 2003 Aug; 73(2):412-9. PubMed ID: 12844285
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia.
Ang SO; Chen H; Hirota K; Gordeuk VR; Jelinek J; Guan Y; Liu E; Sergueeva AI; Miasnikova GY; Mole D; Maxwell PH; Stockton DW; Semenza GL; Prchal JT
Nat Genet; 2002 Dec; 32(4):614-21. PubMed ID: 12415268
[TBL] [Abstract][Full Text] [Related]
5. Mutations in the VHL gene in sporadic apparently congenital polycythemia.
Pastore YD; Jelinek J; Ang S; Guan Y; Liu E; Jedlickova K; Krishnamurti L; Prchal JT
Blood; 2003 Feb; 101(4):1591-5. PubMed ID: 12393546
[TBL] [Abstract][Full Text] [Related]
6. Genetic analysis of von Hippel-Lindau disease.
Nordstrom-O'Brien M; van der Luijt RB; van Rooijen E; van den Ouweland AM; Majoor-Krakauer DF; Lolkema MP; van Brussel A; Voest EE; Giles RH
Hum Mutat; 2010 May; 31(5):521-37. PubMed ID: 20151405
[TBL] [Abstract][Full Text] [Related]
7. Chuvash-type congenital polycythemia in 4 families of Asian and Western European ancestry.
Percy MJ; McMullin MF; Jowitt SN; Potter M; Treacy M; Watson WH; Lappin TR
Blood; 2003 Aug; 102(3):1097-9. PubMed ID: 12702509
[TBL] [Abstract][Full Text] [Related]
8. Allelic deletion and mutation of the von Hippel-Lindau (VHL) tumor suppressor gene in pancreatic microcystic adenomas.
Vortmeyer AO; Lubensky IA; Fogt F; Linehan WM; Khettry U; Zhuang Z
Am J Pathol; 1997 Oct; 151(4):951-6. PubMed ID: 9327728
[TBL] [Abstract][Full Text] [Related]
9. Screening for renal carcinoma associated mutations in the von Hippel-Lindau tumor suppressor gene by temperature gradient gel electrophoresis.
Wenzel M; Enczmann J; Uhrberg M; Hernández A; Wiese U; Ackermann R; Schmitz-Draeger B; Ebert T; Wernet P
Electrophoresis; 1997 Jan; 18(1):45-51. PubMed ID: 9059819
[TBL] [Abstract][Full Text] [Related]
10. Mutations on the von-Hippel-Lindau tumor suppressor gene.
Bergamaschi G
Haematologica; 2005 Jan; 90(1):1. PubMed ID: 15644296
[No Abstract] [Full Text] [Related]
11. The phenotype of polycythemia due to Croatian homozygous VHL (571C>G:H191D) mutation is different from that of Chuvash polycythemia (VHL 598C>T:R200W).
Tomasic NL; Piterkova L; Huff C; Bilic E; Yoon D; Miasnikova GY; Sergueeva AI; Niu X; Nekhai S; Gordeuk V; Prchal JT
Haematologica; 2013 Apr; 98(4):560-7. PubMed ID: 23403324
[TBL] [Abstract][Full Text] [Related]
12. Congenital polycythemia with homozygous and heterozygous mutations of von Hippel-Lindau gene: five new Caucasian patients.
Bento MC; Chang KT; Guan Y; Liu E; Caldas G; Gatti RA; Prchal JT
Haematologica; 2005 Jan; 90(1):128-9. PubMed ID: 15642680
[TBL] [Abstract][Full Text] [Related]
13. Novel Homozygous Mutation of the Internal Translation Initiation Start Site of VHL is Exclusively Associated with Erythrocytosis: Indications for Distinct Functional Roles of von Hippel-Lindau Tumor Suppressor Isoforms.
Bartels M; van der Zalm MM; van Oirschot BA; Lee FS; Giles RH; Kruip MJ; Gitz-Francois JJ; Van Solinge WW; Bierings M; van Wijk R
Hum Mutat; 2015 Nov; 36(11):1039-42. PubMed ID: 26224408
[TBL] [Abstract][Full Text] [Related]
14. The homozygous VHL(D126N) missense mutation is associated with dramatically elevated erythropoietin levels, consequent polycythemia, and early onset severe pulmonary hypertension.
Sarangi S; Lanikova L; Kapralova K; Acharya S; Swierczek S; Lipton JM; Wolfe L; Prchal JT
Pediatr Blood Cancer; 2014 Nov; 61(11):2104-6. PubMed ID: 24729484
[TBL] [Abstract][Full Text] [Related]
15. Somatic mutations in VHL germline deletion kindred correlate with mild phenotype.
Wait SD; Vortmeyer AO; Lonser RR; Chang DT; Finn MA; Bhowmick DA; Pack SD; Oldfield EH; Zhuang Z
Ann Neurol; 2004 Feb; 55(2):236-40. PubMed ID: 14755727
[TBL] [Abstract][Full Text] [Related]
16. Molecular analysis of the von Hippel-Lindau disease tumor suppressor gene in human lung cancer cell lines.
Sekido Y; Bader S; Latif F; Gnarra JR; Gazdar AF; Linehan WM; Zbar B; Lerman MI; Minna JD
Oncogene; 1994 Jun; 9(6):1599-604. PubMed ID: 8183553
[TBL] [Abstract][Full Text] [Related]
17. The worldwide distribution of the VHL 598C>T mutation indicates a single founding event.
Liu E; Percy MJ; Amos CI; Guan Y; Shete S; Stockton DW; McMullin MF; Polyakova LA; Ang SO; Pastore YD; Jedlickova K; Lappin TR; Gordeuk V; Prchal JT
Blood; 2004 Mar; 103(5):1937-40. PubMed ID: 14604959
[TBL] [Abstract][Full Text] [Related]
18. Constitutional von Hippel-Lindau (VHL) gene deletions detected in VHL families by fluorescence in situ hybridization.
Pack SD; Zbar B; Pak E; Ault DO; Humphrey JS; Pham T; Hurley K; Weil RJ; Park WS; Kuzmin I; Stolle C; Glenn G; Liotta LA; Lerman MI; Klausner RD; Linehan WM; Zhuang Z
Cancer Res; 1999 Nov; 59(21):5560-4. PubMed ID: 10554035
[TBL] [Abstract][Full Text] [Related]
19. Multifocal bilateral renal cell carcinoma and retinal angiomas in a patient with de novo von Hippel-Lindau disease: identification of a new germline mutation.
Sessa A; Battini G; Meroni M; Pitingolo F; Righetti M; Ciotti P; Di Maria E; Bellone E; Ajmar F; Mandich P
J Nephrol; 2005; 18(2):209-12. PubMed ID: 15931650
[TBL] [Abstract][Full Text] [Related]
20. Vascular complications in Chuvash polycythemia.
Gordeuk VR; Prchal JT
Semin Thromb Hemost; 2006 Apr; 32(3):289-94. PubMed ID: 16673284
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
