BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

212 related articles for article (PubMed ID: 16604483)

  • 1. [A mutation 1633-26(C-->A) in EXT1 gene causes multiple exostoses].
    Xie ZG; Hu ZM; Pan Q; Zhang RF; Liang DS; Wu LQ; Long ZG; Dai HP; Xia K; Xia JH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Apr; 23(2):147-50. PubMed ID: 16604483
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [EXT1 and EXT2 mutation identified by denaturing high performance liquid chromatograph in three families with hereditary multiple exostoses].
    Zhang M; Liu SG; Li FF; Zhou WH; Jin XH; Ma X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):646-51. PubMed ID: 18067075
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Germline mutations in the EXT1 and EXT2 genes in Korean patients with hereditary multiple exostoses.
    Park KJ; Shin KH; Ku JL; Cho TJ; Lee SH; Choi IH; Phillipe C; Monaco AP; Porter DE; Park JG
    J Hum Genet; 1999; 44(4):230-4. PubMed ID: 10429361
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Novel mutation of Y271H in EXT1 gene causes multiple exostoses].
    Li W; Hu ZM; Xie ZG; He HB; Pan Q; Xia K; Xia JH
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Aug; 32(4):546-50. PubMed ID: 17767039
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [A mutation IVS2+1G>A in EXT2 gene causes hereditary multiple exostoses].
    Hu ZM; Zheng D; Pan Q; Yang YF; Zhao TL; Liu XP; Wu LQ; Jiang DG; Xia K; Xia JH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):97-100. PubMed ID: 15079787
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [From gene to disease; hereditary multiple exostoses].
    Wuyts W; Bovée JV; Hogendoorn PC
    Ned Tijdschr Geneeskd; 2002 Jan; 146(4):162-4. PubMed ID: 11845565
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel EXT1 and EXT2 mutations identified by DHPLC in Italian patients with multiple osteochondromas.
    Pedrini E; De Luca A; Valente EM; Maini V; Capponcelli S; Mordenti M; Mingarelli R; Sangiorgi L; Dallapiccola B
    Hum Mutat; 2005 Sep; 26(3):280. PubMed ID: 16088908
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An optimized DHPLC protocol for molecular testing of the EXT1 and EXT2 genes in hereditary multiple osteochondromas.
    Wuyts W; Radersma R; Storm K; Vits L
    Clin Genet; 2005 Dec; 68(6):542-7. PubMed ID: 16283885
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of autism in two patients with hereditary multiple exostoses caused by novel deletion mutations of EXT1.
    Li H; Yamagata T; Mori M; Momoi MY
    J Hum Genet; 2002; 47(5):262-5. PubMed ID: 12032595
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel EXT1 gene mutation causing hereditary multiple exostoses in a Chinese pedigree.
    Li Y; Wang J; Li H; Wang J; Wang X; Fu Q
    Pathology; 2010 Jan; 42(1):91-3. PubMed ID: 20025490
    [No Abstract]   [Full Text] [Related]  

  • 11. A 651-665delinsTT mutation in EXT1 causes hereditary multiple exostoses.
    Shi YR; Wu JY; Tsai FJ; Lee CC; Tsai CH
    Hum Mutat; 2001 Feb; 17(2):158. PubMed ID: 11180615
    [No Abstract]   [Full Text] [Related]  

  • 12. Mutation screening of EXT1 and EXT2 by direct sequence analysis and MLPA in patients with multiple osteochondromas: splice site mutations and exonic deletions account for more than half of the mutations.
    Vink GR; White SJ; Gabelic S; Hogendoorn PC; Breuning MH; Bakker E
    Eur J Hum Genet; 2005 Apr; 13(4):470-4. PubMed ID: 15586175
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular basis of multiple exostoses: mutations in the EXT1 and EXT2 genes.
    Wuyts W; Van Hul W
    Hum Mutat; 2000; 15(3):220-7. PubMed ID: 10679937
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Denaturant gradient gel electrophoresis in the genetic diagnosis of hereditary multiple exostoses].
    He HB; Hu ZM; Li HJ; Zhu Y; Shi XL; Lei GH; Zhou JN; Li KH
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Apr; 32(2):323-7. PubMed ID: 17478946
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diminished levels of the putative tumor suppressor proteins EXT1 and EXT2 in exostosis chondrocytes.
    Bernard MA; Hall CE; Hogue DA; Cole WG; Scott A; Snuggs MB; Clines GA; Lüdecke HJ; Lovett M; Van Winkle WB; Hecht JT
    Cell Motil Cytoskeleton; 2001 Feb; 48(2):149-62. PubMed ID: 11169766
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosis.
    Xiao CY; Wang J; Zhang SZ; Van Hul W; Wuyts W; Qiu WM; Wu H; Zhang G
    Br J Cancer; 2001 Jul; 85(2):176-81. PubMed ID: 11461073
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis).
    Faiyaz-Ul-Haque M; Ahmad W; Zaidi SH; Hussain S; Haque S; Ahmad M; Cohn DH; Tsui LC
    Clin Genet; 2004 Aug; 66(2):144-51. PubMed ID: 15253765
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses.
    Dobson-Stone C; Cox RD; Lonie L; Southam L; Fraser M; Wise C; Bernier F; Hodgson S; Porter DE; Simpson AH; Monaco AP
    Eur J Hum Genet; 2000 Jan; 8(1):24-32. PubMed ID: 10713884
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses.
    Raskind WH; Conrad EU; Matsushita M; Wijsman EM; Wells DE; Chapman N; Sandell LJ; Wagner M; Houck J
    Hum Mutat; 1998; 11(3):231-9. PubMed ID: 9521425
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary multiple and isolated sporadic exostoses in the same kindred: identification of the causative gene (EXT2) and detection of a new mutation, nt112delAT, that distinguishes the two phenotypes.
    Vujic M; Bergman A; Romanus B; Wahlström J; Martinsson T
    Int J Mol Med; 2004 Jan; 13(1):47-52. PubMed ID: 14654969
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.