BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 25744876)

  • 21. Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostoses.
    Al-Zayed Z; Al-Rijjal RA; Al-Ghofaili L; BinEssa HA; Pant R; Alrabiah A; Al-Hussainan T; Zou M; Meyer BF; Shi Y
    Orphanet J Rare Dis; 2021 Feb; 16(1):100. PubMed ID: 33632255
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Analysis of mutations in EXT1 and EXT2 in Brazilian patients with multiple osteochondromas.
    Santos SCL; Rizzo IMPO; Takata RI; Speck-Martins CE; Brum JM; Sollaci C
    Mol Genet Genomic Med; 2018 May; 6(3):382-392. PubMed ID: 29529714
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Identification of mutation in a candidate gene for hereditary multiple exostoses type II.
    Xu L; Deng H; Xia J; Li H; Zhou J; Wang D; Pan Q; Long Z
    Chin Med J (Engl); 1999 Jan; 112(1):72-5. PubMed ID: 11593646
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Novel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin.
    Vanita V; Sperling K; Sandhu HS; Sandhu PS; Singh JR
    Genet Test Mol Biomarkers; 2009 Feb; 13(1):43-9. PubMed ID: 19309273
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Up-regulation of PTHrP and Bcl-2 expression characterizes the progression of osteochondroma towards peripheral chondrosarcoma and is a late event in central chondrosarcoma.
    Bovée JV; van den Broek LJ; Cleton-Jansen AM; Hogendoorn PC
    Lab Invest; 2000 Dec; 80(12):1925-34. PubMed ID: 11140704
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Multiple osteochondromas.
    Bovée JV
    Orphanet J Rare Dis; 2008 Feb; 3():3. PubMed ID: 18271966
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mutation screening for the EXT1 and EXT2 genes in Chinese patients with multiple osteochondromas.
    Kang QL; Xu J; Zhang Z; He JW; Fu WZ; Zhang ZL
    Arch Med Res; 2013 Oct; 44(7):542-8. PubMed ID: 24120389
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Identification of mutations in EXT1 and EXT2 genes in six Chinese families with multiple osteochondromas.
    Xu Y; Kang Q; Zhang Z
    Mol Med Rep; 2017 Oct; 16(4):5599-5605. PubMed ID: 28849184
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Detection of exostosin glycosyltransferase gene mutations in patients with non-hereditary osteochondromas of the mandibular condyle.
    Zhou Q; Yang C; Chen MJ; Li LZ
    Mol Clin Oncol; 2016 Sep; 5(3):295-299. PubMed ID: 27588195
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cell cycle deregulation and mosaic loss of Ext1 drive peripheral chondrosarcomagenesis in the mouse and reveal an intrinsic cilia deficiency.
    de Andrea CE; Zhu JF; Jin H; Bovée JV; Jones KB
    J Pathol; 2015 Jun; 236(2):210-8. PubMed ID: 25644707
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDG.
    Delgado MA; Martinez-Domenech G; Sarrión P; Urreizti R; Zecchini L; Robledo HH; Segura F; de Kremer RD; Balcells S; Grinberg D; Asteggiano CG
    Sci Rep; 2014 Sep; 4():6407. PubMed ID: 25230886
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Three novel EXT1 and EXT2 gene mutations in Taiwanese patients with multiple exostoses.
    Chen WC; Chi CH; Chuang CC; Jou IM
    J Formos Med Assoc; 2006 May; 105(5):434-7. PubMed ID: 16638657
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Identification of Novel EXT Mutations in Patients with Hereditary Multiple Exostoses Using Whole-Exome Sequencing.
    Liang C; Wang YJ; Wei YX; Dong Y; Zhang ZC
    Orthop Surg; 2020 Jun; 12(3):990-996. PubMed ID: 32293802
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of a novel frameshift mutation of the
    Xia P; Xu H; Shi Q; Li D
    Oncol Lett; 2016 Jan; 11(1):105-110. PubMed ID: 26870176
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [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]  

  • 36. 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]  

  • 37. 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]  

  • 38. The role of EXT1 in nonhereditary osteochondroma: identification of homozygous deletions.
    Hameetman L; Szuhai K; Yavas A; Knijnenburg J; van Duin M; van Dekken H; Taminiau AH; Cleton-Jansen AM; Bovée JV; Hogendoorn PC
    J Natl Cancer Inst; 2007 Mar; 99(5):396-406. PubMed ID: 17341731
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Novel mutation of EXT2 identified in a large family with multiple osteochondromas.
    Chen XJ; Zhang H; Tan ZP; Hu W; Yang YF
    Mol Med Rep; 2016 Nov; 14(5):4687-4691. PubMed ID: 27748933
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A mouse model of chondrocyte-specific somatic mutation reveals a role for Ext1 loss of heterozygosity in multiple hereditary exostoses.
    Matsumoto K; Irie F; Mackem S; Yamaguchi Y
    Proc Natl Acad Sci U S A; 2010 Jun; 107(24):10932-7. PubMed ID: 20534475
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.