These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

347 related articles for article (PubMed ID: 11432960)

  • 1. Genotype-phenotype correlation in hereditary multiple exostoses.
    Francannet C; Cohen-Tanugi A; Le Merrer M; Munnich A; Bonaventure J; Legeai-Mallet L
    J Med Genet; 2001 Jul; 38(7):430-4. PubMed ID: 11432960
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Mutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostoses.
    Philippe C; Porter DE; Emerton ME; Wells DE; Simpson AH; Monaco AP
    Am J Hum Genet; 1997 Sep; 61(3):520-8. PubMed ID: 9326317
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses.
    Wuyts W; Van Hul W; De Boulle K; Hendrickx J; Bakker E; Vanhoenacker F; Mollica F; Lüdecke HJ; Sayli BS; Pazzaglia UE; Mortier G; Hamel B; Conrad EU; Matsushita M; Raskind WH; Willems PJ
    Am J Hum Genet; 1998 Feb; 62(2):346-54. PubMed ID: 9463333
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [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]  

  • 8. Novel mutation in the EXT-1 gene in an Iranian family affected with hereditary multiple exostoses.
    Foroughmand AM; Galehdari H; Rasouli M; Mohammadian G; Mohammadi M
    Pak J Biol Sci; 2008 Apr; 11(7):1037-41. PubMed ID: 18810975
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation analysis of hereditary multiple exostoses in the Chinese.
    Xu L; Xia J; Jiang H; Zhou J; Li H; Wang D; Pan Q; Long Z; Fan C; Deng HX
    Hum Genet; 1999; 105(1-2):45-50. PubMed ID: 10480354
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [A new EXT2 mutation in a Chinese family with hereditary multiple exostoses].
    Zhao WQ; Song SJ; Wei Q; Qiao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):241-4. PubMed ID: 19504431
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Ext-mutation analysis in Italian sporadic and hereditary osteochondromas.
    Gigante M; Matera MG; Seripa D; Izzo AM; Venanzi R; Giannotti A; Digilio MC; Gravina C; Lazzari M; Monteleone G; Monteleone M; Dallapiccola B; Fazio VM
    Int J Cancer; 2001 Nov; 95(6):378-83. PubMed ID: 11668521
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan.
    Shi YR; Wu JY; Hsu YA; Lee CC; Tsai CH; Tsai FJ
    Genet Test; 2002; 6(3):237-43. PubMed ID: 12490068
    [TBL] [Abstract][Full Text] [Related]  

  • 14. EXT genes are differentially expressed in bone and cartilage during mouse embryogenesis.
    Stickens D; Brown D; Evans GA
    Dev Dyn; 2000 Jul; 218(3):452-64. PubMed ID: 10878610
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A splice mutation and mRNA decay of EXT2 provoke hereditary multiple exostoses.
    Tian C; Yan R; Wen S; Li X; Li T; Cai Z; Li X; Du H; Chen H
    PLoS One; 2014; 9(4):e94848. PubMed ID: 24728384
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel EXT1 mutation identified in a pedigree with hereditary multiple exostoses.
    Cao L; Liu F; Kong M; Fang Y; Gu H; Chen Y; Zhao C; Zhang S; Bi Q
    Oncol Rep; 2014 Feb; 31(2):713-8. PubMed ID: 24297320
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ulna/height ratio as clinical parameter separating EXT1 from EXT2 families?
    Leube B; Hardt K; Portier S; Westhoff B; Jäger M; Krauspe R; Royer-Pokora B
    Genet Test; 2008 Mar; 12(1):129-33. PubMed ID: 18373409
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The putative tumour suppressor EXT1 alters the expression of cell-surface heparan sulfate.
    McCormick C; Leduc Y; Martindale D; Mattison K; Esford LE; Dyer AP; Tufaro F
    Nat Genet; 1998 Jun; 19(2):158-61. PubMed ID: 9620772
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 20 novel point mutations and one large deletion in EXT1 and EXT2 genes: report of diagnostic screening in a large Italian cohort of patients affected by hereditary multiple exostosis.
    Ciavarella M; Coco M; Baorda F; Stanziale P; Chetta M; Bisceglia L; Palumbo P; Bengala M; Raiteri P; Silengo M; Caldarini C; Facchini R; Lala R; Cavaliere ML; De Brasi D; Pasini B; Zelante L; Guarnieri V; D'Agruma L
    Gene; 2013 Feb; 515(2):339-48. PubMed ID: 23262345
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Assessing the general population frequency of rare coding variants in the EXT1 and EXT2 genes previously implicated in hereditary multiple exostoses.
    Cousminer DL; Arkader A; Voight BF; Pacifici M; Grant SFA
    Bone; 2016 Nov; 92():196-200. PubMed ID: 27616605
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.