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 *

292 related articles for article (PubMed ID: 7550340)

  • 21. An integrated physical map of 8q22-q24: use in positional cloning and deletion analysis of Langer-Giedion syndrome.
    Hilton MJ; Gutiérrez L; Zhang L; Moreno PA; Reddy M; Brown N; Tan Y; Hill A; Wells DE
    Genomics; 2001 Jan; 71(2):192-9. PubMed ID: 11161813
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Identification of novel mutations in the human EXT1 tumor suppressor gene.
    Wells DE; Hill A; Lin X; Ahn J; Brown N; Wagner MJ
    Hum Genet; 1997 May; 99(5):612-5. PubMed ID: 9150727
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Hereditary multiple exostoses: confirmation of linkage to chromosomes 8 and 11.
    Blanton SH; Hogue D; Wagner M; Wells D; Young ID; Hecht JT
    Am J Med Genet; 1996 Mar; 62(2):150-9. PubMed ID: 8882395
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene family.
    Van Hul W; Wuyts W; Hendrickx J; Speleman F; Wauters J; De Boulle K; Van Roy N; Bossuyt P; Willems PJ
    Genomics; 1998 Jan; 47(2):230-7. PubMed ID: 9479495
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family.
    Wise CA; Clines GA; Massa H; Trask BJ; Lovett M
    Genome Res; 1997 Jan; 7(1):10-6. PubMed ID: 9037597
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24).
    Le Merrer M; Ben Othmane K; Stanescu V; Lyonnet S; Van Maldergem L; Royer G; Munnich A; Maroteaux P
    J Med Genet; 1992 Oct; 29(10):713-5. PubMed ID: 1433231
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Positional cloning of a gene involved in hereditary multiple exostoses.
    Wuyts W; Van Hul W; Wauters J; Nemtsova M; Reyniers E; Van Hul EV; De Boulle K; de Vries BB; Hendrickx J; Herrygers I; Bossuyt P; Balemans W; Fransen E; Vits L; Coucke P; Nowak NJ; Shows TB; Mallet L; van den Ouweland AM; McGaughran J; Halley DJ; Willems PJ
    Hum Mol Genet; 1996 Oct; 5(10):1547-57. PubMed ID: 8894688
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. 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]  

  • 32. Clonal karyotypic abnormalities of the hereditary multiple exostoses chromosomal loci 8q24.1 (EXT1) and 11p11-12 (EXT2) in patients with sporadic and hereditary osteochondromas.
    Bridge JA; Nelson M; Orndal C; Bhatia P; Neff JR
    Cancer; 1998 May; 82(9):1657-63. PubMed ID: 9576285
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Identification and functional characterization of the human EXT1 promoter region.
    Jennes I; Zuntini M; Mees K; Palagani A; Pedrini E; De Cock G; Fransen E; Vanden Berghe W; Sangiorgi L; Wuyts W
    Gene; 2012 Jan; 492(1):148-59. PubMed ID: 22037484
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. [Molecular-genetic characteristics of the deleted region of chromosome 8q24.1 in Langer-Giedion and tricho-rhino-phalangeal type I syndromes].
    Nemtsova MV; Iatsenko AN; Kuleshov NP; Novikov PV; Meerson EM; Zaletaev DV
    Genetika; 1996 Jul; 32(7):978-84. PubMed ID: 8974918
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. [Localization of the gene for 4 hereditary multiple exostoses families].
    Tang Y; Xia JH; Zhou JN; Li HJ; Wang DP; Dai HP; Long ZG; Tang BS; Huang L; Deng HX
    Yi Chuan Xue Bao; 1998; 25(1):1-7. PubMed ID: 9648398
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium.
    Nat Genet; 1995 Oct; 11(2):130-6. PubMed ID: 7550339
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [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]  

  • 40. Characterization and mapping to human chromosome 8q24.3 of Ly-6-related gene 9804 encoding an apparent homologue of mouse TSA-1.
    Shan X; Bourdeau A; Rhoton A; Wells DE; Cohen EH; Landgraf BE; Palfree RG
    J Immunol; 1998 Jan; 160(1):197-208. PubMed ID: 9551972
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.