447 related articles for article (PubMed ID: 11845565)
1. [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]
2. 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]
3. The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes.
Stickens D; Clines G; Burbee D; Ramos P; Thomas S; Hogue D; Hecht JT; Lovett M; Evans GA
Nat Genet; 1996 Sep; 14(1):25-32. PubMed ID: 8782816
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
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. 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]
10. 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]
11. [Molecular cloning of EXT2 and EXT4 gene].
Deng H; Xu L; Ruan Q; Huang L; Xia J
Hunan Yi Ke Da Xue Xue Bao; 1998; 23(6):519-23. PubMed ID: 10806756
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. 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]
16. [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]
17. [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]
18. 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]
19. Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1).
Ahn J; Lüdecke HJ; Lindow S; Horton WA; Lee B; Wagner MJ; Horsthemke B; Wells DE
Nat Genet; 1995 Oct; 11(2):137-43. PubMed ID: 7550340
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
