348 related articles for article (PubMed ID: 10398153)
21. EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas.
Bovée JV; Cleton-Jansen AM; Wuyts W; Caethoven G; Taminiau AH; Bakker E; Van Hul W; Cornelisse CJ; Hogendoorn PC
Am J Hum Genet; 1999 Sep; 65(3):689-98. PubMed ID: 10441575
[TBL] [Abstract][Full Text] [Related]
22. A novel nonsense mutation of the EXT1 gene in an Argentinian patient with multiple hereditary exostoses: a case report.
Delgado MA; Sarrión P; Azar N; Zecchini L; Robledo HH; Segura F; Balcells S; Grinberg D; Dodelson de Kremer R; Asteggiano CG
J Bone Joint Surg Am; 2012 Jun; 94(11):e76. PubMed ID: 22637216
[No Abstract] [Full Text] [Related]
23. 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]
24. EXTra hit for mouse osteochondroma.
Bovée JV
Proc Natl Acad Sci U S A; 2010 Feb; 107(5):1813-4. PubMed ID: 20133829
[No Abstract] [Full Text] [Related]
25. Multiple osteochondromas.
Bovée JV
Orphanet J Rare Dis; 2008 Feb; 3():3. PubMed ID: 18271966
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. The short-lived exostosis induced surgically versus the lasting genetic hereditary multiple exostoses.
Trebicz-Geffen M; Nevo Z; Evron Z; Posternak N; Glaser T; Fridkin M; Kollander Y; Robinson D
Exp Mol Pathol; 2003 Feb; 74(1):40-8. PubMed ID: 12645631
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. A combined analytical approach reveals novel EXT1/2 gene mutations in a large cohort of Italian multiple osteochondromas patients.
Signori E; Massi E; Matera MG; Poscente M; Gravina C; Falcone G; Rosa MA; Rinaldi M; Wuyts W; Seripa D; Dallapiccola B; Fazio VM
Genes Chromosomes Cancer; 2007 May; 46(5):470-7. PubMed ID: 17301954
[TBL] [Abstract][Full Text] [Related]
30. Somatic loss of an EXT2 gene mutation during malignant progression in a patient with hereditary multiple osteochondromas.
Musso N; Caronia FP; Castorina S; Lo Monte AI; Barresi V; Condorelli DF
Cancer Genet; 2015 Mar; 208(3):62-7. PubMed ID: 25744876
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. 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]
33. Similar cytogenetic findings in two synchronous secondary peripheral chondrosarcomas in a patient with multiple osteochondromas.
Kyriazoglou AI; Dimitriadis E; Arnogiannaki N; Brandal P; Heim S; Pandis N
Cancer Genet; 2011 Dec; 204(12):677-81. PubMed ID: 22285020
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. [Multiple exostoses].
Toguchida J; Nagayama S
Nihon Rinsho; 2000 Jul; 58(7):1473-8. PubMed ID: 10921326
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Osteochondromas: review of the clinical, radiological and pathological features.
Kitsoulis P; Galani V; Stefanaki K; Paraskevas G; Karatzias G; Agnantis NJ; Bai M
In Vivo; 2008; 22(5):633-46. PubMed ID: 18853760
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. [Identification of mutations in the human EXT1 and EXT2 genes].
Song G; Zhou J; Xia J; Deng H; Xu L; Ruan Q
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Aug; 16(4):208-10. PubMed ID: 10431043
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
