395 related articles for article (PubMed ID: 21804604)
21. 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]
22. Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patients.
Szuhai K; Jennes I; de Jong D; Bovée JV; Wiweger M; Wuyts W; Hogendoorn PC
Hum Mutat; 2011 Feb; 32(2):E2036-49. PubMed ID: 21280143
[TBL] [Abstract][Full Text] [Related]
23. Loss of heterozygosity and DNA ploidy point to a diverging genetic mechanism in the origin of peripheral and central chondrosarcoma.
Bovée JV; Cleton-Jansen AM; Kuipers-Dijkshoorn NJ; van den Broek LJ; Taminiau AH; Cornelisse CJ; Hogendoorn PC
Genes Chromosomes Cancer; 1999 Nov; 26(3):237-46. PubMed ID: 10502322
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Osteochondroma formation is independent of heparanase expression as revealed in a mouse model of hereditary multiple exostoses.
Mundy C; Chung J; Koyama E; Bunting S; Mahimkar R; Pacifici M
J Orthop Res; 2022 Oct; 40(10):2391-2401. PubMed ID: 34996123
[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. Secondary peripheral chondrosarcoma arising in solitary osteochondroma: variables influencing prognosis and survival.
Righi A; Pacheco M; Cocchi S; Asioli S; Gambarotti M; Donati DM; Evangelista A; Gnoli M; Locatelli M; Mordenti M; Boarini M; Brizola E; Pedrini E; Sangiorgi L
Orphanet J Rare Dis; 2022 Feb; 17(1):74. PubMed ID: 35193636
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. Structural Features of Heparan Sulfate from Multiple Osteochondromas and Chondrosarcomas.
Veraldi N; Parra A; Urso E; Cosentino C; Locatelli M; Corsini S; Pedrini E; Naggi A; Bisio A; Sangiorgi L
Molecules; 2018 Dec; 23(12):. PubMed ID: 30544937
[TBL] [Abstract][Full Text] [Related]
31. EXT-related pathways are not involved in the pathogenesis of dysplasia epiphysealis hemimelica and metachondromatosis.
Bovée JV; Hameetman L; Kroon HM; Aigner T; Hogendoorn PC
J Pathol; 2006 Jul; 209(3):411-9. PubMed ID: 16622899
[TBL] [Abstract][Full Text] [Related]
32. Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies.
Hecht JT; Hogue D; Wang Y; Blanton SH; Wagner M; Strong LC; Raskind W; Hansen MF; Wells D
Am J Hum Genet; 1997 Jan; 60(1):80-6. PubMed ID: 8981950
[TBL] [Abstract][Full Text] [Related]
33. Secondary chondrosarcoma in cartilage bone tumors: report of 32 patients.
Altay M; Bayrakci K; Yildiz Y; Erekul S; Saglik Y
J Orthop Sci; 2007 Sep; 12(5):415-23. PubMed ID: 17909925
[TBL] [Abstract][Full Text] [Related]
34. Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.
Tallini G; Dorfman H; Brys P; Dal Cin P; De Wever I; Fletcher CD; Jonson K; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Samson I; Sciot R; Van den Berghe H; Vanni R; Willén H
J Pathol; 2002 Feb; 196(2):194-203. PubMed ID: 11793371
[TBL] [Abstract][Full Text] [Related]
35. Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11.
Raskind WH; Conrad EU; Chansky H; Matsushita M
Am J Hum Genet; 1995 May; 56(5):1132-9. PubMed ID: 7726169
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. Familial solitary chondrosarcoma resulting from germline EXT2 mutation.
Heddar A; Fermey P; Coutant S; Angot E; Sabourin JC; Michelin P; Parodi N; Charbonnier F; Vezain M; Bougeard G; Baert-Desurmont S; Frébourg T; Tournier I
Genes Chromosomes Cancer; 2017 Feb; 56(2):128-134. PubMed ID: 27636706
[TBL] [Abstract][Full Text] [Related]
39. No haploinsufficiency but loss of heterozygosity for EXT in multiple osteochondromas.
Reijnders CM; Waaijer CJ; Hamilton A; Buddingh EP; Dijkstra SP; Ham J; Bakker E; Szuhai K; Karperien M; Hogendoorn PC; Stringer SE; Bovée JV
Am J Pathol; 2010 Oct; 177(4):1946-57. PubMed ID: 20813973
[TBL] [Abstract][Full Text] [Related]
40. Secondary peripheral chondrosarcoma in multiple osteochondromas: a retrospective single-institution case series.
Gnoli M; Gambarotti M; Righi A; Staals EL; Evangelista A; Tremosini M; Brizola E; Mordenti M; Boarini M; Locatelli M; Pedrini E; Sangiorgi L
Orphanet J Rare Dis; 2024 Feb; 19(1):63. PubMed ID: 38351015
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
