152 related articles for article (PubMed ID: 20662852)
21. 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]
22. 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]
23. [Clinical problems in multiple osteochondroma].
Ham SJ; de Lange J; van der Zwan AL; Schaap GR; van der Woude HJ; Heeg M
Ned Tijdschr Geneeskd; 2012; 156(11):A4254. PubMed ID: 22414670
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. [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]
26. 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]
27. Multiple hereditary exostoses (MHE): elucidating the pathogenesis of a rare skeletal disorder through interdisciplinary research.
Jones KB; Pacifici M; Hilton MJ
Connect Tissue Res; 2014 Apr; 55(2):80-8. PubMed ID: 24409815
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. Investigation of microRNA alterations in leukemias and lymphomas.
Calin GA; Croce CM
Methods Enzymol; 2007; 427():193-213. PubMed ID: 17720486
[TBL] [Abstract][Full Text] [Related]
31. [Osteocartilaginous exostoses (osteochondromas)].
Bulycheva IV; Semenova LA; Makhson AN; Myers JB; Zhukov AG; Iskindirova AK
Arkh Patol; 2008; 70(1):58-61. PubMed ID: 18368814
[TBL] [Abstract][Full Text] [Related]
32. Palovarotene Inhibits Osteochondroma Formation in a Mouse Model of Multiple Hereditary Exostoses.
Inubushi T; Lemire I; Irie F; Yamaguchi Y
J Bone Miner Res; 2018 Apr; 33(4):658-666. PubMed ID: 29120519
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. 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]
35. A splice-site mutation leads to haploinsufficiency of EXT2 mRNA for a dominant trait in a large family with multiple osteochondromas.
Yang L; Hui WS; Chan WC; Ng VC; Yam TH; Leung HC; Huang JD; Shum DK; Jie Q; Cheung KM; Cheah KS; Luo Z; Chan D
J Orthop Res; 2010 Nov; 28(11):1522-30. PubMed ID: 20872591
[TBL] [Abstract][Full Text] [Related]
36. Intronic deletion and duplication proximal of the EXT1 gene: a novel causative mechanism for multiple osteochondromas.
Waaijer CJ; Winter MG; Reijnders CM; de Jong D; John Ham S; Bovée JV; Szuhai K
Genes Chromosomes Cancer; 2013 Apr; 52(4):431-6. PubMed ID: 23341036
[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. 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]
39. Skeletal osteochondromas revisited.
Mavrogenis AF; Papagelopoulos PJ; Soucacos PN
Orthopedics; 2008 Oct; 31(10):. PubMed ID: 19226005
[TBL] [Abstract][Full Text] [Related]
40. An update on the imaging of diaphyseal aclasis.
Ellatif M; Sharif B; Lindsay D; Pollock R; Saifuddin A
Skeletal Radiol; 2021 Oct; 50(10):1941-1962. PubMed ID: 33791832
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
