164 related articles for article (PubMed ID: 20133829)
1. 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]
2. 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]
3. 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]
4. The neoplastic pathogenesis of solitary and multiple osteochondromas.
Porter DE; Simpson AH
J Pathol; 1999 Jun; 188(2):119-25. PubMed ID: 10398153
[TBL] [Abstract][Full Text] [Related]
5. A mouse model of osteochondromagenesis from clonal inactivation of Ext1 in chondrocytes.
Jones KB; Piombo V; Searby C; Kurriger G; Yang B; Grabellus F; Roughley PJ; Morcuende JA; Buckwalter JA; Capecchi MR; Vortkamp A; Sheffield VC
Proc Natl Acad Sci U S A; 2010 Feb; 107(5):2054-9. PubMed ID: 20080592
[TBL] [Abstract][Full Text] [Related]
6. Unsuspected osteochondroma-like outgrowths in the cranial base of Hereditary Multiple Exostoses patients and modeling and treatment with a BMP antagonist in mice.
Sinha S; Mundy C; Bechtold T; Sgariglia F; Ibrahim MM; Billings PC; Carroll K; Koyama E; Jones KB; Pacifici M
PLoS Genet; 2017 Apr; 13(4):e1006742. PubMed ID: 28445472
[TBL] [Abstract][Full Text] [Related]
7. A mouse model of chondrocyte-specific somatic mutation reveals a role for Ext1 loss of heterozygosity in multiple hereditary exostoses.
Matsumoto K; Irie F; Mackem S; Yamaguchi Y
Proc Natl Acad Sci U S A; 2010 Jun; 107(24):10932-7. PubMed ID: 20534475
[TBL] [Abstract][Full Text] [Related]
8. Dysplasia epiphysealis hemimelica (Trevor disease): a rare developmental disorder of bone mimicking osteochondroma of long bones.
Glick R; Khaldi L; Ptaszynski K; Steiner GC
Hum Pathol; 2007 Aug; 38(8):1265-72. PubMed ID: 17490719
[TBL] [Abstract][Full Text] [Related]
9. Cell cycle deregulation and mosaic loss of Ext1 drive peripheral chondrosarcomagenesis in the mouse and reveal an intrinsic cilia deficiency.
de Andrea CE; Zhu JF; Jin H; Bovée JV; Jones KB
J Pathol; 2015 Jun; 236(2):210-8. PubMed ID: 25644707
[TBL] [Abstract][Full Text] [Related]
10. Signaling systems affecting the severity of multiple osteochondromas.
Piombo V; Jochmann K; Hoffmann D; Wuelling M; Vortkamp A
Bone; 2018 Jun; 111():71-81. PubMed ID: 29545125
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Toward an understanding of the short bone phenotype associated with multiple osteochondromas.
Jones KB; Datar M; Ravichandran S; Jin H; Jurrus E; Whitaker R; Capecchi MR
J Orthop Res; 2013 Apr; 31(4):651-7. PubMed ID: 23192691
[TBL] [Abstract][Full Text] [Related]
13. Familial history of bone tumors.
Munoz J; Guo Y
JAMA; 2012 Oct; 308(14):1476-7. PubMed ID: 23047362
[No Abstract] [Full Text] [Related]
14. Re. Review article entitled 'The neoplastic pathogenesis of solitary and multiple osteochondromas'.
Bovée JV; Hogendoorn PC
J Pathol; 2000 Mar; 190(4):516-7. PubMed ID: 10700004
[No Abstract] [Full Text] [Related]
15. Genetic models of osteochondroma onset and neoplastic progression: evidence for mechanisms alternative to EXT genes inactivation.
Zuntini M; Pedrini E; Parra A; Sgariglia F; Gentile FV; Pandolfi M; Alberghini M; Sangiorgi L
Oncogene; 2010 Jul; 29(26):3827-34. PubMed ID: 20418910
[TBL] [Abstract][Full Text] [Related]
16. Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?
Bozzola M; Gertosio C; Gnoli M; Baronio F; Pedrini E; Meazza C; Sangiorgi L
Ital J Pediatr; 2015 Aug; 41():53. PubMed ID: 26239617
[TBL] [Abstract][Full Text] [Related]
17. Secondary peripheral chondrosarcoma evolving from osteochondroma as a result of outgrowth of cells with functional EXT.
de Andrea CE; Reijnders CM; Kroon HM; de Jong D; Hogendoorn PC; Szuhai K; Bovée JV
Oncogene; 2012 Mar; 31(9):1095-104. PubMed ID: 21804604
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Intermediate grade osteosarcoma and chondrosarcoma arising in an osteochondroma. A case report of a patient with hereditary multiple exostoses.
Bovée JV; Sakkers RJ; Geirnaerdt MJ; Taminiau AH; Hogendoorn PC
J Clin Pathol; 2002 Mar; 55(3):226-9. PubMed ID: 11896078
[TBL] [Abstract][Full Text] [Related]
20. Clinical and radiographic analysis of osteochondromas and growth disturbance in hereditary multiple exostoses.
Porter DE; Emerton ME; Villanueva-Lopez F; Simpson AH
J Pediatr Orthop; 2000; 20(2):246-50. PubMed ID: 10739291
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
