BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

107 related articles for article (PubMed ID: 27636706)

  • 21. A novel
    Chen Z; Bi Q; Kong M; Cao L; Ruan W
    Oncol Lett; 2018 Oct; 16(4):5167-5171. PubMed ID: 30250583
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. 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]  

  • 25. Mutation screening of EXT1 and EXT2 by direct sequence analysis and MLPA in patients with multiple osteochondromas: splice site mutations and exonic deletions account for more than half of the mutations.
    Vink GR; White SJ; Gabelic S; Hogendoorn PC; Breuning MH; Bakker E
    Eur J Hum Genet; 2005 Apr; 13(4):470-4. PubMed ID: 15586175
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Mutation screening of EXT genes in Chinese patients with multiple osteochondromas.
    Kang Z; Peng F; Ling T
    Gene; 2012 Sep; 506(2):298-300. PubMed ID: 22820392
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Epiphyseal growth plate and secondary peripheral chondrosarcoma: the neighbours matter.
    de Andrea CE; Hogendoorn PC
    J Pathol; 2012 Jan; 226(2):219-28. PubMed ID: 21956842
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Integrating Morphology and Genetics in the Diagnosis of Cartilage Tumors.
    de Andrea CE; San-Julian M; Bovée JVMG
    Surg Pathol Clin; 2017 Sep; 10(3):537-552. PubMed ID: 28797501
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Novel Mutations in Chinese Patients with Multiple Osteochondromas Identified Using Whole Exome Sequencing.
    Tong Y; Luo J; Zhang Y; Hong Z; Cao L; Chen X; Chen J; Bi Q
    Genet Test Mol Biomarkers; 2021 May; 25(5):361-367. PubMed ID: 34003695
    [No Abstract]   [Full Text] [Related]  

  • 31. 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]  

  • 32. 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]  

  • 33. Usefulness of cytofluorometric DNA ploidy analysis in distinguishing benign cartilaginous tumors from chondrosarcomas.
    Kusuzaki K; Murata H; Takeshita H; Hirata M; Hashiguchi S; Tsuji Y; Nakamura S; Ashihara T; Hirasawa Y
    Mod Pathol; 1999 Sep; 12(9):863-72. PubMed ID: 10496594
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. 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]  

  • 36. Intraosseous atypical chondroid tumor or chondrosarcoma grade 1 in patients with multiple osteochondromas.
    Goud AL; Wuyts W; Bessems J; Bramer J; van der Woude HJ; Ham J
    J Bone Joint Surg Am; 2015 Jan; 97(1):24-31. PubMed ID: 25568391
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb).
    Jennes I; Pedrini E; Zuntini M; Mordenti M; Balkassmi S; Asteggiano CG; Casey B; Bakker B; Sangiorgi L; Wuyts W
    Hum Mutat; 2009 Dec; 30(12):1620-7. PubMed ID: 19810120
    [TBL] [Abstract][Full Text] [Related]  

  • 38. IDH mutation status in a series of 88 head and neck chondrosarcomas: different profile between tumors of the skull base and tumors involving the facial skeleton and the laryngotracheal tract.
    Tallegas M; Miquelestorena-Standley É; Labit-Bouvier C; Badoual C; Francois A; Gomez-Brouchet A; Aubert S; Collin C; Tallet A; de Pinieux G
    Hum Pathol; 2019 Feb; 84():183-191. PubMed ID: 30296521
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. [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]  

    [Previous]   [Next]    [New Search]
    of 6.