Bovée JVMG - Search Results

1

Beyond the Influence of IDH Mutations: Exploring Epigenetic Vulnerabilities in Chondrosarcoma.

Venneker S, Kruisselbrink AB, Baranski Z, Palubeckaite I, Briaire-de Bruijn IH, Oosting J, French PJ, Danen EHJ, Bovée JVMG. Venneker S, et al. Among authors: bovee jvmg. Cancers (Basel). 2020 Nov 30;12(12):3589. doi: 10.3390/cancers12123589. Cancers (Basel). 2020. PMID: 33266275 Free PMC article.

2

Enchondromatosis (Ollier disease, Maffucci syndrome) is not caused by the PTHR1 mutation p.R150C.

Rozeman LB, Sangiorgi L, Briaire-de Bruijn IH, Mainil-Varlet P, Bertoni F, Cleton-Jansen AM, Hogendoorn PC, Bovée JV. Rozeman LB, et al. Hum Mutat. 2004 Dec;24(6):466-73. doi: 10.1002/humu.20095. Hum Mutat. 2004. PMID: 15523647

3

Peripheral chondrosarcoma progression is accompanied by decreased Indian Hedgehog signalling.

Hameetman L, Rozeman LB, Lombaerts M, Oosting J, Taminiau AH, Cleton-Jansen AM, Bovée JV, Hogendoorn PC. Hameetman L, et al. J Pathol. 2006 Aug;209(4):501-11. doi: 10.1002/path.2008. J Pathol. 2006. PMID: 16755518

4

The role of noncartilage-specific molecules in differentiation of cartilaginous tumors: lessons from chondroblastoma and chondromyxoid fibroma.

Romeo S, Oosting J, Rozeman LB, Hameetman L, Taminiau AH, Cleton-Jansen AM, Bovée JV, Hogendoorn PC. Romeo S, et al. Cancer. 2007 Jul 15;110(2):385-94. doi: 10.1002/cncr.22798. Cancer. 2007. PMID: 17559135 Free article.

5

Myxoid tumours of soft tissue: the so-called myxoid extracellular matrix is heterogeneous in composition.

Willems SM, Schrage YM, Baelde JJ, Briaire-de Bruijn I, Mohseny A, Sciot R, Bovée JV, Hogendoorn PC. Willems SM, et al. Histopathology. 2008 Mar;52(4):465-74. doi: 10.1111/j.1365-2559.2008.02967.x. Histopathology. 2008. PMID: 18315599

6

Kinome profiling of chondrosarcoma reveals SRC-pathway activity and dasatinib as option for treatment.

Schrage YM, Briaire-de Bruijn IH, de Miranda NF, van Oosterwijk J, Taminiau AH, van Wezel T, Hogendoorn PC, Bovée JV. Schrage YM, et al. Cancer Res. 2009 Aug 1;69(15):6216-22. doi: 10.1158/0008-5472.CAN-08-4801. Epub 2009 Jul 14. Cancer Res. 2009. PMID: 19602594

7

COX-2 expression in chondrosarcoma: a role for celecoxib treatment?

Schrage YM, Machado I, Meijer D, Briaire-de Bruijn I, van den Akker BE, Taminiau AH, Kalinski T, Llombart-Bosch A, Bovée JV. Schrage YM, et al. Eur J Cancer. 2010 Feb;46(3):616-24. doi: 10.1016/j.ejca.2009.11.002. Epub 2009 Dec 11. Eur J Cancer. 2010. PMID: 20004565

8

Genome-wide analysis of Ollier disease: Is it all in the genes?

Pansuriya TC, Oosting J, Krenács T, Taminiau AH, Verdegaal SH, Sangiorgi L, Sciot R, Hogendoorn PC, Szuhai K, Bovée JV. Pansuriya TC, et al. Orphanet J Rare Dis. 2011 Jan 14;6:2. doi: 10.1186/1750-1172-6-2. Orphanet J Rare Dis. 2011. PMID: 21235737 Free PMC article.

9

Maffucci syndrome: a genome-wide analysis using high resolution single nucleotide polymorphism and expression arrays on four cases.

Pansuriya TC, Oosting J, Verdegaal SH, Flanagan AM, Sciot R, Kindblom LG, Hogendoorn PC, Szuhai K, Bovée JV. Pansuriya TC, et al. Genes Chromosomes Cancer. 2011 Sep;50(9):673-9. doi: 10.1002/gcc.20889. Epub 2011 May 16. Genes Chromosomes Cancer. 2011. PMID: 21584901

10

Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.

Pansuriya TC, van Eijk R, d'Adamo P, van Ruler MA, Kuijjer ML, Oosting J, Cleton-Jansen AM, van Oosterwijk JG, Verbeke SL, Meijer D, van Wezel T, Nord KH, Sangiorgi L, Toker B, Liegl-Atzwanger B, San-Julian M, Sciot R, Limaye N, Kindblom LG, Daugaard S, Godfraind C, Boon LM, Vikkula M, Kurek KC, Szuhai K, French PJ, Bovée JV. Pansuriya TC, et al. Nat Genet. 2011 Nov 6;43(12):1256-61. doi: 10.1038/ng.1004. Nat Genet. 2011. PMID: 22057234 Free PMC article.

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