Bovèe J - Search Results

1

Deletions of the long arm of chromosome 10 in progression of follicular thyroid tumors.

Zedenius J, Wallin G, Svensson A, Bovèe J, Höög A, Bäckdahl M, Larsson C. Zedenius J, et al. Among authors: bovee j. Hum Genet. 1996 Mar;97(3):299-303. doi: 10.1007/BF02185758. Hum Genet. 1996. PMID: 8786068

2

Mutations of codon 918 in the RET proto-oncogene correlate to poor prognosis in sporadic medullary thyroid carcinomas.

Zedenius J, Larsson C, Bergholm U, Bovée J, Svensson A, Hallengren B, Grimelius L, Bäckdahl M, Weber G, Wallin G. Zedenius J, et al. Among authors: bovee j. J Clin Endocrinol Metab. 1995 Oct;80(10):3088-90. doi: 10.1210/jcem.80.10.7559902. J Clin Endocrinol Metab. 1995. PMID: 7559902

3

Genomic profiling of chondrosarcoma: chromosomal patterns in central and peripheral tumors.

Hallor KH, Staaf J, Bovée JV, Hogendoorn PC, Cleton-Jansen AM, Knuutila S, Savola S, Niini T, Brosjö O, Bauer HC, Vult von Steyern F, Jonsson K, Skorpil M, Mandahl N, Mertens F. Hallor KH, et al. Among authors: bovee jv. Clin Cancer Res. 2009 Apr 15;15(8):2685-94. doi: 10.1158/1078-0432.CCR-08-2330. Epub 2009 Mar 31. Clin Cancer Res. 2009. PMID: 19336518 Free article.

4

GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma.

Nord KH, Lilljebjörn H, Vezzi F, Nilsson J, Magnusson L, Tayebwa J, de Jong D, Bovée JV, Hogendoorn PC, Szuhai K. Nord KH, et al. Among authors: bovee jv. Nat Genet. 2014 May;46(5):474-7. doi: 10.1038/ng.2927. Epub 2014 Mar 23. Nat Genet. 2014. PMID: 24658000

5

EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas.

Bovée JV, Cleton-Jansen AM, Wuyts W, Caethoven G, Taminiau AH, Bakker E, Van Hul W, Cornelisse CJ, Hogendoorn PC. Bovée JV, et al. Am J Hum Genet. 1999 Sep;65(3):689-98. doi: 10.1086/302532. Am J Hum Genet. 1999. PMID: 10441575 Free PMC article.

6

Chromosome 9 alterations and trisomy 22 in central chondrosarcoma: a cytogenetic and DNA flow cytometric analysis of chondrosarcoma subtypes.

Bovée JV, Sciot R, Dal Cin P, Debiec-Rychter M, van Zelderen-Bhola SL, Cornelisse CJ, Hogendoorn PC. Bovée JV, et al. Diagn Mol Pathol. 2001 Dec;10(4):228-35. doi: 10.1097/00019606-200112000-00004. Diagn Mol Pathol. 2001. PMID: 11763313

7

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. Hameetman L, et al. Among authors: bovee jv. J Natl Cancer Inst. 2007 Mar 7;99(5):396-406. doi: 10.1093/jnci/djk067. J Natl Cancer Inst. 2007. PMID: 17341731

8

Parent-of-origin tumourigenesis is mediated by an essential imprinted modifier in SDHD-linked paragangliomas: SLC22A18 and CDKN1C are candidate tumour modifiers.

Hoekstra AS, Addie RD, Ras C, Seifar RM, Ruivenkamp CA, Briaire-de Bruijn IH, Hes FJ, Jansen JC, Corssmit EP, Corver WE, Morreau H, Bovée JV, Bayley JP, Devilee P. Hoekstra AS, et al. Among authors: bovee jv. Hum Mol Genet. 2016 Sep 1;25(17):3715-3728. doi: 10.1093/hmg/ddw218. Epub 2016 Jul 8. Hum Mol Genet. 2016. PMID: 27402879

9

Malignant progression in multiple enchondromatosis (Ollier's disease): an autopsy-based molecular genetic study.

Bovée JV, van Roggen JF, Cleton-Jansen AM, Taminiau AH, van der Woude HJ, Hogendoorn PC. Bovée JV, et al. Hum Pathol. 2000 Oct;31(10):1299-303. doi: 10.1053/hupa.2000.19308. Hum Pathol. 2000. PMID: 11070122

10

Loss of NF2 defines a genetic subgroup of non-FOS-rearranged osteoblastoma.

Saba KH, Cornmark L, Hofvander J, Magnusson L, Nilsson J, van den Bos H, Spierings DC, Foijer F, Staaf J, Brosjö O, Sumathi VP, Lam SW, Szuhai K, Bovée JV, Kovac M, Baumhoer D, Styring E, Nord KH. Saba KH, et al. Among authors: bovee jv. J Pathol Clin Res. 2020 Oct;6(4):231-237. doi: 10.1002/cjp2.172. Epub 2020 Jun 16. J Pathol Clin Res. 2020. PMID: 32542935 Free PMC article.

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