Zobrazeno 1 - 9
of 9
pro vyhledávání: '"J V, Bovée"'
Autor:
Suleiman M. Ibramoglu, R. A. de Groen, R. van Eijk, T. van Wezel, R. Raghoo, E. R. de Winter, A. M. Schrader, P. M. Jansen, Briaire-de I. Bruijn, K. Kleiverda, L. Vlasveld, W. F. Posthuma, A. van den Berg, A. Diepstra, P. J. Lugtenburg, J. V. Bovée, A. H. Cleven, J. S. Vermaat
Publikováno v:
HemaSphere. 3:212
Publikováno v:
The Journal of pathology. 193(3)
Reactivation of telomerase, an enzyme which elongates human telomeres, is associated with cell immortilization. In approximately 90% of malignant tumours telomerase activity can be demonstrated, whereas in benign tumours it is mostly absent. Chondros
Autor:
J V, Bovée, A M, Cleton-Jansen, C, Rosenberg, A H, Taminiau, C J, Cornelisse, P C, Hogendoorn
Publikováno v:
The Journal of pathology. 189(4)
Dedifferentiated chondrosarcoma is defined as a high-grade, anaplastic sarcoma adjacent to a low-grade malignant cartilage-forming tumour. Controversy remains as to whether the anaplastic and cartilaginous components are derived from a common precurs
Publikováno v:
Cancer. 86(9)
Enchondroma is the most common primary benign bone tumor of the hand, especially the phalanges, whereas chondrosarcoma is uncommon at this site. Although phalangeal chondrosarcoma may have ominous histologic features, its biologic behavior is relativ
Autor:
J V, Bovée, A M, Cleton-Jansen, N J, Kuipers-Dijkshoorn, L J, van den Broek, A H, Taminiau, C J, Cornelisse, P C, Hogendoorn
Publikováno v:
Genes, chromosomescancer. 26(3)
Chondrosarcomas are malignant cartilaginous tumors arising centrally in bone (central chondrosarcoma), or secondarily within the cartilaginous cap of a hereditary or sporadic exostosis (peripheral chondrosarcoma). Loss of heterozygosity (LOH) was stu
Autor:
S L, van Zelderen-Bhola, J V, Bovée, H W, Wessels, P, Mollevanger, J V, Nijhuis, J D, van Eendenburg, A H, Taminiau, P C, Hogendoorn
Publikováno v:
Cancer genetics and cytogenetics. 105(2)
Chromosome analysis of a chondroblastoma of the right distal femur in a 31-year-old male patient revealed a ring chromosome 4 in approximately one-third of the analyzed cells. The remaining cells had a normal karyotype. These findings were subsequent
Publikováno v:
The Journal of pathology. 184(1)
Adamantinoma of long bones is a rare bone tumour with (immuno-) histological features of epithelial cells, surrounded by various amounts of osteofibrous tissue. Recent studies have indicated that cells with an epithelial phenotype are most probably t
Autor:
J V, Bovée, P C, Hogendoorn
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 141(52)
It is sometimes difficult to make an unequivocal diagnosis of tumours of bone and soft tissue based upon classical morphology alone, which has led to an increased use of additional diagnostic tools. In the past decade new techniques have become avail
Publikováno v:
Biochemical and biophysical research communications. 213(3)
The presence of a t(11;22)(q24;q12) translocation is one of the characteristic features of the Ewing family of tumors. The detection of the fusion gene product by RT-PCR using primers at both sides of the breakpoints has been advocated as a diagnosti