Versteeg R - Search Results

1

Versteeg R, Caron H, Cheng NC, van der Drift P, Slater R, Westerveld A, Voûte PA, Delattre O, Laureys G, Van Roy N, et al. Versteeg R, et al. Eur J Cancer. 1995;31A(4):538-41. doi: 10.1016/0959-8049(95)00037-j. Eur J Cancer. 1995. PMID: 7576962 Review. No abstract available.

2

Detection of recurrent chromosome abnormalities in Ewing's sarcoma and peripheral neuroectodermal tumor cells using bivariate flow karyotyping.

Boschman GA, Rens W, Manders EM, Slater RM, Versteeg R, Aten JA. Boschman GA, et al. Among authors: versteeg r. Genes Chromosomes Cancer. 1992 Nov;5(4):375-84. doi: 10.1002/gcc.2870050413. Genes Chromosomes Cancer. 1992. PMID: 1283326

3

1;17 translocations and other chromosome 17 rearrangements in human primary neuroblastoma tumors and cell lines.

Van Roy N, Laureys G, Cheng NC, Willem P, Opdenakker G, Versteeg R, Speleman F. Van Roy N, et al. Among authors: versteeg r. Genes Chromosomes Cancer. 1994 Jun;10(2):103-14. doi: 10.1002/gcc.2870100205. Genes Chromosomes Cancer. 1994. PMID: 7520263

4

Characterisation of the chromosome breakpoints in a patient with a constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12) and neuroblastoma.

Laureys G, Versteeg R, Speleman F, van der Drift P, Francke U, Opdenakker G, Van Roy N. Laureys G, et al. Among authors: versteeg r. Eur J Cancer. 1995;31A(4):523-6. doi: 10.1016/0959-8049(95)00012-8. Eur J Cancer. 1995. PMID: 7576958

5

Molecular cytogenetic analysis of 1;17 translocations in neuroblastoma.

Van Roy N, Cheng NC, Laureys G, Opdenakker G, Versteeg R, Speleman F. Van Roy N, et al. Among authors: versteeg r. Eur J Cancer. 1995;31A(4):530-5. doi: 10.1016/0959-8049(95)00004-3. Eur J Cancer. 1995. PMID: 7576960

6

Identification of two distinct chromosome 12-derived amplification units in neuroblastoma cell line NGP.

Van Roy N, Forus A, Myklebost O, Cheng NC, Versteeg R, Speleman F. Van Roy N, et al. Among authors: versteeg r. Cancer Genet Cytogenet. 1995 Jul 15;82(2):151-4. doi: 10.1016/0165-4608(95)00034-m. Cancer Genet Cytogenet. 1995. PMID: 7664245

7

Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers.

Laureys G, Speleman F, Versteeg R, van der Drift P, Chan A, Leroy J, Francke U, Opdenakker G, Van Roy N. Laureys G, et al. Among authors: versteeg r. Oncogene. 1995 Mar 16;10(6):1087-93. Oncogene. 1995. PMID: 7700633

8

Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplification.

Cheng NC, Van Roy N, Chan A, Beitsma M, Westerveld A, Speleman F, Versteeg R. Cheng NC, et al. Among authors: versteeg r. Oncogene. 1995 Jan 19;10(2):291-7. Oncogene. 1995. PMID: 7838528

9

A multimegabase cluster of snRNA and tRNA genes on chromosome 1p36 harbours an adenovirus/SV40 hybrid virus integration site.

van der Drift P, Chan A, van Roy N, Laureys G, Westerveld A, Speleman F, Versteeg R. van der Drift P, et al. Among authors: versteeg r. Hum Mol Genet. 1994 Dec;3(12):2131-6. doi: 10.1093/hmg/3.12.2131. Hum Mol Genet. 1994. PMID: 7881409

10

Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity.

Caron H, van Sluis P, van Roy N, de Kraker J, Speleman F, Voûte PA, Westerveld A, Slater R, Versteeg R. Caron H, et al. Among authors: versteeg r. Am J Hum Genet. 1994 Aug;55(2):341-7. Am J Hum Genet. 1994. PMID: 8037211 Free PMC article.

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