Van Roy N - Search Results

1

No evidence for correlation of DDX1 gene amplification with improved survival probability in patients with MYCN-amplified neuroblastomas.

De Preter K, Speleman F, Combaret V, Lunec J, Board J, Pearson A, De Paepe A, Van Roy N, Laureys G, Vandesompele J. De Preter K, et al. Among authors: van roy n. J Clin Oncol. 2005 May 1;23(13):3167-8; author reply 3168-70. doi: 10.1200/JCO.2005.05.346. J Clin Oncol. 2005. PMID: 15860893 No abstract available.

2

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: van der drift p, van roy n. Eur J Cancer. 1995;31A(4):523-6. doi: 10.1016/0959-8049(95)00012-8. Eur J Cancer. 1995. PMID: 7576958

3

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. Eur J Cancer. 1995;31A(4):530-5. doi: 10.1016/0959-8049(95)00004-3. Eur J Cancer. 1995. PMID: 7576960

4

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. Cancer Genet Cytogenet. 1995 Jul 15;82(2):151-4. doi: 10.1016/0165-4608(95)00034-m. Cancer Genet Cytogenet. 1995. PMID: 7664245

5

High-resolution fluorescence mapping of 46 DNA markers to the short arm of human chromosome 1.

Van Roy N, Laureys G, Versteeg R, Opdenakker G, Speleman F. Van Roy N, et al. Genomics. 1993 Oct;18(1):71-8. doi: 10.1006/geno.1993.1427. Genomics. 1993. PMID: 8276418

6

Multiple polysomies in nasal polyps in children.

Speleman F, De Potter C, Van Roy N, Laureys G. Speleman F, et al. Among authors: van roy n. Cancer Genet Cytogenet. 1996 Aug;90(1):86-7. doi: 10.1016/0165-4608(96)00042-8. Cancer Genet Cytogenet. 1996. PMID: 8780754 Review.

7

Reassignment of MYCL1 to human chromosome 1p34.3 by fluorescence in situ hybridization.

Speleman F, Van Camp G, Van Roy N. Speleman F, et al. Among authors: van roy n, van camp g. Cytogenet Cell Genet. 1996;72(2-3):189-90. doi: 10.1159/000134185. Cytogenet Cell Genet. 1996. PMID: 8978772

8

Monosomy 22 in a mixed germ cell-sex cord-stromal tumor of the ovary.

Speleman F, Dermaut B, De Potter CR, Van Gele M, Van Roy N, De Paepe A, Laureys G. Speleman F, et al. Among authors: van gele m, van roy n. Genes Chromosomes Cancer. 1997 Jul;19(3):192-4. Genes Chromosomes Cancer. 1997. PMID: 9219001

9

Comparative genomic hybridization analysis of human neuroblastomas: detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell lines.

Van Roy N, Jauch A, Van Gele M, Laureys G, Versteeg R, De Paepe A, Cremer T, Speleman F. Van Roy N, et al. Among authors: van gele m. Cancer Genet Cytogenet. 1997 Sep;97(2):135-42. doi: 10.1016/s0165-4608(96)00362-7. Cancer Genet Cytogenet. 1997. PMID: 9283597

10

Sensitive and reliable detection of genomic imbalances in human neuroblastomas using comparative genomic hybridisation analysis.

Van Gele M, Van Roy N, Jauch A, Laureys G, Benoit Y, Schelfhout V, De Potter CR, Brock P, Uyttebroeck A, Sciot R, Schuuring E, Versteeg R, Speleman F. Van Gele M, et al. Among authors: van roy n. Eur J Cancer. 1997 Oct;33(12):1979-82. doi: 10.1016/s0959-8049(97)00289-x. Eur J Cancer. 1997. PMID: 9516837

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