Speleman F - Search Results

1

Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma.

Bown N, Cotterill S, Lastowska M, O'Neill S, Pearson AD, Plantaz D, Meddeb M, Danglot G, Brinkschmidt C, Christiansen H, Laureys G, Speleman F, Nicholson J, Bernheim A, Betts DR, Vandesompele J, Van Roy N. Bown N, et al. Among authors: speleman f. N Engl J Med. 1999 Jun 24;340(25):1954-61. doi: 10.1056/NEJM199906243402504. N Engl J Med. 1999. PMID: 10379019 Free article.

2

Molecular cytogenetic delineation of 17q translocation breakpoints in neuroblastoma cell lines.

Lastowska M, Van Roy N, Bown N, Speleman F, Lunec J, Strachan T, Pearson AD, Jackson MS. Lastowska M, et al. Among authors: speleman f. Genes Chromosomes Cancer. 1998 Oct;23(2):116-22. doi: 10.1002/(sici)1098-2264(199810)23:2<116::aid-gcc4>3.0.co;2-5. Genes Chromosomes Cancer. 1998. PMID: 9739014

3

Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastoma.

Lastowska M, Van Roy N, Bown N, Speleman F, Roberts P, Lunec J, Strachan T, Pearson AD, Jackson MS. Lastowska M, et al. Among authors: speleman f. Med Pediatr Oncol. 2001 Jan;36(1):20-3. doi: 10.1002/1096-911X(20010101)36:1<20::AID-MPO1006>3.0.CO;2-E. Med Pediatr Oncol. 2001. PMID: 11464884

4

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: speleman f. Genes Chromosomes Cancer. 1994 Jun;10(2):103-14. doi: 10.1002/gcc.2870100205. Genes Chromosomes Cancer. 1994. PMID: 7520263

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

6

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. Among authors: speleman f. Genomics. 1993 Oct;18(1):71-8. doi: 10.1006/geno.1993.1427. Genomics. 1993. PMID: 8276418

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. Cytogenet Cell Genet. 1996;72(2-3):189-90. doi: 10.1159/000134185. Cytogenet Cell Genet. 1996. PMID: 8978772

8

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: speleman f. Cancer Genet Cytogenet. 1997 Sep;97(2):135-42. doi: 10.1016/s0165-4608(96)00362-7. Cancer Genet Cytogenet. 1997. PMID: 9283597

9

Analysis of 1;17 translocation breakpoints in neuroblastoma: implications for mapping of neuroblastoma genes.

Van Roy N, Laureys G, Van Gele M, Opdenakker G, Miura R, van der Drift P, Chan A, Versteeg R, Speleman F. Van Roy N, et al. Among authors: speleman f. Eur J Cancer. 1997 Oct;33(12):1974-8. doi: 10.1016/s0959-8049(97)00319-5. Eur J Cancer. 1997. PMID: 9516836

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: speleman f. 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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