Slater R - Search Results

1

Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus.

Caron H, van Sluis P, Buschman R, Pereira do Tanque R, Maes P, Beks L, de Kraker J, Voûte PA, Vergnaud G, Westerveld A, Slater R, Versteeg R. Caron H, et al. Among authors: slater r. Hum Genet. 1996 Jun;97(6):834-7. doi: 10.1007/BF02346199. Hum Genet. 1996. PMID: 8641706

2

Chromosome 1p allelic loss in neuroblastoma: prognosis, genomic imprinting and 1;17 translocations.

Caron H, van Sluis P, van Roy N, Beks L, Maes P, Pereira do Tanque R, Slater R, de Kraker J, Speleman F, Voûte PA, et al. Caron H, et al. Among authors: slater r. Prog Clin Biol Res. 1994;385:35-42. Prog Clin Biol Res. 1994. PMID: 7972230 No abstract available.

3

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: slater r. Am J Hum Genet. 1994 Aug;55(2):341-7. Am J Hum Genet. 1994. PMID: 8037211 Free PMC article.

4

Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification.

Caron H, van Sluis P, van Hoeve M, de Kraker J, Bras J, Slater R, Mannens M, Voûte PA, Westerveld A, Versteeg R. Caron H, et al. Among authors: slater r. Nat Genet. 1993 Jun;4(2):187-90. doi: 10.1038/ng0693-187. Nat Genet. 1993. PMID: 8102298

5

Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma.

Caron H, van Sluis P, de Kraker J, Bökkerink J, Egeler M, Laureys G, Slater R, Westerveld A, Voûte PA, Versteeg R. Caron H, et al. Among authors: slater r. N Engl J Med. 1996 Jan 25;334(4):225-30. doi: 10.1056/NEJM199601253340404. N Engl J Med. 1996. PMID: 8531999 Free article.

6

1p36: every subband a suppressor?

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. Among authors: slater r. 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.

7

Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11.

Mannens M, Devilee P, Bliek J, Mandjes I, de Kraker J, Heyting C, Slater RM, Westerveld A. Mannens M, et al. Among authors: slater rm. Cancer Res. 1990 Jun 1;50(11):3279-83. Cancer Res. 1990. PMID: 2159377

8

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours.

Mannens M, Slater RM, Heyting C, Bliek J, de Kraker J, Coad N, de Pagter-Holthuizen P, Pearson PL. Mannens M, et al. Among authors: slater rm. Hum Genet. 1988 Dec;81(1):41-8. doi: 10.1007/BF00283727. Hum Genet. 1988. PMID: 2848758

9

Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors.

Mannens M, Alders M, Redeker B, Bliek J, Steenman M, Wiesmeyer C, de Meulemeester M, Ryan A, Kalikin L, Voûte T, De Kraker J, Hoovers J, Slater R, Feinberg A, Little P, Westerveld A. Mannens M, et al. Among authors: slater r. Med Pediatr Oncol. 1996 Nov;27(5):490-4. doi: 10.1002/(SICI)1096-911X(199611)27:5<490::AID-MPO17>3.0.CO;2-E. Med Pediatr Oncol. 1996. PMID: 8827079 Review.

10

Comparative genomic hybridization analysis of Wilms tumors.

Steenman M, Redeker B, de Meulemeester M, Wiesmeijer K, Voûte PA, Westerveld A, Slater R, Mannens M. Steenman M, et al. Among authors: slater r. Cytogenet Cell Genet. 1997;77(3-4):296-303. doi: 10.1159/000134602. Cytogenet Cell Genet. 1997. PMID: 9284942

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