Slater RM - Search Results

1

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

2

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

3

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. Nat Genet. 1993 Jun;4(2):187-90. doi: 10.1038/ng0693-187. Nat Genet. 1993. PMID: 8102298

4

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. Hum Genet. 1996 Jun;97(6):834-7. doi: 10.1007/BF02346199. Hum Genet. 1996. PMID: 8641706

5

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. 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.

6

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. Cytogenet Cell Genet. 1997;77(3-4):296-303. doi: 10.1159/000134602. Cytogenet Cell Genet. 1997. PMID: 9284942

7

Differences in patterns of allelic loss between two common types of adult cancer, breast and colon carcinoma, and Wilms' tumor of childhood.

Devilee P, van den Broek M, Mannens M, Slater R, Cornelisse CJ, Westerveld A, Khan PM. Devilee P, et al. Int J Cancer. 1991 Apr 1;47(6):817-21. doi: 10.1002/ijc.2910470604. Int J Cancer. 1991. PMID: 1672665

8

Cytogenetics and molecular genetics of Wilms' tumor of childhood.

Slater RM, Mannens MM. Slater RM, et al. Cancer Genet Cytogenet. 1992 Jul 15;61(2):111-21. doi: 10.1016/0165-4608(92)90071-f. Cancer Genet Cytogenet. 1992. PMID: 1322233 Review.

9

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

10

Chromosome number 11 and Wilms' tumor.

Slater RM, de Kraker J. Slater RM, et al. Cancer Genet Cytogenet. 1982 Mar;5(3):237-45. doi: 10.1016/0165-4608(82)90030-9. Cancer Genet Cytogenet. 1982. PMID: 6279277

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