Caron HN - Search Results

1

Stability of PCR targets for monitoring minimal residual disease in neuroblastoma.

Stutterheim J, Zappeij-Kannegieter L, Ora I, van Sluis PG, Bras J, den Ouden E, Versteeg R, Caron HN, van der Schoot CE, Tytgat GA. Stutterheim J, et al. Among authors: caron hn. J Mol Diagn. 2012 Mar-Apr;14(2):168-75. doi: 10.1016/j.jmoldx.2011.12.002. Epub 2012 Jan 16. J Mol Diagn. 2012. PMID: 22251610 Free article.

2

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. 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.

3

Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification.

Caron H, Peter M, van Sluis P, Speleman F, de Kraker J, Laureys G, Michon J, Brugières L, Voûte PA, Westerveld A, et al. Caron H, et al. Hum Mol Genet. 1995 Apr;4(4):535-9. doi: 10.1093/hmg/4.4.535. Hum Mol Genet. 1995. PMID: 7633401

4

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. Prog Clin Biol Res. 1994;385:35-42. Prog Clin Biol Res. 1994. PMID: 7972230 No abstract available.

5

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.

6

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

7

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. N Engl J Med. 1996 Jan 25;334(4):225-30. doi: 10.1056/NEJM199601253340404. N Engl J Med. 1996. PMID: 8531999 Free article.

8

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

9

No mutations found by RET mutation scanning in sporadic and hereditary neuroblastoma.

Hofstra RM, Cheng NC, Hansen C, Stulp RP, Stelwagen T, Clausen N, Tommerup N, Caron H, Westerveld A, Versteeg R, Buys CH. Hofstra RM, et al. Hum Genet. 1996 Mar;97(3):362-4. doi: 10.1007/BF02185773. Hum Genet. 1996. PMID: 8786083

10

An integrated 5-Mb physical, genetic, and radiation hybrid map of a 1p36.1 region implicated in neuroblastoma pathogenesis.

Spieker N, Beitsma M, van Sluis P, Roobeek I, den Dunnen JT, Speleman F, Caron H, Versteeg R. Spieker N, et al. Genes Chromosomes Cancer. 2000 Feb;27(2):143-52. Genes Chromosomes Cancer. 2000. PMID: 10612802

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