Caron HN - Search Results

1

PHOX2B is a novel and specific marker for minimal residual disease testing in neuroblastoma.

Stutterheim J, Gerritsen A, Zappeij-Kannegieter L, Kleijn I, Dee R, Hooft L, van Noesel MM, Bierings M, Berthold F, Versteeg R, Caron HN, van der Schoot CE, Tytgat GA. Stutterheim J, et al. Among authors: caron hn. J Clin Oncol. 2008 Nov 20;26(33):5443-9. doi: 10.1200/JCO.2007.13.6531. Epub 2008 Oct 6. J Clin Oncol. 2008. PMID: 18838715

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

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.

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. 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. 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

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

7

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

8

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

9

SAGE analysis of neuroblastoma reveals a high expression of the human homologue of the Drosophila Delta gene.

van Limpt V, Chan A, Caron H, Sluis PV, Boon K, Hermus MC, Versteeg R. van Limpt V, et al. Med Pediatr Oncol. 2000 Dec;35(6):554-8. doi: 10.1002/1096-911x(20001201)35:6<554::aid-mpo13>3.0.co;2-r. Med Pediatr Oncol. 2000. PMID: 11107116

10

Chromosome bands 1p35-36 contain two distinct neuroblastoma tumor suppressor loci, one of which is imprinted.

Caron H, Spieker N, Godfried M, Veenstra M, van Sluis P, de Kraker J, Voûte P, Versteeg R. Caron H, et al. Genes Chromosomes Cancer. 2001 Feb;30(2):168-74. doi: 10.1002/1098-2264(200102)30:2<168::aid-gcc1072>3.0.co;2-e. Genes Chromosomes Cancer. 2001. PMID: 11135433

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