Westerveld A - Search Results

1

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. Among authors: westerveld a. Int J Cancer. 1991 Apr 1;47(6):817-21. doi: 10.1002/ijc.2910470604. Int J Cancer. 1991. PMID: 1672665

2

Direct assignment of the human beta B2 and beta B3 crystallin genes to 22q11.2----q12: markers for neurofibromatosis 2.

Hulsebos TJ, Bijlsma EK, Geurts van Kessel AH, Brakenhoff RH, Westerveld A. Hulsebos TJ, et al. Among authors: westerveld a. Cytogenet Cell Genet. 1991;56(3-4):171-5. doi: 10.1159/000133080. Cytogenet Cell Genet. 1991. PMID: 2055112

3

DNA repair in human cells: from genetic complementation to isolation of genes.

Bootsma D, Westerveld A, Hoeijmakers JH. Bootsma D, et al. Among authors: westerveld a. Cancer Surv. 1988;7(2):303-15. Cancer Surv. 1988. PMID: 3066477 Review.

4

Cytogenetical characterisation of Chinese hamster 43-3B transferants with the amplified or non-amplified human DNA repair gene ERCC-1.

Darroudi F, Westerveld A, Natarajan AT. Darroudi F, et al. Among authors: westerveld a. Mutat Res. 1989 Jun;212(2):113-22. doi: 10.1016/0027-5107(89)90062-6. Mutat Res. 1989. PMID: 2499774

5

Type III collagen deficiency in saccular intracranial aneurysms. Defect in gene regulation?

van den Berg JS, Pals G, Arwert F, Hennekam RC, Albrecht KW, Westerveld A, Limburg M. van den Berg JS, et al. Among authors: westerveld a. Stroke. 1999 Aug;30(8):1628-31. doi: 10.1161/01.str.30.8.1628. Stroke. 1999. PMID: 10436112

6

Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.

Steenman M, Westerveld A, Mannens M. Steenman M, et al. Among authors: westerveld a. Genes Chromosomes Cancer. 2000 May;28(1):1-13. doi: 10.1002/(sici)1098-2264(200005)28:1<1::aid-gcc1>3.0.co;2-#. Genes Chromosomes Cancer. 2000. PMID: 10738297 Review.

7

Cloning of candidate genes involved in the Beckwith-Wiedemann syndrome and childhood tumors.

Alders M, Bliek J, Redeker B, Ryan A, Feinberg A, Westerveld A, Little P, Mannens M. Alders M, et al. Among authors: westerveld a. Med Pediatr Oncol. 1996 Nov;27(5):495-7. doi: 10.1002/(SICI)1096-911X(199611)27:5<495::AID-MPO18>3.0.CO;2-9. Med Pediatr Oncol. 1996. PMID: 8827080 No abstract available.

8

Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma.

Hermsen MA, Joenje H, Arwert F, Welters MJ, Braakhuis BJ, Bagnay M, Westerveld A, Slater R. Hermsen MA, et al. Among authors: westerveld a. Genes Chromosomes Cancer. 1996 Jan;15(1):1-9. doi: 10.1002/(SICI)1098-2264(199601)15:1<1::AID-GCC1>3.0.CO;2-8. Genes Chromosomes Cancer. 1996. PMID: 8824719

9

A human modifier of methylation for class I HLA genes (MEMO-1) maps to chromosomal bands 1p35-36.1.

Cheng NC, Chan AJ, Beitsma MM, Speleman F, Westerveld A, Versteeg R. Cheng NC, et al. Among authors: westerveld a. Hum Mol Genet. 1996 Mar;5(3):309-17. doi: 10.1093/hmg/5.3.309. Hum Mol Genet. 1996. PMID: 8852654

10

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

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