Williamson KA - Search Results

1

Expression of the Wilms' tumor gene WT1 in human malignant mesothelioma cell lines and relationship to platelet-derived growth factor A and insulin-like growth factor 2 expression.

Langerak AW, Williamson KA, Miyagawa K, Hagemeijer A, Versnel MA, Hastie ND. Langerak AW, et al. Among authors: williamson ka. Genes Chromosomes Cancer. 1995 Feb;12(2):87-96. doi: 10.1002/gcc.2870120203. Genes Chromosomes Cancer. 1995. PMID: 7535092 Free article.

2

The gene for the cyclin-dependent-kinase-4 inhibitor, CDKN2A, is preferentially deleted in malignant mesothelioma.

Prins JB, Williamson KA, Kamp MM, Van Hezik EJ, Van der Kwast TH, Hagemeijer A, Versnel MA. Prins JB, et al. Among authors: williamson ka. Int J Cancer. 1998 Feb 9;75(4):649-53. doi: 10.1002/(sici)1097-0215(19980209)75:4<649::aid-ijc25>3.0.co;2-2. Int J Cancer. 1998. PMID: 9466670 Free article.

3

Genetic interactions between the Wilms' tumor 1 gene and the p53 gene.

Menke AL, Clarke AR, Leitch A, Ijpenberg A, Williamson KA, Spraggon L, Harrison DJ, Hastie ND. Menke AL, et al. Among authors: williamson ka. Cancer Res. 2002 Nov 15;62(22):6615-20. Cancer Res. 2002. PMID: 12438257

4

Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion.

Little MH, Williamson KA, Mannens M, Kelsey A, Gosden C, Hastie ND, van Heyningen V. Little MH, et al. Among authors: williamson ka. Hum Mol Genet. 1993 Mar;2(3):259-64. doi: 10.1093/hmg/2.3.259. Hum Mol Genet. 1993. PMID: 8388765

5

Loss of WT1 function leads to ectopic myogenesis in Wilms' tumour.

Miyagawa K, Kent J, Moore A, Charlieu JP, Little MH, Williamson KA, Kelsey A, Brown KW, Hassam S, Briner J, Hayashi Y, Hirai H, Yazaki Y, van Heyningen V, Hastie ND. Miyagawa K, et al. Among authors: williamson ka. Nat Genet. 1998 Jan;18(1):15-7. doi: 10.1038/ng0198-15. Nat Genet. 1998. PMID: 9425891 No abstract available.

6

Towards an understanding of Wilms' tumour.

Williamson KA, Van Heyningen V. Williamson KA, et al. Int J Exp Pathol. 1994 Jun;75(3):147-55. Int J Exp Pathol. 1994. PMID: 8086311 Free PMC article. Review.

7

Developmental malformations of the eye: the role of PAX6, SOX2 and OTX2.

Hever AM, Williamson KA, van Heyningen V. Hever AM, et al. Among authors: williamson ka. Clin Genet. 2006 Jun;69(6):459-70. doi: 10.1111/j.1399-0004.2006.00619.x. Clin Genet. 2006. PMID: 16712695 Review.

8

Hemolytic uremic syndrome associated with Denys-Drash syndrome.

Sherbotie JR, van Heyningen V, Axton R, Williamson K, Finn LS, Kaplan BS. Sherbotie JR, et al. Pediatr Nephrol. 2000 Oct;14(12):1092-7. doi: 10.1007/s004670000389. Pediatr Nephrol. 2000. PMID: 11045393

9

PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation.

Malandrini A, Mari F, Palmeri S, Gambelli S, Berti G, Bruttini M, Bardelli AM, Williamson K, van Heyningen V, Renieri A. Malandrini A, et al. Clin Genet. 2001 Aug;60(2):151-4. doi: 10.1034/j.1399-0004.2001.600210.x. Clin Genet. 2001. PMID: 11553050

10

Mutations in SOX2 cause anophthalmia.

Fantes J, Ragge NK, Lynch SA, McGill NI, Collin JR, Howard-Peebles PN, Hayward C, Vivian AJ, Williamson K, van Heyningen V, FitzPatrick DR. Fantes J, et al. Nat Genet. 2003 Apr;33(4):461-3. doi: 10.1038/ng1120. Epub 2003 Mar 3. Nat Genet. 2003. PMID: 12612584

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