Edinburgh Research Explorer

Kathy Williamson

Research Fellow

  1. 1987
  2. A new allele of the testosterone-responsive gene, Hdc-a, in the histidine decarboxylase gene complex of the mouse

    Middleton, R. J., Williamson, K. & Bulfield, G., Dec 1987, In: Genetics Research. 50, 3, p. 213-7 5 p.

    Research output: Contribution to journalArticlepeer-review

  3. 1993
  4. Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion

    Little, M. H., Williamson, K. A., Mannens, M., Kelsey, A., Gosden, C., Hastie, N. D. & van Heyningen, V., Mar 1993, In: Human Molecular Genetics. 2, 3, p. 259-64 6 p.

    Research output: Contribution to journalArticlepeer-review

  5. 1994
  6. Towards an understanding of Wilms' tumour

    Williamson, K. A. & Van Heyningen, V., Jun 1994, In: International Journal of Experimental Pathology. 75, 3, p. 147-55 9 p.

    Research output: Contribution to journalReview articlepeer-review

  7. 1995
  8. A high-resolution integrated physical, cytogenetic, and genetic map of human chromosome 11: distal p13 to proximal p15.1

    Fantes, J. A., Oghene, K., Boyle, S., Danes, S., Fletcher, J. M., Bruford, E. A., Williamson, K., Seawright, A., Schedl, A. & Hanson, I., 20 Jan 1995, In: Genomics. 25, 2, p. 447-61 15 p.

    Research output: Contribution to journalArticlepeer-review

  9. 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, A. W., Williamson, K. A., Miyagawa, K., Hagemeijer, A., Versnel, M. A. & Hastie, N. D., Feb 1995, In: Genes, Chromosomes and Cancer. 12, 2, p. 87-96 10 p.

    Research output: Contribution to journalArticlepeer-review

  10. Do children with diffuse mesangial sclerosis in association with mutations of the Wilm's tumour suppressor gene (WT1) require bilateral nephrectomy?

    Webb, N. J., Lewis, M. A., Williamson, K., van Heyningen, V., Bruce, J., Lendon, M. & Postlethwaite, R. J., Apr 1995, In: Pediatric Nephrology. 9, 2, p. 252-3 2 p.

    Research output: Contribution to journalArticlepeer-review

  11. 1998
  12. Loss of WT1 function leads to ectopic myogenesis in Wilms' tumour

    Miyagawa, K., Kent, J., Moore, A., Charlieu, J. P., Little, M. H., Williamson, K. A., Kelsey, A., Brown, K. W., Hassam, S., Briner, J., Hayashi, Y., Hirai, H., Yazaki, Y., van Heyningen, V. & Hastie, N. D., Jan 1998, In: Nature Genetics. 18, 1, p. 15-17 3 p.

    Research output: Contribution to journalArticlepeer-review

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

    Prins, J. B., Williamson, K. A., Kamp, M. M., Van Hezik, E. J., Van der Kwast, T. H., Hagemeijer, A. & Versnel, M. A., 9 Feb 1998, In: International Journal of Cancer. 75, 4, p. 649-53 5 p.

    Research output: Contribution to journalArticlepeer-review

  14. 2000
  15. Hemolytic uremic syndrome associated with Denys-Drash syndrome

    Sherbotie, J. R., van Heyningen, V., Axton, R., Williamson, K., Finn, L. S. & Kaplan, B. S., Oct 2000, In: Pediatric Nephrology. 14, 12, p. 1092-7 6 p.

    Research output: Contribution to journalArticlepeer-review

  16. 2001
  17. PAX6 haploinsufficiency causes cerebral malformation and olfactory dysfunction in humans

    Sisodiya, S. M., Free, S. L., Williamson, K. A., Mitchell, T. N., Willis, C., Stevens, J. M., Kendall, B. E., Shorvon, S. D., Hanson, I. M., Moore, A. T. & van Heyningen, V., Jul 2001, In: Nature Genetics. 28, 3, p. 214-6 3 p.

    Research output: Contribution to journalArticlepeer-review

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