Fergusson WD - Search Results

1

X linked lymphoproliferative disease in a United Kingdom family.

Arkwright PD, Makin G, Will AM, Ayres M, Gokhale DA, Fergusson WD, Taylor GM. Arkwright PD, et al. Among authors: fergusson wd. Arch Dis Child. 1998 Jul;79(1):52-5. doi: 10.1136/adc.79.1.52. Arch Dis Child. 1998. PMID: 9771253 Free PMC article.

2

Infantile osteopetrosis; bone marrow transplantation from a cousin donor.

Taylor GM, Dearden SP, Will AM, Evans DI, Stevens RF, Simon S, Super M, Morrell G, Fergusson WD, Brown IH. Taylor GM, et al. Among authors: fergusson wd. Arch Dis Child. 1995 Nov;73(5):453-5. doi: 10.1136/adc.73.5.453. Arch Dis Child. 1995. PMID: 8554366 Free PMC article.

3

Molecular genetic analysis of a family with a history of Hodgkin's disease and dyschondrosteosis.

Gokhale DA, Evans DG, Crowther D, Woll P, Watson CJ, Dearden SP, Fergusson WD, Stevens RF, Taylor GM. Gokhale DA, et al. Among authors: fergusson wd. Leukemia. 1995 May;9(5):826-33. Leukemia. 1995. PMID: 7769845

4

Lack of association between childhood common acute lymphoblastic leukaemia and an HLA-C locus dimorphism influencing the specificity of natural killer cells.

Ghodsi K, Taylor GM, Gokhale DA, Dearden S, Stevens RF, Birch JM, Fergusson WD, Eden OB, Ollier W. Ghodsi K, et al. Among authors: fergusson wd. Br J Haematol. 1998 Sep;102(5):1279-83. doi: 10.1046/j.1365-2141.1998.00919.x. Br J Haematol. 1998. PMID: 9753057 Free article.

5

A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutations.

Meyer S, Fergusson WD, Oostra AB, Medhurst AL, Waisfisz Q, de Winter JP, Chen F, Carr TF, Clayton-Smith J, Clancy T, Green M, Barber L, Eden OB, Will AM, Joenje H, Taylor GM. Meyer S, et al. Among authors: fergusson wd. Genes Chromosomes Cancer. 2005 Apr;42(4):404-15. doi: 10.1002/gcc.20153. Genes Chromosomes Cancer. 2005. PMID: 15645491

6

Expression of LFA-1 by a lymphoblastoid cell line from a patient with monosomy 21: effects on intercellular adhesion.

Taylor GM, Braddock D, Robson AJ, Fergusson WD, Duckett DP, D'Souza SW, Brenchley P. Taylor GM, et al. Among authors: fergusson wd. Clin Exp Immunol. 1990 Sep;81(3):501-6. doi: 10.1111/j.1365-2249.1990.tb05363.x. Clin Exp Immunol. 1990. PMID: 1975779 Free PMC article.

7

The expression of CD18 is increased on Trisomy 21 (Down syndrome) lymphoblastoid cells.

Taylor GM, Williams A, D'Souza SW, Fergusson WD, Donnai D, Fennell J, Harris R. Taylor GM, et al. Among authors: fergusson wd. Clin Exp Immunol. 1988 Feb;71(2):324-8. Clin Exp Immunol. 1988. PMID: 2964960 Free PMC article.

8

Donor-specific T cell alloreactivity in relation to 1 haplotype-mismatched blood transfusion prior to living-donor renal transplantation.

Bakran A, Taylor GM, Read I, Fergusson W, Johnson RW. Bakran A, et al. Transplant Proc. 1987 Feb;19(1 Pt 1):748-9. Transplant Proc. 1987. PMID: 2978929 Clinical Trial. No abstract available.

9

Strong association of the HLA-DP6 supertype with childhood leukaemia is due to a single allele, DPB1*0601.

Taylor GM, Hussain A, Verhage V, Thompson PD, Fergusson WD, Watkins G, Lightfoot T, Harrison CJ, Birch JM; UKCCS Investigators. Taylor GM, et al. Among authors: fergusson wd. Leukemia. 2009 May;23(5):863-9. doi: 10.1038/leu.2008.374. Epub 2009 Jan 15. Leukemia. 2009. PMID: 19148140

10

Donor-recipient bone-marrow matching by single strand conformation polymorphism analysis.

Summers C, Fergusson W, Gokhale D, Taylor M. Summers C, et al. Lancet. 1992 Mar 7;339(8793):621. doi: 10.1016/0140-6736(92)90911-l. Lancet. 1992. PMID: 1347123 No abstract available.

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