Kelly S - Search Results

1

Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.

Boultwood J, Rack K, Kelly S, Madden J, Sakaguchi AY, Wang LM, Oscier DG, Buckle VJ, Wainscoat JS. Boultwood J, et al. Among authors: kelly s. Proc Natl Acad Sci U S A. 1991 Jul 15;88(14):6176-80. doi: 10.1073/pnas.88.14.6176. Proc Natl Acad Sci U S A. 1991. PMID: 1829836 Free PMC article.

2

Clonality of cell populations in refractory anaemia using combined approach of gene loss and X-linked restriction fragment length polymorphism-methylation analyses.

Abrahamson G, Boultwood J, Madden J, Kelly S, Oscier DG, Rack K, Buckle VJ, Wainscoat JS. Abrahamson G, et al. Among authors: kelly s. Br J Haematol. 1991 Dec;79(4):550-5. doi: 10.1111/j.1365-2141.1991.tb08080.x. Br J Haematol. 1991. PMID: 1685326

3

Homozygous deletion of FMS in a patient with the 5q- syndrome.

Boultwood J, Rack K, Buckle VJ, Kelly S, Madden J, Oscier DG, Wainscoat JS. Boultwood J, et al. Among authors: kelly s. Br J Haematol. 1990 Oct;76(2):310-1. doi: 10.1111/j.1365-2141.1990.tb07892.x. Br J Haematol. 1990. PMID: 2094336 No abstract available.

4

Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q- syndrome: delineation of the critical region on 5q and identification of a 5q- breakpoint.

Boultwood J, Fidler C, Lewis S, Kelly S, Sheridan H, Littlewood TJ, Buckle VJ, Wainscoat JS. Boultwood J, et al. Among authors: kelly s. Genomics. 1994 Feb;19(3):425-32. doi: 10.1006/geno.1994.1090. Genomics. 1994. PMID: 8188284

5

Allelic loss of IRF1 in myelodysplasia and acute myeloid leukemia: retention of IRF1 on the 5q- chromosome in some patients with the 5q- syndrome.

Boultwood J, Fidler C, Lewis S, MacCarthy A, Sheridan H, Kelly S, Oscier D, Buckle VJ, Wainscoat JS. Boultwood J, et al. Among authors: kelly s. Blood. 1993 Nov 1;82(9):2611-6. Blood. 1993. PMID: 8219215 Free article.

6

Translocation 1;7 in hematologic disorders--a report of three further cases. Absence of amplification of the gene for the epidermal growth factor receptor.

Abrahamson GM, Rack K, Buckle VJ, Oscier DG, Kelly S, Wainscoat JS. Abrahamson GM, et al. Among authors: kelly s. Cancer Genet Cytogenet. 1991 May;53(1):91-5. doi: 10.1016/0165-4608(91)90118-e. Cancer Genet Cytogenet. 1991. PMID: 2036643

7

Combined immunophenotyping and FISH identifies the involvement of B-cells in 5q- syndrome.

Jaju RJ, Jones M, Boultwood J, Kelly S, Mason DY, Wainscoat JS, Kearney L. Jaju RJ, et al. Among authors: kelly s. Genes Chromosomes Cancer. 2000 Nov;29(3):276-80. doi: 10.1002/1098-2264(2000)9999:9999<::aid-gcc1035>3.0.co;2-l. Genes Chromosomes Cancer. 2000. PMID: 10992302

8

The impact of dose escalation and resistance modulation in older patients with acute myeloid leukaemia and high risk myelodysplastic syndrome: the results of the LRF AML14 trial.

Burnett AK, Milligan D, Goldstone A, Prentice A, McMullin MF, Dennis M, Sellwood E, Pallis M, Russell N, Hills RK, Wheatley K; United Kingdom National Cancer Research Institute Haematological Oncology Study Group. Burnett AK, et al. Br J Haematol. 2009 May;145(3):318-32. doi: 10.1111/j.1365-2141.2009.07604.x. Epub 2009 Mar 8. Br J Haematol. 2009. PMID: 19291085 Free article. Clinical Trial.

9

Molecular characterization of a novel 10.3 kb deletion causing beta-thalassaemia with unusually high Hb A2.

Craig JE, Kelly SJ, Barnetson R, Thein SL. Craig JE, et al. Among authors: kelly sj. Br J Haematol. 1992 Dec;82(4):735-44. doi: 10.1111/j.1365-2141.1992.tb06952.x. Br J Haematol. 1992. PMID: 1482661

10

Acute myelomonocytic leukaemia following atypical congenital rubella.

Kelly SJ, Gibbs T, Cheetham CH. Kelly SJ, et al. J Clin Pathol. 1993 Aug;46(8):764-5. doi: 10.1136/jcp.46.8.764. J Clin Pathol. 1993. PMID: 8408706 Free PMC article.

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