Rack KA - Search Results

1

Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16.

Wilkie AO, Higgs DR, Rack KA, Buckle VJ, Spurr NK, Fischel-Ghodsian N, Ceccherini I, Brown WR, Harris PC. Wilkie AO, et al. Among authors: rack ka. Cell. 1991 Feb 8;64(3):595-606. doi: 10.1016/0092-8674(91)90243-r. Cell. 1991. PMID: 1991321

2

Characterization of three de novo derivative chromosomes 16 by "reverse chromosome painting" and molecular analysis.

Rack KA, Harris PC, MacCarthy AB, Boone R, Raynham H, McKinley M, Fitchett M, Towe CM, Rudd P, Armour JA, et al. Rack KA, et al. Am J Hum Genet. 1993 May;52(5):987-97. Am J Hum Genet. 1993. PMID: 8488848 Free PMC article.

3

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. Br J Haematol. 1991 Dec;79(4):550-5. doi: 10.1111/j.1365-2141.1991.tb08080.x. Br J Haematol. 1991. PMID: 1685326

4

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. 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.

5

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. Cancer Genet Cytogenet. 1991 May;53(1):91-5. doi: 10.1016/0165-4608(91)90118-e. Cancer Genet Cytogenet. 1991. PMID: 2036643

6

Comparison of cytogenetic and restriction fragment length polymorphism analyses for the detection of loss of chromosome material in clonal hemopoietic disorders.

Abrahamson GM, Rack K, Oscier DG, Fitchett M, Buckle VJ, Wainscoat JS. Abrahamson GM, et al. Am J Hematol. 1993 Feb;42(2):171-6. doi: 10.1002/ajh.2830420206. Am J Hematol. 1993. PMID: 8094942

7

Structure of the human DNA repair gene HAP1 and its localisation to chromosome 14q 11.2-12.

Robson CN, Hochhauser D, Craig R, Rack K, Buckle VJ, Hickson ID. Robson CN, et al. Nucleic Acids Res. 1992 Sep 11;20(17):4417-21. doi: 10.1093/nar/20.17.4417. Nucleic Acids Res. 1992. PMID: 1383925 Free PMC article.

8

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. 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.

9

Structure of the granulocyte macrophage colony-stimulating factor gene in patients with the myelodysplastic syndromes.

Boultwood J, Abrahamson G, Buckle VJ, Rack K, Oscier DG, Wainscoat JS. Boultwood J, et al. Am J Hematol. 1990 Jun;34(2):157-8. doi: 10.1002/ajh.2830340215. Am J Hematol. 1990. PMID: 2187337

10

Hematological features of patients with myelodysplastic syndromes associated with a chromosome 5q deletion.

Lewis S, Oscier D, Boultwood J, Ross F, Fitchett M, Rack K, Abrahamson G, Buckle V, Wainscoat JS. Lewis S, et al. Am J Hematol. 1995 Jul;49(3):194-200. doi: 10.1002/ajh.2830490304. Am J Hematol. 1995. PMID: 7604812

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