Foot NJ - Search Results

1

Novel mutations and polymorphisms in the Fanconi anemia group C gene.

Gibson RA, Morgan NV, Goldstein LH, Pearson IC, Kesterton IP, Foot NJ, Jansen S, Havenga C, Pearson T, de Ravel TJ, Cohn RJ, Marques IM, Dokal I, Roberts I, Marsh J, Ball S, Milner RD, Llerena JC Jr, Samochatova E, Mohan SP, Vasudevan P, Birjandi F, Hajianpour A, Murer-Orlando M, Mathew CG. Gibson RA, et al. Among authors: foot nj. Hum Mutat. 1996;8(2):140-8. doi: 10.1002/(SICI)1098-1004(1996)8:2<140::AID-HUMU6>3.0.CO;2-F. Hum Mutat. 1996. PMID: 8844212

2

The most frequent constitutional translocation in humans, the t(11;22)(q23;q11) is due to a highly specific alu-mediated recombination.

Hill AS, Foot NJ, Chaplin TL, Young BD. Hill AS, et al. Among authors: foot nj. Hum Mol Genet. 2000 Jun 12;9(10):1525-32. doi: 10.1093/hmg/9.10.1525. Hum Mol Genet. 2000. PMID: 10888603

3

Prospective gene expression analysis accurately subtypes acute leukaemia in children and establishes a commonality between hyperdiploidy and t(12;21) in acute lymphoblastic leukaemia.

van Delft FW, Bellotti T, Luo Z, Jones LK, Patel N, Yiannikouris O, Hill AS, Hubank M, Kempski H, Fletcher D, Chaplin T, Foot N, Young BD, Hann IM, Gammerman A, Saha V. van Delft FW, et al. Br J Haematol. 2005 Jul;130(1):26-35. doi: 10.1111/j.1365-2141.2005.05545.x. Br J Haematol. 2005. PMID: 15982341 Free article.

4

Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias.

Raghavan M, Lillington DM, Skoulakis S, Debernardi S, Chaplin T, Foot NJ, Lister TA, Young BD. Raghavan M, et al. Among authors: foot nj. Cancer Res. 2005 Jan 15;65(2):375-8. Cancer Res. 2005. PMID: 15695375

5

A role for mitotic recombination in leukemogenesis.

Young BD, Debernardi S, Lillington DM, Skoulakis S, Chaplin T, Foot NJ, Raghavan M. Young BD, et al. Among authors: foot nj. Adv Enzyme Regul. 2006;46:90-7. doi: 10.1016/j.advenzreg.2006.01.015. Epub 2006 Aug 4. Adv Enzyme Regul. 2006. PMID: 16890980 Review. No abstract available.

6

Assignment of brain acid-soluble protein 1 (BASP1) to human chromosome 5p15.1-->p14, differential expression in human cancer cell lines as a result of alterations in gene dosage.

Fitzgibbon J, Neat MJ, Foot N, Hill AS, Lister TA, Gupta RK. Fitzgibbon J, et al. Cytogenet Cell Genet. 2000;89(3-4):147-9. doi: 10.1159/000015597. Cytogenet Cell Genet. 2000. PMID: 10965107 No abstract available.

7

The characterisation of the lymphoma cell line U937, using comparative genomic hybridisation and multi-plex FISH.

Strefford JC, Foot NJ, Chaplin T, Neat MJ, Oliver RT, Young BD, Jones LK. Strefford JC, et al. Among authors: foot nj. Cytogenet Cell Genet. 2001;94(1-2):9-14. doi: 10.1159/000048774. Cytogenet Cell Genet. 2001. PMID: 11701946

8

Molecular characterisation of the t(1;15)(p22;q22) translocation in the prostate cancer cell line LNCaP.

Strefford JC, Lane TM, Hill A, LeRoux L, Foot NJ, Shipley J, Oliver RT, Lu YJ, Young BD. Strefford JC, et al. Among authors: foot nj. Cytogenet Genome Res. 2006;112(1-2):45-52. doi: 10.1159/000087512. Cytogenet Genome Res. 2006. PMID: 16276089

9

Comparative genomic hybridization and multiplex-fluorescence in situ hybridization: an appraisal in elderly patients with acute myelogenous leukemia.

Dalley CD, Neat MJ, Foot NJ, Burridge M, Byrne L, Amess JA, Rohatiner AZ, Lister A, Young BD, Lillington DM. Dalley CD, et al. Among authors: foot nj. Hematol J. 2002;3(6):290-8. doi: 10.1038/sj.thj.6200194. Hematol J. 2002. PMID: 12522451

10

Detection of chromosome abnormalities pre-high-dose treatment in patients developing therapy-related myelodysplasia and secondary acute myelogenous leukemia after treatment for non-Hodgkin's lymphoma.

Lillington DM, Micallef IN, Carpenter E, Neat MJ, Amess JA, Matthews J, Foot NJ, Young BD, Lister TA, Rohatiner AZ. Lillington DM, et al. Among authors: foot nj. J Clin Oncol. 2001 May 1;19(9):2472-81. doi: 10.1200/JCO.2001.19.9.2472. J Clin Oncol. 2001. PMID: 11331326

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