McKie AB - Search Results

1

Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa.

Bowne SJ, Daiger SP, Hims MM, Sohocki MM, Malone KA, McKie AB, Heckenlively JR, Birch DG, Inglehearn CF, Bhattacharya SS, Bird A, Sullivan LS. Bowne SJ, et al. Among authors: mckie ab. Hum Mol Genet. 1999 Oct;8(11):2121-8. doi: 10.1093/hmg/8.11.2121. Hum Mol Genet. 1999. PMID: 10484783 Free PMC article.

2

Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa.

Keen TJ, Hims MM, McKie AB, Moore AT, Doran RM, Mackey DA, Mansfield DC, Mueller RF, Bhattacharya SS, Bird AC, Markham AF, Inglehearn CF. Keen TJ, et al. Among authors: mckie ab. Eur J Hum Genet. 2002 Apr;10(4):245-9. doi: 10.1038/sj.ejhg.5200797. Eur J Hum Genet. 2002. PMID: 12032732

3

Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).

McKie AB, McHale JC, Keen TJ, Tarttelin EE, Goliath R, van Lith-Verhoeven JJ, Greenberg J, Ramesar RS, Hoyng CB, Cremers FP, Mackey DA, Bhattacharya SS, Bird AC, Markham AF, Inglehearn CF. McKie AB, et al. Hum Mol Genet. 2001 Jul 15;10(15):1555-62. doi: 10.1093/hmg/10.15.1555. Hum Mol Genet. 2001. PMID: 11468273

4

Expression map of human chromosome region 17p13.3, spanning the RP13 dominant retinitis pigmentosa locus, the Miller-Dieker lissencephaly syndrome (MDLS) region, and a putative tumour suppressor locus.

McHale JC, McKie AB, Tarttelin EE, Inglehearn CF. McHale JC, et al. Among authors: mckie ab. Cytogenet Cell Genet. 2000;88(3-4):225-9. doi: 10.1159/000015556. Cytogenet Cell Genet. 2000. PMID: 10828595

5

Abnormalities affecting the APC and MCC tumour suppressor gene loci on chromosome 5q occur frequently in gastric cancer but not in pancreatic cancer.

McKie AB, Filipe MI, Lemoine NR. McKie AB, et al. Int J Cancer. 1993 Oct 21;55(4):598-603. doi: 10.1002/ijc.2910550414. Int J Cancer. 1993. PMID: 8406987

6

Use of DNA fingerprinting to detect genetic rearrangements in human cancer.

Sirivatanauksorn V, Sirivatanauksorn Y, McKie AB, Lemoine NR. Sirivatanauksorn V, et al. Among authors: mckie ab. Methods Mol Med. 2002;68:107-14. doi: 10.1385/1-59259-135-3:107. Methods Mol Med. 2002. PMID: 11901496 No abstract available.

7

Epigenetic inactivation of the human sprouty2 (hSPRY2) homologue in prostate cancer.

McKie AB, Douglas DA, Olijslagers S, Graham J, Omar MM, Heer R, Gnanapragasam VJ, Robson CN, Leung HY. McKie AB, et al. Oncogene. 2005 Mar 24;24(13):2166-74. doi: 10.1038/sj.onc.1208371. Oncogene. 2005. PMID: 15735753

8

Germline mutations in RYR1 are associated with foetal akinesia deformation sequence/lethal multiple pterygium syndrome.

McKie AB, Alsaedi A, Vogt J, Stuurman KE, Weiss MM, Shakeel H, Tee L, Morgan NV, Nikkels PG, van Haaften G, Park SM, van der Smagt JJ, Bugiani M, Maher ER. McKie AB, et al. Acta Neuropathol Commun. 2014 Dec 5;2:148. doi: 10.1186/s40478-014-0148-0. Acta Neuropathol Commun. 2014. PMID: 25476234 Free PMC article.

9

Abnormalities of the RB1 and DCC tumor suppressor genes: uncommon in human pancreatic adenocarcinoma.

Barton CM, McKie AB, Hogg A, Bia B, Elia G, Phillips SM, Ding SF, Lemoine NR. Barton CM, et al. Among authors: mckie ab. Mol Carcinog. 1995 Jun;13(2):61-9. doi: 10.1002/mc.2940130202. Mol Carcinog. 1995. PMID: 7605581

10

Alu-polymerase chain reaction genomic fingerprinting technique identifies multiple genetic loci associated with pancreatic tumourigenesis.

McKie AB, Iwamura T, Leung HY, Hollingsworth MA, Lemoine NR. McKie AB, et al. Genes Chromosomes Cancer. 1997 Jan;18(1):30-41. doi: 10.1002/(sici)1098-2264(199701)18:1<30::aid-gcc4>3.0.co;2-2. Genes Chromosomes Cancer. 1997. PMID: 8993978

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