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Construction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type 1 diabetes.
BMC Genet. 2005 Feb 18;6:9. doi: 10.1186/1471-2156-6-9.
BMC Genet. 2005.
PMID: 15720714
Free PMC article.
Haplotype tag single nucleotide polymorphism analysis of the human orthologues of the rat type 1 diabetes genes Ian4 (Lyp/Iddm1) and Cblb.
Payne F, Smyth DJ, Pask R, Barratt BJ, Cooper JD, Twells RC, Walker NM, Lam AC, Smink LJ, Nutland S, Rance HE, Todd JA.
Payne F, et al. Among authors: pask r.
Diabetes. 2004 Feb;53(2):505-9. doi: 10.2337/diabetes.53.2.505.
Diabetes. 2004.
PMID: 14747305
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Investigating the utility of combining phi29 whole genome amplification and highly multiplexed single nucleotide polymorphism BeadArray genotyping.
Pask R, Rance HE, Barratt BJ, Nutland S, Smyth DJ, Sebastian M, Twells RC, Smith A, Lam AC, Smink LJ, Walker NM, Todd JA.
Pask R, et al.
BMC Biotechnol. 2004 Jul 27;4:15. doi: 10.1186/1472-6750-4-15.
BMC Biotechnol. 2004.
PMID: 15279678
Free PMC article.
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No evidence of association or interaction between the IL4RA, IL4, and IL13 genes in type 1 diabetes.
Maier LM, Chapman J, Howson JM, Clayton DG, Pask R, Strachan DP, McArdle WL, Twells RC, Todd JA.
Maier LM, et al. Among authors: pask r.
Am J Hum Genet. 2005 Mar;76(3):517-21. doi: 10.1086/428387. Epub 2005 Jan 19.
Am J Hum Genet. 2005.
PMID: 15660293
Free PMC article.
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No evidence for association of the TATA-box binding protein glutamine repeat sequence or the flanking chromosome 6q27 region with type 1 diabetes.
Payne F, Smyth DJ, Pask R, Cooper JD, Masters J, Wang WY, Godfrey LM, Bowden G, Szeszko J, Smink LJ, Lam AC, Burren O, Walker NM, Nutland S, Rance H, Undlien DE, Rønningen KS, Guja C, Ionescu-Tîrgovişte C, Todd JA, Twells RC.
Payne F, et al. Among authors: pask r.
Biochem Biophys Res Commun. 2005 Jun 3;331(2):435-41. doi: 10.1016/j.bbrc.2005.03.203.
Biochem Biophys Res Commun. 2005.
PMID: 15850778
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Population structure, differential bias and genomic control in a large-scale, case-control association study.
Clayton DG, Walker NM, Smyth DJ, Pask R, Cooper JD, Maier LM, Smink LJ, Lam AC, Ovington NR, Stevens HE, Nutland S, Howson JM, Faham M, Moorhead M, Jones HB, Falkowski M, Hardenbol P, Willis TD, Todd JA.
Clayton DG, et al. Among authors: pask r.
Nat Genet. 2005 Nov;37(11):1243-6. doi: 10.1038/ng1653. Epub 2005 Oct 9.
Nat Genet. 2005.
PMID: 16228001
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No evidence for a major effect of two common polymorphisms of the catalase gene in type 1 diabetes susceptibility.
Pask R, Cooper JD, Walker NM, Nutland S, Hutchings J, Dunger DB, Nejentsev S, Todd JA.
Pask R, et al.
Diabetes Metab Res Rev. 2006 Sep-Oct;22(5):356-60. doi: 10.1002/dmrr.628.
Diabetes Metab Res Rev. 2006.
PMID: 16453382
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Candidate gene association study of solute carrier family 11a members 1 (SLC11A1) and 2 (SLC11A2) genes in Alzheimer's disease.
Jamieson SE, White JK, Howson JM, Pask R, Smith AN, Brayne C, Evans JG, Xuereb J, Cairns NJ, Rubinsztein DC, Blackwell JM.
Jamieson SE, et al. Among authors: pask r.
Neurosci Lett. 2005 Feb 10;374(2):124-8. doi: 10.1016/j.neulet.2004.10.038.
Neurosci Lett. 2005.
PMID: 15644277
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