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Molecular modelling of the C-terminal domains of factor H of human complement: a correlation between haemolytic uraemic syndrome and a predicted heparin binding site.
Perkins SJ, Goodship TH. Perkins SJ, et al. Among authors: goodship th. J Mol Biol. 2002 Feb 15;316(2):217-24. doi: 10.1006/jmbi.2001.5337. J Mol Biol. 2002. PMID: 11851332
Solution structures of complement components by X-ray and neutron scattering and analytical ultracentrifugation.
Perkins SJ, Gilbert HE, Aslam M, Hannan J, Holers VM, Goodship TH. Perkins SJ, et al. Among authors: goodship th. Biochem Soc Trans. 2002 Nov;30(Pt 6):996-1001. doi: 10.1042/bst0300996. Biochem Soc Trans. 2002. PMID: 12440960 Review.
The role of ADAMTS-13 activity and complement mutational analysis in differentiating acute thrombotic microangiopathies.
Phillips EH, Westwood JP, Brocklebank V, Wong EK, Tellez JO, Marchbank KJ, McGuckin S, Gale DP, Connolly J, Goodship TH, Kavanagh D, Scully MA. Phillips EH, et al. Among authors: goodship th. J Thromb Haemost. 2016 Jan;14(1):175-85. doi: 10.1111/jth.13189. Epub 2016 Jan 11. J Thromb Haemost. 2016. PMID: 26559391 Free PMC article.
Successful renal transplantation in factor H autoantibody associated HUS with CFHR1 and 3 deficiency and CFH variant G2850T.
Waters AM, Pappworth I, Marchbank K, Bockenhauer D, Tullus K, Pickering MC, Strain L, Sebire N, Shroff R, Marks SD, Goodship TH, Rees L. Waters AM, et al. Among authors: goodship th. Am J Transplant. 2010 Jan;10(1):168-72. doi: 10.1111/j.1600-6143.2009.02870.x. Epub 2009 Nov 16. Am J Transplant. 2010. PMID: 19951285
Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN.
Wong EK, Anderson HE, Herbert AP, Challis RC, Brown P, Reis GS, Tellez JO, Strain L, Fluck N, Humphrey A, Macleod A, Richards A, Ahlert D, Santibanez-Koref M, Barlow PN, Marchbank KJ, Harris CL, Goodship TH, Kavanagh D. Wong EK, et al. Among authors: goodship th. J Am Soc Nephrol. 2014 Nov;25(11):2425-33. doi: 10.1681/ASN.2013070732. Epub 2014 Apr 10. J Am Soc Nephrol. 2014. PMID: 24722444 Free PMC article.
Chromosomal rearrangement-A rare cause of complement factor I associated atypical haemolytic uraemic syndrome.
Gleeson PJ, Wilson V, Cox TE, Sharma SD, Smith-Jackson K, Strain L, Lappin D, McHale T, Kavanagh D, Goodship TH. Gleeson PJ, et al. Among authors: goodship th. Immunobiology. 2016 Oct;221(10):1124-30. doi: 10.1016/j.imbio.2016.05.002. Epub 2016 May 10. Immunobiology. 2016. PMID: 27268256
Is complement factor H a susceptibility factor for IgA nephropathy?
Edey M, Strain L, Ward R, Ahmed S, Thomas T, Goodship TH. Edey M, et al. Among authors: goodship th. Mol Immunol. 2009 Apr;46(7):1405-8. doi: 10.1016/j.molimm.2008.12.002. Epub 2009 Jan 21. Mol Immunol. 2009. PMID: 19162324
Factor H autoantibodies in membranoproliferative glomerulonephritis.
Goodship TH, Pappworth IY, Toth T, Denton M, Houlberg K, McCormick F, Warland D, Moore I, Hunze EM, Staniforth SJ, Hayes C, Cavalcante DP, Kavanagh D, Strain L, Herbert AP, Schmidt CQ, Barlow PN, Harris CL, Marchbank KJ. Goodship TH, et al. Mol Immunol. 2012 Oct;52(3-4):200-6. doi: 10.1016/j.molimm.2012.05.009. Epub 2012 Jun 20. Mol Immunol. 2012. PMID: 22721707
Complement therapy in atypical haemolytic uraemic syndrome (aHUS).
Wong EK, Goodship TH, Kavanagh D. Wong EK, et al. Among authors: goodship th. Mol Immunol. 2013 Dec 15;56(3):199-212. doi: 10.1016/j.molimm.2013.05.224. Epub 2013 Jun 28. Mol Immunol. 2013. PMID: 23810412 Free PMC article. Review.
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