PDB/2G7I[Secondary Source ID] - Search Results

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Structure of complement factor H carboxyl-terminus reveals molecular basis of atypical haemolytic uremic syndrome.

Jokiranta TS, Jaakola VP, Lehtinen MJ, Pärepalo M, Meri S, Goldman A. Jokiranta TS, et al. EMBO J. 2006 Apr 19;25(8):1784-94. doi: 10.1038/sj.emboj.7601052. Epub 2006 Apr 6. EMBO J. 2006. PMID: 16601698 Free PMC article.

Two distinct conformations of factor H regulate discrete complement-binding functions in the fluid phase and at cell surfaces.

Osborne AJ, Nan R, Miller A, Bhatt JS, Gor J, Perkins SJ. Osborne AJ, et al. J Biol Chem. 2018 Nov 2;293(44):17166-17187. doi: 10.1074/jbc.RA118.004767. Epub 2018 Sep 14. J Biol Chem. 2018. PMID: 30217822 Free PMC article.

Disturbed sialic acid recognition on endothelial cells and platelets in complement attack causes atypical hemolytic uremic syndrome.

Hyvärinen S, Meri S, Jokiranta TS. Hyvärinen S, et al. Blood. 2016 Jun 2;127(22):2701-10. doi: 10.1182/blood-2015-11-680009. Epub 2016 Mar 22. Blood. 2016. PMID: 27006390 Free article.

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