Matthew C. Pickering
Centre for Complement and Inflammation Research
Imperial College
London
United Kingdom
Name/email consistency: high
- A Hybrid CFHR3-1 Gene Causes Familial C3 Glomerulopathy. Malik, T.H., Lavin, P.J., Goicoechea de Jorge, E., Vernon, K.A., Rose, K.L., Patel, M.P., de Leeuw, M., Neary, J.J., Conlon, P.J., Winn, M.P., Pickering, M.C. J. Am. Soc. Nephrol. (2012)
- Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals. Pickering, M.C., Cook, H.T. Clin. Exp. Immunol. (2008)
- Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains. Pickering, M.C., de Jorge, E.G., Martinez-Barricarte, R., Recalde, S., Garcia-Layana, A., Rose, K.L., Moss, J., Walport, M.J., Cook, H.T., de Córdoba, S.R., Botto, M. J. Exp. Med. (2007)
- Prevention of C5 activation ameliorates spontaneous and experimental glomerulonephritis in factor H-deficient mice. Pickering, M.C., Warren, J., Rose, K.L., Carlucci, F., Wang, Y., Walport, M.J., Cook, H.T., Botto, M. Proc. Natl. Acad. Sci. U.S.A. (2006)
