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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1980 1
1991 1
1994 3
1996 4
1997 2
1998 4
1999 6
2000 6
2001 9
2002 6
2003 5
2004 9
2005 12
2006 30
2007 18
2008 13
2009 16
2010 11
2011 11
2012 5
2013 7
2014 5
2015 4
2016 6
2017 2
2018 1
2019 1
2020 1
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Similar Articles for PMID: 16338962

179 results
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Page 1
Factor H and atypical hemolytic uremic syndrome: mutations in the C-terminus cause structural changes and defective recognition functions.
Józsi M, Heinen S, Hartmann A, Ostrowicz CW, Hälbich S, Richter H, Kunert A, Licht C, Saunders RE, Perkins SJ, Zipfel PF, Skerka C. Józsi M, et al. J Am Soc Nephrol. 2006 Jan;17(1):170-7. doi: 10.1681/ASN.2005080868. Epub 2005 Dec 7. J Am Soc Nephrol. 2006. PMID: 16338962 Free article.
Mutations of factor H impair regulation of surface-bound C3b by three mechanisms in atypical hemolytic uremic syndrome.
Lehtinen MJ, Rops AL, Isenman DE, van der Vlag J, Jokiranta TS. Lehtinen MJ, et al. J Biol Chem. 2009 Jun 5;284(23):15650-8. doi: 10.1074/jbc.M900814200. Epub 2009 Apr 7. J Biol Chem. 2009. PMID: 19351878 Free PMC article.
An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutations.
Saunders RE, Goodship TH, Zipfel PF, Perkins SJ. Saunders RE, et al. Hum Mutat. 2006 Jan;27(1):21-30. doi: 10.1002/humu.20268. Hum Mutat. 2006. PMID: 16281287
Hemolytic uremic syndrome: a factor H mutation (E1172Stop) causes defective complement control at the surface of endothelial cells.
Heinen S, Józsi M, Hartmann A, Noris M, Remuzzi G, Skerka C, Zipfel PF. Heinen S, et al. J Am Soc Nephrol. 2007 Feb;18(2):506-14. doi: 10.1681/ASN.2006091069. Epub 2007 Jan 17. J Am Soc Nephrol. 2007. PMID: 17229916 Free article.
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome.
Manuelian T, Hellwage J, Meri S, Caprioli J, Noris M, Heinen S, Jozsi M, Neumann HP, Remuzzi G, Zipfel PF. Manuelian T, et al. J Clin Invest. 2003 Apr;111(8):1181-90. doi: 10.1172/JCI16651. J Clin Invest. 2003. PMID: 12697737 Free PMC article.
Both domain 19 and domain 20 of factor H are involved in binding to complement C3b and C3d.
Bhattacharjee A, Lehtinen MJ, Kajander T, Goldman A, Jokiranta TS. Bhattacharjee A, et al. Mol Immunol. 2010 May;47(9):1686-91. doi: 10.1016/j.molimm.2010.03.007. Epub 2010 Apr 7. Mol Immunol. 2010. PMID: 20378178
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. J Mol Biol. 2002 Feb 15;316(2):217-24. doi: 10.1006/jmbi.2001.5337. J Mol Biol. 2002. PMID: 11851332
De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome.
Heinen S, Sanchez-Corral P, Jackson MS, Strain L, Goodship JA, Kemp EJ, Skerka C, Jokiranta TS, Meyers K, Wagner E, Robitaille P, Esparza-Gordillo J, Rodriguez de Cordoba S, Zipfel PF, Goodship TH. Heinen S, et al. Hum Mutat. 2006 Mar;27(3):292-3. doi: 10.1002/humu.9408. Hum Mutat. 2006. PMID: 16470555
The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models.
Saunders RE, Abarrategui-Garrido C, Frémeaux-Bacchi V, Goicoechea de Jorge E, Goodship TH, López Trascasa M, Noris M, Ponce Castro IM, Remuzzi G, Rodríguez de Córdoba S, Sánchez-Corral P, Skerka C, Zipfel PF, Perkins SJ. Saunders RE, et al. Hum Mutat. 2007 Mar;28(3):222-34. doi: 10.1002/humu.20435. Hum Mutat. 2007. PMID: 17089378
The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20.
Caprioli J, Bettinaglio P, Zipfel PF, Amadei B, Daina E, Gamba S, Skerka C, Marziliano N, Remuzzi G, Noris M; Itaslian Registry of Familial and Recurrent HUS/TTP. Caprioli J, et al. J Am Soc Nephrol. 2001 Feb;12(2):297-307. J Am Soc Nephrol. 2001. PMID: 11158219 Free article.
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