Similar articles for PMID: 16281287

Year	Number of Results
1984	1
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2002	11
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2013	7
2014	8
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2024	0

1

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

2

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

3

A user's guide to the interactive Web database of factor H-associated hemolytic uremic syndrome.

Saunders RE, Perkins SJ. Saunders RE, et al. Semin Thromb Hemost. 2006 Mar;32(2):160-8. doi: 10.1055/s-2006-939772. Semin Thromb Hemost. 2006. PMID: 16575691

4

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

5

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

6

Crystallographic determination of the disease-associated T1184R variant of complement regulator factor H.

Morgan HP, Jiang J, Herbert AP, Kavanagh D, Uhrin D, Barlow PN, Hannan JP. Morgan HP, et al. Acta Crystallogr D Biol Crystallogr. 2011 Jul;67(Pt 7):593-600. doi: 10.1107/S0907444911015423. Epub 2011 Jun 11. Acta Crystallogr D Biol Crystallogr. 2011. PMID: 21697597

7

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

8

Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome.

Sellier-Leclerc AL, Fremeaux-Bacchi V, Dragon-Durey MA, Macher MA, Niaudet P, Guest G, Boudailliez B, Bouissou F, Deschenes G, Gie S, Tsimaratos M, Fischbach M, Morin D, Nivet H, Alberti C, Loirat C; French Society of Pediatric Nephrology. Sellier-Leclerc AL, et al. J Am Soc Nephrol. 2007 Aug;18(8):2392-400. doi: 10.1681/ASN.2006080811. Epub 2007 Jun 28. J Am Soc Nephrol. 2007. PMID: 17599974

9

Factor XI deficiency database: an interactive web database of mutations, phenotypes, and structural analysis tools.

Saunders RE, O'Connell NM, Lee CA, Perry DJ, Perkins SJ. Saunders RE, et al. Hum Mutat. 2005 Sep;26(3):192-8. doi: 10.1002/humu.20214. Hum Mutat. 2005. PMID: 16086308

10

Comparison of surface recognition and C3b binding properties of mouse and human complement factor H.

Cheng ZZ, Hellwage J, Seeberger H, Zipfel PF, Meri S, Jokiranta TS. Cheng ZZ, et al. Mol Immunol. 2006 Mar;43(7):972-9. doi: 10.1016/j.molimm.2005.05.011. Epub 2005 Jul 14. Mol Immunol. 2006. PMID: 16023208

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