Skerka C - Search Results

1

Factor I and factor H deficiency in renal diseases: similar defects in the fluid phase have a different outcome at the surface of the glomerular basement membrane.

Zipfel PF, Smith RJ, Skerka C. Zipfel PF, et al. Among authors: skerka c. Nephrol Dial Transplant. 2009 Feb;24(2):385-7. doi: 10.1093/ndt/gfn652. Epub 2008 Dec 4. Nephrol Dial Transplant. 2009. PMID: 19056782 Free PMC article. Review. No abstract available.

2

FHL-1/reconectin: a human complement and immune regulator with cell-adhesive function.

Zipfel PF, Skerka C. Zipfel PF, et al. Among authors: skerka c. Immunol Today. 1999 Mar;20(3):135-40. doi: 10.1016/s0167-5699(98)01432-7. Immunol Today. 1999. PMID: 10203705 Review.

3

Complement factor H and hemolytic uremic syndrome.

Zipfel PF, Skerka C, Caprioli J, Manuelian T, Neumann HH, Noris M, Remuzzi G. Zipfel PF, et al. Among authors: skerka c. Int Immunopharmacol. 2001 Mar;1(3):461-8. doi: 10.1016/s1567-5769(00)00047-3. Int Immunopharmacol. 2001. PMID: 11367530 Review.

4

Factor H family proteins: on complement, microbes and human diseases.

Zipfel PF, Skerka C, Hellwage J, Jokiranta ST, Meri S, Brade V, Kraiczy P, Noris M, Remuzzi G. Zipfel PF, et al. Among authors: skerka c. Biochem Soc Trans. 2002 Nov;30(Pt 6):971-8. doi: 10.1042/bst0300971. Biochem Soc Trans. 2002. PMID: 12440956 Review.

5

FHR-4A: a new factor H-related protein is encoded by the human FHR-4 gene.

Józsi M, Richter H, Löschmann I, Skerka C, Buck F, Beisiegel U, Erdei A, Zipfel PF. Józsi M, et al. Among authors: skerka c. Eur J Hum Genet. 2005 Mar;13(3):321-9. doi: 10.1038/sj.ejhg.5201324. Eur J Hum Genet. 2005. PMID: 15562282

6

Complement and diseases: defective alternative pathway control results in kidney and eye diseases.

Zipfel PF, Heinen S, Józsi M, Skerka C. Zipfel PF, et al. Among authors: skerka c. Mol Immunol. 2006 Jan;43(1-2):97-106. doi: 10.1016/j.molimm.2005.06.015. Mol Immunol. 2006. PMID: 16026839 Review.

7

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. Among authors: skerka c. 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

8

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. Among authors: skerka c. Hum Mutat. 2006 Mar;27(3):292-3. doi: 10.1002/humu.9408. Hum Mutat. 2006. PMID: 16470555

9

The role of defective complement control in hemolytic uremic syndrome.

Zipfel PF, Misselwitz J, Licht C, Skerka C. Zipfel PF, et al. Among authors: skerka c. Semin Thromb Hemost. 2006 Mar;32(2):146-54. doi: 10.1055/s-2006-939770. Semin Thromb Hemost. 2006. PMID: 16575689 Review.

10

Complement dysfunction in hemolytic uremic syndrome.

Zipfel PF, Skerka C. Zipfel PF, et al. Among authors: skerka c. Curr Opin Rheumatol. 2006 Sep;18(5):548-55. doi: 10.1097/01.bor.0000240370.47336.ae. Curr Opin Rheumatol. 2006. PMID: 16896298 Review.

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