Józsi M - Search Results

1

Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II).

Licht C, Heinen S, Józsi M, Löschmann I, Saunders RE, Perkins SJ, Waldherr R, Skerka C, Kirschfink M, Hoppe B, Zipfel PF. Licht C, et al. Among authors: jozsi m. Kidney Int. 2006 Jul;70(1):42-50. doi: 10.1038/sj.ki.5000269. Epub 2006 Apr 12. Kidney Int. 2006. PMID: 16612335 Free article.

2

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: jozsi m. Mol Immunol. 2006 Jan;43(1-2):97-106. doi: 10.1016/j.molimm.2005.06.015. Mol Immunol. 2006. PMID: 16026839 Review.

3

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

4

Factor H family proteins and human diseases.

Józsi M, Zipfel PF. Józsi M, et al. Trends Immunol. 2008 Aug;29(8):380-7. doi: 10.1016/j.it.2008.04.008. Epub 2008 Jul 2. Trends Immunol. 2008. PMID: 18602340 Review.

5

Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease).

Abrera-Abeleda MA, Nishimura C, Smith JL, Sethi S, McRae JL, Murphy BF, Silvestri G, Skerka C, Józsi M, Zipfel PF, Hageman GS, Smith RJ. Abrera-Abeleda MA, et al. Among authors: jozsi m. J Med Genet. 2006 Jul;43(7):582-9. doi: 10.1136/jmg.2005.038315. Epub 2005 Nov 18. J Med Genet. 2006. PMID: 16299065 Free PMC article.

6

The C-terminus of complement regulator Factor H mediates target recognition: evidence for a compact conformation of the native protein.

Oppermann M, Manuelian T, Józsi M, Brandt E, Jokiranta TS, Heinen S, Meri S, Skerka C, Götze O, Zipfel PF. Oppermann M, et al. Among authors: jozsi m. Clin Exp Immunol. 2006 May;144(2):342-52. doi: 10.1111/j.1365-2249.2006.03071.x. Clin Exp Immunol. 2006. PMID: 16634809 Free PMC article.

7

Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies Conference.

Goodship TH, Cook HT, Fakhouri F, Fervenza FC, Frémeaux-Bacchi V, Kavanagh D, Nester CM, Noris M, Pickering MC, Rodríguez de Córdoba S, Roumenina LT, Sethi S, Smith RJ; Conference Participants. Goodship TH, et al. Kidney Int. 2017 Mar;91(3):539-551. doi: 10.1016/j.kint.2016.10.005. Epub 2016 Dec 16. Kidney Int. 2017. PMID: 27989322 Free article.

8

Genetic screening in haemolytic uraemic syndrome.

Zipfel PF, Neumann HP, Józsi M. Zipfel PF, et al. Among authors: jozsi m. Curr Opin Nephrol Hypertens. 2003 Nov;12(6):653-7. doi: 10.1097/00041552-200311000-00014. Curr Opin Nephrol Hypertens. 2003. PMID: 14564205 Review.

9

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. Eur J Hum Genet. 2005 Mar;13(3):321-9. doi: 10.1038/sj.ejhg.5201324. Eur J Hum Genet. 2005. PMID: 15562282

10

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. Among authors: jozsi m. 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

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