Zhang Y - Search Results

1

Mutation of complement factor B causing massive fluid-phase dysregulation of the alternative complement pathway can result in atypical hemolytic uremic syndrome.

Zhang Y, Kremsdorf RA, Sperati CJ, Henriksen KJ, Mori M, Goodfellow RX, Pitcher GR, Benson CL, Borsa NG, Taylor RP, Nester CM, Smith RJH. Zhang Y, et al. Kidney Int. 2020 Nov;98(5):1265-1274. doi: 10.1016/j.kint.2020.05.028. Epub 2020 Jun 12. Kidney Int. 2020. PMID: 32540405 Free PMC article.

2

A comparative study of Eya1 and Eya4 protein function and its implication in branchio-oto-renal syndrome and DFNA10.

Zhang Y, Knosp BM, Maconochie M, Friedman RA, Smith RJ. Zhang Y, et al. J Assoc Res Otolaryngol. 2004 Sep;5(3):295-304. doi: 10.1007/s10162-004-4044-3. Epub 2004 Jun 24. J Assoc Res Otolaryngol. 2004. PMID: 15492887 Free PMC article.

3

Inactivation of NADPH oxidase organizer 1 results in severe imbalance.

Kiss PJ, Knisz J, Zhang Y, Baltrusaitis J, Sigmund CD, Thalmann R, Smith RJ, Verpy E, Bánfi B. Kiss PJ, et al. Among authors: zhang y. Curr Biol. 2006 Jan 24;16(2):208-13. doi: 10.1016/j.cub.2005.12.025. Curr Biol. 2006. PMID: 16431374 Free article.

4

Sensorineural deafness and male infertility: a contiguous gene deletion syndrome.

Zhang Y, Malekpour M, Al-Madani N, Kahrizi K, Zanganeh M, Lohr NJ, Mohseni M, Mojahedi F, Daneshi A, Najmabadi H, Smith RJ. Zhang Y, et al. J Med Genet. 2007 Apr;44(4):233-40. doi: 10.1136/jmg.2006.045765. Epub 2006 Nov 10. J Med Genet. 2007. PMID: 17098888 Free PMC article.

5

Genetic male infertility and mutation of CATSPER ion channels.

Hildebrand MS, Avenarius MR, Fellous M, Zhang Y, Meyer NC, Auer J, Serres C, Kahrizi K, Najmabadi H, Beckmann JS, Smith RJ. Hildebrand MS, et al. Among authors: zhang y. Eur J Hum Genet. 2010 Nov;18(11):1178-84. doi: 10.1038/ejhg.2010.108. Epub 2010 Jul 21. Eur J Hum Genet. 2010. PMID: 20648059 Free PMC article. Review.

6

Dense deposit disease associated with monoclonal gammopathy of undetermined significance.

Sethi S, Sukov WR, Zhang Y, Fervenza FC, Lager DJ, Miller DV, Cornell LD, Krishnan SG, Smith RJ. Sethi S, et al. Among authors: zhang y. Am J Kidney Dis. 2010 Nov;56(5):977-82. doi: 10.1053/j.ajkd.2010.06.021. Epub 2010 Sep 15. Am J Kidney Dis. 2010. PMID: 20832153 Free PMC article.

7

A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome.

Maga TK, Meyer NC, Belsha C, Nishimura CJ, Zhang Y, Smith RJ. Maga TK, et al. Among authors: zhang y. Nephrol Dial Transplant. 2011 Feb;26(2):739-41. doi: 10.1093/ndt/gfq658. Epub 2010 Oct 25. Nephrol Dial Transplant. 2011. PMID: 20974643 Free PMC article.

8

Proliferative glomerulonephritis secondary to dysfunction of the alternative pathway of complement.

Sethi S, Fervenza FC, Zhang Y, Nasr SH, Leung N, Vrana J, Cramer C, Nester CM, Smith RJ. Sethi S, et al. Among authors: zhang y. Clin J Am Soc Nephrol. 2011 May;6(5):1009-17. doi: 10.2215/CJN.07110810. Epub 2011 Mar 17. Clin J Am Soc Nephrol. 2011. PMID: 21415311 Free PMC article.

9

Sensorineural deafness and male infertility: a contiguous gene deletion syndrome.

Zhang Y, Malekpour M, Al-Madani N, Kahrizi K, Zanganeh M, Mohseni M, Mojahedi F, Daneshi A, Najmabadi H, Smith RJ. Zhang Y, et al. BMJ Case Rep. 2009;2009:bcr08.2008.0645. doi: 10.1136/bcr.08.2008.0645. Epub 2009 Jan 23. BMJ Case Rep. 2009. PMID: 21686705 Free PMC article.

10

Allelic variants of complement genes associated with dense deposit disease.

Abrera-Abeleda MA, Nishimura C, Frees K, Jones M, Maga T, Katz LM, Zhang Y, Smith RJ. Abrera-Abeleda MA, et al. Among authors: zhang y. J Am Soc Nephrol. 2011 Aug;22(8):1551-9. doi: 10.1681/ASN.2010080795. Epub 2011 Jul 22. J Am Soc Nephrol. 2011. PMID: 21784901 Free PMC article.

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