Smith RJH - Search Results

1

Factor B and C4b2a Autoantibodies in C3 Glomerulopathy.

Hauer JJ, Shao D, Zhang Y, Nester CM, Smith RJH. Hauer JJ, et al. Among authors: smith rjh. Front Immunol. 2019 Apr 4;10:668. doi: 10.3389/fimmu.2019.00668. eCollection 2019. Front Immunol. 2019. PMID: 31024533 Free PMC article. Review.

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

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.

4

A claudin-9-based ion permeability barrier is essential for hearing.

Nakano Y, Kim SH, Kim HM, Sanneman JD, Zhang Y, Smith RJ, Marcus DC, Wangemann P, Nessler RA, Bánfi B. Nakano Y, et al. PLoS Genet. 2009 Aug;5(8):e1000610. doi: 10.1371/journal.pgen.1000610. Epub 2009 Aug 21. PLoS Genet. 2009. PMID: 19696885 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. 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. 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. 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. 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

Dense deposit disease.

Smith RJ, Harris CL, Pickering MC. Smith RJ, et al. Mol Immunol. 2011 Aug;48(14):1604-10. doi: 10.1016/j.molimm.2011.04.005. Epub 2011 May 24. Mol Immunol. 2011. PMID: 21601923 Free PMC article. Review.

10

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.

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