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Items: 1 to 20 of 124


Do the mutations of C1GALT1C1 gene play important roles in the genetic susceptibility to Chinese IgA nephropathy?

Li GS, Nie GJ, Zhang H, LV JC, Shen Y, Wang HY.

BMC Med Genet. 2009 Sep 24;10:101. doi: 10.1186/1471-2350-10-101.


Variants of C1GALT1 gene are associated with the genetic susceptibility to IgA nephropathy.

Li GS, Zhang H, Lv JC, Shen Y, Wang HY.

Kidney Int. 2007 Mar;71(5):448-53. Epub 2007 Jan 17.


No evidence for a role of cosmc-chaperone mutations in European IgA nephropathy patients.

Malycha F, Eggermann T, Hristov M, Schena FP, Mertens PR, Zerres K, Floege J, Eitner F.

Nephrol Dial Transplant. 2009 Jan;24(1):321-4. doi: 10.1093/ndt/gfn538. Epub 2008 Oct 7.


The role of C1GALT1C1 in lipopolysaccharide-induced IgA1 aberrant O-glycosylation in IgA nephropathy.

Xie LS, Qin W, Fan JM, Huang J, Xie XS, Li Z.

Clin Invest Med. 2010 Feb 1;33(1):E5-13.


External suppression causes the low expression of the Cosmc gene in IgA nephropathy.

Qin W, Zhong X, Fan JM, Zhang YJ, Liu XR, Ma XY.

Nephrol Dial Transplant. 2008 May;23(5):1608-14. doi: 10.1093/ndt/gfm781. Epub 2008 Jan 17.


Genetic variant of C1GalT1 contributes to the susceptibility to IgA nephropathy.

Pirulli D, Crovella S, Ulivi S, Zadro C, Bertok S, Rendine S, Scolari F, Foramitti M, Ravani P, Roccatello D, Savoldi S, Cerullo G, Lanzilotta SG, Bisceglia L, Zelante L, Floege J, Alexopoulos E, Kirmizis D, Ghiggeri GM, FrascĂ  G, Schena FP, Amoroso A; European IgAN Consortium.

J Nephrol. 2009 Jan-Feb;22(1):152-9.


Association of -27T>C and its haplotype at the putative promoter for IgA-specific receptor gene with IgA nephropathy among the Chinese Han population.

Huang W, Gu H, Li R, Lou T, Zhang J, Shi W, Ye Z, Zhou Y, Li C, Xiong S, Li L, Wu C, Leung JC, Lam MF, Lai KN, Wang Y.

Nephrol Dial Transplant. 2011 Aug;26(8):2537-44. doi: 10.1093/ndt/gfq765. Epub 2011 Jan 27.


Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with the progression of IgA nephropathy in Chinese.

Cheng W, Zhou X, Zhu L, Shi S, Lv J, Liu L, Zhang H.

Nephrol Dial Transplant. 2011 Aug;26(8):2544-9. doi: 10.1093/ndt/gfq768. Epub 2011 Jan 18.


Variants of the ST6GALNAC2 promoter influence transcriptional activity and contribute to genetic susceptibility to IgA nephropathy.

Li GS, Zhu L, Zhang H, Lv JC, Ding JX, Zhao MH, Shen Y, Wang HY.

Hum Mutat. 2007 Oct;28(10):950-7.


Toll-like receptor 1 gene polymorphisms in childhood IgA nephropathy: a case-control study in the Korean population.

Lee JS, Park HK, Suh JS, Hahn WH, Kang SW, Park HJ, Kim MJ, Chung JH, Cho BS.

Int J Immunogenet. 2011 Apr;38(2):133-8. doi: 10.1111/j.1744-313X.2010.00978.x. Epub 2010 Nov 25.


[Association of single nucleotide polymorphism of megsin gene with IgA nephropathy].

Wang ZH, Chen N, Pan XX, Ren H, Wang WM, Zhang W, Hao CL, Zhu J, Lu Y, Han B.

Zhonghua Yi Xue Za Zhi. 2006 May 23;86(19):1337-41. Chinese.


Association of C-509T and T869C polymorphisms of transforming growth factor-beta1 gene with susceptibility to and progression of IgA nephropathy.

Lim CS, Kim YS, Chae DW, Ahn C, Han JS, Kim S, Lee JS, Kim IS.

Clin Nephrol. 2005 Feb;63(2):61-7.


The effects of both single-locus and multi-locus interaction on the clinical manifestations of IgA nephropathy in Southern Han Chinese.

Wang W, Sun Y, Fu Y, Yu X, Li M.

Nephrol Dial Transplant. 2014 Mar;29(3):550-5. doi: 10.1093/ndt/gft468. Epub 2013 Nov 21.


Interaction of C1GALT1-IL5RA on the susceptibility to IgA nephropathy in Southern Han Chinese.

Wang W, Sun Y, Fu Y, Yu X, Li M.

J Hum Genet. 2013 Jan;58(1):40-6. doi: 10.1038/jhg.2012.133. Epub 2012 Nov 29.


Association of systemic lupus erythematosus susceptibility genes with IgA nephropathy in a Chinese cohort.

Zhou XJ, Cheng FJ, Zhu L, Lv JC, Qi YY, Hou P, Zhang H.

Clin J Am Soc Nephrol. 2014 Apr;9(4):788-97. doi: 10.2215/CJN.01860213. Epub 2014 Jan 23.


The enabled homolog gene polymorphisms are associated with susceptibility and progression of childhood IgA nephropathy.

Hahn WH, Suh JS, Cho BS, Kim SD.

Exp Mol Med. 2009 Nov 30;41(11):793-801. doi: 10.3858/emm.2009.41.11.085.


Aberrant galactosylation of IgA1 is involved in the genetic susceptibility of Chinese patients with IgA nephropathy.

Lin X, Ding J, Zhu L, Shi S, Jiang L, Zhao M, Zhang H.

Nephrol Dial Transplant. 2009 Nov;24(11):3372-5. doi: 10.1093/ndt/gfp294. Epub 2009 Jun 16.


FCGR2B and FCRLB gene polymorphisms associated with IgA nephropathy.

Zhou XJ, Cheng FJ, Qi YY, Zhao YF, Hou P, Zhu L, Lv JC, Zhang H.

PLoS One. 2013 Apr 12;8(4):e61208. doi: 10.1371/journal.pone.0061208. Print 2013.


DNA methylation in Cosmc promoter region and aberrantly glycosylated IgA1 associated with pediatric IgA nephropathy.

Sun Q, Zhang J, Zhou N, Liu X, Shen Y.

PLoS One. 2015 Feb 3;10(2):e0112305. doi: 10.1371/journal.pone.0112305. eCollection 2015.


Association of gene polymorphism of polymeric immunoglobulin receptor and IgA nephropathy.

Narita I, Kondo D, Goto S, Saito N, Watanabe Y, Yamazaki H, Sakatsume M, Saito A, Gejyo F.

Intern Med. 2001 Sep;40(9):867-72.

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