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Results: 6

Related Articles by Review for PubMed (Select 19778426)

1.

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.

2.

Association of megsin 2093C/T, 2180C/T and C25663G gene polymorphism with the risk of IgA nephropathy.

Mao S, Ren X, Huang S, Zhang A.

Ren Fail. 2014 Jun;36(5):817-22. doi: 10.3109/0886022X.2014.890058. Epub 2014 Feb 27. Review.

PMID:
24575807
3.

Association of T869, C509T, G915C gene polymorphism of transforming growth factor-β1 with IgA nephropathy risk.

Zhou TB, Guo XF, Yin SS.

Ren Fail. 2014 Jun;36(5):823-8. doi: 10.3109/0886022X.2014.890059. Epub 2014 Feb 24. Review.

PMID:
24564406
4.

Genetic studies of IgA nephropathy: past, present, and future.

Kiryluk K, Julian BA, Wyatt RJ, Scolari F, Zhang H, Novak J, Gharavi AG.

Pediatr Nephrol. 2010 Nov;25(11):2257-68. doi: 10.1007/s00467-010-1500-7. Epub 2010 Apr 13. Review.

5.

[Progression in the mechanism of the Cosmc in IgA nephropathy].

Zhou N, Shen Y.

Zhonghua Er Ke Za Zhi. 2013 Jul;51(7):549-51. Review. Chinese. No abstract available.

PMID:
24267143
6.

Pathogenesis of immunoglobulin A nephropathy: recent insight from genetic studies.

Kiryluk K, Novak J, Gharavi AG.

Annu Rev Med. 2013;64:339-56. doi: 10.1146/annurev-med-041811-142014. Epub 2012 Oct 16. Review.

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