Complement C3 activation in cyst fluid and urine from autosomal dominant polycystic kidney disease patients-Reference-Cited by-同舟云学术

Complement C3 activation in cyst fluid and urine from autosomal dominant polycystic kidney disease patients

Published:2014-09-30 Issue:5 Volume:276 Page:539-540
ISSN:0954-6820
Container-title:Journal of Internal Medicine
language:en
Short-container-title:J Intern Med

Author:

Mrug M.¹²,Zhou J.¹,Mrug S.³,Guay‐Woodford L. M.⁴,Yoder B. K.⁵,Szalai A. J.⁶

Affiliation:

1. Division of Nephrology Nephrology Research and Training Center University of Alabama at BirminghamUniversity of Alabama at BirminghamBirmingham AL USA

2. Department of Veterans Affairs Medical CenterUniversity of Alabama at BirminghamBirmingham AL USA

3. Department of Psychology University of Alabama at Birmingham Birmingham AL USA

4. Center for Translational Science Children's National Health System Washington DCUSA

5. Department of Cell, Developmental and Integrative BiologyUniversity of Alabama at BirminghamBirmingham AL USA

6. Division of Rheumatology Department of Medicine University of Alabama at Birmingham Birmingham AL USA

Publisher

Wiley

Subject

Internal Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/joim.12307

Reference9 articles.

1. Excessive activation of the alternative complement pathway in autosomal dominant polycystic kidney disease

2. Kidney injury accelerates cystogenesis via pathways modulated by heme oxygenase and complement;Zhou J;J Am Soc Nephrol,2012

3. C3 polymorphisms and outcomes of renal allografts;Mrug M;N Engl J Med,2009

4. Overexpression of innate immune response genes in a model of recessive polycystic kidney disease;Mrug M;Kidney Int,2008

5. Systems biology of autosomal dominant polycystic kidney disease (ADPKD): computational identification of gene expression pathways and integrated regulatory networks;Song XW;Hum Mol Genet,2009

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