Targeting new cellular disease pathways in autosomal dominant polycystic kidney disease-Reference-Cited by-同舟云学术

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Targeting new cellular disease pathways in autosomal dominant polycystic kidney disease

Published:2017-08-29 Issue:8 Volume:33 Page:1310-1316
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:

Author:

Chang Ming-Yang¹,C.M. Ong Albert²³

Affiliation:

1. Kidney Research Center, Department of Nephrology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan

2. Kidney Genetics Group, Academic Nephrology Unit, University of Sheffield Medical School, Sheffield, UK

3. Sheffield Kidney Institute, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK

Funder

Chang Gung Memorial Hospital

Ministry of Science and Technology of Taiwan

Kidney Research UK

Sheffield Kidney Research Foundation

European Union

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/33/8/1310/25198337/gfx262.pdf

Reference84 articles.

1. Molecular diagnostics for autosomal dominant polycystic kidney disease;Harris;Nat Rev Nephrol,2010

2. Predictors of autosomal dominant polycystic kidney disease progression;Schrier;J Am Soc Nephrol,2014

3. A polycystin-centric view of cyst formation and disease: the polycystins revisited;Ong;Kidney Int,2015

4. Making sense of polycystic kidney disease;Ong;Lancet,2017

5. Mechanism-based therapeutics for autosomal dominant polycystic kidney disease: recent progress and future prospects;Chang;Nephron Clin Pract,2012

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