eBook - ePub
Polycystic Kidney Disease
Jinghua Hu,Yong Yu
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- 346 pages
- English
- ePUB (mobile friendly)
- Available on iOS & Android
eBook - ePub
Polycystic Kidney Disease
Jinghua Hu,Yong Yu
Book details
Table of contents
Citations
About This Book
This volume focuses on the investigatory methods applied to autosomal dominant polycystic kidney disease (ADPKD), one of the most common human genetic diseases. ADPKD is caused by mutations in PKD1 and TRPP2, two integral membrane proteins that function as receptor/ion channels in primary cilia of tubular epithelial cells. Thus, ADPKD belongs to ciliopathies, a group of disorders caused by abnormal cilia formation or function. This proposed book will cover the state-of-the-art methods ranging from molecular biology, biochemistry, electrophysiology, to tools in model animal studies.
Key Features
- Explores the role of cilia in polycystic kidney disease
- Focuses on myriad state-of-the-art methods and techniques
- Reviews specific mutations integral to this autosomal genetic disease
- Includes discussions of model systems
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Table of contents
Citation styles for Polycystic Kidney Disease
APA 6 Citation
Hu, J., & Yu, Y. (2019). Polycystic Kidney Disease (1st ed.). CRC Press. Retrieved from https://www.perlego.com/book/1493610/polycystic-kidney-disease-pdf (Original work published 2019)
Chicago Citation
Hu, Jinghua, and Yong Yu. (2019) 2019. Polycystic Kidney Disease. 1st ed. CRC Press. https://www.perlego.com/book/1493610/polycystic-kidney-disease-pdf.
Harvard Citation
Hu, J. and Yu, Y. (2019) Polycystic Kidney Disease. 1st edn. CRC Press. Available at: https://www.perlego.com/book/1493610/polycystic-kidney-disease-pdf (Accessed: 14 October 2022).
MLA 7 Citation
Hu, Jinghua, and Yong Yu. Polycystic Kidney Disease. 1st ed. CRC Press, 2019. Web. 14 Oct. 2022.