Structural and molecular basis of the assembly of the TRPP2/PKD1 complex-Reference-Cited by-同舟云学术

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Structural and molecular basis of the assembly of the TRPP2/PKD1 complex

Published:2009-06-25 Issue:28 Volume:106 Page:11558-11563
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:PNAS

Author:

Yu Yong,Ulbrich Maximilian H.,Li Ming-Hui,Buraei Zafir,Chen Xing-Zhen,Ong Albert C. M.,Tong Liang,Isacoff Ehud Y.,Yang Jian

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference42 articles.

1. Molecular pathogenesis of ADPKD: The polycystin complex gets complex

2. Molecular Genetics and Mechanism of Autosomal Dominant Polycystic Kidney Disease

3. Polycystic Kidney Disease

4. The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains

5. The versatile nature of the calcium‐permeable cation channel TRPP2

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1. Cilia-enriched oxysterol 7β,27-DHC is required for polycystin ion channel activation;Nature Communications;2024-07-31

2. Mastigoneme structure reveals insights into the O-linked glycosylation code of native hydroxyproline-rich helices;Cell;2024-04

3. Molecular and structural basis of the dual regulation of the polycystin-2 ion channel by small-molecule ligands;Proceedings of the National Academy of Sciences;2024-03-14

4. Autosomal Dominant Polycystic Kidney Disease: Extrarenal Involvement;International Journal of Molecular Sciences;2024-02-22

5. Polycystin-2 Ion Channel Function and Pathogenesis in Autosomal Dominant Polycystic Kidney;PROG BIOCHEM BIOPHYS;2024

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