Back to search

Article

Regulation of the PKD2 channel function and associated disease phenotypes by RASSF4

2025-06-26

Abstract excerpt

<title>Abstract</title> <p>ADPKD is caused by mutations in receptor PKD1 and ion channel PKD2. As no effective treatment is available for ADPKD, further studies on the function and regulation of PKD1 and PKD2 are required. Using biotin-neighborhood labeling in HEK293T cells and mass spectrometry analysis, we identified Ras association domain family member-4 (RASSF4) as a potential PKD2-binding protein. Our co-imm...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
d487d466-0f8f-58f9-9d2f-3e0bdc331fb7
DOI
10.21203/rs.3.rs-6884050/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Regulation of the PKD2 channel function and associated disease phenotypes by RASSF4DOI 10.21203/rs.3.rs-6884050/v1
Select a neighboring publication to make it the new centre.