Back to search

Article

A unique subset of pericystic endothelium associates with aberrant microvascular remodelling and impaired blood perfusion early in polycystic kidney disease

2024-03-06

Abstract excerpt

<h4>ABSTRACT</h4> Hallmarks of autosomal dominant polycystic kidney disease (ADPKD), the most common hereditary kidney anomaly, include expanding fluid-filled epithelial cysts, inflammation, and fibrosis. Despite previous work showing the potential of vascular-based therapies, renal microvascular alterations in ADPKD, and their timing, are poorly understood. Using single-cell transcriptomics of human kidney micro...

Topics

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

Identifiers and source

Literature Corpus work
9aa642fc-236a-5e49-a18b-0d089e69c49a
DOI
10.1101/2024.03.03.583132
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.
A unique subset of pericystic endothelium associates with aberrant microvascular remodelling and impaired blood perfusion early in polycystic kidney diseaseDOI 10.1101/2024.03.03.583132
Select a neighboring publication to make it the new centre.