PubMed Central
metadata only
CC BY 4.0
Ultrasound-guided renal artery administration of angiopoietin-1 RNA therapy slows the progression of preclinical WT1 glomerular disease
Mutations in the transcription factor Wilms Tumour 1 (WT1) are one of the leading causes of congenital glomerular disease, characterised by severe urinary protein loss and glomerular scarring. Currently no disease modifying therapies exist for WT1 glomerulopathies and affected children rely on dialy
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- Treatment of Renal Angiomyolipomas in Tuberous Sclerosis by Beta-blockers#1114232
- EMILIN1 emerges as a TGFβ/SETDB1-regulated secreted biomarker in Duchenne muscular dystrophy#273947
- Study of Genome-associated Mechanisms of Diabetic Nephropathy and Evaluation of Nephroprotective Therapy in Patients With Type 2 Diabetes Mellitus in the Kazakh Population#1085544
- Efficacy and Safety of Dapagliflozin in Children With Proteinuria#1229680
- THERAPEUTIC GENOME EDITING FOR HEREDITARY CONNECTIVE TISSUE DISORDERS#929422
Record · ID 1347273
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive