Reduction of elevated Gli3 does not alter the progression of autosomal recessive polycystic kidney disease
Abstract Polycystic kidney diseases (PKD) are genetic disorders which disrupt kidney architecture and function. Autosomal recessive PKD (ARPKD) is a rare form of PKD, caused by mutations in PKHD1, and clinically more severe than the more common autosomal dominant PKD (ADPKD). Prior studies have impl...
Saved in:
Main Authors: | Lauren G. Russell, Maria Kolatsi‐Joannou, Laura Wilson, Jennifer C. Chandler, Nuria Perretta Tejedor, Georgie Stagg, Karen L. Price, Christopher J. Rowan, Tessa Crompton, Norman D. Rosenblum, Paul J. D. Winyard, David A. Long |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2025-01-01
|
Series: | Physiological Reports |
Subjects: | |
Online Access: | https://doi.org/10.14814/phy2.70191 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Unilateral focal choroidal excavation in autosomal recessive bestrophinopathy
by: Neha Goel
Published: (2025-01-01) -
Differential Expression of -Associated Genes in Autosomal Dominant Polycystic Kidney Disease
by: Yeon Joo Yook, et al.
Published: (2012-03-01) -
Mucopolysaccharidosis: A rare case from ophthalmology perspective
by: Santosh Singh Patel, et al.
Published: (2025-01-01) -
Trajectory of human migration: insights from autosomal and non-autosomal variant clustering patterns
by: Samayeta Sarkar Tuli, et al.
Published: (2025-03-01) -
Spot Versus 24-Hour Urine Osmolality Measurement in Autosomal Dominant Polycystic Kidney Disease: A Diagnostic Test Study
by: Ayub Akbari, et al.
Published: (2025-03-01)