Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

NEPHRONOPHTHISIS 9

Known as: NPHP9 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Polycystic kidney disease (PKD) encompasses a spectrum of inherited disorders that lead to end-stage renal disease (ESRD). There… Expand
2016
2016
We studied two brothers who presented in the newborn period with cardiac, renal, and hepatic anomalies that were initially… Expand
2016
2016
The disease-modifying effects of target of rapamycin complex 1 (TORC1) inhibitors during different stages of polycystic kidney… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • table 1
Highly Cited
2013
Highly Cited
2013
Nephronophthisis is an autosomal recessive cystic kidney disease that leads to renal failure in childhood or adolescence. Most… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Highly Cited
2012
Highly Cited
2012
Nephronophthisis (NPH) is a genetically heterogenous kidney disease and represents the most common genetic cause for end-stage… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Highly Cited
2010
Highly Cited
2010
A primary cilium is an antenna‐like structure extending from the surface of most vertebrate cells. It is structurally divided… Expand
Highly Cited
2008
Highly Cited
2008
Nephronophthisis, an autosomal recessive kidney disease, is the most frequent genetic cause of chronic renal failure in the first… Expand
  • figure 1
  • table 1
  • figure 3
  • figure 2