NEPHRONOPHTHISIS 9

Known as: NPHP9 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2008-2016
01220082016

Papers overview

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2016
2016
The disease-modifying effects of target of rapamycin complex 1 (TORC1) inhibitors during different stages of polycystic kidney… (More)
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2016
2016
We studied two brothers who presented in the newborn period with cardiac, renal, and hepatic anomalies that were initially… (More)
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2013
2013
Nephronophthisis is an autosomal recessive cystic kidney disease that leads to renal failure in childhood or adolescence. Most… (More)
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Review
2013
Review
2013
POLYCYSTIC KIDNEY DISEASE comprises a number of genetically disparate disorders including autosomal dominant polycystic kidney… (More)
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2012
2012
Nephronophthisis (NPH) is a genetically heterogenous kidney disease and represents the most common genetic cause for end-stage… (More)
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2010
2010
A primary cilium is an antenna-like structure extending from the surface of most vertebrate cells. It is structurally divided… (More)
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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… (More)
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