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NEK9 protein, human

Known as: Nercc1 protein, human, Serine/Threonine-Protein Kinase Nek9, Nek8 
Serine/threonine-protein kinase Nek9 (979 aa, ~107 kDa) is encoded by the human NEK9 gene. This protein is involved in the progression of mitosis and… Expand
National Institutes of Health

Papers overview

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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
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Highly Cited
2013
Highly Cited
2013
Renal ciliopathies are a leading cause of kidney failure, but their exact etiology is poorly understood. NEK8/NPHP9 is a ciliary… Expand
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Review
2012
Review
2012
Summary Genetic screens for cell division cycle mutants in the filamentous fungus Aspergillus nidulans led to the discovery of… Expand
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Highly Cited
2010
Highly Cited
2010
Background Nephronophthisis associated ciliopathies (NPHP-AC) comprise a group of autosomal recessive cystic kidney diseases that… 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
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Highly Cited
2008
Highly Cited
2008
Nek8 is a serine/threonine kinase that is mutated in the jck (juvenile cystic kidneys) mouse, a model of autosomal recessive… Expand
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Review
2005
Review
2005
The Nek family of cell-cycle kinases is widely represented in eukaryotes and includes numerous proteins that were described only… Expand
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Highly Cited
2004
Highly Cited
2004
Polycystic kidney disease and related syndromes involve dysregulation of cell proliferation in conjunction with ciliary defects… Expand
2004
2004
Autosomal dominant polycystic kidney disease (ADPKD) is a commonly inherited disorder (1/1000) in humans characterized by fluid… Expand
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Highly Cited
2002
Highly Cited
2002
We describe the isolation, cloning, and characterization of human Nek8, a new mammalian NIMA-related kinase, and its candidate… Expand