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… (More)
National Institutes of Health

Papers overview

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2016
2016
Ciliopathies are a group of genetic multi-systemic disorders related to dysfunction of the primary cilium, a sensory organelle… (More)
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2013
2013
Renal ciliopathies are a leading cause of kidney failure, but their exact etiology is poorly understood. NEK8/NPHP9 is a ciliary… (More)
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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… (More)
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2013
2013
Mutations affecting the integrity and function of cilia have been identified in various genes over the last decade accounting for… (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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2012
2012
Mutations in the never-in-mitosis A-related kinase, Nek8, are associated with cystic kidney disease in both humans and mice, with… (More)
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Highly Cited
2011
Highly Cited
2011
BACKGROUND Nephronophthisis associated ciliopathies (NPHP-AC) comprise a group of autosomal recessive cystic kidney diseases that… (More)
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2007
2007
Mutations in the human NIMA (Never in Mitosis gene A)-related kinase 8 (Nek8) are associated with a rare form of the juvenile… (More)
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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… (More)
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2004
2004
The family of human Nek (NIMA Related Kinase) kinases currently contains 11 members. We have identified Nek8 as a new member of… (More)
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