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NEK9 protein, human
Known as:
Nercc1 protein, human
, Serine/Threonine-Protein Kinase Nek9
, Nek8
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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…
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National Institutes of Health
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Related topics
Related topics
12 relations
Casein Kinase I Isoform Delta, human
Cell Cycle Progression
Chromosome Segregation
Enzyme Gene
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Broader (1)
NIMA-Related Kinases
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2013
Highly Cited
2013
ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3
Sylvia Hoff
,
J. Halbritter
,
+38 authors
S. Lienkamp
Nature Genetics
2013
Corpus ID: 15821960
Nephronophthisis is an autosomal recessive cystic kidney disease that leads to renal failure in childhood or adolescence. Most…
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Highly Cited
2013
Highly Cited
2013
NEK8 links the ATR-regulated replication stress response and S phase CDK activity to renal ciliopathies.
Hyo Jei Claudia Choi
,
Jia-Ren Lin
,
+8 authors
K. Cimprich
Molecules and Cells
2013
Corpus ID: 4102774
Highly Cited
2013
Highly Cited
2013
Mutations in NEK8 link multiple organ dysplasia with altered Hippo signalling and increased c-MYC expression.
V. Frank
,
S. Habbig
,
+19 authors
C. Bergmann
Human Molecular Genetics
2013
Corpus ID: 17710603
Mutations affecting the integrity and function of cilia have been identified in various genes over the last decade accounting for…
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Review
2012
Review
2012
Cell cycle regulation by the NEK family of protein kinases
A. Fry
,
Laura O'Regan
,
Sarah R. Sabir
,
R. Bayliss
Journal of Cell Science
2012
Corpus ID: 3673251
Summary Genetic screens for cell division cycle mutants in the filamentous fungus Aspergillus nidulans led to the discovery of…
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Highly Cited
2010
Highly Cited
2010
Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy
E. Otto
,
G. Ramaswami
,
+16 authors
F. Hildebrandt
Journal of Medical Genetics
2010
Corpus ID: 2451007
Background Nephronophthisis associated ciliopathies (NPHP-AC) comprise a group of autosomal recessive cystic kidney diseases that…
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Highly Cited
2008
Highly Cited
2008
NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis.
E. Otto
,
Melissa L Trapp
,
U. Schultheiss
,
Juliana Helou
,
L. Quarmby
,
F. Hildebrandt
Journal of the American Society of Nephrology
2008
Corpus ID: 3220964
Nephronophthisis, an autosomal recessive kidney disease, is the most frequent genetic cause of chronic renal failure in the first…
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Highly Cited
2008
Highly Cited
2008
Nek8 regulates the expression and localization of polycystin-1 and polycystin-2.
E. Sohara
,
Ying Luo
,
Jingjing Zhang
,
Danielle K. Manning
,
D. Beier
,
Jing Zhou
Journal of the American Society of Nephrology
2008
Corpus ID: 10839197
Nek8 is a serine/threonine kinase that is mutated in the jck (juvenile cystic kidneys) mouse, a model of autosomal recessive…
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Review
2005
Review
2005
Caught Nek-ing: cilia and centrioles
L. Quarmby
,
M. Mahjoub
Journal of Cell Science
2005
Corpus ID: 10797911
The Nek family of cell-cycle kinases is widely represented in eukaryotes and includes numerous proteins that were described only…
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Highly Cited
2004
Highly Cited
2004
Nek8, a NIMA family kinase member, is overexpressed in primary human breast tumors.
Alex J. Bowers
,
J. Boylan
Gene
2004
Corpus ID: 19985144
Highly Cited
2004
Highly Cited
2004
A NIMA-related kinase, Fa2p, localizes to a novel site in the proximal cilia of Chlamydomonas and mouse kidney cells.
M. Mahjoub
,
M. Qasim Rasi
,
L. Quarmby
Molecular Biology of the Cell
2004
Corpus ID: 41085645
Polycystic kidney disease and related syndromes involve dysregulation of cell proliferation in conjunction with ciliary defects…
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