INPP5E gene

Known as: INOSITOL POLYPHOSPHATE-5-PHOSPHATASE, 72-KD, PPI5PIV, CORS1 
 
National Institutes of Health

Papers overview

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2017
2017
ARL13B (a small GTPase) and INPP5E (a phosphoinositide 5-phosphatase) are ciliary proteins encoded by causative genes of Joubert… (More)
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2017
2017
Phosphoinositides, a family of phosphorylated derivatives of phosphatidylinositol (PtdIns), are tightly regulated both temporally… (More)
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2017
2017
Sonic Hedgehog (SHH) signaling at primary cilia drives the proliferation and progression of a subset of medulloblastomas, the… (More)
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2017
2017
The partially understood phosphoinositide signaling cascade regulates multiple aspects of cellular metabolism. Previous studies… (More)
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2017
2017
The life cycle of a primary cilium begins in quiescence and ends prior to mitosis. In quiescent cells, the primary cilium… (More)
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2016
2016
Defective primary cilia are causative to a wide spectrum of human genetic disorders, termed ciliopathies. Although the regulation… (More)
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2016
2016
Polycystic kidney disease (PKD) is a common cause of renal failure with few effective treatments. INPP5E is an inositol… (More)
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2015
2015
Mutations in inositol polyphosphate 5-phosphatase E (INPP5E) cause the ciliopathies known as Joubert and MORM syndromes; however… (More)
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Highly Cited
2012
Highly Cited
2012
Mutations affecting ciliary components cause a series of related genetic disorders in humans, including nephronophthisis (NPHP… (More)
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2006
2006
Only a few approaches are available to address the mechanisms of cell death in vivo which are induced by anticancer treatment in… (More)
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