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PDE6D gene

Known as: PHOSPHODIESTERASE 6D, cGMP-SPECIFIC, ROD, DELTA, JBTS22, PDE-DELTA 
 
National Institutes of Health

Papers overview

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2015
2015
Ciliary dysfunction underlies multiple human genetic diseases, and mechanisms of protein trafficking to cilia are an area of… Expand
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2015
2015
The retinitis pigmentosa 2 polypeptide (RP2) functions as a GTPase‐activating protein (GAP) for ARL3 (Arf‐like protein 3), a… Expand
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Highly Cited
2014
Highly Cited
2014
Joubert syndrome (JS) is characterized by a distinctive cerebellar structural defect, namely the « molar tooth sign ». JS is… Expand
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2014
2014
Enterohemorrhagic E. coli (EHEC) manipulate their human host through at least 39 effector proteins which hijack host processes… Expand
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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… Expand
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2010
2010
BackgroundIdiopathic Pulmonary Fibrosis (IPF) is an unresolved clinical issue. Phosphodiesterases (PDEs) are known therapeutic… Expand
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2010
2010
Earlier we have shown that exogenous expression of HIPPI, a molecular partner of Huntingtin interacting protein HIP-1, induces… Expand
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2003
2003
A cyclic nucleotide phosphodiesterase, PdeE, that harbors two cyclic nucleotide binding motifs and a binuclear Zn2+-binding… Expand
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2002
2002
StmF mutants are chemotactic mutants that are defective in a cGMP phosphodiesterase (PDE) activity. We identified a novel gene… Expand
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1998
1998
The mammalian multisubunit photoreceptor cGMP phosphodiesterase PDE alpha beta gamma 2 (PDE6 family) is a peripherally membrane… Expand
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