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… (More)
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2015
2015
PDEδ is a small protein that binds and controls the trafficking of RAS subfamily proteins. Its inhibition protects initiation of… (More)
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2014
2014
Joubert syndrome (JS) is characterized by a distinctive cerebellar structural defect, namely the << molar tooth sign >>. JS is… (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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2010
2010
Earlier we have shown that exogenous expression of HIPPI, a molecular partner of Huntingtin interacting protein HIP-1, induces… (More)
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2007
2007
PURPOSE Canine X-linked progressive retinal atrophy (XLPRA) is caused by mutations in RPGR exon ORF15, which is also a mutation… (More)
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2003
2003
A cyclic nucleotide phosphodiesterase, PdeE, that harbors two cyclic nucleotide binding motifs and a binuclear Zn(2+)-binding… (More)
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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… (More)
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2002
2002
The δ and γ subunits of the cGMP-phosphodiesterase (PDE6D, PDE6G) genes were screened in order to identify mutations causing… (More)
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1998
1998
The mammalian multisubunit photoreceptor cGMP phosphodiesterase PDE alpha beta gamma 2 (PDE6 family) is a peripherally membrane… (More)
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