PHYH gene

Known as: PAHX, LNAP1, MOUSE, HOMOLOG OF, PHYTANOYL-CoA HYDROXYLASE 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1987-2016
02419872016

Papers overview

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2008
2008
Refsum disease is caused by a deficiency of phytanoyl-CoA hydroxylase (PHYH), the first enzyme of the peroxisomal alpha-oxidation… (More)
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2008
2008
Interactions between the gene products encoded by the mitochondrial and nuclear genomes play critical roles in eukaryotic… (More)
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2006
2006
The transcription of neuron-specific genes must be repressed in nonneuronal cells. REST/NRSF is a transcription factor that… (More)
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2005
2005
Refsum disease (RD), a neurological syndrome characterized by adult onset retinitis pigmentosa, anosmia, sensory neuropathy, and… (More)
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2004
2004
Herein, we exploit the power of global lipidomics to identify the critical role of peroxisomal processing of fatty acids in… (More)
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2003
2003
Refsum disease is a peroxisomal disorder characterized by adult-onset retinitis pigmentosa, anosmia, sensory neuropathy, ataxia… (More)
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2002
2002
Since it possesses a 3-methyl group, phytanic acid is degraded by a peroxisomal alpha-oxidation pathway, the first step of which… (More)
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2001
2001
Previously, PAHX-AP1 (PAHX-associated protein 1) was isolated as a novel protein to interact with Refsum disease gene product… (More)
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2001
2001
Refsum's disease is a neurological syndrome characterized by adult-onset retinitis pigmentosa, anosmia, sensory neuropathy and… (More)
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Highly Cited
1997
Highly Cited
1997
Refsum disease is an autosomal recessive disorder characterized by retinitis pigmentosa, peripheral poly neuropathy, cerebellar… (More)
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