PEX6 gene

Known as: PEROXIN 6, PEX6, PEROXISOMAL ASSEMBLY FACTOR 2 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2018
02419962018

Papers overview

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2016
2016
Deafblindness is part of several genetic disorders. We investigated a consanguineous Egyptian family with two siblings affected… (More)
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2015
2015
Pex1 and Pex6 are Type-2 AAA+ ATPases required for the de novo biogenesis of peroxisomes. Mutations in Pex1 and Pex6 account for… (More)
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2015
2015
Members of the AAA family of ATPases assemble into hexameric double rings and perform vital functions, yet their molecular… (More)
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2014
2014
Turnover of damaged, dysfunctional, or excess organelles is critical to cellular homeostasis. We screened mutants disturbed in… (More)
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2014
2014
BACKGROUND Zellweger spectrum disorder is an autosomal recessively inherited multisystem disorder caused by one of the 13… (More)
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2011
2011
Proteins are targeted to the peroxisome matrix via processes that are mechanistically distinct from those used by other… (More)
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2007
2007
Jasmonic acid (JA) is an important regulator of plant development and stress responses. Several enzymes involved in the… (More)
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Highly Cited
2000
Highly Cited
2000
Peroxisomes are independent organelles found in virtually all eukaryotic cells. Genetic studies have identified more than 20 PEX… (More)
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Highly Cited
1996
Highly Cited
1996
In humans, defects in peroxisome assembly result in the peroxisome biogenesis disorders (PBDs), a group of genetically… (More)
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1996
1996
Isolation of human disease genes is a challenging process and can often only be achieved by labor-intensive positional cloning… (More)
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