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PEX16 gene

Known as: PEX16, peroxisomal biogenesis factor 16, PEROXISOME BIOGENESIS FACTOR 16 
 
National Institutes of Health

Papers overview

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Highly Cited
2017
Highly Cited
2017
Peroxisomes function together with mitochondria in a number of essential biochemical pathways, from bile acid synthesis to fatty… Expand
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2015
2015
Peroxisomes rely on a diverse array of mechanisms to ensure the specific targeting of their protein constituents. Peroxisomal… Expand
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2014
2014
The endoplasmic reticulum (ER) is required for the de novo biogenesis of peroxisomes in mammalian cells. However, its role in… Expand
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2011
2011
Sec16 plays a key role in the formation of coat protein II vesicles, which mediate protein transport from the endoplasmic… Expand
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2010
2010
BACKGROUND Zellweger syndrome spectrum disorders are caused by mutations in any of at least 12 different PEX genes. This includes… Expand
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Review
2009
Review
2009
With every cell division, peroxisomes duplicate and are segregated between progeny cells. Here, we discuss the different modes of… Expand
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Highly Cited
2006
Highly Cited
2006
Peroxisomes are ubiquitous organelles that proliferate under different physiological conditions and can form de novo in cells… Expand
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Highly Cited
1999
Highly Cited
1999
Zellweger syndrome and related diseases are caused by defective import of peroxisomal matrix proteins. In all previously reported… Expand
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Highly Cited
1998
Highly Cited
1998
Peroxisome-biogenesis disorders (PBDs), including Zellweger syndrome (ZS), are autosomal recessive diseases caused by a… Expand
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Highly Cited
1997
Highly Cited
1997
Pex mutants of the yeast Yarrowia lipolytica are defective in peroxisome assembly. The mutant strain pex16-1 lacks… Expand
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