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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
Highly Cited
2011
Highly Cited
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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Highly Cited
2010
Highly Cited
2010
Background Zellweger syndrome spectrum disorders are caused by mutations in any of at least 12 different PEX genes. This includes… Expand
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
2002
Highly Cited
2002
Previously we isolated human PEX16encoding 336-amino acid-long peroxin Pex16p and showed that its dysfunction was responsible for… Expand
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
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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