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COG4 gene

Known as: DKFZP586E1519, COMPONENT OF OLIGOMERIC GOLGI COMPLEX 4, COD1 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
The conserved oligomeric Golgi (COG) complex is involved in intracellular vesicular transport, and is composed of eight subunits… Expand
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2015
2015
The conserved oligomeric Golgi (COG) complex is involved in intra‐Golgi retrograde trafficking, and mutations in six of its eight… Expand
2014
2014
The conserved oligomeric Golgi complex is a peripheral membrane protein complex that orchestrates the tethering and fusion of… Expand
2011
2011
Mutations in the Conserved Oligomeric Golgi (COG) complex give rise to type II congenital disorders of glycosylation (CDG). Thus… Expand
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Highly Cited
2009
Highly Cited
2009
The proper glycosylation of proteins trafficking through the Golgi apparatus depends upon the conserved oligomeric Golgi (COG… Expand
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Highly Cited
2009
Highly Cited
2009
The conserved oligomeric Golgi (COG) complex is a hetero-octameric complex essential for normal glycosylation and intra-Golgi… Expand
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Highly Cited
2009
Highly Cited
2009
The conserved oligomeric Golgi (COG) complex is a tethering factor composed of eight subunits that is involved in the retrograde… Expand
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Highly Cited
2002
Highly Cited
2002
The internal environment of the ER is regulated to accommodate essential cellular processes, yet our understanding of this… Expand
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1998
1998
Progressive X-linked cone-rod dystrophy (COD1) is a retinal disease affecting primarily the cone photoreceptors. The COD1 locus… Expand
1994
1994
X-linked progressive cone dystrophy (COD1) causes progressive deterioration of visual acuity, deepening of central scotomas… Expand