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COG4 gene

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

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COG4 protein, S cerevisiae

Papers overview

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2017
2017
Severe infantile acute encephalopathy and COG4 mutation: CDG IIJ
2016
2016
A High Copy Suppressor Screen for Autophagy Defects in Saccharomyces arl1Δ and ypt6Δ Strains
In Saccharomyces cerevisiae, Arl1 and Ypt6, two small GTP-binding proteins that regulate membrane traffic in the secretory and… 
2015
2015
A7.11 IGA autoantigens – a link between the gut and the anti-TNF therapy response in rheumatoid arthritis patients analysed in two independent clinical trials
Background So far no mechanism for non response to biologicals targeting TNFα has been described, despite one third of rheumatoid… 
2014
2014
Identified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese population
Diabetic nephropathy (DN) has become one of the most common causes of end-stage renal disease (ESRD) in many countries, such as… 
2011
2011
Searching For Meaningful Use Of Health Information Technology A Study Of Cardiovascular Disease Care In Veterans General Hospitals
2009
2009
A mutation in a COG4 homologue affects polarity establishment in the fungus Aspergillus nidulans
We have identified a mutation in the fungus Aspergillus nidulans, designated swoP (for swollen cell phenotype), causing a… 
2001
2001
Identification, genomic structure, and screening of the vacuolar proton-ATPase membrane sector-associated protein M8-9 gene within the COD1 critical region (Xp11.4).
PURPOSE Our goal is to identify the gene responsible for X-linked cone-rod dystrophy (COD1) that has been localized to a limited… 
2001
2001
AN INVESTIGATION INTO NAVIER-STOKES SOLUTIONS OF THE FLOW AROUND WING-BODY GEOMETRIES
In this paper the commercial CFD packages Star-CD and Flo++ was used to investigate the suitability of the Navier-Stokes method… 
1997
1997
A Family with X-Linked Cone Dystrophy Showing a Tapetal-Like Reflex
X-linked cone dystrophy (XLCD) is an infrequent cause of progressive central visual loss in males. Other clinical features… 
1994
1994
Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
X-linked progressive cone dystrophy (COD1) causes progressive deterioration of visual acuity, deepening of central scotomas… 
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