Conserved oligomeric Golgi complex specifically regulates the maintenance of Golgi glycosylation machinery

Differential effects of lobe A and lobe B of the Conserved Oligomeric Golgi complex on the stability of β1,4-galactosyltransferase 1 and α2,6-sialyltransferase 1

(2010) Romain Peanne et al.   GLYCOBIOLOGY

Interaction of Golgin-84 with the COG Complex Mediates the Intra-Golgi Retrograde Transport

(2010) Miwa Sohda et al.   TRAFFIC

Localization of Golgi-resident glycosyltransferases

(2009) Linna Tu et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

A new mutation in COG7 extends the spectrum of COG subunit deficiencies

(2009) Renate Zeevaert et al.   European Journal of Medical Genetics

Sorting out glycosylation enzymes in the Golgi apparatus

(2009) Tommy Nilsson et al.   FEBS LETTERS

Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation

(2009) P. Paesold-Burda et al.   HUMAN MOLECULAR GENETICS

Golgi function and dysfunction in the first COG4-deficient CDG type II patient

(2009) Ellen Reynders et al.   HUMAN MOLECULAR GENETICS

Glycoproteomics Analysis of Human Liver Tissue by Combination of Multiple Enzyme Digestion and Hydrazide Chemistry

(2009) Rui Chen et al.   JOURNAL OF PROTEOME RESEARCH

Structural basis for a human glycosylation disorder caused by mutation of the COG4 gene

(2009) B. C. Richardson et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The COG Complex, Rab6 and COPI Define a Novel Golgi Retrograde Trafficking Pathway that is Exploited by SubAB Toxin

(2009) Richard D. Smith et al.   TRAFFIC

COG defects, birth and rise!

(2008) François Foulquier   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Role of the conserved oligomeric Golgi (COG) complex in protein glycosylation

(2008) Richard D. Smith et al.   CARBOHYDRATE RESEARCH

Golgi Localization of Glycosyltransferases Requires a Vps74p Oligomer

(2008) Karl R. Schmitz et al.   DEVELOPMENTAL CELL

Cerebrocostomandibular-like syndrome and a mutation in the conserved oligomeric Golgi complex, subunit 1

(2008) R. Zeevaert et al.   HUMAN MOLECULAR GENETICS

Signal-Mediated Dynamic Retention of Glycosyltransferases in the Golgi

(2008) L. Tu et al.   SCIENCE

Deficiencies in subunits of the Conserved Oligomeric Golgi (COG) complex define a novel group of Congenital Disorders of Glycosylation

(2007) Renate Zeevaert et al.   MOLECULAR GENETICS AND METABOLISM