Glycosylation disorders of membrane trafficking

The V-ATPase proteolipid cylinder promotes the lipid-mixing stage of SNARE-dependent fusion of yeast vacuoles

(2011) Bernd Strasser et al.   EMBO JOURNAL

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

(2011) Irina D Pokrovskaya et al.   GLYCOBIOLOGY

Passage through the Golgi

(2010) Akihiko Nakano et al.   CURRENT OPINION IN CELL BIOLOGY

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

Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation

(2010) J. Lubbehusen et al.   HUMAN MOLECULAR GENETICS

Identification of the first COG–CDG patient of Indian origin

(2010) Bobby G. Ng et al.   MOLECULAR GENETICS AND METABOLISM

Membrane Fusion: Role of SNAREs and Calcium

(2010) Bhanu Jena   PROTEIN AND PEPTIDE LETTERS

Membrane Traffic Within the Golgi Apparatus

(2009) Benjamin S. Glick et al.   Annual Review of Cell and Developmental Biology

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

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

Role of vesicle tethering factors in the ER-Golgi membrane traffic

(2009) Elizabeth Sztul 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

Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in theSEC23Bgene

(2009) Paola Bianchi et al.   HUMAN MUTATION

Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II

(2009) Klaus Schwarz et al.   NATURE GENETICS

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

Transport through the Golgi Apparatus by Rapid Partitioning within a Two-Phase Membrane System

(2008) George H. Patterson et al.   CELL

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

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

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