A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1-Cog8 interaction in COG complex formation (Q33269052)

24 July 2017

title

A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1-Cog8 interaction in COG complex formation (English)

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24 July 2017

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François Foulquier

1

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Daniel Ungar

object named as

Daniel Ungar

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author name string

Ellen Reynders

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24 July 2017

Renate Zeevaert

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24 July 2017

Philippa Mills

5

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24 July 2017

Maria Teresa García-Silva

6

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24 July 2017

Paz Briones

7

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24 July 2017

Bryan Winchester

8

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24 July 2017

Willy Morelle

9

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24 July 2017

Monty Krieger

10

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24 July 2017

Willem Annaert

11

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24 July 2017

Gert Matthijs

12

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24 July 2017

language of work or name

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12 January 2007

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24 July 2017

published in

Human Molecular Genetics

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24 July 2017

volume

16

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24 July 2017

issue

7

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24 July 2017

page(s)

717-730

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Cisternal maturation and vesicle transport: join the band wagon! (Review).

24 July 2017

cites work

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https://api.crossref.org/works/10.1093%2FHMG%2FDDL476

Retrograde transport on the COG railway.

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Congenital disorders of glycosylation: a review

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Komrower Lecture. Congenital disorders of glycosylation (CDG): it's all in it!

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Genetic defects in the human glycome

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Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder

21 January 2018

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Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II.

21 January 2018

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The Sec34/35 Golgi transport complex is related to the exocyst, defining a family of complexes involved in multiple steps of membrane traffic

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDL476

Characterization of a mammalian Golgi-localized protein complex, COG, that is required for normal Golgi morphology and function

21 January 2018

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Cog1p plays a central role in the organization of the yeast conserved oligomeric Golgi complex.

21 January 2018

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Genetic analysis of the subunit organization and function of the conserved oligomeric golgi (COG) complex: studies of COG5- and COG7-deficient mammalian cells

21 January 2018

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The binary interacting network of the conserved oligomeric Golgi tethering complex

21 January 2018

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Apolipoprotein C-III isofocusing in the diagnosis of genetic defects in O-glycan biosynthesis

21 January 2018

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Mass spectrometric analysis of glycans in elucidating the pathogenesis of CDG type IIx .

21 January 2018

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Three types of low density lipoprotein receptor-deficient mutant have pleiotropic defects in the synthesis of N-linked, O-linked, and lipid-linked carbohydrate chains

21 January 2018

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Subunit architecture of the conserved oligomeric Golgi complex

21 January 2018

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LDLC encodes a brefeldin A-sensitive, peripheral Golgi protein required for normal Golgi function

21 January 2018

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Cog3p depletion blocks vesicle-mediated Golgi retrograde trafficking in HeLa cells.

21 January 2018

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The COG and COPI complexes interact to control the abundance of GEARs, a subset of Golgi integral membrane proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL476

COG-7-deficient Human Fibroblasts Exhibit Altered Recycling of Golgi Proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL476

Rapid redistribution of Golgi proteins into the ER in cells treated with brefeldin A: evidence for membrane cycling from Golgi to ER

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL476

COG complex-mediated recycling of Golgi glycosyltransferases is essential for normal protein glycosylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL476

IntraGolgi distribution of the Conserved Oligomeric Golgi (COG) complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL476

21 January 2018

Identifiers

DOI

10.1093/HMG/DDL476

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24 July 2017

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