More than just sugars: Conserved oligomeric Golgi complex deficiency causes glycosylation-independent cellular defects.

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More than just sugars: Conserved oligomeric Golgi complex deficiency causes glycosylation-independent cellular defects.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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More than just sugars: Conserv ...... -independent cellular defects.

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More than just sugars: Conserv ...... -independent cellular defects.

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More than just sugars: Conserv ...... -independent cellular defects.

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More than just sugars: Conserv ...... -independent cellular defects.

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More than just sugars: Conserv ...... -independent cellular defects.

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More than just sugars: Conserv ...... -independent cellular defects.

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P1476

More than just sugars: Conserv ...... -independent cellular defects.

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P2093

Irina Pokrovskaya

http://www.w3.org/2001/XMLSchema#string

Jessica B Blackburn

http://www.w3.org/2001/XMLSchema#string

Tetyana Kudlyk

http://www.w3.org/2001/XMLSchema#string

P2860

Purification and characterization of a novel 13 S hetero-oligomeric protein complex that stimulates in vitro Golgi transport

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

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

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

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

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

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

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

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

Requirement of the human GARP complex for mannose 6-phosphate-receptor-dependent sorting of cathepsin D to lysosomes

P31

scholarly article

P356

10.1111/TRA.12564

http://www.w3.org/2001/XMLSchema#string

P50

Vladimir Lupashin

P577

2018-03-23T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29573151

http://www.w3.org/2001/XMLSchema#string

P921

glycosylation

P932

5948163

http://www.w3.org/2001/XMLSchema#string