(Q54455138)

30 May 2018

title

Large protein complexes retained in the ER are dislocated by non-COPII vesicles and degraded by selective autophagy. (English)

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30 May 2018

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Valerie Le Fourn

1

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30 May 2018

Sujin Park

2

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30 May 2018

Insook Jang

3

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30 May 2018

Katarina Gaplovska-Kysela

4

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30 May 2018

Bruno Guhl

5

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30 May 2018

Yangsin Lee

6

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30 May 2018

Jin Won Cho

7

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30 May 2018

Christian Zuber

8

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30 May 2018

Jürgen Roth

9

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30 May 2018

publication date

22 January 2013

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30 May 2018

Cellular and Molecular Life Sciences

published in

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30 May 2018

volume

70

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30 May 2018

issue

11

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30 May 2018

page(s)

1985-2002

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30 May 2018

https://scigraph.springernature.com/pub.10.1007/s00018-012-1236-6

exact match

0 references

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Proteasome-dependent endoplasmic reticulum-associated protein degradation: an unconventional route to a familiar fate

21 January 2018

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Protein translocation by the Sec61/SecY channel

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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The mechanism of Z alpha 1-antitrypsin accumulation in the liver

21 January 2018

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Aggregated myocilin induces russell bodies and causes apoptosis: implications for the pathogenesis of myocilin-caused primary open-angle glaucoma

21 January 2018

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Simian Virus 40 depends on ER protein folding and quality control factors for entry into host cells

21 January 2018

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Murine polyomavirus requires the endoplasmic reticulum protein Derlin-2 to initiate infection

21 January 2018

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Assembly and secretion of fibrinogen. Degradation of individual chains

21 January 2018

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12 December 2020

Mott cells are plasma cells defective in immunoglobulin secretion

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12 December 2020

Intracellular inclusions containing mutant alpha1-antitrypsin Z are propagated in the absence of autophagic activity

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Glucosidase II, a protein of the endoplasmic reticulum with high mannose oligosaccharide chains and a rapid turnover.

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High-resolution visualization of fibrinogen molecules and fibrin fibers with atomic force microscopy

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The endoplasmic reticulum degradation pathway for mutant secretory proteins alpha1-antitrypsin Z and S is distinct from that for an unassembled membrane protein

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In vitro assembly of the component chains of fibrinogen requires endoplasmic reticulum factors

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A naturally occurring nonpolymerogenic mutant of alpha 1-antitrypsin characterized by prolonged retention in the endoplasmic reticulum

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Developmental regulation of alpha beta T cell antigen receptor expression results from differential stability of nascent TCR alpha proteins within the endoplasmic reticulum of immature and mature T cells.

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The structure and biological features of fibrinogen and fibrin.

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A specific inhibitor of phosphatidylinositol 3-kinase, 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY294002)

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Disulfide bridges in the middle part of human fibrinogen

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The degradation of nascent fibrinogen chains is mediated by the ubiquitin proteasome pathway

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Intracisternal granules in the exocrine cells of the pancreas

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The alpha chain of the T cell antigen receptor is degraded in the cytosol

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12 December 2020

Biosynthesis of human fibrinogen. Subunit interactions and potential intermediates in the assembly

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Studies on the assembly and secretion of fibrinogen

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Prevention of non-specific interactions of gold-labeled reagents on tissue sections

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Identification and mass analysis of human fibrinogen molecules and their domains by scanning transmission electron microscopy

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Fibrinogen biosynthesis. Assembly, intracellular degradation, and association with lipid synthesis and secretion

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Fibrinogen precursors. Order of assembly of fibrinogen chains

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12 December 2020

10.1007/S00018-012-1236-6

Identifiers

DOI

1 reference

30 May 2018

1 reference

30 May 2018