ER exit sites are physical and functional core autophagosome biogenesis components. - sprookjes - yvandenbroek - TriplyDB

ER exit sites are physical and functional core autophagosome biogenesis components.

ER exit sites are physical and functional core autophagosome biogenesis components.

http://www.wikidata.org/entity/Q37167928

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Architecture and dynamics of the autophagic phosphatidylinositol 3-kinase complex Advances in Autophagy Regulatory Mechanisms Autophagy signal transduction by ATG proteins: from hierarchies to networks Atomistic autophagy: the structures of cellular self-digestion A Role for Macro-ER-Phagy in ER Quality Control.Ltc1 is an ER-localized sterol transporter and a component of ER-mitochondria and ER-vacuole contacts.Yip1A, a novel host factor for the activation of the IRE1 pathway of the unfolded protein response during Brucella infection Autophagosome biogenesis in primary neurons follows an ordered and spatially regulated pathway.Ypt1/Rab1 regulates Hrr25/CK1δ kinase activity in ER-Golgi traffic and macroautophagy.AMPK and vacuole-associated Atg14p orchestrate μ-lipophagy for energy production and long-term survival under glucose starvation TOR complex 2-Ypk1 signaling is an essential positive regulator of the general amino acid control response and autophagy.Golgi compartmentation and identity.Phosphatidylinositol 3-kinase and COPII generate LC3 lipidation vesicles from the ER-Golgi intermediate compartment.Ultrastructural relationship of the phagophore with surrounding organelles.Functional Diversity of Haloacid Dehalogenase Superfamily Phosphatases from Saccharomyces cerevisiae: BIOCHEMICAL, STRUCTURAL, AND EVOLUTIONARY INSIGHTS.Autophagy initiation by ULK complex assembly on ER tubulovesicular regions marked by ATG9 vesicles VMP1 Establishes ER-Microdomains that Regulate Membrane Contact Sites and Autophagy ULK1 phosphorylates Sec23A and mediates autophagy-induced inhibition of ER-to-Golgi traffic.Structure and function of the ULK1 complex in autophagy The Noncanonical Role of ULK/ATG1 in ER-to-Golgi Trafficking Is Essential for Cellular Homeostasis.Subcellular Evidence for Biogenesis of Autophagosomal Membrane during Spermiogenesis In vivo.The EM structure of the TRAPPIII complex leads to the identification of a requirement for COPII vesicles on the macroautophagy pathway.TMEM166/EVA1A interacts with ATG16L1 and induces autophagosome formation and cell death.Calcium channel regulator Mid1 links TORC2-mediated changes in mitochondrial respiration to autophagy.New findings of silica nanoparticles induced ER autophagy in human colon cancer cell.A proteolytic pathway that controls glucose uptake in fat and muscle.A current perspective of autophagosome biogenesis.Organellophagy: eliminating cellular building blocks via selective autophagy.Regulation of autophagy by amino acid availability in S. cerevisiae and mammalian cells.Getting ready for building: signaling and autophagosome biogenesis.Dynamics of autophagosome formation: a pulse and a sequence of waves.TBC1D14 regulates autophagy via the TRAPP complex and ATG9 traffic Autophagy in neuronal cells: general principles and physiological and pathological functions.Systems biology of the secretory pathway: what have we learned so far?The changing nature of the Brucella-containing vacuole.Autophagy and proteins involved in vesicular trafficking.Remodeling of ER-exit sites initiates a membrane supply pathway for autophagosome biogenesis.Autophagosome formation is initiated at phosphatidylinositol synthase-enriched ER subdomains.Autophagy in the test tube: In vitro reconstitution of aspects of autophagosome biogenesis.An overview of macroautophagy in yeast.

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ER exit sites are physical and functional core autophagosome biogenesis components.

http://www.wikidata.org/entity/Q37167928

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

@tr

scientific article published on 31 July 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

ER exit sites are physical and functional core autophagosome biogenesis components.

@en

ER exit sites are physical and functional core autophagosome biogenesis components.

@nl

type

label

ER exit sites are physical and functional core autophagosome biogenesis components.

@en

ER exit sites are physical and functional core autophagosome biogenesis components.

@nl

prefLabel

ER exit sites are physical and functional core autophagosome biogenesis components.

@en

ER exit sites are physical and functional core autophagosome biogenesis components.

@nl

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MBC.E13-07-0381

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Molecular Biology of the Cell

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ER exit sites are physical and functional core autophagosome biogenesis components.

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Christopher Graham

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

Jodi Nunnari

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

Jonathan R Friedman

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

Martin Graef

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

Mohan Babu

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

P2860

Disruption of Toxoplasma gondii parasitophorous vacuoles by the mouse p47-resistance GTPases.

A subdomain of the endoplasmic reticulum forms a cradle for autophagosome formation

Autophagosomes form at ER-mitochondria contact sites

Network organization of the human autophagy system

The pre-autophagosomal structure organized by concerted functions of APG genes is essential for autophagosome formation

An evolutionary proteomics approach identifies substrates of the cAMP-dependent protein kinase

Organization of the pre-autophagosomal structure responsible for autophagosome formation

Formation process of autophagosome is traced with Apg8/Aut7p in yeast

Tor-mediated induction of autophagy via an Apg1 protein kinase complex

Two mammalian Sec16 homologues have nonredundant functions in endoplasmic reticulum (ER) export and transitional ER organization

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2918-2931

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scholarly article

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10.1091/MBC.E13-07-0381

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18

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24

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2013-07-31T00:00:00Z

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23904270

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3771953

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