Further assembly required: construction and dynamics of the endoplasmic reticulum network. - Wikidata - wikimedia - TriplyDB

Further assembly required: construction and dynamics of the endoplasmic reticulum network.

Further assembly required: construction and dynamics of the endoplasmic reticulum network.

http://www.wikidata.org/entity/Q33962105

about

Protrudin binds atlastins and endoplasmic reticulum-shaping proteins and regulates network formation Endoplasmic reticulum stress-mediated pathways to both apoptosis and autophagy: Significance for melanoma treatment Cell death and survival through the endoplasmic reticulum-mitochondrial axis Membrane-shaping disorders: a common pathway in axon degeneration Review: biogenesis of the multifunctional lipid droplet: lipids, proteins, and sites Arl6IP1 has the ability to shape the mammalian ER membrane in a reticulon-like fashion Protrudin regulates endoplasmic reticulum morphology and function associated with the pathogenesis of hereditary spastic paraplegia The kinase inhibitor SFV785 dislocates dengue virus envelope protein from the replication complex and blocks virus assembly REEPs are membrane shaping adapter proteins that modulate specific g protein-coupled receptor trafficking by affecting ER cargo capacity Spg20-/- mice reveal multimodal functions for Troyer syndrome protein spartin in lipid droplet maintenance, cytokinesis and BMP signaling Direct association of the reticulon protein RTN1A with the ryanodine receptor 2 in neurons Biogenesis and functions of lipid droplets in plants: Thematic Review Series: Lipid Droplet Synthesis and Metabolism: from Yeast to Man Endoplasmic reticulum-mediated signalling in cellular microdomains.Phosphoregulation of STIM1 leads to exclusion of the endoplasmic reticulum from the mitotic spindle Inhibition of TFG function causes hereditary axon degeneration by impairing endoplasmic reticulum structure.Acyl-CoA synthetase 3 promotes lipid droplet biogenesis in ER microdomains Inward cholesterol gradient of the membrane system in P. falciparum-infected erythrocytes involves a dilution effect from parasite-produced lipids.Emerging themes of ER organization in the development and maintenance of axons.STIM proteins and the endoplasmic reticulum-plasma membrane junctions.SLC33A1/AT-1 protein regulates the induction of autophagy downstream of IRE1/XBP1 pathway Pharmacologic rescue of axon growth defects in a human iPSC model of hereditary spastic paraplegia SPG3A.Connecting the cytoskeleton to the endoplasmic reticulum and Golgi.ERMO3/MVP1/GOLD36 is involved in a cell type-specific mechanism for maintaining ER morphology in Arabidopsis thaliana Membrane tethering by the atlastin GTPase depends on GTP hydrolysis but not on forming the cross-over configuration.Phosphatidylethanolamines modified by γ-ketoaldehyde (γKA) induce endoplasmic reticulum stress and endothelial activation.Increased ER-mitochondrial coupling promotes mitochondrial respiration and bioenergetics during early phases of ER stress A conserved amphipathic helix is required for membrane tubule formation by Yop1p A Novel Microtubule-Disrupting Agent Induces Endoplasmic Reticular Stress-Mediated Cell Death in Human Hepatocellular Carcinoma Cells.Endoplasmic Reticulum-Localized Transmembrane Protein Dpy19L1 Is Required for Neurite Outgrowth.XBP1 depletion precedes ubiquitin aggregation and Golgi fragmentation in TDP-43 transgenic rats.Hereditary spastic paraplegia-causing mutations in atlastin-1 interfere with BMPRII trafficking.Untangling the web: mechanisms underlying ER network formation.Why do proteins aggregate? "Intrinsically insoluble proteins" and "dark mediators" revealed by studies on "insoluble proteins" solubilized in pure water.Assembly of Dynamic P450-Mediated Metabolons-Order Versus Chaos.Plasmodesmata viewed as specialised membrane adhesion sites.Patterns and processes in the evolution of the eukaryotic endomembrane system.Cellular pathways of hereditary spastic paraplegia.Rab proteins of the endoplasmic reticulum: functions and interactors.Lysine acetylation in the lumen of the ER: a novel and essential function under the control of the UPR.The role of reticulons in neurodegenerative diseases.

P2860

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P2860

Further assembly required: construction and dynamics of the endoplasmic reticulum network.

http://www.wikidata.org/entity/Q33962105

description

2010 nî lūn-bûn

@nan

2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Further assembly required: con ...... endoplasmic reticulum network.

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Craig Blackstone

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Seong H Park

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P2860

Cellular localization, oligomerization, and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastin

Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance

Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network

Reshaping of the endoplasmic reticulum limits the rate for nuclear envelope formation

Spastin couples microtubule severing to membrane traffic in completion of cytokinesis and secretion

Atlastin GTPases are required for Golgi apparatus and ER morphogenesis.

A class of dynamin-like GTPases involved in the generation of the tubular ER network

Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy

An ER-mitochondria tethering complex revealed by a synthetic biology screen

Subdomain-specific localization of CLIMP-63 (p63) in the endoplasmic reticulum is mediated by its luminal alpha-helical segment

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515-521

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scholarly article

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10.1038/EMBOR.2010.92

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7

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11

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20559323

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endoplasmic reticulum

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2897125

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