About: Recent advances in p97/VCP/Cdc48 cellular functions

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scientific article published on 12 July 2011

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) наукова стаття, опублікована в липні 2011 (uk) مقالة علمية نشرت في 12 يوليو 2011 (ar) scientific article published on 12 July 2011 (en) 2011 թվականի հուլիսի 12-ին հրատարակված գիտական հոդված (hy) artículu científicu espublizáu en xunetu de 2011 (ast)
publication date	wds:Q37904023-6D2A8FC5-AB3D-435C-AAF2-F65507C8687F
publication date	2011-07-12 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37904023-E9EF0CC1-EF5D-4275-89A9-306BC99DD6EB
language of work or name	English
cites work	wds:Q37904023-B5C77AA9-A02B-4FA3-91DD-F055C2BAA9D7
cites work	Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
author name string	wds:Q37904023-0B1C3F29-0FE8-4761-A56F-C34FF23B80CB wds:Q37904023-605C43E4-1B18-482F-8BE0-B4AE112329F2 wds:Q37904023-92EF0228-EF01-428F-93A8-10DA567F2875
author name string	Kunitoshi Yamanaka Teru Ogura Yohei Sasagawa
rdfs:label	Recent advances in p97/VCP/Cdc48 cellular functions (en) Recent advances in p97/VCP/Cdc48 cellular functions (nl)
skos:prefLabel	Recent advances in p97/VCP/Cdc48 cellular functions (en) Recent advances in p97/VCP/Cdc48 cellular functions (nl)
name	Recent advances in p97/VCP/Cdc48 cellular functions (en) Recent advances in p97/VCP/Cdc48 cellular functions (nl)
title	wds:Q37904023-B1AF66DC-FDBD-4384-A230-9108CA142970
title	Recent advances in p97/VCP/Cdc48 cellular functions (en)
page(s)	wds:Q37904023-446F1963-904C-486E-BFAB-A0A612BF4BFF
page(s)	130-137
instance of	wds:Q37904023-29028e59-3212-4709-bf7f-ab5ca89f8652 wds:Q37904023-550C1A16-549F-4993-A009-0AEC45FF5B0B
instance of	review article scholarly article
PubMed ID	wds:Q37904023-BD2C782A-22DB-4B8E-A969-735C7DAE1075
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/21781992
PubMed ID	21781992
published in	wds:Q37904023-2ECFEBF6-E02D-4B5F-901E-32A21E5B3192
published in	Biochimica et Biophysica Acta
issue	wds:Q37904023-FC1A6BC9-7B41-4B60-888C-D39860B12845
volume	wds:Q37904023-C8D2EC59-6369-46DE-AC65-7889FE386ED5
issue	1
volume	1823
DOI	wds:Q37904023-4CDCE006-17AC-41BC-9DF2-09F39D4939F5
DOI	http://dx.doi.org/10.1016/J.BBAMCR.2011.07.001
DOI	10.1016/J.BBAMCR.2011.07.001
ResearchGate publication ID	wds:Q37904023-B1A238B7-8A1F-431E-95DA-6C1C62AF84D9
ResearchGate publication ID	51514320
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37904023
is cites work of	Functional chromatography reveals three natural products that target the same protein with distinct mechanisms of action. Pathogenesis/genetics of frontotemporal dementia and how it relates to ALS. Atad2 is a generalist facilitator of chromatin dynamics in embryonic stem cells Aggrephagy: selective disposal of protein aggregates by macroautophagy. Caveolae as plasma membrane sensors, protectors and organizers. Lysine methylation of VCP by a member of a novel human protein methyltransferase family Altered ribostasis: RNA-protein granules in degenerative disorders A non-canonical role of the p97 complex in RIG-I antiviral signaling Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levels Progranulin: at the interface of neurodegenerative and metabolic diseases Mitochondrial function in neuronal cells depends on p97/VCP/Cdc48-mediated quality control The p97-UBXD8 complex destabilizes mRNA by promoting release of ubiquitinated HuR from mRNP Effects of 1.8 GHz radiofrequency radiation on protein expression in human lens epithelial cells Proteomic analysis of saliva in HIV-positive heroin addicts reveals proteins correlated with cognition The p97/VCP ATPase is critical in muscle atrophy and the accelerated degradation of muscle proteins Regulation of proteasome activity in health and disease Direct and/or Indirect Roles for SUMO in Modulating Alpha-Synuclein Toxicity Comprehensive cell-specific protein analysis in early and late pollen development from diploid microsporocytes to pollen tube growth Functional genomic screen and network analysis reveal novel modifiers of tauopathy dissociated from tau phosphorylation Single base substitution in OsCDC48 is responsible for premature senescence and death phenotype in rice Protein interaction profiling of the p97 adaptor UBXD1 points to a role for the complex in modulating ERGIC-53 trafficking Control of p97 function by cofactor binding Lys11- and Lys48-linked ubiquitin chains interact with p97 during endoplasmic-reticulum-associated degradation Yeast prions and human prion-like proteins: sequence features and prediction methods Pro178 and Pro183 of selenoprotein S are essential residues for interaction with p97(VCP) during endoplasmic reticulum-associated degradation Selenoprotein S-dependent Selenoprotein K Binding to p97(VCP) Protein Is Essential for Endoplasmic Reticulum-associated Degradation Structure and function of the AAA+ ATPase p97/Cdc48p Dual recruitment of Cdc48 (p97)-Ufd1-Npl4 ubiquitin-selective segregase by small ubiquitin-like modifier protein (SUMO) and ubiquitin in SUMO-targeted ubiquitin ligase-mediated genome stability functions Immunoreactivity of valosin-containing protein in sporadic amyotrophic lateral sclerosis and in a case of its novel mutant The VCP/p97 system at a glance: connecting cellular function to disease pathogenesis. Inhibitors of the AAA+ chaperone p97 Autophagy Mechanism, Regulation, Functions, and Disorders Arginine methylation of HSP70 regulates retinoid acid-mediated RARβ2 gene activation MHC class I antigen presentation of DRiP-derived peptides from a model antigen is not dependent on the AAA ATPase p97 Combined inhibition of p97 and the proteasome causes lethal disruption of the secretory apparatus in multiple myeloma cells Five Questions (with their Answers) on ER-Associated Degradation METTL21B Is a Novel Human Lysine Methyltransferase of Translation Elongation Factor 1A: Discovery by CRISPR/Cas9 Knockout. Association between SNPs and haplotypes in the METTL21C gene and peak bone mineral density and body composition in Chinese male nuclear families. Ubiquitin-binding site 2 of ataxin-3 prevents its proteasomal degradation by interacting with Rad23 Dual Unnatural Amino Acid Incorporation and Click-Chemistry Labeling to Enable Single-Molecule FRET Studies of p97 Folding Combining valosin-containing protein (VCP) inhibition and suberanilohydroxamic acid (SAHA) treatment additively enhances the folding, trafficking, and function of epilepsy-associated γ-aminobutyric acid, type A (GABAA) receptors

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