about
The proteasomal de-ubiquitinating enzyme POH1 promotes the double-strand DNA break responseThe ubiquitin proteasomal system: a potential target for the management of Alzheimer's diseaseThe role of the ubiquitin proteasome system in cerebellar development and medulloblastomaThe role of targeted protein degradation in early neural developmentEfficient and biologically relevant consensus strategy for Parkinson's disease gene prioritization.Niclosamide prevents the formation of large ubiquitin-containing aggregates caused by proteasome inhibitionSolution Structure and Rpn1 Interaction of the UBL Domain of Human RNA Polymerase II C-Terminal Domain PhosphataseAntiviral activity of a small molecule deubiquitinase inhibitor occurs via induction of the unfolded protein responseOral administration of the pimelic diphenylamide HDAC inhibitor HDACi 4b is unsuitable for chronic inhibition of HDAC activity in the CNS in vivoBassoon and Piccolo maintain synapse integrity by regulating protein ubiquitination and degradationEnhancement of proteasome activity by a small-molecule inhibitor of USP14Ubiquitin conjugation triggers misfolded protein sequestration into quality control foci when Hsp70 chaperone levels are limiting.Overexpression of ALS-associated p.M337V human TDP-43 in mice worsens disease features compared to wild-type human TDP-43 mice.Alteration in basal and depolarization induced transcriptional network in iPSC derived neurons from Timothy syndrome.Validation of microarray data in human lymphoblasts shows a role of the ubiquitin-proteasome system and NF-kB in the pathogenesis of Down syndrome.Transcriptional analysis implicates endoplasmic reticulum stress in bovine spongiform encephalopathyA novel role for ATM in regulating proteasome-mediated protein degradation through suppression of the ISG15 conjugation pathway.Targeting the ubiquitin-proteasome pathway with inorganic compounds to fight cancer: a challenge for the future.Somatic intronic microsatellite loci differentiate glioblastoma from lower-grade gliomas.Intellectual disability and autism spectrum disorders: causal genes and molecular mechanisms.Withaferin A induces proteasome inhibition, endoplasmic reticulum stress, the heat shock response and acquisition of thermotolerance.Quantitative analysis of α-synuclein solubility in living cells using split GFP complementationMutation in E1, the ubiquitin activating enzyme, reduces Drosophila lifespan and results in motor impairment.Ubiquitin-positive intranuclear inclusions in neuronal and glial cells in a mouse model of the fragile X premutation.Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis.Induced pluripotent stem cell-derived neuronal cells from a sporadic Alzheimer's disease donor as a model for investigating AD-associated gene regulatory networks.Ube3a imprinting impairs circadian robustness in Angelman syndrome modelsUBE2E ubiquitin-conjugating enzymes and ubiquitin isopeptidase Y regulate TDP-43 protein ubiquitination.Ubiquitination in postsynaptic function and plasticityProteasomal dysfunction and endoplasmic reticulum stress enhance trafficking of prion protein aggregates through the secretory pathway and increase accumulation of pathologic prion proteinDictyostelium discoideum has a highly Q/N-rich proteome and shows an unusual resilience to protein aggregation.Investigation of Gene Regulatory Networks Associated with Autism Spectrum Disorder Based on MiRNA Expression in China.Insights from cerebellar transcriptomic analysis into the pathogenesis of ataxia.Indirect inhibition of 26S proteasome activity in a cellular model of Huntington's disease.Cysteine cathepsins are essential in lysosomal degradation of α-synuclein.Pathophysiology of protein aggregation and extended phenotyping in filaminopathy.Effect of divalent metals on the neuronal proteasomal system, prion protein ubiquitination and aggregation.Monitoring of ubiquitin-proteasome activity in living cells using a Degron (dgn)-destabilized green fluorescent protein (GFP)-based reporter protein.Dysregulation of core components of SCF complex in poly-glutamine disordersISG15 deregulates autophagy in genotoxin-treated ataxia telangiectasia cells.
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
The ubiquitin proteasome system in neuropathology
@ast
The ubiquitin proteasome system in neuropathology
@en
The ubiquitin proteasome system in neuropathology
@nl
type
label
The ubiquitin proteasome system in neuropathology
@ast
The ubiquitin proteasome system in neuropathology
@en
The ubiquitin proteasome system in neuropathology
@nl
prefLabel
The ubiquitin proteasome system in neuropathology
@ast
The ubiquitin proteasome system in neuropathology
@en
The ubiquitin proteasome system in neuropathology
@nl
P2860
P921
P3181
P1476
The ubiquitin proteasome system in neuropathology
@en
P2093
Norman L Lehman
P2860
P2888
P304
P3181
P356
10.1007/S00401-009-0560-X
P407
P577
2009-07-14T00:00:00Z
P5875
P6179
1038312087