scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1033502926 |
P356 | DOI | 10.1186/1471-2202-11-95 |
P932 | PMC publication ID | 2928238 |
P698 | PubMed publication ID | 20704702 |
P5875 | ResearchGate publication ID | 45639178 |
P2093 | author name string | Tao Liu | |
Peng Xie | |||
Ming Chang | |||
Linsen Hu | |||
Yihong Hu | |||
Jinhua Piao | |||
Yingjiu Zhang | |||
Xing'an Li | |||
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Immunocytochemical co-localization of the proteasome in ubiquitinated structures in neurodegenerative diseases and the elderly. | Q53216133 | ||
In situ and in vitro study of colocalization and segregation of alpha-synuclein, ubiquitin, and lipids in Lewy bodies | Q64764806 | ||
Cu/Zn superoxide dismutase-like immunoreactivity is present in Lewy bodies from Parkinson disease: a light and electron microscopic immunocytochemical study | Q72064008 | ||
Cu/Zn superoxide dismutase-like immunoreactivity in Lewy body-like inclusions of sporadic amyotrophic lateral sclerosis | Q72520333 | ||
Chromatin condensation is not associated with apoptosis | Q77229025 | ||
Subcellular fractionation | Q79436481 | ||
Peptide fragment intensity statistical modeling | Q80830941 | ||
Chaperone proteins identified from synthetic proteasome inhibitor-induced inclusions in PC12 cells by proteomic analysis | Q81237748 | ||
Tubulin seeds alpha-synuclein fibril formation | Q24291881 | ||
A Product of the Human Gene Adjacent to parkin Is a Component of Lewy Bodies and Suppresses Pael Receptor-induced Cell Death | Q24297163 | ||
Parkin accumulation in aggresomes due to proteasome impairment | Q24308757 | ||
Regulation of type II collagen synthesis during osteoarthritis by prolyl-4-hydroxylases: possible influence of low oxygen levels | Q24671477 | ||
A simple technique for quantifying apoptosis in 96-well plates | Q24810168 | ||
alpha-Synuclein shares physical and functional homology with 14-3-3 proteins | Q28139698 | ||
Superoxide dismutase--applications and relevance to human diseases | Q28198204 | ||
Inhibition of proteasomes induces accumulation, phosphorylation, and recruitment of HSP27 and alphaB-crystallin to aggresomes | Q28211937 | ||
Aggresome formation and neurodegenerative diseases: therapeutic implications | Q28265926 | ||
Protein aggregation and neurodegenerative disease | Q28273600 | ||
Rat pheochromocytoma tyrosine hydroxylase is phosphorylated on serine 40 by an associated protein kinase | Q28282891 | ||
A single polypeptide acts both as the beta subunit of prolyl 4-hydroxylase and as a protein disulfide-isomerase | Q28288295 | ||
Regional assignment of the human gene coding for a multifunctional polypeptide (P4HB) acting as the β-subunit of prolyl 4-hydroxylase and the enzyme protein disulfide isomerase to 17q25 | Q28296844 | ||
ER chaperones in mammalian development and human diseases | Q28300625 | ||
Proteomic changes of PC12 cells treated with proteasomal inhibitor PSI | Q28569104 | ||
Proteasomal inhibition-induced inclusion formation and death in cortical neurons require transcription and ubiquitination | Q28570666 | ||
Parkin binds to alpha/beta tubulin and increases their ubiquitination and degradation | Q28572388 | ||
Proteomic analysis of ubiquitin-proteasome effects: insight into the function of eukaryotic initiation factor 5A | Q28586364 | ||
Proteotoxic stress and inducible chaperone networks in neurodegenerative disease and aging | Q29614783 | ||
The minimum information about a proteomics experiment (MIAPE) | Q29615391 | ||
Parkinson's disease transgenic mitochondrial cybrids generate Lewy inclusion bodies. | Q30312062 | ||
A proteomic survey of rat cerebral cortical synaptosomes | Q31163203 | ||
Increased expression and altered subunit composition of proteasomes induced by continuous proteasome inhibition establish apoptosis resistance and hyperproliferation of Burkitt lymphoma cells | Q33285275 | ||
An update on data standards for gel electrophoresis | Q33300248 | ||
Hepatitis B virus X protein suppressing adriamycin-induced apoptosis of HepG2 cells | Q33316883 | ||
Neuroprotective effect of the natural iron chelator, phytic acid in a cell culture model of Parkinson's disease | Q33318606 | ||
Specificity in intracellular protein aggregation and inclusion body formation | Q33949081 | ||
Proteasome inhibitor-induced apoptosis is mediated by positive feedback amplification of PKCdelta proteolytic activation and mitochondrial translocation | Q34214022 | ||
Tyrosine hydroxylase protein in Lewy bodies of parkinsonian and senile brains | Q42447562 | ||
Effect of proteasome inhibition on cellular oxidative damage, antioxidant defences and nitric oxide production | Q43658583 | ||
Proteasomal inhibition leads to formation of ubiquitin/alpha-synuclein-immunoreactive inclusions in PC12 cells | Q43718632 | ||
Characterization of cytoplasmic alpha-synuclein aggregates. Fibril formation is tightly linked to the inclusion-forming process in cells | Q43758292 | ||
Ubiquitination of soluble and membrane-bound tyrosine hydroxylase and degradation of the soluble form | Q43902847 | ||
Selective loss of 20S proteasome alpha-subunits in the substantia nigra pars compacta in Parkinson's disease | Q44048965 | ||
Aggresome-related biogenesis of Lewy bodies | Q44242992 | ||
Immunohistochemical localization of 14.3.3 zeta protein in amyloid plaques in human spongiform encephalopathies | Q44295928 | ||
Effect of proteasome inhibitor on cultured mesencephalic dopaminergic neurons | Q44308146 | ||
Enhanced oligomerization of the alpha-synuclein mutant by the Cu,Zn-superoxide dismutase and hydrogen peroxide system. | Q44379856 | ||
Ubiquitination of alpha-synuclein in Lewy bodies is a pathological event not associated with impairment of proteasome function | Q44552114 | ||
Fine Structure and Biochemical Mechanisms Underlying Nigrostriatal Inclusions and Cell Death after Proteasome Inhibition | Q44605313 | ||
Methamphetamine produces neuronal inclusions in the nigrostriatal system and in PC12 cells. | Q44693092 | ||
Analysis of alpha-synuclein-associated proteins by quantitative proteomics | Q44964546 | ||
Generalized brain and skin proteasome inhibition in Huntington's disease | Q45045405 | ||
A proteasomal stress response: pre-treatment with proteasome inhibitors increases proteasome activity and reduces neuronal vulnerability to oxidative injury | Q45138331 | ||
Oxidative modifications and aggregation of Cu,Zn-superoxide dismutase associated with Alzheimer and Parkinson diseases | Q45230472 | ||
VCP/p97 in abnormal protein aggregates, cytoplasmic vacuoles, and cell death, phenotypes relevant to neurodegeneration | Q45304146 | ||
Huntingtin inclusions do not deplete polyglutamine-containing transcription factors in HD mice | Q45305847 | ||
Angiotensin-(1-7) through AT receptors mediates tyrosine hydroxylase degradation via the ubiquitin-proteasome pathway | Q46138698 | ||
Proteasome inhibition by lactacystin in primary neuronal cells induces both potentially neuroprotective and pro-apoptotic transcriptional responses: a microarray analysis | Q46578554 | ||
Phosphorylation of Ser-129 is the dominant pathological modification of alpha-synuclein in familial and sporadic Lewy body disease | Q46593989 | ||
Apoptosis and the conformational change of Bax induced by proteasomal inhibition of PC12 cells are inhibited by bcl-xL and bcl-2. | Q46679719 | ||
Ultrasonic extraction and separation of anthraquinones from Rheum palmatum L. | Q46749006 | ||
Proteasome inhibition: an early or late event in nitric oxide-induced neuronal death? | Q46851350 | ||
Proteomic identification of novel proteins in cortical lewy bodies | Q48227693 | ||
An early cytoplasmic change before Lewy body maturation: an ultrastructural study of the substantia nigra from an autopsy case of juvenile parkinsonism | Q48352469 | ||
Potential oxidative pathways of brain catecholamines | Q48410486 | ||
Neural heme oxygenase-1 expression in idiopathic Parkinson's disease | Q48503937 | ||
Unfolding the role of chaperones and chaperonins in human disease | Q34348757 | ||
Proteasomal dysfunction in sporadic Parkinson's disease | Q34529359 | ||
Hassles with taking out the garbage: aggravating aggresomes. | Q34637179 | ||
Substrate recognition by the protein disulfide isomerases | Q34692501 | ||
How the ubiquitin-proteasome system controls transcription | Q35075758 | ||
Part II: alpha-synuclein and its molecular pathophysiological role in neurodegenerative disease. | Q35157623 | ||
The role of the ubiquitin/proteasome system in cellular responses to radiation | Q35208807 | ||
Ubiquitin-proteasome system and proteasome inhibition: new strategies in stroke therapy. | Q35760480 | ||
Autophagy, proteasomes, lipofuscin, and oxidative stress in the aging brain. | Q35869366 | ||
Roles of molecular chaperones in protein degradation | Q36236478 | ||
Gene expression profiling of sporadic Parkinson's disease substantia nigra pars compacta reveals impairment of ubiquitin-proteasome subunits, SKP1A, aldehyde dehydrogenase, and chaperone HSC-70. | Q36265331 | ||
Protein aggregation in the pathogenesis of familial and sporadic Parkinson's disease | Q36278180 | ||
Sequential assistance of molecular chaperones and transient formation of covalent complexes during protein degradation from the ER. | Q36323835 | ||
Expanding insights of mitochondrial dysfunction in Parkinson's disease. | Q36404133 | ||
Protein quality control: the who's who, the where's and therapeutic escapes | Q36432134 | ||
Protein misfolding disorders: pathogenesis and intervention | Q36501365 | ||
Mechanisms of disease II: cellular protein quality control. | Q36748835 | ||
Abnormal proteins can form aggresome in yeast: aggresome-targeting signals and components of the machinery | Q37072429 | ||
Proteomic identification of novel proteins associated with Lewy bodies | Q37146740 | ||
From hatching to dispatching: the multiple cellular roles of the Hsp70 molecular chaperone machinery | Q37292909 | ||
Ubiquitin-dependent and -independent mitochondrial protein quality controls: implications in ageing and neurodegenerative diseases | Q37329440 | ||
Think locally: control of ubiquitin-dependent protein degradation in neurons | Q37349687 | ||
Oxidative modifications, mitochondrial dysfunction, and impaired protein degradation in Parkinson's disease: how neurons are lost in the Bermuda triangle | Q37509229 | ||
Proteasome inhibitor induced gene expression profiles reveal overexpression of transcriptional regulators ATF3, GADD153 and MAD1. | Q38310990 | ||
Ubiquitin crosstalk connecting cellular processes | Q38702950 | ||
Mitochondria and ubiquitin-proteasomal system interplay: relevance to Parkinson's disease | Q39962524 | ||
Proteasome inhibition blocks caspase-8 degradation and sensitizes prostate cancer cells to death receptor-mediated apoptosis | Q40036325 | ||
Effects of proteasome inhibitor, MG132, on proteasome activity and oxidative status of rat liver | Q40128812 | ||
Small heat shock proteins protect against alpha-synuclein-induced toxicity and aggregation | Q40212840 | ||
Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stress | Q40262236 | ||
Alpha-synuclein activation of protein phosphatase 2A reduces tyrosine hydroxylase phosphorylation in dopaminergic cells | Q40395753 | ||
Identification of the ubiquitin-proteasome pathway in the regulation of the stability of eukaryotic elongation factor-2 kinase | Q40427685 | ||
Identification of the protein disulfide isomerase family member PDIp in experimental Parkinson's disease and Lewy body pathology | Q40518177 | ||
Simultaneous inhibition of hsp 90 and the proteasome promotes protein ubiquitination, causes endoplasmic reticulum-derived cytosolic vacuolization, and enhances antitumor activity. | Q40556399 | ||
Proteasome inhibition alters neural mitochondrial homeostasis and mitochondria turnover | Q40595923 | ||
Inhibition of proteasome activity induces concerted expression of proteasome genes and de novo formation of Mammalian proteasomes | Q40658264 | ||
Aggresomes protect cells by enhancing the degradation of toxic polyglutamine-containing protein | Q40662036 | ||
Regulation of translation elongation factor-2 by insulin via a rapamycin-sensitive signalling pathway | Q41064925 | ||
Neuropathology of Parkinson's disease | Q41095404 | ||
Expression of K6W-ubiquitin in lens epithelial cells leads to upregulation of a broad spectrum of molecular chaperones. | Q41822888 | ||
Histone carbonylation in vivo and in vitro | Q42244057 | ||
P4510 | describes a project that uses | ImageQuant | Q112270642 |
P304 | page(s) | 95 | |
P577 | publication date | 2010-08-12 | |
P1433 | published in | BMC Neuroscience | Q15766477 |
P1476 | title | Proteomic characterization of an isolated fraction of synthetic proteasome inhibitor (PSI)-induced inclusions in PC12 cells might offer clues to aggresomes as a cellular defensive response against proteasome inhibition by PSI. | |
P478 | volume | 11 |