scholarly article | Q13442814 |
P819 | ADS bibcode | 2018NatCo...9.1738L |
P356 | DOI | 10.1038/S41467-018-04117-8 |
P932 | PMC publication ID | 5928105 |
P698 | PubMed publication ID | 29712894 |
P50 | author | Vadim Arshavsky | Q59675789 |
Mikael Klingeborn | Q59687016 | ||
Ekaterina S. Lobanova | Q79115801 | ||
P2093 | author name string | Jing Li | |
Raymond J Deshaies | |||
Stella Finkelstein | |||
Nikolai P Skiba | |||
Ying Hao | |||
Amanda M Travis | |||
P2860 | cites work | Increased proteasome activity in human embryonic stem cells is regulated by PSMD11 | Q24298544 |
Proteasome assembly | Q28245575 | ||
Iron homeostasis and toxicity in retinal degeneration | Q28252419 | ||
Ubiquitin-independent proteasomal degradation | Q28290917 | ||
Transducin gamma-subunit sets expression levels of alpha- and beta-subunits and is crucial for rod viability | Q28508147 | ||
Massive light-driven translocation of transducin between the two major compartments of rod cells: a novel mechanism of light adaptation | Q28577839 | ||
Retinitis pigmentosa | Q29616538 | ||
Enhancement of proteasome activity by a small-molecule inhibitor of USP14 | Q29616735 | ||
Mechanistic basis for the failure of cone transducin to translocate: why cones are never blinded by light | Q33904030 | ||
PA28αβ: the enigmatic magic ring of the proteasome? | Q33912635 | ||
The ubiquitin-proteasome system in neurodegenerative diseases: precipitating factor, yet part of the solution | Q33980214 | ||
Properties of the hybrid form of the 26S proteasome containing both 19S and PA28 complexes. | Q34088438 | ||
The ATP-binding cassette transporter ABCA4: structural and functional properties and role in retinal disease | Q34092691 | ||
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa | Q34168407 | ||
Beyond counting photons: trials and trends in vertebrate visual transduction | Q34465227 | ||
Enhancement of proteasome function by PA28α overexpression protects against oxidative stress. | Q34592321 | ||
Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations | Q34695879 | ||
Enhancement of proteasomal function protects against cardiac proteinopathy and ischemia/reperfusion injury in mice | Q35187068 | ||
Membrane attachment is key to protecting transducin GTPase-activating complex from intracellular proteolysis in photoreceptors | Q35513856 | ||
General pathophysiology in retinal degeneration | Q35515194 | ||
Short-lived green fluorescent proteins for quantifying ubiquitin/proteasome-dependent proteolysis in living cells | Q61788079 | ||
Dissecting the dark-adapted electroretinogram | Q73109716 | ||
Characterization of recombinant REGalpha, REGbeta, and REGgamma proteasome activators | Q73770368 | ||
Monitoring activity and inhibition of 26S proteasomes with fluorogenic peptide substrates | Q81453964 | ||
Spatial arrangement and functional role of α subunits of proteasome activator PA28 in hetero-oligomeric form | Q86045061 | ||
cAMP-induced phosphorylation of 26S proteasomes on Rpn6/PSMD11 enhances their activity and the degradation of misfolded proteins. | Q36435295 | ||
Subcellular distribution and dynamics of active proteasome complexes unraveled by a workflow combining in vivo complex cross-linking and quantitative proteomics. | Q36666357 | ||
Proteasome overload is a common stress factor in multiple forms of inherited retinal degeneration | Q36932207 | ||
Mechanistic insights into Bardet-Biedl syndrome, a model ciliopathy | Q37111349 | ||
Protein sorting, targeting and trafficking in photoreceptor cells | Q37138123 | ||
Review: retinal degeneration: focus on the unfolded protein response. | Q37195781 | ||
Dry age-related macular degeneration: mechanisms, therapeutic targets, and imaging | Q37395303 | ||
Rescue of mutant rhodopsin traffic by metformin-induced AMPK activation accelerates photoreceptor degeneration | Q37701985 | ||
Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators | Q37726645 | ||
Loss of daylight vision in retinal degeneration: are oxidative stress and metabolic dysregulation to blame? | Q37954832 | ||
Structural biology of the proteasome | Q38081952 | ||
The proteasome: from basic mechanisms to emerging roles | Q38096863 | ||
Tuning the proteasome to brighten the end of the journey | Q38559265 | ||
Mammalian proteasome subtypes: Their diversity in structure and function | Q38685306 | ||
Degradation of oxidized proteins by the proteasome: Distinguishing between the 20S, 26S, and immunoproteasome proteolytic pathways. | Q38828129 | ||
A challenge to the striking genotypic heterogeneity of retinitis pigmentosa: a better understanding of the pathophysiology using the newest genetic strategies | Q38937867 | ||
Proteome complexity and the forces that drive proteome imbalance. | Q38954697 | ||
Label-free quantitative proteomics reveals the dynamics of proteasome complexes composition and stoichiometry in a wide range of human cell lines. | Q38997541 | ||
A proteomic atlas of insulin signalling reveals tissue-specific mechanisms of longevity assurance. | Q41676470 | ||
Phosducin regulates transmission at the photoreceptor-to-ON-bipolar cell synapse. | Q42153063 | ||
Decreased proteasomal activity causes photoreceptor degeneration in mice | Q42757671 | ||
Capzimin is a potent and specific inhibitor of proteasome isopeptidase Rpn11. | Q42791381 | ||
Robust Endoplasmic Reticulum-Associated Degradation of Rhodopsin Precedes Retinal Degeneration. | Q43214685 | ||
A transgenic mouse model of the ubiquitin/proteasome system | Q44519483 | ||
Phosducin facilitates light-driven transducin translocation in rod photoreceptors. Evidence from the phosducin knockout mouse | Q44770010 | ||
Tissue-specific and developmental regulation of rod opsin chimeric genes in transgenic mice | Q45967554 | ||
The Mammalian Proteasome Activator PA28 Forms an Asymmetric α4β3 Complex | Q46312642 | ||
Dopamine-dependent sensitization of rod bipolar cells by GABA is conveyed through wide-field amacrine cells. | Q46443740 | ||
Preparation of hybrid (19S-20S-PA28) proteasome complexes and analysis of peptides generated during protein degradation | Q46794658 | ||
Characterization of the proteasome using native gel electrophoresis | Q46794661 | ||
RPN-6 determines C. elegans longevity under proteotoxic stress conditions | Q46942610 | ||
The role of the ER stress-response protein PERK in rhodopsin retinitis pigmentosa | Q47647015 | ||
Proteasomes. A molecular census of 26S proteasomes in intact neurons | Q48364209 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | photoreceptor protein | Q7187894 |
P304 | page(s) | 1738 | |
P577 | publication date | 2018-04-30 | |
P1433 | published in | Nature Communications | Q573880 |
P1476 | title | Increased proteasomal activity supports photoreceptor survival in inherited retinal degeneration | |
P478 | volume | 9 |