| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.3390/IJMS16036076 |
| P8608 | Fatcat ID | release_bqt5u4a2vvdpfe3j2v4oo67xwy |
| P932 | PMC publication ID | 4394520 |
| P698 | PubMed publication ID | 25785563 |
| P5875 | ResearchGate publication ID | 273951481 |
| P50 | author | Kazuhiro Nagata | Q11550232 |
| Masataka Kinjo | Q55763114 | ||
| Akira Kitamura | Q48061805 | ||
| P2860 | cites work | Application of the fluorescence resonance energy transfer method for studying the dynamics of caspase-3 activation during UV-induced apoptosis in living HeLa cells | Q73886949 |
| Polyglutamine protein aggregates are dynamic | Q78315034 | ||
| HDAC6 and microtubules are required for autophagic degradation of aggregated huntingtin | Q24337155 | ||
| RNA sequence- and shape-dependent recognition by proteins in the ribonucleoprotein particle | Q24537188 | ||
| Structure-guided evolution of cyan fluorescent proteins towards a quantum yield of 93%. | Q24606976 | ||
| Prions, protein homeostasis, and phenotypic diversity | Q24610666 | ||
| Misfolded proteins partition between two distinct quality control compartments | Q24651093 | ||
| RNA granules | Q24683783 | ||
| Protein folding and quality control in the ER | Q26823157 | ||
| HDAC6 as a target for neurodegenerative diseases: what makes it different from the other HDACs? | Q27015801 | ||
| Ligand binding and aggregation of pathogenic SOD1 | Q27677527 | ||
| The 1.6 Å resolution structure of a FRET-optimized Cerulean fluorescent protein | Q27677934 | ||
| A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. | Q27860836 | ||
| Spreading of pathology in neurodegenerative diseases: a focus on human studies | Q28082279 | ||
| Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis | Q28131672 | ||
| Protein misfolding, functional amyloid, and human disease | Q28131732 | ||
| Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis | Q28131805 | ||
| Adapting proteostasis for disease intervention | Q28131818 | ||
| Protein aggregation and neurodegenerative disease | Q28273600 | ||
| Proteasomes activate aggresome disassembly and clearance by producing unanchored ubiquitin chains | Q28298487 | ||
| Molecular chaperones in protein folding and proteostasis | Q29547715 | ||
| Proteotoxic stress and inducible chaperone networks in neurodegenerative disease and aging | Q29614783 | ||
| Aggresomes, inclusion bodies and protein aggregation | Q29615253 | ||
| Rapid caspase-3 activation during apoptosis revealed using fluorescence-resonance energy transfer | Q30475824 | ||
| A novel fluorescent sensor protein for visualization of redox states in the cytoplasm and in peroxisomes. | Q30495884 | ||
| Spatial sequestration of misfolded proteins by a dynamic chaperone pathway enhances cellular fitness during stress | Q30585884 | ||
| Chaperonin TRiC promotes the assembly of polyQ expansion proteins into nontoxic oligomers. | Q50715387 | ||
| Direct detection of caspase-3 activation in single live cells by cross-correlation analysis. | Q50784503 | ||
| Cytosolic chaperonin prevents polyglutamine toxicity with altering the aggregation state. | Q52573641 | ||
| The interaction of Hsp104 with yeast prion Sup35 as analyzed by fluorescence cross-correlation spectroscopy. | Q54624492 | ||
| Studying protein dynamics in living cells | Q30674118 | ||
| Expanded dynamic range of fluorescent indicators for Ca(2+) by circularly permuted yellow fluorescent proteins. | Q30769723 | ||
| Fluorescence cross-correlation spectroscopy in living cells | Q33232364 | ||
| Sensitivity of CFP/YFP and GFP/mCherry pairs to donor photobleaching on FRET determination by fluorescence lifetime imaging microscopy in living cells | Q33255796 | ||
| Dimerization, oligomerization, and aggregation of human amyotrophic lateral sclerosis copper/zinc superoxide dismutase 1 protein mutant forms in live cells | Q33652243 | ||
| The chaperonin TRiC controls polyglutamine aggregation and toxicity through subunit-specific interactions | Q33693921 | ||
| Quantitative study of synthetic Hox transcription factor-DNA interactions in live cells | Q33732788 | ||
| Organismal proteostasis: role of cell-nonautonomous regulation and transcellular chaperone signaling | Q33917420 | ||
| Quantitative in vivo fluorescence cross-correlation analyses highlight the importance of competitive effects in the regulation of protein-protein interactions | Q34056400 | ||
| Protein aggregation and pathogenesis of Huntington's disease: mechanisms and correlations | Q34081469 | ||
| Amyloid structure: conformational diversity and consequences | Q34175001 | ||
| An orange fluorescent protein with a large Stokes shift for single-excitation multicolor FCCS and FRET imaging | Q34225444 | ||
| Dysregulation of the proteasome increases the toxicity of ALS-linked mutant SOD1. | Q34391529 | ||
| How the nucleus copes with proteotoxic stress | Q34391566 | ||
| Misfolded proteins impose a dosage-dependent fitness cost and trigger a cytosolic unfolded protein response in yeast | Q34490441 | ||
| Imaging spatiotemporal dynamics of neuronal signaling using fluorescence resonance energy transfer and fluorescence lifetime imaging microscopy | Q34565908 | ||
| Determination of dissociation constant of the NFκB p50/p65 heterodimer using fluorescence cross-correlation spectroscopy in the living cell | Q34764549 | ||
| Retarded PDI diffusion and a reductive shift in poise of the calcium depleted endoplasmic reticulum | Q35047388 | ||
| Long-distance integration of nuclear ERK signaling triggered by activation of a few dendritic spines | Q35053685 | ||
| Visualization of the spatial and temporal dynamics of intracellular signaling | Q35085294 | ||
| Hsp70 and hsp40 chaperones can inhibit self-assembly of polyglutamine proteins into amyloid-like fibrils | Q35169533 | ||
| The ubiquitin proteasome system in neurodegenerative diseases: sometimes the chicken, sometimes the egg. | Q35558459 | ||
| Compartmentalization of superoxide dismutase 1 (SOD1G93A) aggregates determines their toxicity | Q36300695 | ||
| Structural properties and neuronal toxicity of amyotrophic lateral sclerosis-associated Cu/Zn superoxide dismutase 1 aggregates. | Q36320449 | ||
| Fluorescence as a method to reveal structures and membrane-interactions of amyloidogenic proteins | Q36817510 | ||
| Prefoldin protects neuronal cells from polyglutamine toxicity by preventing aggregation formation | Q37000637 | ||
| Red fluorescent proteins: chromophore formation and cellular applications | Q37079629 | ||
| Highly sensitive and quantitative FRET-FLIM imaging in single dendritic spines using improved non-radiative YFP | Q37170554 | ||
| Quantitative comparison of different fluorescent protein couples for fast FRET-FLIM acquisition. | Q37392567 | ||
| Fluorescent protein-based redox probes | Q37678406 | ||
| Amyloid oligomers: dynamics and toxicity in the cytosol and nucleus | Q37690821 | ||
| Nucleolar aggresomes as counterparts of cytoplasmic aggresomes in proteotoxic stress. Proteasome inhibitors induce nuclear ribonucleoprotein inclusions that accumulate several key factors of neurodegenerative diseases and cancer | Q37855730 | ||
| Quality control of mitochondrial proteostasis | Q37882863 | ||
| Proteostasis in endoplasmic reticulum--new mechanisms in kidney disease | Q38206090 | ||
| Histone deacetylases and their inhibitors in cancer, neurological diseases and immune disorders | Q38240733 | ||
| Control of systemic proteostasis by the nervous system. | Q38244932 | ||
| Lost after translation: missorting of Tau protein and consequences for Alzheimer disease | Q38249863 | ||
| Failure of ubiquitin proteasome system: risk for neurodegenerative diseases | Q38270078 | ||
| Minimum set of mutations needed to optimize cyan fluorescent proteins for live cell imaging. | Q39236322 | ||
| Mutant SOD1 detoxification mechanisms in intact single cells | Q40054229 | ||
| Soluble polyglutamine oligomers formed prior to inclusion body formation are cytotoxic | Q40065738 | ||
| Cellular toxicity of polyglutamine expansion proteins: mechanism of transcription factor deactivation | Q40540661 | ||
| Monitoring protein conformations and interactions by fluorescence resonance energy transfer between mutants of green fluorescent protein | Q40846791 | ||
| Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias | Q41269608 | ||
| Genetically encoded probes for measurement of intracellular calcium | Q41964161 | ||
| Endoplasmic reticulum Ca2+ increases enhance mutant glucocerebrosidase proteostasis. | Q41976836 | ||
| Oxygen-induced maturation of SOD1: a key role for disulfide formation by the copper chaperone CCS. | Q41987289 | ||
| Architecture of polyglutamine-containing fibrils from time-resolved fluorescence decay | Q42141160 | ||
| Peroxisomal proteostasis involves a Lon family protein that functions as protease and chaperone. | Q42322296 | ||
| Complementary methods for studies of protein interactions in living cells | Q42380047 | ||
| Intact protein folding in the glutathione-depleted endoplasmic reticulum implicates alternative protein thiol reductants | Q42746408 | ||
| Spatio-temporal activation of caspase revealed by indicator that is insensitive to environmental effects | Q42916419 | ||
| Binding modes of thioflavin-T to the single-layer beta-sheet of the peptide self-assembly mimics | Q43267891 | ||
| Single-cell fluorescence resonance energy transfer analysis demonstrates that caspase activation during apoptosis is a rapid process. Role of caspase-3. | Q43966285 | ||
| An ultramarine fluorescent protein with increased photostability and pH insensitivity | Q45021033 | ||
| Amyotrophic lateral sclerosis mutations have the greatest destabilizing effect on the apo- and reduced form of SOD1, leading to unfolding and oxidative aggregation. | Q45251257 | ||
| Detection of polyglutamine protein oligomers in cells by fluorescence correlation spectroscopy | Q45305431 | ||
| Firefly luciferase mutants as sensors of proteome stress | Q45362617 | ||
| Huntingtin and mutant SOD1 form aggregate structures with distinct molecular properties in human cells | Q46863333 | ||
| A high-throughput method for development of FRET-based indicators for proteolysis | Q47441149 | ||
| An intersubunit disulfide bond prevents in vitro aggregation of a superoxide dismutase-1 mutant linked to familial amytrophic lateral sclerosis | Q47700139 | ||
| Redox sensor proteins for highly sensitive direct imaging of intracellular redox state | Q50218475 | ||
| P275 | copyright license | Creative Commons Attribution | Q6905323 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Förster resonance energy transfer | Q367473 |
| protein aggregation | Q7251455 | ||
| protein | Q8054 | ||
| P304 | page(s) | 6076-92 | |
| P577 | publication date | 2015-03-16 | |
| P1433 | published in | International Journal of Molecular Sciences | Q3153277 |
| P1476 | title | Conformational analysis of misfolded protein aggregation by FRET and live-cell imaging techniques | |
| P478 | volume | 16 |
| Q48359218 | AgHalo: A Facile Fluorogenic Sensor to Detect Drug-Induced Proteome Stress |
| Q48061730 | Different aggregation states of a nuclear localization signal-tagged 25-kDa C-terminal fragment of TAR RNA/DNA-binding protein 43 kDa |
| Q36204164 | Longitudinal reference ranges for maternal plasma laeverin, and its role as a potential biomarker of preeclampsia |
| Q62129243 | Modulation of Fluorescent Protein Chromophores To Detect Protein Aggregation with Turn-On Fluorescence |
| Q55287168 | State-of-the-Art Fluorescence Fluctuation-Based Spectroscopic Techniques for the Study of Protein Aggregation. |
| Q48260487 | Stoichiometric analysis of oligomeric states of three class-A GPCRs, chemokine-CXCR4, dopamine-D2, and prostaglandin-EP1 receptors, on living cells |
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