Characterization of one- and two-photon excitation fluorescence resonance energy transfer microscopy.
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Endocytosis of apolipoprotein A-V by members of the low density lipoprotein receptor and the VPS10p domain receptor familiesFluorescence resonance energy transfer (FRET) microscopy imaging of live cell protein localizationsIntravital microscopy: a practical guide on imaging intracellular structures in live animalsDevelopmentally regulated GTP-binding protein 2 coordinates Rab5 activity and transferrin recycling.Parallelized TCSPC for dynamic intravital fluorescence lifetime imaging: quantifying neuronal dysfunction in neuroinflammationThree-color confocal Förster (or fluorescence) resonance energy transfer microscopy: Quantitative analysis of protein interactions in the nucleation of actin filaments in live cells.Confocal FRET microscopy to measure clustering of ligand-receptor complexes in endocytic membranes.Studying Nuclear Receptor Complexes in the Cellular Environment.Automated selection of regions of interest for intensity-based FRET analysis of transferrin endocytic trafficking in normal vs. cancer cellsIQGAP1 interactome analysis by in vitro reconstitution and live cell 3-color FRET microscopy.Förster resonance energy transfer microscopy and spectroscopy for localizing protein-protein interactions in living cells.Transmembrane domain IV of the Gallus gallus VT2 vasotocin receptor is essential for forming a heterodimer with the corticotrophin releasing hormone receptorNon-invasive in vivo imaging of near infrared-labeled transferrin in breast cancer cells and tumors using fluorescence lifetime FRET.Myosin-Va-dependent cell-to-cell transfer of RNA from Schwann cells to axons.Three-Color FRET expands the ability to quantify the interactions of several proteins involved in actin filament nucleation.FRET microscopy in 2010: the legacy of Theodor Förster on the 100th anniversary of his birthFörster resonance energy transfer as a tool to study photoreceptor biologyThree-color spectral FRET microscopy localizes three interacting proteins in living cellsImaging molecular interactions in living cells.Characterization of spectral FRET imaging microscopy for monitoring nuclear protein interactions.Quantitative imaging of protein interactions in the cell nucleus.Pdx1 and BETA2/NeuroD1 participate in a transcriptional complex that mediates short-range DNA looping at the insulin gene.Receptor complexes cotransported via polarized endocytic pathways form clusters with distinct organizations.Energy migration alters the fluorescence lifetime of Cerulean: implications for fluorescence lifetime imaging Forster resonance energy transfer measurementsProtein interaction quantified in vivo by spectrally resolved fluorescence resonance energy transferA white light confocal microscope for spectrally resolved multidimensional imaging.Intravital two-photon microscopy: focus on speed and time resolved imaging modalities.Exploiting the superior protein resistance of polymer brushes to control single cell adhesion and polarisation at the micron scale.GABA transporter function, oligomerization state, and anchoring: correlates with subcellularly resolved FRETOne-photon scattering by an atomic chain in a two-mode resonator: cyclic conditions.Fluorescent fusion proteins of soluble guanylyl cyclase indicate proximity of the heme nitric oxide domain and catalytic domain.A Bayesian method for inferring quantitative information from FRET data.Dual-color fluorescence lifetime correlation spectroscopy to quantify protein-protein interactions in live cell.GPR54 (KISS1R) transactivates EGFR to promote breast cancer cell invasiveness.Recent advances in dynamic intravital multi-photon microscopy.The fluorescent protein palette: tools for cellular imaging.On the analyses of fluorescence depolarisation data in the presence of electronic energy migration. Part I: Theory and general description.On the analyses of fluorescence depolarisation data in the presence of electronic energy migration. Part II: Applying and evaluating two-photon excited fluorescence.Photobleaching-corrected FRET efficiency imaging of live cells.Heme oxygenase isoforms differ in their subcellular trafficking during hypoxia and are differentially modulated by cytochrome P450 reductase.
P2860
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P2860
Characterization of one- and two-photon excitation fluorescence resonance energy transfer microscopy.
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
name
Characterization of one- and t ...... ce energy transfer microscopy.
@ast
Characterization of one- and t ...... ce energy transfer microscopy.
@en
type
label
Characterization of one- and t ...... ce energy transfer microscopy.
@ast
Characterization of one- and t ...... ce energy transfer microscopy.
@en
prefLabel
Characterization of one- and t ...... ce energy transfer microscopy.
@ast
Characterization of one- and t ...... ce energy transfer microscopy.
@en
P2093
P1433
P1476
Characterization of one- and t ...... ce energy transfer microscopy.
@en
P2093
Ammasi Periasamy
Horst Wallrabe
Masilamani Elangovan
Richard N Day
P356
10.1016/S1046-2023(02)00283-9
P577
2003-01-01T00:00:00Z