Breaking the diffraction barrier in fluorescence microscopy at low light intensities by using reversibly photoswitchable proteins. - Wikidata - wikimedia - TriplyDB

Breaking the diffraction barrier in fluorescence microscopy at low light intensities by using reversibly photoswitchable proteins.

Breaking the diffraction barrier in fluorescence microscopy at low light intensities by using reversibly photoswitchable proteins.

http://www.wikidata.org/entity/Q33228029

about

Multi-photon excitation microscopy Multicolor fluorescence nanoscopy in fixed and living cells by exciting conventional fluorophores with a single wavelength Super-resolution fluorescence microscopy Fluorescence microscopy below the diffraction limit Ultra-high resolution imaging by fluorescence photoactivation localization microscopy rsEGFP2 enables fast RESOLFT nanoscopy of living cells Focusing super resolution on the cytoskeleton Twinkle, twinkle little star: photoswitchable fluorophores for super-resolution imaging Photocontrollable fluorescent proteins for superresolution imaging Photoswitchable fluorescent proteins: ten years of colorful chemistry and exciting applications Nano-scale measurement of biomolecules by optical microscopy and semiconductor nanoparticles Super-resolution imaging strategies for cell biologists using a spinning disk microscope Insulin regulates Glut4 confinement in plasma membrane clusters in adipose cells Highly photostable, reversibly photoswitchable fluorescent protein with high contrast ratio for live-cell superresolution microscopy STED nanoscopy with time-gated detection: theoretical and experimental aspects Chromophore protonation state controls photoswitching of the fluoroprotein asFP595 Breaking the Diffraction Barrier in Fluorescence Microscopy by Optical Shelving Structural basis for reversible photobleaching of a green fluorescent protein homologue.Structural characterization of IrisFP, an optical highlighter undergoing multiple photo-induced transformations A reversibly photoswitchable GFP-like protein with fluorescence excitation decoupled from switching A Structural Basis for Reversible Photoswitching of Absorbance Spectra in Red Fluorescent Protein rsTagRFP Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM)Applications of phototransformable fluorescent proteins for tracking the dynamics of cellular components STED nanoscopy: a glimpse into the future Axial resolution enhancement by 4Pi confocal fluorescence microscopy with two-photon excitation RESOLFT Nanoscopy of Fixed Cells Using a Z-Domain Based Fusion Protein for Labelling Achieving λ/10 resolution CW STED nanoscopy with a Ti:Sapphire oscillator Light microscopy: an ongoing contemporary revolution Stimulated emission depletion (STED) nanoscopy of a fluorescent protein-labeled organelle inside a living cell.Diverse protocols for correlative super-resolution fluorescence imaging and electron microscopy of chemically fixed samples.Photoswitchable non-fluorescent thermochromic dye-nanoparticle hybrid probes.Reversibly switchable fluorescence microscopy with enhanced resolution and image contrast.Directed molecular evolution to design advanced red fluorescent proteins Single cell optical imaging and spectroscopy.Two-photon excitation and photoconversion of EosFP in dual-color 4Pi confocal microscopy Differential evanescence nanometry: live-cell fluorescence measurements with 10-nm axial resolution on the plasma membrane Investigating intracellular dynamics of FtsZ cytoskeleton with photoactivation single-molecule tracking Advances in light microscopy for neuroscience.Rational design, synthesis, and characterization of highly fluorescent optical switches for high-contrast optical lock-in detection (OLID) imaging microscopy in living cells.Nonlinear structured-illumination microscopy with a photoswitchable protein reveals cellular structures at 50-nm resolution.

P2860

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P2860

Breaking the diffraction barrier in fluorescence microscopy at low light intensities by using reversibly photoswitchable proteins.

http://www.wikidata.org/entity/Q33228029

description

2005 nî lūn-bûn

@nan

2005 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2005年の論文

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2005年論文

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2005年論文

@zh-hant

2005年論文

@zh-hk

2005年論文

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2005年論文

@zh-tw

2005年论文

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name

Breaking the diffraction barri ...... ibly photoswitchable proteins.

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Breaking the diffraction barri ...... ibly photoswitchable proteins.

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type

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Breaking the diffraction barri ...... ibly photoswitchable proteins.

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Breaking the diffraction barri ...... ibly photoswitchable proteins.

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Breaking the diffraction barri ...... ibly photoswitchable proteins.

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Breaking the diffraction barri ...... ibly photoswitchable proteins.

@en

P1433

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PNAS.0506010102

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Breaking the diffraction barri ...... ibly photoswitchable proteins.

@en

P2093

Michael Hofmann

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P2860

Photostability of a fluorescent marker under pulsed excited-state depletion through stimulated emission

Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy

Fluorescence microscopy with diffraction resolution barrier broken by stimulated emission

Structure and mechanism of the reversible photoswitch of a fluorescent protein.

Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy.

True optical resolution beyond the Rayleigh limit achieved by standing wave illumination.

Synthesis and properties of the chromophore of the asFP595 chromoprotein from Anemonia sulcata.

Molecular photobleaching kinetics of Rhodamine 6G by one- and two-photon induced confocal fluorescence microscopy.

Reversible single-molecule photoswitching in the GFP-like fluorescent protein Dronpa

Reversible molecular photoswitches: a key technology for nanoscience and fluorescence imaging.

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17565-17569

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scholarly article

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10.1073/PNAS.0506010102

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49

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102

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Christian Eggeling

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