Measuring and interpreting point spread functions to determine confocal microscope resolution and ensure quality control. - Wikidata - wikimedia - TriplyDB

Measuring and interpreting point spread functions to determine confocal microscope resolution and ensure quality control.

Measuring and interpreting point spread functions to determine confocal microscope resolution and ensure quality control.

http://www.wikidata.org/entity/Q34074267

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A high performance, cost-effective, open-source microscope for scanning two-photon microscopy that is modular and readily adaptable In vivo subcellular resolution optical imaging in the lung reveals early metastatic proliferation and motility Diffusive Promotion by Velocity Gradient of Cytoplasmic Streaming (CPS) in Nitella Internodal Cells Advanced light microscopy core facilities: Balancing service, science and career Dimensional metrology of lab-on-a-chip internal structures: a comparison of optical coherence tomography with confocal fluorescence microscopy Survey statistics of automated segmentations applied to optical imaging of mammalian cells.Fluorescence microscopy gets faster and clearer: roles of photochemistry and selective illumination Any Way You Slice It-A Comparison of Confocal Microscopy Techniques.Fluorescence fluctuation approaches to the study of adhesion and signaling Improving spinning disk confocal microscopy by preventing pinhole cross-talk for intravital imaging.Fabrication and operation of GRIN probes for in vivo fluorescence cellular imaging of internal organs in small animals Optical imaging. Expansion microscopy.Localized nuclear and perinuclear Ca(2+) signals in intact mouse skeletal muscle fibers.Investigation of the Viability, Adhesion, and Migration of Human Fibroblasts in a Hyaluronic Acid/Gelatin Microgel-Reinforced Composite Hydrogel for Vocal Fold Tissue Regeneration.3D structure tensor analysis of light microscopy data for validating diffusion MRI.Epi-fluorescence microscopy Fluorescence correlation spectroscopy analysis of serotonin, adrenergic, muscarinic, and dopamine receptor dimerization: the oligomer number puzzle Unraveling the Thousand Word Picture: An Introduction to Super-Resolution Data Analysis.Migration and vascular lumen formation of endothelial cells in cancer cell spheroids of various sizes.Quality control protocol for confocal systems.Confocal microscopy for astrocyte in vivo imaging: Recycle and reuse in microscopy Phase-retrieved pupil function and coherent transfer function in confocal microscopy.The Gray Institute 'open' high-content, fluorescence lifetime microscopes.International test results for objective lens quality, resolution, spectral accuracy and spectral separation for confocal laser scanning microscopes.ConfocalCheck--a software tool for the automated monitoring of confocal microscope performance.Development and experimental testing of an optical micro-spectroscopic technique incorporating true line-scan excitation.Impact of immersion oils and mounting media on the confocal imaging of dendritic spines.Direct imaging of phase objects enables conventional deconvolution in bright field light microscopy.Calibration of wide-field deconvolution microscopy for quantitative fluorescence imaging.A multi-axis confocal rheoscope for studying shear flow of structured fluids.On the role of the gap junction protein Cx43 (GJA1) in human cardiac malformations with Fallot-pathology. a study on paediatric cardiac specimen.An improved procedure for subcellular spatial alignment during live-cell CLEM Native serotonin 5-HT2C receptors are expressed as homodimers on the apical surface of choroid plexus epithelial cells Quantitative high dynamic range beam profiling for fluorescence microscopy.High numerical aperture Fourier ptychography: principle, implementation and characterization.Superresolution live imaging of plant cells using structured illumination microscopy.Fluorescent Microspheres as Point Sources: A Localization Study.Imaging fluorescence (cross-) correlation spectroscopy in live cells and organisms.Motion-free endoscopic system for brain imaging at variable focal depth using liquid crystal lenses.Comparison of the structure, function and autophagic maintenance of mitochondria in nigrostriatal and tuberoinfundibular dopamine neurons.

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P2860

Measuring and interpreting point spread functions to determine confocal microscope resolution and ensure quality control.

http://www.wikidata.org/entity/Q34074267

description

2011 nî lūn-bûn

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2011 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Measuring and interpreting poi ...... on and ensure quality control.

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Measuring and interpreting poi ...... on and ensure quality control.

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Measuring and interpreting poi ...... on and ensure quality control.

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Measuring and interpreting poi ...... on and ensure quality control.

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Measuring and interpreting poi ...... on and ensure quality control.

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Nature Protocols

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Measuring and interpreting poi ...... on and ensure quality control.

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P2093

Richard W Cole

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Tushare Jinadasa

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P2860

Fluctuation correlation spectroscopy with a laser-scanning microscope: exploiting the hidden time structure.

Raster image correlation spectroscopy (RICS) for measuring fast protein dynamics and concentrations with a commercial laser scanning confocal microscope.

Paxillin dynamics measured during adhesion assembly and disassembly by correlation spectroscopy.

Measuring fast dynamics in solutions and cells with a laser scanning microscope

Experimental test of an analytical model of aberration in an oil-immersion objective lens used in three-dimensional light microscopy.

Determination of three-dimensional imaging properties of a light microscope system. Partial confocal behavior in epifluorescence microscopy.

Live cell imaging using wide-field microscopy and deconvolution.

Evaluating optical aberration using fluorescent microspheres: methods, analysis, and corrective actions.

Light-emitting diodes are better illumination sources for biological microscopy than conventional sources.

Spatial mapping of integrin interactions and dynamics during cell migration by image correlation microscopy.

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1929-1941

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10.1038/NPROT.2011.407

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12

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6

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2011-11-10T00:00:00Z

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51797897

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1045004690

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22082987

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quality control