Robert Feulgen Prize Lecture 1995. Electronic light microscopy: present capabilities and future prospects (Q36788166)

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scientific article published on August 1995

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English	Robert Feulgen Prize Lecture 1995. Electronic light microscopy: present capabilities and future prospects	scientific article published on August 1995

Statements

instance of

scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

8536077

retrieved

16 August 2017

review article

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Europe PubMed Central

title

Robert Feulgen Prize Lecture 1995. Electronic light microscopy: present capabilities and future prospects (English)

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stated in

Europe PubMed Central

PubMed publication ID

8536077

retrieved

16 August 2017

author

David Shotton

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8536077

retrieved

16 August 2017

publication date

1 August 1995

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stated in

Europe PubMed Central

PubMed publication ID

8536077

retrieved

16 August 2017

published in

Histochemistry and Cell Biology

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stated in

Europe PubMed Central

PubMed publication ID

8536077

retrieved

16 August 2017

volume

104

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stated in

Europe PubMed Central

PubMed publication ID

8536077

retrieved

16 August 2017

issue

2

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stated in

Europe PubMed Central

PubMed publication ID

8536077

retrieved

16 August 2017

page(s)

97-137

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Europe PubMed Central

PubMed publication ID

8536077

retrieved

16 August 2017

cites work

The point-spread function of a confocal microscope: its measurement and use in deconvolution of 3-D data

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Actions of cytochalasins on the organization of actin filaments and microtubules in a neuronal growth cone

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Tracking kinesin-driven movements with nanometre-scale precision

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PubMed

reference URL

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12 December 2020

based on heuristic

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Characterization of low-light-level cameras for digitized video microscopy.

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PubMed

reference URL

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12 December 2020

based on heuristic

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Monoclonal antibodies detect a spectrin-like protein in normal and dystrophic human skeletal muscle

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8536077

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12 December 2020

based on heuristic

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Two-photon laser scanning fluorescence microscopy

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8536077

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12 December 2020

based on heuristic

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Two-photon molecular excitation provides intrinsic 3-dimensional resolution for laser-based microscopy and microphotochemistry

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8536077

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Cytoskeletal reorganization underlying growth cone motility

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PubMed

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Movement of organelles along filaments dissociated from the axoplasm of the squid giant axon

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reference URL

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12 December 2020

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Direct observation of kinesin stepping by optical trapping interferometry

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Gliding movement of and bidirectional transport along single native microtubules from squid axoplasm: evidence for an active role of microtubules in cytoplasmic transport.

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The three-dimensional structure of human erythrocyte aquaporin CHIP

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Use of ferro-electric liquid crystal shutters for time-resolved fluorescence microscopy

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Automated detection and tracking of individual and clustered cell surface low density lipoprotein receptor molecules

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Five-parameter fluorescence imaging: wound healing of living Swiss 3T3 cells

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Simultaneous confocal recording of multiple fluorescent labels with improved channel separation.

1 reference

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Video image processing greatly enhances contrast, quality, and speed in polarization-based microscopy

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Three-dimensional optical microscopy using tilted views

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Different axoplasmic proteins generate movement in opposite directions along microtubules in vitro

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Nanovid tracking: a new automatic method for the study of mobility in living cells based on colloidal gold and video microscopy

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Dynamic instability of individual microtubules analyzed by video light microscopy: rate constants and transition frequencies

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Lateral diffusion and retrograde movements of individual cell surface components on single motile cells observed with Nanovid microscopy

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Video-enhanced light microscopy and its applications in cell biology.

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Lymphocyte locomotion in three-dimensional collagen gels. Comparison of three quantitative methods for analysing cell trajectories

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Viewing single microtubules by video light microscopy

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New Reflected-Light Microscope for Viewing Unstained Brain and Ganglion Cells

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The use of submicroscopic gold particles combined with video contrast enhancement as a simple molecular probe for the living cell

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Atomic force microscopy produces faithful high-resolution images of protein surfaces in an aqueous environment

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Dynamic behavior of the transferrin receptor followed in living epidermoid carcinoma (A431) cells with nanovid microscopy

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Multiple colors by fluorescence in situ hybridization using ratio-labelled DNA probes create a molecular karyotype

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The application of real-time confocal microscopy to the study of high-speed dental-bur-tooth-cutting interactions.

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New observations on cell architecture and dynamics by video-enhanced contrast optical microscopy

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Fluorescent analog cytochemistry of contractile proteins

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Image intensification applied to biological problems

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Video-enhanced microscopy with a computer frame memory

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A system for fluorescence metaphase finding and scoring of chromosomal translocations visualized by in situ hybridization

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A comparison of the detection sensitivity of lymphocyte membrane antigens using fluorescein and phosphor immunoconjugates

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Imaging in scanning microscopes with slit-shaped detectors.

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Fluorescence microscopy in three dimensions.

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Applicability of a noncooled video-rated CCD camera for detection of fluorescence in situ hybridization signals

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Organelle, bead, and microtubule translocations promoted by soluble factors from the squid giant axon

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Ultrastructural identification of type 1 fibres in human skeletal muscle

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Fluorescent analog cytochemistry: tracing functional protein components in living cells

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Direct observation of microtubule dynamics in living cells

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A unified approach to analysing cell motility.

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Multiple fluorescence in situ hybridization.

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High-resolution three-dimensional images from confocal scanning laser microscopy. Quantitative study and mathematical correction of the effects from bleaching and fluorescence attenuation in depth.

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Single myosin molecule mechanics: piconewton forces and nanometre steps

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Actin-dependent organelle movement in squid axoplasm

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Fluorescence ratio measurements of double-labeled probes for multiple in situ hybridization by digital imaging microscopy

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Image intensification techniques for detection of proteins in cultured cells

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Fluorescence ratio imaging microscopy

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Three-dimensional architecture of a polytene nucleus

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Real-time observations of microtubule dynamic instability in living cells

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Optical sectioning microscopy: cellular architecture in three dimensions

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Lateral Movements of Membrane Glycoproteins Restricted by Dynamic Cytoplasmic Barriers

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In vivo confocal imaging: general principles and applications

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Spatial organization of the Drosophila nucleus: a three-dimensional cytogenetic study

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Confocal scanning microscopy: three-dimensional biological imaging

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Three-color fluorescence in situ hybridization for the simultaneous detection of multiple nucleic acid sequences

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Identification of a novel force-generating protein, kinesin, involved in microtubule-based motility

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Quantification of fluorescence in situ hybridization signals by image cytometry

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Single microtubules from squid axoplasm support bidirectional movement of organelles

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Multiple spectral parameter imaging

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Direct observation of brownian motion of lipids in a membrane

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Fast axonal transport in squid giant axon

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Identifiers

DOI

10.1007/BF01451571

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8536077

retrieved

16 August 2017

PubMed publication ID

8536077

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8536077

retrieved

16 August 2017

 

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