Results 11 to 20 of about 768,563 (305)

Improved-throughput traction microscopy based on fluorescence micropattern for manual microscopy. [PDF]

open access: yesPLoS ONE, 2013
Traction force microscopy (TFM) is a quantitative technique for measuring cellular traction force, which is important in understanding cellular mechanotransduction processes.
Kai Liu   +6 more
doaj   +1 more source

Advanced Fluorescence Microscopy Techniques-FRAP, FLIP, FLAP, FRET and FLIM [PDF]

open access: yes, 2012
Fluorescence microscopy provides an efficient and unique approach to study fixed and living cells because of its versatility, specificity, and high sensitivity.
Ankerhold, Richard   +5 more
core   +1 more source

Can a Proper T-Cell Development Occur in an Altered Thymic Epithelium? Lessons From EphB-Deficient Thymi

open access: yesFrontiers in Endocrinology, 2018
For a long time, the effects of distinct Eph tyrosine kinase receptors and their ligands, ephrins on the structure, immunophenotype, and development of thymus and their main cell components, thymocytes (T) and thymic epithelial cells (TECs), have been ...
Juan José Muñoz   +6 more
doaj   +1 more source

Evaluating performance in three-dimensional fluorescence microscopy [PDF]

open access: yes, 2007
In biological fluorescence microscopy, image contrast is often degraded by a high background arising from out of focus regions of the specimen. This background can be greatly reduced or eliminated by several modes of thick specimen microscopy, including ...
JOHN M. MURRAY   +7 more
core   +1 more source

Multiple airy beams light-sheet fluorescence microscopy

open access: yesFrontiers in Physics, 2022
Light-sheet fluorescence microscopy (LSFM) is a kind of volumetric imaging methodology suited for long term living specimens at high temporal-spatial resolution.
Shuangyu Gu   +9 more
doaj   +1 more source

Bleaching‐Resistant Super‐Resolution Fluorescence Microscopy

open access: yesAdvanced Science, 2022
Photobleaching is the permanent loss of fluorescence after extended exposure to light and is a major limiting factor in super‐resolution microscopy (SRM) that restricts spatiotemporal resolution and observation time.
Jiwoong Kwon   +2 more
doaj   +1 more source

Deep-learning-based methods for super-resolution fluorescence microscopy

open access: yesJournal of Innovative Optical Health Sciences, 2023
The algorithm used for reconstruction or resolution enhancement is one of the factors affecting the quality of super-resolution images obtained by fluorescence microscopy. Deep-learning-based algorithms have achieved state-of-the-art performance in super-
Jianhui Liao   +3 more
doaj   +1 more source

Label-free 3D visualization of cellular and tissue structures in intact muscle with second and third harmonic generation microscopy. [PDF]

open access: yes, 2011
Second and Third Harmonic Generation (SHG and THG) microscopy is based on optical effects which are induced by specific inherent physical properties of a specimen.
Krombach Fritz   +11 more
core   +1 more source

Fluorescence Microscopy of the HIV-1 Envelope

open access: yesViruses, 2020
Human immunodeficiency virus (HIV) infection constitutes a major health and social issue worldwide. HIV infects cells by fusing its envelope with the target cell plasma membrane.
Pablo Carravilla   +2 more
doaj   +1 more source

Computational based time-resolved multispectral fluorescence microscopy

open access: yesAPL Photonics, 2023
Multispectral imaging and time-resolved imaging are two common acquisition schemes in fluorescence microscopy, and their combination can be beneficial to increase specificity.
Alberto Ghezzi   +8 more
doaj   +1 more source

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