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  1. AU="Douglas J Kelly"
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  1. Article ; Online: Marcksl1 modulates endothelial cell mechanoresponse to haemodynamic forces to control blood vessel shape and size

    Igor Kondrychyn / Douglas J. Kelly / Núria Taberner Carretero / Akane Nomori / Kagayaki Kato / Jeronica Chong / Hiroyuki Nakajima / Satoru Okuda / Naoki Mochizuki / Li-Kun Phng

    Nature Communications, Vol 11, Iss 1, Pp 1-

    2020  Volume 18

    Abstract: During lumen formation in blood vessels, endothelial cells become exposed to hemodynamic forces that induce membrane blebbing and changes in cell shape. Here, the authors show endothelial cells develop an actin-based protective mechanism in the cell ... ...

    Abstract During lumen formation in blood vessels, endothelial cells become exposed to hemodynamic forces that induce membrane blebbing and changes in cell shape. Here, the authors show endothelial cells develop an actin-based protective mechanism in the cell cortex that prevents excessive blebbing to control cell shape and vessel diameter.
    Keywords Science ; Q
    Language English
    Publishing date 2020-10-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Marcksl1 modulates endothelial cell mechanoresponse to haemodynamic forces to control blood vessel shape and size

    Igor Kondrychyn / Douglas J. Kelly / Núria Taberner Carretero / Akane Nomori / Kagayaki Kato / Jeronica Chong / Hiroyuki Nakajima / Satoru Okuda / Naoki Mochizuki / Li-Kun Phng

    Nature Communications, Vol 11, Iss 1, Pp 1-

    2020  Volume 18

    Abstract: During lumen formation in blood vessels, endothelial cells become exposed to hemodynamic forces that induce membrane blebbing and changes in cell shape. Here, the authors show endothelial cells develop an actin-based protective mechanism in the cell ... ...

    Abstract During lumen formation in blood vessels, endothelial cells become exposed to hemodynamic forces that induce membrane blebbing and changes in cell shape. Here, the authors show endothelial cells develop an actin-based protective mechanism in the cell cortex that prevents excessive blebbing to control cell shape and vessel diameter.
    Keywords Science ; Q
    Language English
    Publishing date 2020-10-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Rapid global fitting of large fluorescence lifetime imaging microscopy datasets.

    Sean C Warren / Anca Margineanu / Dominic Alibhai / Douglas J Kelly / Clifford Talbot / Yuriy Alexandrov / Ian Munro / Matilda Katan / Chris Dunsby / Paul M W French

    PLoS ONE, Vol 8, Iss 8, p e

    2013  Volume 70687

    Abstract: Fluorescence lifetime imaging (FLIM) is widely applied to obtain quantitative information from fluorescence signals, particularly using Förster Resonant Energy Transfer (FRET) measurements to map, for example, protein-protein interactions. Extracting ... ...

    Abstract Fluorescence lifetime imaging (FLIM) is widely applied to obtain quantitative information from fluorescence signals, particularly using Förster Resonant Energy Transfer (FRET) measurements to map, for example, protein-protein interactions. Extracting FRET efficiencies or population fractions typically entails fitting data to complex fluorescence decay models but such experiments are frequently photon constrained, particularly for live cell or in vivo imaging, and this leads to unacceptable errors when analysing data on a pixel-wise basis. Lifetimes and population fractions may, however, be more robustly extracted using global analysis to simultaneously fit the fluorescence decay data of all pixels in an image or dataset to a multi-exponential model under the assumption that the lifetime components are invariant across the image (dataset). This approach is often considered to be prohibitively slow and/or computationally expensive but we present here a computationally efficient global analysis algorithm for the analysis of time-correlated single photon counting (TCSPC) or time-gated FLIM data based on variable projection. It makes efficient use of both computer processor and memory resources, requiring less than a minute to analyse time series and multiwell plate datasets with hundreds of FLIM images on standard personal computers. This lifetime analysis takes account of repetitive excitation, including fluorescence photons excited by earlier pulses contributing to the fit, and is able to accommodate time-varying backgrounds and instrument response functions. We demonstrate that this global approach allows us to readily fit time-resolved fluorescence data to complex models including a four-exponential model of a FRET system, for which the FRET efficiencies of the two species of a bi-exponential donor are linked, and polarisation-resolved lifetime data, where a fluorescence intensity and bi-exponential anisotropy decay model is applied to the analysis of live cell homo-FRET data. A software package implementing ...
    Keywords Medicine ; R ; Science ; Q
    Subject code 006 ; 530
    Language English
    Publishing date 2013-01-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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