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  1. Article ; Online: Hypothesis-driven quantitative fluorescence microscopy - the importance of reverse-thinking in experimental design.

    Wait, Eric C / Reiche, Michael A / Chew, Teng-Leong

    Journal of cell science

    2020  Volume 133, Issue 21

    Abstract: One of the challenges in modern fluorescence microscopy is to reconcile the conventional utilization of microscopes as exploratory instruments with their emerging and rapidly expanding role as a quantitative tools. The contribution of microscopy to ... ...

    Abstract One of the challenges in modern fluorescence microscopy is to reconcile the conventional utilization of microscopes as exploratory instruments with their emerging and rapidly expanding role as a quantitative tools. The contribution of microscopy to observational biology will remain enormous owing to the improvements in acquisition speed, imaging depth, resolution and biocompatibility of modern imaging instruments. However, the use of fluorescence microscopy to facilitate the quantitative measurements necessary to challenge hypotheses is a relatively recent concept, made possible by advanced optics, functional imaging probes and rapidly increasing computational power. We argue here that to fully leverage the rapidly evolving application of microscopes in hypothesis-driven biology, we not only need to ensure that images are acquired quantitatively but must also re-evaluate how microscopy-based experiments are designed. In this Opinion, we present a reverse logic that guides the design of quantitative fluorescence microscopy experiments. This unique approach starts from identifying the results that would quantitatively inform the hypothesis and map the process backward to microscope selection. This ensures that the quantitative aspects of testing the hypothesis remain the central focus of the entire experimental design.
    MeSH term(s) Microscopy, Fluorescence ; Optics and Photonics ; Research Design
    Language English
    Publishing date 2020-11-05
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2993-2
    ISSN 1477-9137 ; 0021-9533
    ISSN (online) 1477-9137
    ISSN 0021-9533
    DOI 10.1242/jcs.250027
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Actin cables and comet tails organize mitochondrial networks in mitosis.

    Moore, Andrew S / Coscia, Stephen M / Simpson, Cory L / Ortega, Fabian E / Wait, Eric C / Heddleston, John M / Nirschl, Jeffrey J / Obara, Christopher J / Guedes-Dias, Pedro / Boecker, C Alexander / Chew, Teng-Leong / Theriot, Julie A / Lippincott-Schwartz, Jennifer / Holzbaur, Erika L F

    Nature

    2021  Volume 591, Issue 7851, Page(s) 659–664

    Abstract: Symmetric cell division requires the even partitioning of genetic information and cytoplasmic contents between daughter cells. Whereas the mechanisms coordinating the segregation of the genome are well known, the processes that ensure organelle ... ...

    Abstract Symmetric cell division requires the even partitioning of genetic information and cytoplasmic contents between daughter cells. Whereas the mechanisms coordinating the segregation of the genome are well known, the processes that ensure organelle segregation between daughter cells remain less well understood
    MeSH term(s) Actin Cytoskeleton/chemistry ; Actin Cytoskeleton/metabolism ; Actins/chemistry ; Actins/metabolism ; Animals ; Cell Division ; Cell Line ; Cytokinesis ; Endoplasmic Reticulum/metabolism ; Hippocampus/cytology ; Hippocampus/embryology ; Humans ; Mitochondria/chemistry ; Mitochondria/metabolism ; Mitosis ; Neurons ; Rats
    Chemical Substances Actins
    Language English
    Publishing date 2021-03-03
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 120714-3
    ISSN 1476-4687 ; 0028-0836
    ISSN (online) 1476-4687
    ISSN 0028-0836
    DOI 10.1038/s41586-021-03309-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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