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High-speed imaging of transient metabolic dynamics using two-photon fluorescence lifetime imaging microscopy

Two-photon fluorescence lifetime imaging microscopy (2P-FLIM) of autofluorescent metabolic coenzymes has been widely used to investigate energetic perturbations in living cells and tissues in a label-free manner with subcellular resolution. While the currently used state-of-the-art instruments are h...

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Foilsithe in:Optica
Main Authors: Bower, Andrew J., Li, Joanne, Chaney, Eric J., Marjanovic, Marina, Spillman, Darold R., Boppart, Stephen A.
Formáid: Artigo
Teanga:Inglês
Foilsithe: 2018
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6457362/
https://ncbi.nlm.nih.gov/pubmed/30984802
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1364/OPTICA.5.001290
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