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Live-cell imaging of dendritic spines by STED microscopy

Time lapse fluorescence imaging has become one of the most important approaches in neurobiological research. In particular, both confocal and two-photon microscopy have been used to study activity-dependent changes in synaptic morphology. However, the diffraction-limited resolution of light microsco...

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Autors principals: Nägerl, U. Valentin, Willig, Katrin I., Hein, Birka, Hell, Stefan W., Bonhoeffer, Tobias
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 2008
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2585941/
https://ncbi.nlm.nih.gov/pubmed/19028874
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0810028105
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