Despite recent improvements in microscopy, it is still difficult to apply super-resolution microscopy for deep imaging due to the deterioration of light convergence properties in thick specimens. As a strategy to avoid such optical limitations for deep super-resolution imaging, we focused on super-resolution radial fluctuation (SRRF), a super-resolution technique based on image analysis. In this study, we applied SRRF to two-photon microscopy (2P-SRRF) and characterized its spatial resolution, suitability for deep observation, and morphological reproducibility in real brain tissue. By the comparison with structured illumination microscopy (SIM), it was confirmed that 2P-SRRF exhibited two-point resolution and morphological reproducibility c...
Fluorescence imaging in biology has become a fundamental tool to understanding structure and functio...
Imaging synapses in the brain is difficult due to the diffraction limit of light microscopy, which ...
We developed adaptive optical (AO) two-photon excitation microscopy by introducing a spatial light m...
Pilger C, Pospisil J, Müller M, et al. Super-resolution fluorescence microscopy by line-scanning wit...
AbstractMany cellular structures and organelles are too small to be properly resolved by conventiona...
Super-resolution radial fluctuations (SRRF) is a combination of temporal fluctuation analysis and lo...
The brain is complex and dynamic. The spatial scales of interest to the neurobiologist range from in...
The brain is complex and dynamic. The spatial scales of interest to the neurobiologist range from in...
The ability to visualize deep brain structures in vivo with high spatial resolution is of rising int...
Abstract Visualization of axons and dendritic spines is crucial in neuroscience research. However, t...
Super-resolution fluorescence microscopy techniques have enabled dramatic development in modern biol...
SummaryTwo-photon laser scanning microscopy (2PLSM) has allowed unprecedented fluorescence imaging o...
A number of new Correlative Light and Electron Microscopy approaches have been developed over the pa...
Two-photon microscopy has enabled high-resolution imaging of single cells in the brain of anaestheti...
The understanding of the biological processes at the cellular and subcellular level requires the abi...
Fluorescence imaging in biology has become a fundamental tool to understanding structure and functio...
Imaging synapses in the brain is difficult due to the diffraction limit of light microscopy, which ...
We developed adaptive optical (AO) two-photon excitation microscopy by introducing a spatial light m...
Pilger C, Pospisil J, Müller M, et al. Super-resolution fluorescence microscopy by line-scanning wit...
AbstractMany cellular structures and organelles are too small to be properly resolved by conventiona...
Super-resolution radial fluctuations (SRRF) is a combination of temporal fluctuation analysis and lo...
The brain is complex and dynamic. The spatial scales of interest to the neurobiologist range from in...
The brain is complex and dynamic. The spatial scales of interest to the neurobiologist range from in...
The ability to visualize deep brain structures in vivo with high spatial resolution is of rising int...
Abstract Visualization of axons and dendritic spines is crucial in neuroscience research. However, t...
Super-resolution fluorescence microscopy techniques have enabled dramatic development in modern biol...
SummaryTwo-photon laser scanning microscopy (2PLSM) has allowed unprecedented fluorescence imaging o...
A number of new Correlative Light and Electron Microscopy approaches have been developed over the pa...
Two-photon microscopy has enabled high-resolution imaging of single cells in the brain of anaestheti...
The understanding of the biological processes at the cellular and subcellular level requires the abi...
Fluorescence imaging in biology has become a fundamental tool to understanding structure and functio...
Imaging synapses in the brain is difficult due to the diffraction limit of light microscopy, which ...
We developed adaptive optical (AO) two-photon excitation microscopy by introducing a spatial light m...