Most methods to observe three-dimensional processes in living samples are based on imaging a single plane that is sequentially scanned through the sample. Sequential scanning is inherently slow, which can make it difficult to capture objects moving quickly in three dimensions. Here we present a novel method, multiple point-of-view microscopy (MPoVM), that allows simultaneous capturing of the front and side views of a sample with high resolution. MPoVM can be implemented in most fluorescence microscopes, offering new opportunities in the study of dynamic biological processes in three dimensions
We have developed a real-time imaging method for two-color wide-field fluorescence microscopy using ...
In this paper, we present a new multi-focus microscope (MFM) system based on a phase mask and HiLo a...
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Emp...
The imaging of cellular dynamics in three dimensions using a standard microscope is severely limited...
Due to the classical conflict between spatial and temporal resolution, microscopy studies of fast ev...
Fluorescence microscopy provides an unparalleled tool for imaging biological samples. However, produ...
The conventional optical microscope is an inherently two-dimensional (2D) imaging tool. The objectiv...
Live-cell microscopy faces two challenges when neither the spatial nor the temporal in-formation abo...
The distance separating two biomolecules in close proximity is an important determinant of the natur...
Fluorescent observation of cells generally suffers from the limited axial resolution due to the elon...
Optical microscopes allow us to study highly dynamic events from the molecular scale up to the whole...
International audienceABSTRACT Understanding how development is coordinated in multiple tissues and ...
Fluorescence microscopy is an indispensable tool in the areas of cell biology, histology and materia...
Conventional acquisition of three-dimensional (3D) microscopy data requires sequential z scanning an...
The current image speed of multi-photon microscopy is not enough for fast biological processes such ...
We have developed a real-time imaging method for two-color wide-field fluorescence microscopy using ...
In this paper, we present a new multi-focus microscope (MFM) system based on a phase mask and HiLo a...
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Emp...
The imaging of cellular dynamics in three dimensions using a standard microscope is severely limited...
Due to the classical conflict between spatial and temporal resolution, microscopy studies of fast ev...
Fluorescence microscopy provides an unparalleled tool for imaging biological samples. However, produ...
The conventional optical microscope is an inherently two-dimensional (2D) imaging tool. The objectiv...
Live-cell microscopy faces two challenges when neither the spatial nor the temporal in-formation abo...
The distance separating two biomolecules in close proximity is an important determinant of the natur...
Fluorescent observation of cells generally suffers from the limited axial resolution due to the elon...
Optical microscopes allow us to study highly dynamic events from the molecular scale up to the whole...
International audienceABSTRACT Understanding how development is coordinated in multiple tissues and ...
Fluorescence microscopy is an indispensable tool in the areas of cell biology, histology and materia...
Conventional acquisition of three-dimensional (3D) microscopy data requires sequential z scanning an...
The current image speed of multi-photon microscopy is not enough for fast biological processes such ...
We have developed a real-time imaging method for two-color wide-field fluorescence microscopy using ...
In this paper, we present a new multi-focus microscope (MFM) system based on a phase mask and HiLo a...
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Emp...