Networks of neurons are inherently three-dimensional in nature, whereas conventional imaging methods, such as laser scanning two-photon microscopy, usually provide only fast two-dimensional imaging. Rapid volumetric imaging would however be preferable for imaging neurons. To get a more complete picture of the dynamics of the neuron-to-neuron interactions, we have developed a pseudo-parallelised multi-plane two-photon excitation imaging system through the incorporation of an acousto-optic switching and a remote focusing technique into a resonant scanning microscope. This permits the recording of millisecond scale fluorescence transients of calcium indicators from large populations of neurons upon neural firing events at multiple chosen axial...
Multifocal two-photon microscopy (MTPM) increases imaging speed over single-focus scanning by parall...
The first ever demonstration of temporal focusing with Short Wave InfraRed (SWIR) excitation and emi...
Kurtz R, Fricke M, Kalb J, Tinnefeld P, Sauer M. Application of multiline two-photon microscopy to f...
Networks of neurons are inherently three-dimensional in nature, whereas conventional imaging methods...
Networks of neurons are inherently three-dimensional in nature, whereas conventional imaging methods...
Two-photon excitation fluorescence microscopy is widely used to study the activity of neuronal circu...
Two-photon excitation fluorescence microscopy is widely used to study the activity of neuronal circu...
Two-photon excitation fluorescence microscopy is widely used to study the activity of neuronal circu...
Recording of the concerted activity of neuronal assemblies and the dendritic and axonal signal integ...
Multiphoton excitation of molecular probes has become an important tool in experimental neurobiology...
This is the final version of the article. Available from SPIE via the DOI in this record.Optical sec...
The progress of neuroscience is limited by the instrumentation available to it for studying the bra...
Brain is composed of complex neural networks that work in concert to underlie the animal’s cognition...
The understanding of brain computations requires methods that read out neural activity on different...
AbstractBackgroundTwo-photon microscopy is widely used to study brain function, but conventional mic...
Multifocal two-photon microscopy (MTPM) increases imaging speed over single-focus scanning by parall...
The first ever demonstration of temporal focusing with Short Wave InfraRed (SWIR) excitation and emi...
Kurtz R, Fricke M, Kalb J, Tinnefeld P, Sauer M. Application of multiline two-photon microscopy to f...
Networks of neurons are inherently three-dimensional in nature, whereas conventional imaging methods...
Networks of neurons are inherently three-dimensional in nature, whereas conventional imaging methods...
Two-photon excitation fluorescence microscopy is widely used to study the activity of neuronal circu...
Two-photon excitation fluorescence microscopy is widely used to study the activity of neuronal circu...
Two-photon excitation fluorescence microscopy is widely used to study the activity of neuronal circu...
Recording of the concerted activity of neuronal assemblies and the dendritic and axonal signal integ...
Multiphoton excitation of molecular probes has become an important tool in experimental neurobiology...
This is the final version of the article. Available from SPIE via the DOI in this record.Optical sec...
The progress of neuroscience is limited by the instrumentation available to it for studying the bra...
Brain is composed of complex neural networks that work in concert to underlie the animal’s cognition...
The understanding of brain computations requires methods that read out neural activity on different...
AbstractBackgroundTwo-photon microscopy is widely used to study brain function, but conventional mic...
Multifocal two-photon microscopy (MTPM) increases imaging speed over single-focus scanning by parall...
The first ever demonstration of temporal focusing with Short Wave InfraRed (SWIR) excitation and emi...
Kurtz R, Fricke M, Kalb J, Tinnefeld P, Sauer M. Application of multiline two-photon microscopy to f...