AbstractWe describe an experimental system to visualize the soma and processes of mammalian neurons and glia in living and fixed preparations by using a recombinant adenovirus vector to transfer the jellyfish green fluorescent protein (GFP) into postmitotic neural cells both in vitro and in vivo. We have introduced several modifications of GFP that enhance its fluorescence intensity in mammalian axons and dendrites. This method should be useful for studying the dynamic processes of cell migration and the development of neuronal connections, as well as for analyzing the function of exogenous genes introduced into cells using the adenovirus vector
The green fluorescent fusion protein and its isoforms are extensively used to monitor gene expressio...
The possibility of directly converting non-neuronal cells into neurons in situ in the brain would op...
AbstractWe generated transgenic mice in which red, green, yellow, or cyan fluorescent proteins (toge...
We describe an experimental system to visualize the soma and processes of mammalian neurons and glia...
AbstractWe describe an experimental system to visualize the soma and processes of mammalian neurons ...
We here describe various approaches using GFP that are being used in the morphological and functiona...
Neural stem cells (NSC’s) often follow the same path of migration throughout the brain, traveling fr...
Visualization of neurons is indispensable for the investigation of neuronal circuits in the central ...
To visualize the movements of cells and their processes in developing vertebrates, we constructed re...
Abstract: For the evaluation of a possible adenovirus-mediated gene transfer into cells of the CNS a...
Visualizing the precise morphology of closely juxtaposed cells and their interactions can be highly ...
In this paper a detailed protocol is presented for neuroscientists planning to start work on first g...
AbstractTwo methods are described for using the jellyfish green fluorescent protein (GFP) as a repor...
To detect subtle changes in neuronal morphology in response to changes in experience, one must image...
Background Ex vivo gene therapy and cell replacement in the nervous system may provide therapeutic o...
The green fluorescent fusion protein and its isoforms are extensively used to monitor gene expressio...
The possibility of directly converting non-neuronal cells into neurons in situ in the brain would op...
AbstractWe generated transgenic mice in which red, green, yellow, or cyan fluorescent proteins (toge...
We describe an experimental system to visualize the soma and processes of mammalian neurons and glia...
AbstractWe describe an experimental system to visualize the soma and processes of mammalian neurons ...
We here describe various approaches using GFP that are being used in the morphological and functiona...
Neural stem cells (NSC’s) often follow the same path of migration throughout the brain, traveling fr...
Visualization of neurons is indispensable for the investigation of neuronal circuits in the central ...
To visualize the movements of cells and their processes in developing vertebrates, we constructed re...
Abstract: For the evaluation of a possible adenovirus-mediated gene transfer into cells of the CNS a...
Visualizing the precise morphology of closely juxtaposed cells and their interactions can be highly ...
In this paper a detailed protocol is presented for neuroscientists planning to start work on first g...
AbstractTwo methods are described for using the jellyfish green fluorescent protein (GFP) as a repor...
To detect subtle changes in neuronal morphology in response to changes in experience, one must image...
Background Ex vivo gene therapy and cell replacement in the nervous system may provide therapeutic o...
The green fluorescent fusion protein and its isoforms are extensively used to monitor gene expressio...
The possibility of directly converting non-neuronal cells into neurons in situ in the brain would op...
AbstractWe generated transgenic mice in which red, green, yellow, or cyan fluorescent proteins (toge...