Showing papers in "NeuroImage in 1993"

TL;DR: It is concluded that significant and inconsistent errors can be introduced by using shape-based stereological methods for estimating neuronal somal volumes in phrenic moto-neuron somal volume.

TL;DR: Slice cultures provide a favorable opportunity to investigate [Ca2+]i responses in individual neurons maintained in an organotypic synaptic environment, taking advantage of high-resolution optical techniques.

TL;DR: It is proposed that preferential adhesion involved a signal transduction mechanism that discriminated between positively charged and uncharged molecules, which could contribute to pathfinding by neuroblasts and growth cones along extracellular matrix proteins in vivo.

TL;DR: A prototype combined optical fluorescence/atomic force microscope (OFAFM) designed for use in neurobiology and related disciplines has been constructed and used to study filamentous actin and other cellular structures in fixed Xenopus retinal glial cells (XR1 glial cell line) as mentioned in this paper.

TL;DR: A new method for realizing direct stereoscopic views of thick microscopic sections employs multiple oblique illuminating beams and a single objective lens to achieve excellent 3D images in the higher magnification range, where conventional stereo microscopes no longer function.

TL;DR: Golgi-impregnated neurons of the human or animal central nervous system were studied with a confocal laser scanning microscope (CLSM), and a true and complete three-dimensional reconstruction of neurons can be obtained using an extended RAM and quick elaboration combined with the rotation of the reconstructed image in the different planes.

TL;DR: The parametric model presented here facilitates the process of performing quantitative analysis of hybridized neurons based on predetermined and unbiased morphological criteria.

TL;DR: Three-dimensional wireframe reconstructions revealed a functional organization of the cerebral blood flow responses which was not apparent in two-dimensional coronal sections of the dorsal raphe nucleus (DRN).