𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Velocity estimation of spots in three-dimensional confocal image sequences of living cells

✍ Scribed by C.B.J. Bergsma; G.J. Streekstra; A.W.M. Smeulders; E.M.M. Manders


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
356 KB
Volume
43
Category
Article
ISSN
0196-4763

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Quantitative three-dimensional confocal
✍ Toshiyuki Hosokawa; Timothy V. P. Bliss; Alan Fine πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 881 KB

In order to study changes in synaptic structure that accompany learning and memory, we have developed optical methods to visualize dendritic spines and presynaptic terminals in living, electrically monitored brain slices maintained in vitro. Focal microapplication of the fluorescent lipophilic dye D

Three-dimensional analysis of complex br
✍ Mahnaz Maddah; Hamid Soltanian-Zadeh; Ali Afzali-Kusha; Ali Shahrokni; Zheng G. πŸ“‚ Article πŸ“… 2005 πŸ› Elsevier Science 🌐 English βš– 532 KB

The characteristic of confocal microscopy (CM) vascular data is that it contains many tiny vessels with branching and complex structure. In this work, an automated method for quantitative analysis and reconstruction of cerebral vessels from CM images is presented in which the extracted centerline of

Three-dimensional quantification of moss
✍ Tzu-Ping Yu; Thomas H. Brown πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 872 KB

Confocal laser scanning microscopy (CLSM) was used to visualize presynaptic elements of mossy-fiber synapses in living rat hippocampal slices. Mossy fiber (mf) axons and their boutons were labeled in transverse hippocampal slices by injecting one of three fluorescent dyes (diI, diA, or fast diI) int

Three-dimensional tracking and temporal
✍ Feng-Ching Tsai; Lin-Ai Tai; Yu-Jing Wang; Jian-Long Xiao; Tsi-Hsuan Hsu; Chung- πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 661 KB

## Abstract Gold nanoparticles (AuNPs) confined in liposomes of diameters around 200 nm produce strong scattering signal owing to surface plasmon resonance, and therefore bright‐field optical tracking of the AuNP‐encapsulating liposomes can be conducted in living cells. Using an optical profiling t