- About
-
The Global ETD Search service is a free service for researchers
to find electronic theses and dissertations. This service is
provided by the
Networked Digital Library of Theses and Dissertations.
Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
Search results
Showing 211 to 220 of 6651 (0.048 seconds)| 211 |
Electron energy loss and cathodoluminescence of rare earthsYuan, Jun January 1987 (has links)
No description available.
|
| 212 |
Fresnel and high resolution techniques for the characterisation of ultrathin semiconductor layersDunin-Borkowski, Rafal Edward January 1994 (has links)
No description available.
|
| 213 |
A study of shear-force microscopy and its application to liquid-crystal and biological systemsBrereton, Luke James January 1998 (has links)
No description available.
|
| 214 |
Characterisation of the native rat GABAâ†B receptor and the recombinant GABAâ†B receptor transiently expressed in COS cellsKeir, Miranda J. January 1999 (has links)
No description available.
|
| 215 |
The Use of Scanning Electron Microscopy as a Tool in DendrochronologyRevel, Richard D. January 1982 (has links)
No description available.
|
| 216 |
An investigation of fabrication routes for multilayer all ceramic capacitorsMaltman, David William January 1994 (has links)
No description available.
|
| 217 |
Study of porous materials by scanning probe microscopyNugues, Steven January 1996 (has links)
No description available.
|
| 218 |
Plastic deformation of MoSiâ‚‚ single crystals and polycrystalline Mo(Si,Al)â‚‚Jiao, Chengge January 2000 (has links)
No description available.
|
| 219 |
Total internal reflection microscopy studies on colloidal particle endocytosis by living cellsByrne, Gerard January 2009 (has links)
The purpose of this study was to develop novel optical microscopy techniques in order to investigate colloidal drug particle endocytosis by mammalian cells. A total internal reflection microscope (TIRM) was initially developed for high resolution cellular imaging. TIRM is a non-fluorescent imaging technique based on the principle of ‘scattering’ of the evanescent field created when a light beam undergoes total internal reflection at an interface between two media with different refractive indices, such as glass and air. The key design considerations with respect to development of a TIRM instrument are discussed. The technique is also compared and contrasted to the more commonly known non-fluorescent RICM (Reflection Interference Contrast Microscopy) technique using computer simulations. Time-lapse video TIRM is applied to imaging the interaction between A549 and 3T3 cells, and a polylysine coated substrate. Real-time label-free visualisation of 0.5 and 1 m polystyrene particle endocytosis by living cells is then demonstrated. Modifications to the TIRM system to include a dual-colour fluorescent TIRF (Total Internal Reflection Fluorescence) microscope are described in detail. Results are shown which demonstrate the ability of a combined TIRM/TIRF instrument to selectively image the basal cell membrane both label-free and fluorescently. 3T3 fibroblast cells were genetically modified using standard molecular biology protocols to express the fluorescent fusion protein EGFP-Clathrin LCa (enhanced green fluorescent protein clathrin light chain a). Finally, colloidal particle endocytosis by the genetically modified cell was imaged using the TIRM/TIRF microscope. Direct visualisation of the internalisation of 500 nm particles via clathrin coated pits in 3T3 cells was shown for the first time.
|
| 220 |
Application of image analysis to fungal fermentationsCox, Philip William January 2000 (has links)
No description available.
|
Page generated in 0.0533 seconds