By Wolfgang Kuehnel
The totally revised and up to date fourth variation comprises 745 full-color illustrations - virtually two hundred greater than have been incorporated within the 3rd version. fantastic, top quality microphotographs and pathologic stains are observed through legends, informative texts, and various cross-references.
Key beneficial properties of the up-to-date fourth version:
* greater than seven hundred fine quality illustrations utilizing complicated recommendations in histology and electron microscopy * sensible, details * Concise and concentrated textual content * Key recommendations and concepts illustrated in under 550 pages
Ideal for examination instruction, this world-class ebook is an integral visible examine software for clinical, dental and biology scholars. it will probably additionally function an exceptional evaluate and refresher text.
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Extra resources for Color Atlas of Cytology, Histology and Microscopic Anatomy (Thieme Flexibook)
These filaments, named stress fibers, improve the adhesion of endothelial cells and protect them from the shearing forces of the bloodstream. Fluorescence microscopy; magnification: × 690 55 Intermediary Filaments—the Tonofilament System In addition to actin filaments and microtubules, intermediary filaments (tonofilaments) are the third system making up the intracellular cytoskeleton of eukaryotic cells. Their diameter is 7–11 nm. This makes them thicker than microfilaments (5–7 nm) and thinner than microtubules (20–25 nm).
Usage subject to terms and conditions of license. Cells 45 Lysosomes C. de Duve identified lysosomes as unique cell organelles relatively late—only in 1955. 0. These enzymes are specific to lysosomes and can be used as marker enzymes. Histochemical identification of these marker enzymes allows it to localize and visualize lysosomes using light microscopy. Due to their acid hydrolase content, lysosomal cell compartments play an important role in the intracellular digestion or degradation of endogenous substances (autophagy) and phagocytosed substances (heterophagy).
The structure of microvilli is static and without any particular organization. However, protrusions from the plasmalemma increase the cell surface area. Scanning electron microscopy provides a method of examining the outer elements of the tissue surface in detail. This figure offers a view of the surface of the uterine cavum epithelium. The cells are either polygonal or round and covered with short stub-like microvilli. The image is that of small patches of lawn. The dark lines between the cells are cell borders.