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Lining cells

Russian production may be going to a flow line cell concept (35). In this process, dehydrated camaOite is fed to a chamber where it is mixed with spent electrolyte coming from the electrolytic cells. The spent electrolyte first enters a metal collection chamber, where the molten magnesium is separated. The electrolyte is then enriched with camaOite and any iasoluble impurities are allowed to settle. The enriched electrolyte is then returned to the electrolytic cells. The result is that most of the remaining impurities are removed ia the first electrolytic cell. [Pg.319]

Heat build up Design discharge to avoid bridging, provide reli-due to plugged able instrumentation to detect full receiver (load discharge line. cells or level probe) Check lines to ensure they are clear before startup Monitor and alarm temperature CCPS G-f2 CCPS G-23 CCPS G-29 CCPS G-39... [Pg.97]

Osteoblasts are the primary cells responsible for bone formation. They are derived from mesenchymal (stromal) cells that first differentiate into pre-osteoblasts and then into mature, bone matrix producing osteoblasts. Inactivated or resting osteoblasts become lining cells and thus a reservoir for bone forming cells to be activated at the next remodelling cycle. Osteoblasts trapped and embedded in the mineralised matrix are called osteocyts, and are important for many properties of living bone. [Pg.278]

Animal experiments into the effect of ingestion of chryso-tile asbestos demonstrated an accumulation of cellular debris within the lumen of the ileum and colon consistent with cytotoxic changes of the mucosal lining cells (Jacobs etal., 1978). The question as to whether asbestos causes tumours in the gastrointestinal tract in humans is a topic of concern, however, the evidence remains equivocal (Levine, 1985). [Pg.251]

Cell Line Cell Type Source Receptor... [Pg.441]

The uptake of radiocerium by intestinal lining cells is not unique but may be expected to occur in similar chemical compounds that form colloids or large complexes within the intestine (Sullivan, 1966). Macromolecules are known to be easily absorbed by the intestinal cells of newborn animals through the process of pinocytosis (Clark, 1959). Polyvinylpyrrolidone (PVP) has been shown to be taken into the intestinal cells of rats less than 18 days old (Clarke and Hardy, 1969). [Pg.22]

Rat intratracheal AMAD 1.35-1.42 pm o, 1.7-1.9 "CeCli, pH 3 — 130 edema, fibrosis, proliferation of alveolar Lining cells, thickening of interal- No No No (1974) Korolev (1969a ... [Pg.57]

Chang T, Hughes-Fulford (2009) Monolayer and spheroid culture of human liver hepatocellular carcinoma cell line cells demonstrate distinct global gene expression patterns and functional phenotypes. Tissue Eng Part A 15 559-567... [Pg.166]

Information metabolism provides a way to store and retrieve the information that guides the development of cellular structure, communication, and regulation. Like other metabolic pathways, this process is highly regulated. Information is stored by the process of DNA replication and meiosis, in which we form our germ-line cells. These processes are limited to specific portions of the cell cycle. Information is retrieved by the transcription of DNA into RNA and the ultimate translation of the signals in the mRNA into protein. [Pg.53]

ParfittAM (2001) The bone remodeling compartment a circulatory function for bone lining cells. J Bone Miner Res 16 1583-1585... [Pg.187]

Ringerike, T. et al., Detection of immunotoxicity using T-cell based cytokine reporter cell lines ( Cell Chip ), Toxicology, 206, 257, 2005. [Pg.20]

Established cell lines, cell strains or primary cell cultures may be used. The most often used are Chinese hamster cell lines and human peripheral blood lymphocytes. The merits of these two cell lines have been reported (Ishidate and Hamois, 1987 Kirkland and Gamer, 1987). The cell system must be validated and consistently sensitive to known clastogens. [Pg.217]

Cell Lines. Cell lines, derived from tissue of various species, are commercially available from tissue culture banks. These cell populations are immortalized in that they possess the capacity to permanently proliferate in culture. Such cellular models can be studied in short-term suspension (hours) or longer-term monolayer culture (days, weeks, months). Since cell lines have been extensively cultured or passaged for multiple generations, the degree or retention (or loss) of kidney-specific morphology and function is an important limitation that is not thoroughly addressed for a number of renal cell lines. One renal cell line that has been relatively well characterized is the pig kidney cell line, LLC-PK,. [Pg.670]

Figure 2D. Cell counts normalized by control cells at starting point A, continuous line show control cell number, B dotted line GI50 after 24h C) broken line, cell number at starting (T0) point. Figure 2D. Cell counts normalized by control cells at starting point A, continuous line show control cell number, B dotted line GI50 after 24h C) broken line, cell number at starting (T0) point.
There are four different drug products under Part II chemical active substance(s), radiopharmaceutical products, biological medicinal products, and vegetable medicinal products. For example, the GMP production report for biological medicinal products includes description of the genes used, strain of cell line, cell bank system, fermentation and harvesting, purification, characterization, analytical method development, process validation, impurities, and batch analysis (GMP production of biopharmaceuticals is described in Chapter 10). A DMF (Exhibit 8.8) is submitted. [Pg.258]

In two dominant lethal studies, neither heptachlor nor heptachlor epoxide proved to be clastogenic in the germ-line cells of male Charles River or Swiss mice (Arnold et al. 1977 Epstein et al. 1972). [Pg.43]

There are very few in vivo genotoxicity studies. Only two in vivo studies were located, and both assessed the dominant lethal effects. The results were negative for both studies, implying that neither heptachlor nor heptachlor epoxide are genotoxic to the germ-line cells of male mice when tested alone or as a mixture (Arnold et al. 1977 Epstein et al. 1972). Refer to Table 2- 3 for a summary of these results of in vivo studies. [Pg.56]


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See also in sourсe #XX -- [ Pg.164 , Pg.165 , Pg.177 ]




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