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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 1 (1968), S. 488-491 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 141 (1967), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Antonie van Leeuwenhoek 36 (1970), S. 119-128 
    ISSN: 1572-9699
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Filar micrometer measurements of the central body during its conversion to the vegetative cell indicated an initial spherical body of about 1.7 microns in diameter. The central body first increases in diameter then elongates such that its length is 2–2.5 times the diameter. Central bodies supplemented with casein hydrolysate in addition to sucrose formed vegetative cells in only 8 hr instead of the usual 12. Central bodies were quite susceptible to lysis by EDTA-lysozyme or citrate-lysozyme, but relatively insensitive to citrate-EDTA or single employment of EDTA or citrate. Comparative electron microscopy of cysts and central bodies following sonication revealed little alteration in cysts but reduction of central bodies to cellular debris after only 2 min. Central bodies were resistant to bacteriophage adsorption at 0 hr and required about 4 hr incubation before adsorption could occur.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 156 (1974), S. 1-20 
    ISSN: 1432-0878
    Keywords: Exocrine pancreas ; Cell membrane regulation ; Coated vesicles, Multivesicular bodies ; Endocytosis ; Autoradiography, Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Stimulation of secretion by pilocarpine results in a 70% loss of zymogen granules from pancreatic acinar cell during the first hr after injection of the drug. In previous work (Geuze and Poort, 1973), we found that the amount of membrane stored in the surface of the microvilli and of the numerous infoldings present in highly stimulated cells, increases during the first 2 hr and then decreases again during the 3rd hr after stimulation, concurrently with maximal endocytosis of sorbitol-[su14C]. Further observations on the fine structure of stimulated cells at various time intervals after injection of pilocarpine showed that during the first hr numerous smooth vesicles and multivesicular bodies (mvb's) appear in the apical cytoplasm, while the number of coated vesicles and their relative total volume increase significantly 3 hr after stimulation. By infusion of ferritin in the pancreatic duct system in vivo and application of cytochemical techniques (osmium impregnation, electron microscope autoradiography and acid phosphatase cytochemistry) it could be established that after stimulated exocytotic secretion, redundant apical cell membrane is withdrawn by at least two routes: 1) During the initial rapid increase of the amount of apical cell membrane, withdrawal is accomplished by interiorization of luminal invaginations into smooth endocytotic vesicles, which in turn give rise to mvb's by infolding and subsequent fission of their limiting membrane. 2) Once the bulk of stored secretion granules has been discharged, endocytotic coated vesicles become gradually more prominent as carriers for redundant cell membrane. The contents of endocytotic structures ultimately become incorporated in residual bodies, suggesting lysosomal degradation of cell membrane prior to eventual reutilization. Coated vesicles also originate by pinching off from mature Golgi cisternae and condensing vacuoles. A possible function of the coated membranes in the concentration of exportable protein within forming secretory granules is discussed.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 85 (1968), S. 206-209 
    ISSN: 1432-0878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary By means of an autoradiographic method we verified the moment of stemcell renewal proposed by different authors for rats and mice. We found that in rats and mice the stemcells arise as daughter cells of the A4 spermatogonia. The hypothesis is put forward that in general stemcells for the next spermatogenetic cycle arise on the moment of morphological differentiation of the A spermatogonia.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 86 (1968), S. 163-170 
    ISSN: 1432-0878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. The cells of the peri-insular acini have larger nuclei and zymogen regions and are refractory to the secretion stimulating action of pilocarpine, in contrast to the cells of the common acini (the halo phenomenon). 2. In addition to the data in the literature suggesting a relation between the presence of insulin producing B-cells in the islets and the halo phenomenon, we have shown that the destruction of the B-cells by alloxan results in a disappearance of the haloes. 3. The peri-insular cells incorporate more leucine-3H than the cells of the common acini. The larger mass of ergastoplasm mainly accounts for this increased protein synthesis, the incorporation per unit volume of ergastoplasm not being substantially increased. 4. This great protein synthesis in cells maximally filled with zymogen granules is in accordance with our finding (Kramer and Poort, 1968) that the rate of protein synthesis in the cells of the rat pancreas is a constant one, independent of the phase of the secretory cycle. As in common acini, 90 per cent of the protein synthesized during 45 min, in the peri-insular acini of a “resting”, non stimulated gland is lost from the cells within 24 hours. As much protein must leave the cell as is synthesized in order to prevent overfilling. 5. A short discussion is given on the influence insulin can have on the secretion and on the protein synthesis in the acinar cells.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 92 (1968), S. 400-405 
    ISSN: 1432-0878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary With the help of the alkylating agent Myleran we confirmed our finiding that in the rat, mouse and golden hamster the spermatogonial stem cells are daughter cells of the last generation of A spermatogonia.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 86 (1968), S. 475-486 
    ISSN: 1432-0878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Rats were starved for 48 hrs and stimulated to secrete by means of pilocarpine. The rate of synthesis of protein was determined both biochemically and autoradiographically by the assessment of leucine-3H incorporation during 10 min after its administration at various intervals (up to 7 hrs) after the pilocarpine stimulation. Care was taken to assess the incorporation with reference to the number of cells present, not to the total dry matter content nor to the protein content, as the latter tend to vary with the physiological state of the organ. Depletion of a pancreas filled with zymogen granules by means of pilocarpine gives rise to a transitory decrease in its rate of protein synthesis. After 1 hr the rate of synthesis reverts to the value found in fasting, unstimulated rats. Studies of pancreas slices taken from the rats after killing show that the in vitro synthetic capacity (leucine-14C) of the gland is unaffected by either fasting or stimulation. Peri-insular acini do not lose their zymogen granules upon pilocarpine stimulation as do the other acini. Yet, the rate of protein synthesis in both types of acini follows the same course after fasting and subsequent stimulation. Protein synthesized during fasting is largely lost from the gland during the next 24 hrs of continued fasting, either through catabolism or secretion. The results are discussed with a view on conflicting reports in the literature on the possibility of enhancing the rate of protein synthesis in the pancreas by stimulation of the secretion. A concept is given of a secretory cycle combined with a continuous protein synthesis at a constant rate in the cells of the rat pancreas, the cycle being divided into four phases.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 78 (1966), S. 215-216 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 5 (1966), S. 263-263 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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