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  • Electronic Resource  (9)
  • 1980-1984  (7)
  • 1965-1969  (2)
  • 1
    ISSN: 1520-4804
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Neuroscience 6 (1983), S. 381-418 
    ISSN: 0147-006X
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 292 (1981), S. 836-838 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Our findings are based on immunofluorescent localization of IF proteins using previously characterized antisera against FIF protein the 180,000-molecular weight (MW)10'21 and 70,000-MW21 NIF proteins, and IF proteins characteristic of astrocytes21 and muscle cells23'24. Cryostat sections were taken ...
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Preliminary studies were carried out with hypothalamus from female rats at random stages of the oestrous cycle and from male animals. Figure 1 shows the basal release of immunoreactive LH-RH from synaptosomes, during a 30-min incubation period. Levels of LH-RH in the incubation medium were ...
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 165 (1969), S. 543-557 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Light and electron microscopic radioautographs of the tissues of young rats which were sacrificed at various times after a single 3H-ribose injection revealed a wide distribution of the label.Nuclear reactions were seen over hepatocytes and other cell types. After removal of RNA by treatment with RNAse, most nuclear reactions were absent; they were, therefore, attributed to the incorporation of label into newly-synthesized RNA. In about 2% of the nuclei, however, labeling persisted after RNAse, but was absent after DNAse treatment, indicating uptake into newly-synthesized DNA. Hence, ribose may be taken up into nucleic acidsundergoing synthesis.In cells of liver and cartilage as well as in some muscle fibers, moderate reaction appeared over glycogen areas. Removal of the label by salivary amylase confirmed its uptake into glycogen.In mucous and other secretory cells, amylase resistant radioautographic reactions appeared over the Golgi region and later over secretion products. Presumably the label was incorporated into the glycoproteinmoieties of these secretions.Many, if not all, cells in the body appear to be able to utilize free exogenous ribose. It is presumed that ribose is first phosphorylated and then either incorporated into the RNA and DNA being synthesized in the nucleus or converted into the glucose or fructose derivatives used for glycogen and glycoprotein synthesis in the cytoplasm. That these pathways may play a significant physiological role is suggested by the recent finding of free ribose in the blood.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 13 (1969), S. 2371-2381 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The viscosity-average molecular weight, Mv, of a polymer is given operationally through its limiting viscosity number [η] and the Mark-Houwink equation [η] = KMvα, where K and α are empirical constants. If [η] is measured under different conditions, α and Mv will vary for the same sample. Mvα is the α-order moment about the origin of the differential weight distribution of the polymer. Practically, the results of a series of Mv measurements on the same polymer are equivalent to a cluster of fractional moments of the weight distribution, with orders between 0.55 and 0.80. It is shown that the first moment of this distribution, Mw, may be estimated reliably by a straightline plot of Mv against α-extrapolated to α equals 1. This simple expedient is effective although there are probably no molecular weight distributions in which the relation is strictly linear and there are no mathematical distributions for which the αth root of the αth moment is a linear function of α for all α. The deviation from linearity is small enough, however, that the real curve can be represented by a straight line over a short range of α. Thus, Mw can be measured accurately, but Mn, Mz, or the breadth of the distribution is not accessible by this method. Experimental and literature examples show that the precision of Mw estimated by this method compares well with that of primary methods for measuring this molecular weight average. If a linear relationship is observed with reliable α values, this appears to be a sufficient condition for estimation of a valid Mw.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Young (40 gm) rats were given a single intravenous injection of colchicine (4.0 mg) or vinblastine (2.0 mg). At 10 min after colchicine and 30 min after vinblastine administration, the rats were injected with 3H-fucose. Control rats received 3H-fucose only. All rats were sacrificed 90 min after 3H-fucose injection and their tissues processed for radioautography.In thyroid follicular cells of control animals, at this time interval, 57% of the total label was associated with colloid and secretory vesicles in the apical cytoplasm while 27% was localized in the Golgi apparatus and neighboring vesicles. In experimental animals, the proportion of label in colloid and apical vesicles was reduced by more than 69% after colchicine and more than 83% after vinblastine treatment. The proportion of label in the Golgi region, on the other hand, increased by more than 125% after colchicine and more than 179% after vinblastine treatment. Within the Golgi region, the great majority of the label was associated with secretory vesicles which accumulated adjacent to the trans face of the Golgi stacks. It is concluded that the drugs do not interfere with passage of newly synthesized thyroglobulin from the Golgi saccules to nearby secretory vesicles, but do inhibit intracellular migration of these vesicles to the cell apex. In most cells the number of vesicles in the apical cytoplasm diminished, but this was not always the case, suggesting that exocytosis may also be partially inhibited. The loss of microtubules in drug-treated cells suggests that the microtubules may be necessary for intracellular transport of thyroglobulin.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Previous studies have shown that colchicine and vinblastine inhibit secretion in many cell types by interrupting the normal intracellular migration of secretory products. In the present work, radioautography has been used to study the effects of these drugs on migration of membrane and secretory glycoproteins in a variety of cell types. Young (40 gm) rats were given a single intravenous injection of colchicine (4.0 mg) or vinblastine (2.0 mg). At 10 min after colchicine and 30 min after vinblastine administration, the rats were injected with 3H-fucose. Control rats received 3H-fucose only. All rats were sacrificed 90 min after 3H-fucose injection and their tissues processed for light microscope radioautography.Examination of secretory cell types such as ameloblasts and thyroid follicular cells in control animals revealed reactions of approximately equal intensity over the Golgi region and over extracellular secretion products, while in drug-treated rats most of the reaction was confined to the Golgi region. In a variety of other cell types, including endocrine cells (e.g., hepatocytes) and cells generally considered as nonsecretory (e.g., intestinal columnar cells), reaction in control animals occurred both over the Golgi region and over various portions of the cell surface. In drug-treated animals, a strong Golgi reaction was present, but reaction over the cell surface was weak or absent.These results indicate that in many cell types, colchicine and vinblastine inhibit migration out of the Golgi region not only of secretory glycoproteins, but also of membrane glycoproteins destined for the plasma membrane.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: In the first paper of this series (Bennett et al., 1984), lightmicroscope radioautographic studies showed that colchicine or vinblastine inhibited intracellular migration of glycoproteins out of the Golgi region in a variety of cell types. In the present work, the effects of these drugs on migration of membrane glycoproteins have been examined at the ultrastructural level in duodenal villous columnar cells and hepatocytes.Young (40 gm) rats were given a single intravenous injection of colchicine (4.0 mg) or vinblastine (2.0 mg). At 10 min after colchicine and 30 min after vinblastine administration, the rats were injected with 3H-fucose. Control rats received 3H-fucose only. All rats were sacrificed 90 min after 3H-fucose injection and their tissues processed for radioautography.In duodenal villous columnar cells, 3H-fucose labeling of the apical plasma membrane was reduced by 51% after colchicine and by 67% after vinblastine treatment; but there was little change in labeling of the lateral plasma membrane. Labeling of the Golgi apparatus increased. This suggests that labeled glycoproteins destined for the apical plasma membrane were inhibited from leaving the Golgi region, while migration to the lateral plasma membrane was not impaired. In hepatocytes, labeling of the sinusoidal plasma membrane was reduced by 83% after colchicine and by 85% after vinblastine treatment. Labeling of the lateral plasma membrane also decreased, although not so dramatically. Labeling of the Golgi apparatus and neighboring secretory vesicles increased. This indicates that the drugs inhibited migration of membrane glycoproteins from the Golgi region to the various portions of the plasma membrane. Accumulation of secretory vesicles at the sinusoidal front suggests that exocytosis may also have been partially inhibited. In both cell types, microtubules almost completely disappeared after drug treatment. Microtubules may, therefore, be necessary for intracellular transport of membrane glycoproteins, although the possibility of a direct action of these drugs on Golgi or plasma membranes must also be considered.
    Additional Material: 21 Ill.
    Type of Medium: Electronic Resource
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