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  • 1975-1979  (12)
  • 1965-1969  (6)
  • 11
    facet.materialart.
    Unknown
    Harlow, etc. : Periodicals Archive Online (PAO)
    English Historical Review. 82:325 (1967:Oct.) 726 
    Library Location Call Number Volume/Issue/Year Availability
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  • 12
    facet.materialart.
    Unknown
    London : Periodicals Archive Online (PAO)
    Journal of theological studies. n.s.:20 (1969) 697 
    ISSN: 0022-5185
    Topics: Theology and Religious Studies
    Notes: AUTHORS AND BOOKS REVIEWED OR NOTICED
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Probability theory and related fields 34 (1976), S. 135-155 
    ISSN: 1432-2064
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 254 (1976), S. 768-768 
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular histology 9 (1977), S. 393-417 
    ISSN: 1573-6865
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Synopsis The three major types of glycoproteins present in animal cells, that is, the secretory, lysosomal and plasma membrane glycoproteins, were examined with regard to the sites of synthesis of their carbohydrate side chains and to their subsequent migration within cells. The site at which a monosaccharide is added to a growing glycoprotein depends on the position of that monosaccharide in the carbohydrate side-chain. Thus, radiauutography of thyroid cells within minutes of the intravenous injection of labelled mannose, a sugar located near the base of the larger side-chains, reveals that it is incorporated in rough endoplasmic reticulum, whereas the more distally located galactose and fucose are incorporated in the Golgi apparatus. Recently [3H]N-acetylmannosamine, a specific precursor for the terminally located sialic acid residues, was shown to be also added in the Golgi apparatus. Presumably synthesis of glycoproteins is completed in this organelle. Radioautographs of animals sacrificed a few hours after injection of [3H]N-acetylmannosamine show that, in many secretory cells, labelled glycoproteins pass into secretory products. In these cells, as well as in non-secretory cells, the label may also appear within lysosomes and at the cell surface. In the latter site, it is presumably included within the plasma membrane glycoproteins whose carbohydrate side-chains form the cell coat. The continual migration of glycoproteins from Golgi apparatus to cell surface implies turnover of plasma membrane glycoproteins. Radioautographic quantitation of [3H]fucose label at the surface of proximal tubule cells in the kidney of singly-injected adult mice have shown that, after an initial peak, cell surface labelling decreases at a rate indicating a half-life of plasma membrane glycoproteins of about three days.
    Type of Medium: Electronic Resource
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  • 16
    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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  • 17
    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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  • 18
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Antibody against the intermediate-sized filaments from gizzard smooth muscle was used to determine the presence or absence of reacting 10-nm filaments in different cell types. The antibody against gizzard 10-nm filaments reacted with filaments in cultured smooth muscle cells, skeletal myotubes and postmitotic skeletal myoblasts. It did not bind to the 10-nm filaments present in replicating presumptive myoblasts and fibroblasts, or the 10-nm filaments in spinal ganglion cells.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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