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  • 1980-1984  (17)
  • 1965-1969  (4)
  • 1910-1914  (1)
  • 11
    facet.materialart.
    Unknown
    New York, etc. : Periodicals Archive Online (PAO)
    The Art Bulletin. 47:3 (1965:Sept.) 375 
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  • 12
    facet.materialart.
    Unknown
    New York, etc. : Periodicals Archive Online (PAO)
    The Art Bulletin. 47:3 (1965:Sept.) 377 
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 258 (1980), S. 794-794 
    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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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 308 (1982), S. 301-313 
    ISSN: 1434-601X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Excitation functions of (α,xn yp) reactions on93Nb withy≦6 andx≦10 have been measured in four different irradiations from 16 to 171 MeV bombarding energy by Ge(Li) spectroscopy of the residual activity of stacked foils. Similarly, previous measurements of181Ta(α,x n y p) reactions from 15 to 103 MeV were extended up to 170 MeVα-energy for residual nuclei withy≦4 andx≦12. Including isomeric states a total number of 37 residual activities could be identified in93Nb+α. From the rather complexγ-decay spectra altogether 28 different excitation functions of sizable length could be established. For181Ta+α 10 different residual activities were analyzed so that together with the former data a set of 15 excitation functions is available. The whole set of excitation functions provides a large data basis for probing the validity of combined equilibrium and preequilibrium reaction models in a wide energy range.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Springer
    Digestive diseases and sciences 26 (1981), S. 485-497 
    ISSN: 1573-2568
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Clinical and pathologic features of three patients with chronic intrahepatic cholestasis from birth are described. Each patient exhibited a paucity and hypoplasia of interlobular bile ducts, unusual facies, short stature, a pulmonary ejection systolic murmur, and structural anomalies of vertebrae. This constellation of defects constitutes a distinct syndrome to which the terms arteriohepatic dysplasia and syndromatic hepatic ductular hypoplasia are applied. Clinically, cholestasis was not progressive and, although the SGPT was chronically elevated (122–520 units/liter), features of liver cell failure did not develop. Changes in plasma lipids and lipoproteins and serum bile acids were consistent with chronic cholestasis. Liver biopsies from the three cases revealed pseudoxanthomatous change, increased stainable copper and mild hepatocellular degenerative changes. Electron microscopy of one of the liver biopsies revealed extension of thick bundles of collagen from portal areas into hepatic lobules with obliteration of the space of Mall. With increasing age, portal tracts contained fewer bile ducts. This apparent progression of the lesion was not associated with an inflammatory cell infiltrate, progressive fibrosis, or the development of cirrhosis.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Acta informatica 14 (1980), S. 243-255 
    ISSN: 1432-0525
    Source: Springer Online Journal Archives 1860-2000
    Topics: Computer Science
    Notes: Summary Every alternating t(n)-time bounded multitape Turing machine can be simulated by an alternating t(n)-time bounded 1-tape Turing machine. Every nondeterministic t(n)-time bounded 1-tape Turing machine can be simulated by an alternating (n + (t(n)) 1/2)-timebounded 1-tape Turing machine. For wellbehaved functions t(n) every nondeterministic t(n)-time bounded 1-tape Turing machine can be simulated by a deterministic ((nlogn)1/2 + (t(n))1/2)-tape bounded off-line Turing machine. These results improve or extend results by Chandra-Stockmeyer, Lipton-Tarjan and Paterson.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 68 (1965), S. 795-817 
    ISSN: 1432-0878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Giant epithelial cells are a conspicuous feature of the anterior segment of the vas deferens of Porcellio. Smaller epithelial cells (prismatic cells) are distributed between the giant cells. The giant cells may possibly form by hypertrophy of prismatic cells. Large nuclei with clumped heterochromatin are the most conspicuous feature of giant cells. Numerous large dictyosomes are distributed in the cytoplasm. These dictyosomes are comprised of closely packed, agranular cisternae and numerous vesicles. Anastomosing cisternae of endoplasmic reticulum fill the entire cytoplasmic region. These cisternae are often considerably dilated. The giant cells probably secrete a mucoprotein which binds sperm in the lumen of the vas into spermatophores. The probable mechanism of formation and extrusion of the secretory product is discussed for these cells, which apparently do not form secretory droplets. The presence of a prominent brush border on these supposedly secretory cells suggests the possibility that secretion may be transported in molecular form across the increased surface provided by the microvilli. Prismatic cells are recognizable by their less dilated endoplasmic reticulum, smaller nuclei with fewer heterochromatin clumps, and less conspicuous dictyosomes. In addition, dense granules are often found in association with the dictyosomes of these cells.
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 317 (1984), S. 626-627 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 92 (1980), S. 429-444 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Glykogen-Phosphorylasen katalysieren den Abbau von Glykogen durch Phosphat (oder Arsenat) zu Glucose-1-phosphat (bzw. Glucose + Arsenat). Alle Glykogen-Phosphorylasen enthalten Pyridoxal-5′-phosphat, ein Vitamin-B6-Derivat, als Cofaktor. Es ist im Enzym durch eine Doppelbindung mit der ∊-Aminogruppe eines Lysinrestes verbunden. Wird der Cofaktor vom Enzymprotein abgetrennt, erhält man inaktives Apoenzym. Das Enzym bleibt jedoch aktiv, wenn man die Doppelbindung mit NaBH4 reduziert. Sollte daher Pyridoxalphosphat an der Katalyse der Glykogen-Phosphorylasen beteiligt sein, so müßte es eine andere Funktion als in allen anderen „klassischen“ Pyridoxalphosphat-abhängigen Enzymen haben, denn diese werden durch Reduktion inaktiviert. Die 31P-NMR-Spektroskopie hat gezeigt, daß die Phosphatgruppe von Pyridoxalphosphat in den katalytisch aktiven Formen der Glykogen-Phosphorylasen als Dianion in einer hydrophoben Umgebung vorliegt. Die kovalente und allosterische Aktivierung der Muskel-Glykogen-Phosphorylasen wird von der Umwandlung der monoprotonierten Form der Phosphatgruppe des Cofaktors in die dianionische Form begleitet. Wir fanden nun derartige Ionisierungsänderungen auch bei den nichtregulierten aktiven Kartoffel- und E. -coli-Maltodextrin-Phosphorylasen, und zwar bei der Bindung von Glucose und Oligosacchariden sowie bei katalytischem Umsatz, d. h. Arsenolyse der α-1,4-glykosidischen Bindungen. (Maltodextrin-Phosphorylasen gehören wie Glykogen-Phosphorylasen zur Klasse der α-Glucan-Phosphorylasen.) Versuche unserer Gruppe sowie neuere Befunde über die Raumstruktur der kristallinen Muskel-Glykogen-Phosphorylase legen es nahe, die dianionische Phosphatgruppe als Protonenacceptor beim Glucosyltransfer vom und zum Glucosylacceptor anzusehen. Wenn dies auch nicht die einzige Erklärung der Befunde sein mag, so kann doch nicht mehr daran gezweifelt werden, daß die dianionische Phosphatgruppe des Cofaktors der Glykogen-Phosphorylasen eine katalytische Funktion ausübt.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 95 (1983), S. 336-337 
    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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