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  • 2000-2004
  • 1965-1969  (3)
  • 1925-1929  (6)
  • 1967  (3)
  • 1929  (6)
Material
Years
  • 2000-2004
  • 1965-1969  (3)
  • 1925-1929  (6)
Year
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 32 (1967), S. 2412-2416 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of medicinal chemistry 10 (1967), S. 556-564 
    ISSN: 1520-4804
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    facet.materialart.
    Unknown
    Stuttgart, etc. : Periodicals Archive Online (PAO)
    Deutsche Vierteljahrsschrift für Literaturwissenschaft und Geistesgeschichte. 7 (1929) 682 
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 8 (1929), S. 2332-2333 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 8 (1929), S. 937-938 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-2013
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Zusammenfassung 1. Für die Beurteilung der Achsenzylinderhüllen ist die ultramikroskopische Untersuchung wegen der in hohem Ma\e störenden BeugungsphÄnomene im allgemeinen im Nachteil gegenüber der gewöhnlichen Beobachtung im Hellfeld. Dagegen erlaubt sie einen tieferen Einblick in die Struktur des Achsenzylinders, wenigstens in dem negativen Sinne, da\ kontinuierliche, aus gleichmÄ\ig dichter Substanz bestehende Primitivfibrillen nicht gefunden werden. Die Partikelchen, die des öfteren in Reihen angeordnet erscheinen, sind vielleicht gar nicht als prÄexistente Formelemente (Micellarstruktur) anzusprechen, denn es bleibt immerhin möglich, da\ man es bei ihnen schon mit einer SchÄdigung der Nervenfaser und dem Beginn einer Koagulation zu tun hat. 2. Infolge des Umstandes, da\ sich etwaige Absterbeprozesse wÄhrend der ultramikroskopischen Durchmusterung der PrÄparate der Kontrolle entziehen und auch die Nervenfasern eines und desselben PrÄparates keinen einheitlichen Charakter zeigen, ermangeln RückschlÄge auf eine kolloidale Beeinflussung durch Natrium- und Kaliumionen oder durch die Narkotica einer genügend zuverlÄssigen Grundlage. 3. Hingegen gelingt am fixierten PrÄparate auch bei Berücksichtigung aller Kautelen der Nachweis für die Richtigkeit der FeststellungHöbers bezüglich der Differenzen zwischen den Achsenzylindern des Natrium- und Kaliumnerven. Allerdings handelt es sich dabei kaum um so einfache kolloidale ZustandsÄnderungen wie Verdichtung bzw. Auflockerung, sondern sehr wahrscheinlich um eine chemische Reaktion, nÄmlich die Bildung von Proteinaten. 4. Die Narkose ist, wie sich bei geeigneter Methodik gleichfalls am fixierten PrÄparate, und zwar auf direktem Wege, dartun lÄ\t, mit kolloidalen VerÄnderungen im Axoplasma verbunden. Es ist anzunehmen, da\ das Axoplasma im allgemeinen in der Narkose gerinnungsfördernden Einflüssen in stÄrkerem Grade unterliegt, vielleicht auch umgekehrt auflockernden Faktoren einen grö\eren Widerstand entgegensetzt. — Die kolloidale Einwirkung erstreckt sich über den Gesamtquerschnitt des Achsenzylinders; man ist nicht berechtigt, das histologische Substrat vorbehaltlos für eine Theorie über das Verhalten von Grenzmembranen zu verwerten. 5. Das Axoplasma erfÄhrt bei der Narkose nicht lediglich sekundÄr eine Einengung durch Quellung der Markscheide oder eine Retraktion infolge verÄnderter OberflÄchenspannung, verrÄt vielmehr eine hiervon unabhÄngige selbstÄndige Reaktion.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 17 (1929), S. 84-85 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Documenta ophthalmologica 22 (1967), S. 1-71 
    ISSN: 1573-2622
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. The wave pattern of the normal ERG elicited by flash stimuli, its recovery from a preliminary light adaptation, and a possible interaction between scotopic and photopic activity were studied. 2. a. In the course of dark adaptation photopic and scotopic components greatly overlap in the ERG, so that detail cannot be clearly discerned. Scotopic dark adaptation was, therefore, impeded so that the recovery of the primarily photopic response could be followed while the scotopic response was limited. This was helped by cutting off part of the low-pass filters in the preamplifiers. b. The recovery of the primarily scotopic response was followed during undisturbed dark adaptation in an ERG elicited by weak light stimuli which did not suppress the recovery of the scotopic reponse but were too weak to produce a full photopic response. 3. a. The recovery of photopic electrical activity was characterized by a fast increase in the positive amplitude of the primarily photopic wave within the first minute in the dark which was followed by a decrease in amplitude. b. The scotopic recovery was characterized by a continuous increase in the positive amplitude of the scotopic wave for about 25 minutes which eventually dominated the ERG. 4. When dark adaptation was undisturbed, the amplitude of the photopic wave remained constant after the decrease. It increased again, however, when scotopic recovery was impeded. 5.During undisturbed dark adaptation, the negative photopic and scotopic components exhibited a similar recovery as the respective positive components. 6.The phenomena were explained by assuming an inhibitory influence on photopic recovery by the scotopic activity. 7. As in the light, the primarily photopic ERG is characterized by a number of negative and positive peaks with a fixed latency. They are regularly spaced along the time axis at a frequency of around 140 cps, and are considered to be due to oscillatory potentials, which summate with the negative wave and the positive photopic wave. 8. A slow oscillatory potential at a frequency of 50 cps was observed in light adaptation. It is less clearly visible under conditions of dark adaptation. 9. The appearance of the fast oscillatory potentials and the extent of their superimposition upon the photopic main wave seem to depend on the latency of the latter. Their changes in amplitude are explained by a shortening or lengthening in the latency of the photopic main wave which occur both during the course of dark adaptation and with the change in stimulus intensity.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 76 (1929), S. 67-77 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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