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  • Chemistry  (3)
  • Optic neuropile  (1)
  • MAN/SYSTEM TECHNOLOGY AND LIFE SUPPORT
  • Polymer and Materials Science
  • 1980-1984  (4)
  • 1983  (4)
Collection
Keywords
Publisher
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  • 1980-1984  (4)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 233 (1983), S. 305-317 
    ISSN: 1432-0878
    Keywords: Freeze fracture ; HVEM ; Retina ; Optic neuropile ; Drosophila
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The developmental mutant of Drosophila (ora JK84) is characterized by nonfunctional photoreceptor cells (R1–6), while the R7/R8 cells are normal. A fundamental question is: Does the near absence of photosensitive membranes inhibit development of the Rl-6 axons and their synapses at the other end of the cell? The retina and first optic neuropile (lamina ganglionaris) were examined with freeze-fracture technique and high voltage electron microscopy. R1–6 have reduced rhabdomere caps; rhabdomeric microvilli have about 50% of the normal diameter and 20% of the normal length. Affected cells exhibit prominent vacuoles which appear to communicate with some highly convoluted microvillar membranes. Almost no P-face particles (putative rhodopsin molecules) are present in the R1–6 rhabdomeres, and particle densities are lower in R7 than previously reported. Near the rhabdomere caps, microvilli of R1–6 are fairly normal, but at more proximal levels they are greatly diminished in length and changed in orientation, while at still more proximal levels they are lost. R1–6, R7, and R8 axons from each ommatidium are bundled into normal pseudocartridges beneath the basement membrane. No abnormalities are found in the lamina ganglionaris, and all synaptic associations as well as the presumed “virgin” synapses (of R1–6) appear normal. No glial anomalies are present, and R7/R8 axons project through the lamina in the usual fashion. These fine structural findings are correlated with known electrophysiological, biochemical, and behavioral correlates of both sets of photoreceptors (R1–6, and R7/R8).
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1983 (1983), S. 1446-1447 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Neue Umlagerung von 1,2:4,8-Diepoxy-p-menthanErhitzen von 1,2:4,8-Diepoxy-p-methan (1) mit Aluminiumoxid in Toluol induziert eine Fragmentierung zum 6-Ethenyl-5,6-dihydro-2,2,6-trimethyl-2H-pyran-3(4H)-on (2).
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Naturstoffe werden seit Jahrmilliarden in Tieren, Pflanzen oder Mikroorganismen synthetisiert. Sie treten in der Regel enantiomerenrein auf. Ihre Chiralität kommt ihrer Verwendung als Nahrungsmittel oder als biologischer Wirkstoff zugute. Wo Naturstoffe nach Menge oder Qualität nicht ausreichen, beginnt man neuerdings, sie unverändert oder abgewandelt durch biologische Synthese zugänglich zu machen; auch dabei entstehen sie enantiomerenrein. Die chemische Synthese ist in den letzten zwanzig Jahren zu einer Haupttätigkeit für Organiker geworden. Ihre Zielverbindungen sind in erster Linie enantiomerenreine Naturstoffe oder deren Varianten mit biologischer Wirkung.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0570-0833
    Keywords: Stereoselectivity ; Natural products ; Natural products ; Estrone ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Natural products have been synthesized for billions of years in animals, plants, and microorganisms. As a rule they occur enantiomerically pure. Their chiral character corroborates their use in metabolism or as biologically active agents. Natural products may be insufficient in quality or quantity. They have recently begun to become accessible, either unchanged or modified, by biological synthesis; here, too, they are obtained enantiomerically pure. In the last twenty years chemical synthesis has become a major concern of organic chemists. Their target compounds are primarily enantiomerically pure natural products or biologically active variants thereof.
    Type of Medium: Electronic Resource
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