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  • 1985-1989  (3)
  • 1905-1909
  • 1987  (3)
  • Life and Medical Sciences  (2)
  • Cell isolation  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 250 (1987), S. 543-549 
    ISSN: 1432-0878
    Keywords: Olfactory sensilla ; Sensory neurons ; Morphogenesis ; Cell isolation ; Antheraea polyphemus, Antheraea pernyi (Insecta, Lepidoptera)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary By combined enzymatic and mechanical treatment, it was possible to dissociate the sensory epithelium of developing antennae of male Antheraea polyphemus and A. pernyi silkmoths from the stage of separation of the antennal branches up to the early stages of cuticle deposition. Large numbers of entire developing trichoid sensilla were isolated. These are characterized by a large trichogen cell with a long apical, hair-forming process and a large nucleus. A cluster of 2–3 sensory neurons, enclosed by the thecogen cell, is situated in the basal region. The dendrites run past the nucleus of the trichogen cell into the apical process from which they protrude laterally. The nuclei of the tormogen and a 4th enveloping cell can be distinguished near the base of the prospective hair. After further dissociation, only the neuron clusters remain, still enclosed by their thecogen cell and often attached to the antennal branch nerve via their axons. It is finally possible to disrupt the thecogen cells and the axons, leaving the sensory neurons with inner dendritic segments and axon stumps. The majority of these neurons can be expected to be olfactory.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 131 (1987), S. 36-42 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Treatment of murine peritoneal macrophages for 30 min with lipopolysaccharide (LPS) resulted in a transient increase in c-fos proto-oncogene mRNA levels (Introna et al., 1986). After 2 h from the initial treatment, c-fos mRNA could no longer be detected and its expression could not be restimulated either by LPS or by other signals including colony stimulating factor-1 (CSF-1) and phorbol myristate acetate (PMA), both of which are able to induce expression of the c-fos gene in unstimulated macrophages. When LPS was removed after an initial 30 min incubation, responsiveness to a second exposure to LPS began to reappear after 3 h and was completely restored by 20 h. The same pattern of desensitization of c-fos induction was observed when CSF-1 stimulated macrophages were subsequently exposed to LPS. The loss of sensitivity to PMA following pretreatment with LPS was selective for c-fos expression as LPS treated macrophages remained responsive to PMA with respect to the ability to stimulate secretion of H2O2. The mechanism of desensitization was localized, at least in part, at the level of transcription as demonstrated by analysis of c-fos transcripts in nuclei isolated from macrophages pretreated and restimulated with LPS.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ [u.a.] : Wiley-Blackwell
    Journal of Orthopaedic Research 5 (1987), S. 150-153 
    ISSN: 0736-0266
    Keywords: Laser Doppler flowmetry ; Blood cell flux ; Cruciate blood flow ; Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The purpose of this study was to quantitate the blood flow of the anterior cruciate ligament in vivo. Functional flow was evaluated using laser Doppler flowmetry (LDF), for which the output signal, blood cell flux (BCF), is expressed in terms of volts. Ten patients undergoing routine arthroscopic surgery with clinically intact anterior cruciate ligaments were selected at random for participation in the study. Under arthroscopic visualization, a 2.2-mm probe was placed through a trocar sleeve into the anterior cruciate ligament after the arthroscopic procedure. Pulsatile flow within the ligament was observed in all patients. The mean maximum BCF value ranged from 101 to 274 mV; SD range was + 3-9 mV. The mean minimum BCF ranged from 75 to 197 mV; SD range was + 0 to 9 mV. Laser Doppler flowmetry offers significant promise as a method for measurement of in vivo anterior cruciate and cruciate substitution blood flow.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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