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  • 1965-1969  (4)
  • 1
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 98 (1969), S. 538-549 
    ISSN: 1432-0878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. The technique of cultivation of dissociated neurons from chick spinal ganglia in Maximow assembly is described. 2. Three different techniques for preparation of neurons from spinal ganglia were compared: “hand-free dissection”, separation with nylon sieves and trypsinisation. All these techniques were useful. But the best results (working with 15 days chick embryo) were obtained by “hand-free dissection”. 3. The highest number of newly formed nerve processes was observed with spinal ganglia neurons from 12 to 16-day sold chick embryos. Under optimal conditions an average of 40% of the dissociated neurons formed processes. 4. Cells isolated from young (6 to 7-days old) embryos and embryos older than 19 days are not able to form new processes in culture, in our experimental conditions. 5. The influence of the composition of the medium in which the cells are cultivated was tested. A stimulatory effect on the outgrowth of new processes by 10–20% brain extract from 10-days chick embryos was demonstrated. The highest effect was observed with neurons isolated from 14 to 17-days old embryos. The presence of nerve growth factor (NGF) increased the number of processes newly formed in cultures from 8 to 17-days old embryos. With both brain extract and NGF, the length and ramifications of the fibres were greater.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 82 (1967), S. 65-81 
    ISSN: 1432-0878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary During the development of the chick embryo from the 6th to the 15th day of incubation, the cell types in cerebral hemispheres undergo differentiation. During this period the indifferent cells of the germinal layer migrate away from the neural cavity to form the mantle layer. These cells differentiate into neuroblasts and spongioblasts. RNA biosynthesis is very active in the cells of the germmal layer of the young embryos. From the 10th day on, it decreased becoming very weak in the 15-days old embryos. The RNA is stored in the nucleus and its passage to cytoplasm is very slow. In 6 and 8-days old embryos the RNA biosynthesis in the mantle layer is not very active but increases during embryonic development as the germinal cells differentiate. The biosynthesis is always more intense in the neuroblasts than in the spongioblasts. The RNA is stored in the nucleus and its passage to cytoplasm is slow in the young neuroblasts and the spongioblasts. The formation of Nissl bodies in neuroblasts and the differentiation of neuroblasts into neurons, which corresponds to the development of axons and dendrites, both are accompanied by an activation of the RNA passage from the nucleus into the cytoplasm.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A method of fractionation of neuroblasts and spongioblasts perikarya from developing chick embryo cerebral hemispheres is described. The tissue, treated by a mixture of acetone-glycerol-water is dissociated through a nylon sieve. Differential centrifugation on sucrose 1.3 M and 1.8 M has been used to obtain fractions enriched in neuroblasts (80% purity) and spongioblasts (90% purity). The duration of the whole operation is two hours. The evolution and distribution of the cells was studied on dissociated tissue from the 6th day of embryonic life to hatching. The proportion of neuroblasts varies from 13% at 6 days to 36% at 12 days. At the same period the proportion of the sum of indifferent cells and spongioblasts decreases from 81 to 58%, whereas the ependymal cells show little variation (6 to 9%). At hatching these proportions have not changed greatly: neuroblasts, spongioblasts and ependymal cells represent respectively 33, 65 and 2% of the total cells. The cellular differentiation proceeds from the 6th day to hatching. The size of neuroblasts increases and many of them become multipolar. The number of spindle-like cells and small indifferent cells whose origin is probably the germinal layer, decreases together with the thickness of this layer. Early spongioblasts appear only at 10 days and, later on, differentiate into oligodendroblasts and astroblasts.
    Type of Medium: Electronic Resource
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