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  • Articles: DFG German National Licenses  (8)
  • Electronic Resource  (8)
  • 1
    Electronic Resource
    Electronic Resource
    Cambridge : Cambridge University Press
    Modern Asian studies 11 (1977), S. 310-311 
    ISSN: 0026-749X
    Source: Cambridge Journals Digital Archives
    Topics: Ethnic Sciences , History , Political Science , Economics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] We have previously described a MAP2 complementary DNA clone, 38a, which hybridizes to the 6-kilobase (kb) mRNA that encodes MAP2c (ref. 3). The nucleotide sequence of this clone was determined and the deduced ammo-acid sequence was compared with that of high-molecular weight MAP2 from juvenile ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 336 (1988), S. 674-677 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Fig. 1 The location of mRNAs for MAP2 (a) and tubulin (d) in six-day-old rat cerebral cortex revealed by in situ hybridization with cDNA probes. The location of label is shown by the white autoradiographic grains. The positions of cells in the same sections are shown by bisbenzimide fluorescent ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Development genes and evolution 200 (1991), S. 108-112 
    ISSN: 1432-041X
    Keywords: Tenascin ; Embryogenesis ; Feather germ ; mRNA ; In situ hybridization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary I have studied the distribution of tenascin and its transcript during feather germ morphogenesis using immunohistochemistry and in situ hybridization. Anti-tenascin staining is intense in the periphery of dermal core condensations in both the feather rudiment and bud. There is faint anti-tenascin immunoreactivity in the overlying epithelium, but the apex of the bud is unstained. The appearance of tenascin in the developing feather is transient, as no significant anti-tenascin staining can be detected in the feather shaft or follicle at later stages of development. In situ hybridization with a tenascin cDNA probe reveals tenascin mRNA in the epithelial placode of the feather rudiment and early bud. In contrast, tenascin mRNA is concentrated in the dermis in the late feather bud. Therefore, at the time when inductive events are taking place, the expression of tenascin flips from the epithelium overlying tenascin-rich mesenchyme to the mesenchyme itself.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Development genes and evolution 199 (1990), S. 169-173 
    ISSN: 1432-041X
    Keywords: Tenascin ; Embryogenesis ; Mesenchyme ; Cell motility
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary We have used polyclonal antisera raised against vertebrate tenascin to identify and localize tenascin-like proteins in the developing sea urchin. These antisera recognize high-molecular weight proteins on immunoblots of sea urchin embryo homogenates that are similar in size and appearance to tenascin from vertebrates. These proteins appear as a doublet with an apparent molecular weight of 150 kDa and a larger, broad band with an apparent molecular weight of 350 kDa. Whole mounts of sea urchin embryos and larvae were stained with one of these antisera. The anti-tenascin stained the surface of primary mesenchyme cells during their phase of active migration. This staining was sensitive to detergent, suggesting that the protein recognized by the antiserum was associated with the cell surface. During later stages of development, the bulk of the antitenascin staining was found dispersed throughout the blastocoel matrix, and was no longer sensitive to detergent. We conclude that sea urchins express tenascin-like proteins during early stages of development, and that these proteins may play a role associated with primary mesenchyme cell morphogenesis.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1573-5117
    Keywords: predation ; reactive distance ; parthenogenic eggs ; Daphnia magna ; Lepomis macrochirus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The distance at which the bluegill sunfish (Lepomis macrochirus) can locate Daphnia magna with parthenogenic eggs is shown to be significantly greater than the reactive distance for non-gravid Daphnia of the same size. This difference is due to greater visibility of the gravid prey and not to different locomotor behavior, since there was no correlation between the number of eggs carried by a Daphnia and the antennal beat frequency. Based on this experiment and other observations, an explanation is given for selective predation of polymorphic cladoceran populations.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Human ecology 19 (1991), S. 99-113 
    ISSN: 1572-9915
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Ethnic Sciences
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Developmental Dynamics 203 (1995), S. 477-490 
    ISSN: 1058-8388
    Keywords: Thrombospondin ; Development ; Extracellular matrix ; In situ hybridization ; Chondrogenesis ; Osteogenesis ; Cornea ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The thrombospondins are a family of related glycoproteins found in the embryonic extracellular matrix. To date, five members of this family have been identified. Thrombospondin-1 and thrombospondin-2 have similar primary structure, but are expressed in different tissues at different times during development. Thrombospondins-3, -4, and cartilage oligomeric protein belong to a second thrombospondin subgroup in which the carboxyl-half of each molecule is most similar to thrombospondin-1 and -2. Here, we report the cloning and sequencing of a novel probe to avian thrombospondin-4. We have used this probe to determine the origins of thrombospondin-4 in the chick embryo by in situ hybridization. Thrombospondin-4 transcripts first appear in the mesenchyme surrounding bone anlage coinciding with the initial stages of osteogenesis. The expression in osteogenic tissues is transient: thrombospondin-4 mRNAs are not seen in the osteoblasts of bone collars in developing long bones. This pattern is distinct from avian thrombospondin-2, which is expressed in perichondrium and embryonic fibrous connective tissues. Our observations indicate that connective tissues are the principal site of thrombospondin-4 expression in the chick. The diverse origins of different thrombospondin gene family members imply distinctive roles for these proteins related to the growth and differentiation of cartilage, tendons, and bone. ©1995 Wiley-Liss, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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