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  • 1
    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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  • 2
    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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