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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 364 (1993), S. 196-196 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] SIR - Tabin and Laufer1 present a thought-provoking model for the evolution of the tetrapod limb, but nevertheless leave untackled some important issues. First, it has long been known that the axial level of the paired appendages of fishes is plastic, in that the specific level of ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Development genes and evolution 198 (1989), S. 103-113 
    ISSN: 1432-041X
    Keywords: Morphogenesis ; Keratan sulfate ; Glycosaminoglycan ; Craniofacial morphogenesis ; Chondrogenesis ; Placodes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Using the monoclonal antibody MZ15 in immunocytochemical and ultrastructural studies we have been able to determine the spatiotemporal pattern of keratan sulfate (KS) distribution during quail craniofacial morphogenesis. KS-containing proteoglycans are found associated with invaginating placodes (olfactory, lens and otic), in developing pronephric tubules, notochord, pharynx and endocardium, and display developmental regulation. The appearance of such proteoglycans (PGs) during placode morphogenesis is particularly striking and we suggest that they may be an important component of the extracellular matrix which has been previously implicated in mediating the morphogenetic interactions and cell movements occurring at these sites. The otic vesicle during stage 18–22 displays a notable asymmetric distribution of KS-containing PGs. The role that these molecules may play and the reasons for this regionalization are, as yet, unclear but it is conceivable that the distribution of proteoglycans at this stage reflects subsequent differentiative events during otocyst development. Furthermore, our ultrastructural observations indicate that over the developmental period studied (H & H stages 8–22) keratan sulfate exists in at least two proteoglycan forms. Some spatiotemporal correlation has been found to exist between the distributions of KS-containing PGs and type II collagen as previously reported by Thorogood et al. (1986). We suggest that the proteoglycan detected at such sites is cartilage-specific proteoglycan and that it plays an important role, together with type II collagen, in the “signalling” mechanism which specifies the subsequent pattern of the chondrocranium. It is proposed that this interaction at epithelio-mesenchymal interfaces in the developing head parallels the matrix-mediated tissue interaction between notochord and somites which results in the formation of the cartilaginous primordia of the vertebrae from the sclerotomes as reported by Lash and Vasan (1978).
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Development genes and evolution 203 (1994), S. 445-449 
    ISSN: 1432-041X
    Keywords: RAR-β, RXR-γ ; Retinoids ; Neural crest ; Craniofacial development
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In situ hybridization reveals that RAR-β and RXR-γ genes in mesencephalic neural crest cultures are independently regulated. RAR-β transcripts are found in all cells, with a slight increase in signal/cell with time in culture. In contrast, the distribution of RXR-γ transcript is initially uniform but becomes increasingly heterogeneous, so that after 72 h in culture, a significant proportion of cells lack transcripts while a small subpopulation contains very high levels of message. These differences in the behaviour of the RARβ and RXRγ genes in vitro can be related to differences in their expression patterns in vivo.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 241 (1985), S. 165-169 
    ISSN: 1432-0878
    Keywords: Cell migration ; Neural crest ; Contact inhibition ; Coturnix coturnix japonica (Aves)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary When grown in confrontation culture on a planar substratum, avian neural crest cells and somite cells display both homotypic and heterotypic contact inhibition of movement as judged by analysis of time-lapse video recordings of locomotory and contact behaviour, and by use of a nuclear overlap assay. It is therefore unlikely that migration of neural crest cells within the embryo, and within embryonic tissues, can be explained on the basis of a lack of contact inhibition. The results are discussed in the general context of cell invasiveness.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular histology 13 (1981), S. 631-642 
    ISSN: 1573-6865
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Conclusions Evidently it is the circumstances of tissue association which are important with regard to the differentiation of NC-derived cells into primary cartilage and membrane bone. Tissue interactions of this sort apparently do not play a role in the differentiation of secondary cartilage, where simply theposition of NC-derived cells and their progeny within the early membrane bone primordium determines whether or not those cells will subsequently express a secondary chondrogenic potential. Whether we are considering the type of tissue association generated or the ‘specification’ of cell positioning, both are controlled by the parameter of NC cell migration. Thus disturbances in the conditions of migration, for instance retarded migration or incorrect timing, will generate anomalies of cranio-facial morphogenesis and of skull development, (Johnstonet al., 1977; Morriss & Thorogood, 1978). Furthermore, as phylogenetic differences in (skull) form are generated by changes in developmental mechanisms, simple quantitative changes in such parameters as NC migration and proliferation will have profound evolutionary consequences (see, for example, Kollar & Fisher, 1980). This review started by asking the question ‘How, in a developmental sense, does one build a skull?’ That question has not been answered but a few suggestions have been provided as to the rules of the developmental programme whereby the various skeletal tissues are laid down in a skull-specific pattern. It seems that these rules can be defined in terms of timing, circumstances of tissue association and spatial positioning of cells. A comprehensive identification and fuller recognition of rules such as these is, I propose, a pre-requisite to understanding this particular developmental programme.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Developmental Dynamics 201 (1994), S. 151-167 
    ISSN: 1058-8388
    Keywords: Morphogenesis ; Pattern formation ; Somite ; Notochord ; Teleost ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: We have made a detailed analysis of cell behaviour using high resolution timelapse microscopy of the earliest cellular interactions taking place during morphogenesis of the notochord and somites in intact teleost embryos. Notochord formation is typified by active intercalation of paraxial mesenchyme cells into the lateral surfaces of the primordium. Following this recruitment phase, complete immiscibility develops between cells of the notochord and the presomitic mesenchyme. Dorso-ventral and rostro-caudal expansion of the notochord is characterised by translocation of cells within dorsoventral planes of section and is supported by elongation of the remaining cells and reduction in width across its latero-medial axis. A lateral pallisading of paraxial mesenchyme against the lateral aspects of the notochord precedes overt segmentation. Intersomitic furrows form by localised de-adhesion at small foci at the nascent intersomitic planes, which are consolidated by coalescence of such areas by de-adhesion to produce the interface. It is not possible to predict precisely where cells would initiate de-adhesion since there is a stochastic element to the phenomenon. Once formed, boundaries between somites are stable and provide no opportunity for mixing, except across the first formed furrow, which disintegrates at the 4-6 somite stage. The first ten somites form at a constant rate of 2.3 somites/hr, during which time we recorded constant relative displacement of the segmental plate against the rostro-caudally elongating notochord. Unlike teleost epiboly and gastrulation, no large-scale movements of individual cells can be detected during elaboration of the embryonic axis. © 1994 Wiley-Liss, Inc.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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