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  • Antarctic Peninsula; ANT-XXVIII/4; Bottom trawl; BT; Comment; CT; Curator/sampler; Date; Date/Time of event; Eggs; Eggs, diameter; Eggs, length; Eggs weight, fresh; Event label; Gonad, mass; Identification; Latitude of event; Length, mantle; Longitude of event; Mass; Maturation stage; MUC; MultiCorer; Ovary, diameter; Oviducal gland, diameter; Polarstern; PS79; PS79/190-1; PS79/191-1; PS79/197-1; PS79/198-1; PS79/206-1; PS79/219-1; PS79/221-1; PS79/222-1; PS79/228-1; PS79/235-1; PS79/236-1; PS79/237-1; PS79/238-1; PS79/242-1; PS79/243-1; PS79/244-1; PS79/247-2; PS79/254-1; PS79/258-1; PS79/259-1; PS79/286-1; PS79/290-1; PS79/4-track; Scotia Sea; Species; Underway cruise track measurements  (1)
  • Morphogenesis  (1)
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  • 1
    Publication Date: 2024-04-25
    Description: All information is related to the cruise POLARSTERN PS79 - ANTXXVIII-4 to the Antarctic Peninsula between March and April 2012. Animals were collected, identified and labelled by Dr. Christoph Noever during the 2012 cruise. In laboratory all animals were re-examined by Richard Schwarz.
    Keywords: Antarctic Peninsula; ANT-XXVIII/4; Bottom trawl; BT; Comment; CT; Curator/sampler; Date; Date/Time of event; Eggs; Eggs, diameter; Eggs, length; Eggs weight, fresh; Event label; Gonad, mass; Identification; Latitude of event; Length, mantle; Longitude of event; Mass; Maturation stage; MUC; MultiCorer; Ovary, diameter; Oviducal gland, diameter; Polarstern; PS79; PS79/190-1; PS79/191-1; PS79/197-1; PS79/198-1; PS79/206-1; PS79/219-1; PS79/221-1; PS79/222-1; PS79/228-1; PS79/235-1; PS79/236-1; PS79/237-1; PS79/238-1; PS79/242-1; PS79/243-1; PS79/244-1; PS79/247-2; PS79/254-1; PS79/258-1; PS79/259-1; PS79/286-1; PS79/290-1; PS79/4-track; Scotia Sea; Species; Underway cruise track measurements
    Type: Dataset
    Format: text/tab-separated-values, 28176 data points
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of mathematical biology 35 (1996), S. 97-113 
    ISSN: 1432-1416
    Keywords: Key words: Tendon ; Cell density ; Morphogenesis ; Collagen ; Cell proliferation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Mathematics
    Notes: Abstract.  A mathematical model of tendon morphogenesis is presented that is consistent with the dramatic transitions seen in this tissue as it progresses from rapid growth early in development to no growth in the adult. To accomplish this change, the embryonic chick tendon is hypercellular with each cell dedicating half of its protein production to procollagen but over time, as growth subsides, the tissue gradually becomes hypocellular with each cell producing only about 1% procollagen. Making this transition from the embryonic to the adult state, forming a roughly cylindrical tissue composed of ∼90% collagen, and linking the correct muscle to the right bone, is a complex task. The proposed solution requires only two factors: an activator of growth and an inhibitor complex, composed of the activator and another molecule that modifies the activity of the activator. From a diverse set of cell culture observations, these two factors were deduced as the primary components of the mechanism that allows cells to signal their presence to their neighbors. Since cell density signaling is the principal regulator of both collagen synthesis and cell proliferation, its components should play the key role in tendon development. A mathematical model based on the changes in the concentrations of these factors with cell density correlates well with the transitions observed in vivo. Furthermore, the model predicts that in the maturing chicken there should be a high cell density region at the muscle tendon interface. Experimental observations of frozen sections of tendon from a 4 month old chicken confirm this prediction.
    Type of Medium: Electronic Resource
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