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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 30 (1991), S. 3118-3120 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1520-6041
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 111 (1989), S. 7659-7661 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK and Malden, USA : Blackwell Science Ltd
    BJOG 112 (2005), S. 0 
    ISSN: 1471-0528
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Physiology 62 (2000), S. 649-671 
    ISSN: 0066-4278
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Medicine , Biology
    Notes: Abstract Regulated assembly of a highly specialized interconnecting network of vascular endothelial and supportive cells is fundamental to embryonic development and organogenesis, as well as to postnatal tissue repair in metazoans. This review advances an "endotheliocentric" model that defines tasks required of endothelial cells and describes molecular controls that regulate steps in activation, assembly, and maturation of new vessels. In addition to the classical assembly mechanisms-angiogenesis and vasculogenesis-endothelial cells are also recruited into vascular structures from the circulatory system in adult animals and from resident mesenchymally derived progenitors during organogenesis of kidney and other organs. Paracrine signaling cascades regulated by hypoxia initiate a sequentially coordinated series of endothelial responses, including matrix degradation, migration, proliferation, and morphogenetic remodeling. Surface receptors on committed endothelial lineage progenitors transduce cues from extracellular-matrix-associated proteins and cell-cell contact to direct migration, matrix attachment, proliferation, targeting and cell-cell assembly, and vessel maturation. Through their capacity to spatially segregate and temporally integrate a diverse range of extracellular signals, endothelial cells determine their migratory paths, cellular partners, and life-or-death responses to local cues.
    Type of Medium: Electronic Resource
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  • 6
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    Unknown
    Columbia, Mo., etc. : Periodicals Archive Online (PAO)
    Sociological quarterly. 36:3 (1995:Summer) 505 
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  • 7
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The most detailed long-term record of seawater chemistry known to the authors is the Panulirus Station 4S' data set, collected by the Bermuda Biological Station from south of Bermuda at monthly intervals from 1952 to the present1. Although this record has proved valuable in many oceano-graphic ...
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-1939
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary To explore the mechanical determinants of feeding strategies for nectar feeders, we develop a fluid dynamical and behavioral model describing the mechanics and energetics of capillary feeding in hummingbirds. Behavioral and morphological data for Calypte and Archilochus are used to test and illustrate this model. We emphasize the important differences between capillary and suction mechanisms of fluid feeding. Model predictions of nectar intake rates and nectar volumes per lick are consistent with observed values for Calypte anna. The optimal nectar concentration maximizing rate of energy intake depends on tongue morphology and licking behavior. For hummingbirds exhibiting optimal licking behavior, the optimal nectar concentration is 35–40% sucrose for feeding on large nectar volumes. For small nectar volumes, the optimal concentration is 20–25%. The model also identifies certain tongue morphologies and licking frequencies maximizing energy intake, that are consistent with available observations on licking behavior and tongue design in nectar feeding birds. These predictions differ qualitatively from previous results for suction feeding in butterflies. The model predicts that there is a critical food canal radius above which suction feeding is superior to capillary feeding in maximizing the rate of energy intake; the tongues of most hummingbirds and sunbirds fall above this critical radius. The development of suction feeding by nectarivorous birds may be constrained by the elastic properties of their flexible tongues. Our results show that, in terms of morphology, scaling, and energetics, different mechanisms of feeding on the same food resource can lead to qualitatively different predictions about optimal design and feeding strategies.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-1939
    Keywords: Pieris ; Nectivory ; Optimal foraging ; Muscle mechanics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary We develop a mechanistic model for nectar feeding in butterflies that integrates the two basic components of the feeding process: the fluid dynamics of nectar flow through the food canal and the contractile mechanics of the muscular, cibarial pump. We use the model to predict the relation between rate of energy intake during feeding and nectar concentration. We then identify nectar concentations that maximize energy intake rates (the optimal concentrations). We illustrate the model using measurements of the food canal and cibarium of Pieris butterflies. The model predicts an overall optimal range of nectar concentration of 31–39% sucrose for butterflies, which is in agreement with previously reported laboratory values. The model also predicts an interaction among the geometries of the food canal, the cibarial cavity, and the cibarial muscles, that allows us to identify the combinations of food canal, cibarium, and muscle dimensions that yield the highest rates of energy intake. Nectar-feeding is “functionally equivalent” in butterflies and hummingbirds: two physically different feeding mechanisms can yield identical energy intake rates. This equivalence results from a mathematical and physical similarity between quasi-steady-state fluid flow in hummingbrid tongues and the force-velocity characteristics of contracting cibarial muscle in butterflies.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1573-2592
    Keywords: Western blot ; autoantibodies ; cryptic endothelial antigens ; thrombotic microangiopathies
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Autoantibodies detected by immunofluorescence, ELISA, and complement-fixation techniques have provided discriminatory markers for many human diseases. However, these commonly applied assays may fail to detect antibodies against antigenic sites which are either inaccessible or not displayed in recognizable cellular structures. Moreover, molecular identities of recognized antigen(s) are not determined with such methods. We have used Western blot analysis of cellular proteins derived from human renal microvascular endothelial cells (HRMEC) to identify autoantibodies in patients with pathological endothelial injury. Exploring the possibility that endothelial injury may expose cryptic endothelial antigens to immune recognition, we detected antibodies binding a number of distinct HRMEC proteins. Among these, antibodies recognizing specific HRMEC proteins of 43 kDa were commonly detected in plasmas from patients with thrombotic thrombocytopenic purpura (TTP) (13 of 14) and hemolytic uremic syndrome (HUS) (4 of 5) but were absent in 9 of 10 healthy subjects and 11 patients with a range of diseases not associated with endothelial injury of insult. Antibodies binding 43-kDa HRMEC antigens were detected in individual patients with systemic lupus erythematosus, anti-glomerular basement membrane nephropathy, and heparin-associated thrombocytopenia, as well as in one of three patients with immune thrombocytopenic purpura. Similar antibodies were detected in one hypercholesterolemic subject. Antibodies from four TTP patients were affinity purified and shown by two-dimensional analysis to recognize 43-kDa proteins having identical pl's (5.9, 6.0, and 6.1). Subcellular fractionation localized these antigens to cytosolic and nuclear compartments, sites presumably protected from immune recognition in the absence of endothelial injury. Western blot recognition of antiendothelial antibodies offers opportunities to define molecular characteristics and cellular distribution of antigens while generating reagents useful in their purification.
    Type of Medium: Electronic Resource
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