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  • 1
    Keywords: Volcanism North Atlantic Ocean ; Geology, Stratigraphic Tertiary ; Sea-floor spreading North Atlantic Ocean ; North-east Atlantic Ocean. Bed. Geological features ; Geology++North Atlantic Ocean ; geology ; volcanism ; geology, stratigraphic ; seafloor spreading ; Tertiary ; North Atlantic Ocean ; Konferenzschrift ; Atlantischer Ozean Nordost ; Geologie ; Vulkanismus ; Tertiär ; Seafloor spreading ; Atlantischer Ozean Nordost ; Geologie ; Vulkanismus ; Tertiär ; Seafloor spreading ; Submariner Vulkanismus ; Britische Inseln ; Island ; Grönland ; Färöer ; Barentssee ; Magmatismus ; Geologie ; Tertiär ; Vulkanismus ; Aufschluss
    Type of Medium: Book
    Pages: XII, 477 S.
    Edition: 1. publ.
    ISBN: 0632021713
    Series Statement: Special publication / Geological Society 39
    DDC: 551.7/8/091821
    RVK:
    Language: English
    Note: Includes bibliography and index
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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] Despite the concentration of members of the deep-sea drilling community around the North Atlantic, surprisingly few Deep Sea Drilling Project sites have been drilled that are suitable for even a cursory study of North Atlantic palaeoenvironments. Until recently the best sites in which to study the ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Oecologia 53 (1982), S. 105-110 
    ISSN: 1432-1939
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary As a preliminary to a population study using markrelease-recapture techniques, specimens of the Satyrid buttfly Melanargia galathea (L.) were subjected to a number of marking and capture techniques. Although the adults are thought to display both aposematic and cryptic coloration, the use of marks of different sizes and colours had no significant effect on recapture frequencies. However, repeated disturbance due to capture was found to significantly reduce recapture frequency. The influence of the different techniques on recapture frequencies could not be detected reliably by excessively low recapture rates, or by comparisons to Poisson distributions. It is suggested that these comparisons are of limited value as measures of the suitability of a marking or handling scheme. Subsequent work showed that capture affected recapture rates of several other species. Moreover, these effects could not be readily predicted from knowledge of the biology of these species. The implications of these findings are discussed.
    Type of Medium: Electronic Resource
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  • 4
    Publication Date: 2016-02-05
    Description: Rationale: Platelets shed microRNAs (miRNAs). Plasma miRNAs change on platelet inhibition. It is unclear whether plasma miRNA levels correlate with platelet function. Objective: To link small RNAs to platelet reactivity. Methods and Results: Next-generation sequencing of small RNAs in plasma revealed 2 peaks at 22 to 23 and 32 to 33 nucleotides corresponding to miRNAs and YRNAs, respectively. Among YRNAs, predominantly, fragments of RNY4 and RNY5 were detected. Plasma miRNAs and YRNAs were measured in 125 patients with a history of acute coronary syndrome who had undergone detailed assessment of platelet function 30 days after the acute event. Using quantitative real-time polymerase chain reactions, 92 miRNAs were assessed in patients with acute coronary syndrome on different antiplatelet therapies. Key platelet-related miRNAs and YRNAs were correlated with platelet function tests. MiR-223 ( r p =0.28; n=121; P =0.002), miR-126 ( r p =0.22; n=121; P =0.016), and other abundant platelet miRNAs and YRNAs showed significant positive correlations with the vasodilator-stimulated phosphoprotein phosphorylation assay. YRNAs, miR-126, and miR-223 were also among the small RNAs showing the greatest dependency on platelets and strongly correlated with plasma levels of P-selectin, platelet factor 4, and platelet basic protein in the population-based Bruneck study (n=669). A single-nucleotide polymorphism that facilitates processing of pri-miR-126 to mature miR-126 accounted for a rise in circulating platelet activation markers. Inhibition of miR-126 in mice reduced platelet aggregation. MiR-126 directly and indirectly affects ADAM9 and P2Y 12 receptor expression. Conclusions: Levels of platelet-related plasma miRNAs and YRNAs correlate with platelet function tests in patients with acute coronary syndrome and platelet activation markers in the general population. Alterations in miR-126 affect platelet reactivity.
    Keywords: Platelets, Secondary Prevention, Functional Genomics, Treatment
    Print ISSN: 0009-7330
    Electronic ISSN: 1524-4571
    Topics: Medicine
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  • 5
    Publication Date: 2015-02-08
    Description: Aims Acute coronary syndromes (ACSs) are driven by inflammation within coronary plaque. Interleukin-1 (IL-1) has an established role in atherogenesis and the vessel-response to injury. ACS patients have raised serum markers of inflammation. We hypothesized that if IL-1 is a driving influence of inflammation in non-ST elevation ACS (NSTE-ACS), IL-1 inhibition would reduce the inflammatory response at the time of ACS. Methods and results A phase II, double-blinded, randomized, placebo-controlled, study recruited 182 patients with NSTE-ACS, presenting 〈48 h from onset of chest pain. Treatment was 1:1 allocation to daily, subcutaneous IL-1receptor antagonist (IL-1ra) or placebo for 14 days. Baseline characteristics were well matched. Treatment compliance was 85% at 7 days. The primary endpoint (area-under-the-curve for C-reactive protein over the first 7 days) was: IL-1ra group, 21.98 mg day/L (95%CI 16.31–29.64); placebo group, 43.5 mg day/L (31.15–60.75) (geometric mean ratio = 0.51 mg/L; 95%CI 0.32–0.79; P = 0.0028). In the IL-1ra group, 14-day achieved high-sensitive C-reactive protein ( P 〈 0.0001) and IL-6 levels ( P = 0.02) were lower than Day 1. Sixteen days after discontinuation of treatment (Day 30) high-sensitive C-reactive protein levels had risen again in the IL-1ra group [IL-1ra; 3.50 mg/L (2.65–4.62): placebo; 2.21 mg/L (1.67–2.92), P = 0.022]. MACE at Day 30 and 3 months was similar but at 1 year there was a significant excess of events in the IL-1ra group. Conclusion IL-1 drives C-reactive protein elevation at the time of NSTE-ACS. Following 14 days IL-1ra treatment inflammatory markers were reduced. These results show the importance of IL-1 as a target in ACS, but also indicate the need for additional studies with anti-IL-1 therapy in ACS to assess duration and safety. Clinical Trial Registration EUCTR: 2006-001767-31-GB: www.clinicaltrialsregister.eu/ctr-search/trial/2006-001767-31/GB .
    Print ISSN: 0195-668X
    Electronic ISSN: 1522-9645
    Topics: Medicine
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