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  • 11
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Prostaglandins 34 (1987), S. 685-696 
    ISSN: 0090-6980
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Physiology 57 (1995), S. 771-790 
    ISSN: 0066-4278
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Medicine , Biology
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 36 (1992), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Molecules encoded by the class I major histocompatibility genes bind short (nonameric) peptides produced by inlracellular proleolysis of antigens. These complexes formed intraeellularly are then expressed on membranes of target eells and recognized by the anligen receptor of eytolylic T cells. No binding of externally added peptides could so far be monitored directly on the antigen presenting cells, although cytotoxicity experiments and indirect binding assays provided evidence for its existence. Here we report experiments where specific binding to class I molecules, of externally added peptides, has been monitored on living cells, N-terminal biottn-labelled Kd-restricted peptides (residues 147-155, residues 147-158, and an analogue lacking the arginine at position 156. derived from the sequence of the influenza A virus nucleoprotein) were incubated with murine H-2Kd mastocytoma cells (line P815)dt 4°C. The binding on surface of hve, intact cells was then demonstrated fluoro metrically via ihe inieraction ofa streptavidin-phycoerythrin conjugate with the biotin-labelled peptides. Thus, this binding does not involve processing, and its specificity in terms of peptide structure was established by competition with the respective unmodified peptides. The specificity ofbinding to class I molecules was demonstrated by blocking experiments u.sing monoclonal antibodies specific for H-2Kd. Finally, a correlation was observed between the results of peptide binding measurements and those ofcytotoxieity assays.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 306 (1978), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 177 (1995), S. 427-437 
    ISSN: 1432-1351
    Keywords: Cockroach ; Escape behavior ; Giant interneuron ; Coordination ; Motor outputs
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract In the escape behavior of the cockroach, all six legs begin to make directed movements nearly simultaneously. The sensory stimulus that evokes these leg movements is a wind puff. Posterior wind receptors excite giant interneurons that carry a multi-cellular code for stimulus direction — and thus for turn direction-to the three thoracic ganglia, which innervate the three pairs of legs. We have attemptd to discriminate among various possible ways that the directional information in the giant interneurons could be distributed to each leg's motor circuit. Do the giant interneurons, for instance, inform separately each thoracic ganglion of wind direction? Or is there one readout system that conveys this information to all three ganglia, and if so, might the identified thoracic interneurons, which are postsynaptic to the giant interneurons, subserve this function? We made mid-sagittal lesions in one or two thoracic ganglia, thus severing the initial segments of all the known thoracic interneurons in these ganglia, and thus causing their projection axons to the other thoracic ganglia to degenerate. This lesion did not sever the giant interneurons, however (Fig. 5). Following such lesions, the legs innervated by the intact thoracic ganglia made normally directed leg movements (Figs. 4, 6, 7). Thus, the projection axons of the thoracic interneurons are not necessary for normal leg movements. Rather, the giant interneurons appear to specify to each thoracic ganglion in which direction to move the pair of legs it innervates.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 23 (1967), S. 66-67 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Riassunto È stato dimostrato che l'istamina ha un effetto sulle cellule del nodo seno-atriale del cuore di coniglio. Tale effetto consiste in un marcato aumento della velocità di depolarizzazione del potenziale «pacemaker», cui consegue un effetto cronotropo positivo.
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    Springer
    Inflammation research 36 (1992), S. C187 
    ISSN: 1420-908X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We had found that histamine (HA)-induced relaxation of cavian pulmonary artery is selectively inhibited by Nω-methyl-l-arginine (NMA) and thus depends on the synthesis ofl-arginine (ARG)-derived EDRF/nitric oxide (NO). We have now assessed whether ARG-derived NO also mediates the coronary-vasodilating effect of HA in the intact heart. Langendorff guinea pig hearts, vasoconstricted by the thromboxane agonist U46619 (86 nM), responded to HA (bolus intra-aortic injections of 1–30 μg) with dose-dependent increases in coronary flow (20–90%), heart rate and contractility. NMA (92 μM) markedly inhibited the HA-induced increase in coronary flow, but not its positive inotropic and chronotropic effects. A similar inhibition was obtained with the NO scavenging compound, Fe2+-myoglobin. ARG (1 mM) reestablished the coronary-dilating effects of HA in the presence of NMA. Thus, ARG-derived NO contributes significantly to HA-induced coronary-vasodilatation. Inasmuch as the ultimate HA effect on the coronaries depends on the balance between constriction and relaxation, mediated by smooth muscle and endothelial H1-receptors, respectively, as well as relaxation due to smooth muscle H2-receptors, dysfunction of the NO system is likely to precipitate HA-induced vasospasm.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    Springer
    Inflammation research 25 (1988), S. 296-306 
    ISSN: 1420-908X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Release of cardiac histamine by immunologic and pharmacologic stimuli is known to provoke ventricular arrhythmias. Augmented histamine efflux from ischemic myocardium has been proposed but remains controversial. The purpose of this study was to determine whether cardiac histamine efflux is precipitated by coronary artery occlusion and if so, whether histamine efflux is associated with the development of early ischemic ventricular arrhythmias. The left anterior descending coronary artery was occluded while recording a continuous electrocardiogram and coronary sinus blood was sampled frequently during the first 30 min of coronary artery occlusion in pentobarbital-anesthetized, openchest dogs. Coronary sinus histamine concentration rose from a mean baseline of 0.06±0.10 ng/ml (±SD) before coronary artery occlusion to a mean peak of 0.61±0.40 ng/ml after coronary artery occlusion (p〈0.0001;n=14). The median peak coronary sinus histamine concentration was significantly greater in dogs that suffered ventricular fibrillation after coronary artery occlusion (n=4) than in those that did not (n=10) (0.86 ng/ml vs. 0.37 ng/ml;p=0.05). The area under the coronary sinus histamine concentration-vs.-time curve (“total cardiac histamine efflux”) correlated directly with the total number of ventricular premature contractions during the first 30 min after coronary artery occlusion (r=0.81;p〈0.005;n=10), and with infarct size (r=0.91;p〈0.01;n=6). Thus, during acute myocardial ischemia, the coronary sinus histamine concentration increases simultaneously with the development of early ischemic ventricular arrhythmias and in proportion to their severity.
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 93 (1933), S. 307-310 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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