70 research outputs found

    ゾル−ゲル転移を示す生体適合ポリマー材料の開発と応用 (2)

    Get PDF
    (1) Title: Bulk pH Responsive DNA Quadruplex Hydrogels Prepared by Liquid-Phase Large Scale DNA SynthesisJournal: ACS Macro Letters(2) Title: Communication—DNA Quadruplex Hydrogel Beads Showing Peroxidase ActivityJournal: Journal of The Electrochemical SocietyDOI: http://dx.doi.org/10.1149/2.0441909je

    Investigation of inter-annual variation in the feeding habits of Japanese sardine (Sardinops melanostictus) and mackerels (Scomber spp.) in the Western North Pacific based on bulk and amino acid stable isotopes

    Get PDF
    Inter-annual variation in the feeding habits and food sources of Japanese sardine and mackerel at age-0 and age-1+ caught in the Kuroshio-Oyashio transition zone of the Western North Pacific were investigated based on analyses of bulk stable isotopes (δ13C, δ15N) and amino acid nitrogen isotopes (δ15NAA). Differences in δ13C and δ15N between Japanese sardine and mackerel were small for age-0, and inter-annual variation trends were similar, suggesting they depend on similar food sources in the same food web at this age. In contrast, inter-annual variation in δ13C and δ15N were significantly different between both species at age-1+, and both δ15N of phenylalanine (δ15NPhe: an indicator of nitrogen source) and trophic position estimated from δ15NAA (TPAA) were higher in mackerel, suggesting that the two species depend on distinct food webs as they age. Inter-annual variations in δ15NPhe were considered to have different causes for the two species; differences in food web structure due to the degree of southward intrusion of the Oyashio Current for Japanese sardine, compared to a shift in migration area and depth for mackerel. Furthermore, competition for food due to the recent increases in the population densities of both fishes appeared to be reflected in increased TPAA of mackerel. Although they are caught in the same region, the mechanism of variation in food sources differs because of differences in migration area, depth, and feeding habits. Differences in the feeding habits of Japanese sardine and mackerel may affect trophic status and spawning characteristics, potentially leading to different shifts in stock abundances

    P-selectin glycoprotein ligand-1 contributes to wound healing predominantly as a p-selectin ligand and partly as an e-selectin ligand.

    Get PDF
    Cell adhesion molecules are critical to wound healing through leukocyte recruitment. Although P-selectin glycoprotein ligand-1 (PSGL-1) regulates leukocyte rolling by binding P-selectin, but also binding E- and L-selectins with lower affinity, little is known about a role of PSGL-1 in wound healing. To clarify a role of PSGL-1 and its interaction with E- and P-selectins in wound healing, we investigated cutaneous wound healing in PSGL-1-deficient (PSGL-1(-/-)) mice in comparison with E-selectin(-/-), P-selectin(-/-), and P-selectin(-/-) mice treated with an anti-E-selectin antibody. PSGL-1 deficiency inhibited early wound healing, which was accompanied by decreased inflammatory cell infiltration and growth factor expression. By contrast, E-selectin deficiency did not affect wound healing. In general, the inhibitory effect of PSGL-1 deficiency on wound healing was similar to that of P-selectin deficiency either alone or with E-selectin blockade. However, early granulation tissue formation, late angiogenesis, and early infiltration of neutrophils and macrophages in PSGL-1(-/-) mice were inhibited beyond the inhibition in P-selectin(-/-) mice, but to a similar level of inhibition in P-selectin(-/-) mice with E-selectin blockade. These results suggest that PSGL-1 contributes to wound healing predominantly as a P-selectin ligand and partly as an E-selectin ligand by mediating infiltration of inflammatory cells

    A note on a formalized arithmetic with function symbols ' and +

    No full text

    A theorem on the formalized arithmetic with function symbols ' and +

    No full text

    Taking out LK

    No full text

    Short proofs of tautologies using the schema of equivalence

    No full text
    corecore