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MDH enzymes from a diversity of organisms
2020-08-03

MDH enzymes from a TAK-715 of organisms have been extensively studied. MDH enzymes catalyze an oxidation reaction that converts malate to OAA, and the reverse reaction also occurs [11]. This catalytic reaction is accompanied by the reduction of NAD+ to generate NADH. Based on phylogenetic analysis,
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While crystal structures of DDR and DDR
2020-08-03

While crystal structures of DDR1 and DDR2 have revealed the molecular basis for extracellular collagen interaction [5], [36], a structural description of the kinase domain fold is lacking. Here, we present the crystal structures of the kinase domain of human DDR1 in complexes with the inhibitors ima
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Enzyme inhibition may increase the
2020-08-03

Enzyme inhibition may increase the drug concentration in blood circulation which may potentiate drug induced toxicity. It is important to quantify the phytomolecule present in the extract. It is important to select biomarker (biologically active constituent) which possesses pharmacological property
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Icariin a main bioactive flavonoid of
2020-07-31

Icariin, a main bioactive flavonoid of Epimedium sagittatum (Siebold & Zucc.) Maxim (Berberidaceae family), is a traditional Chinese herb frequently used to treat the kidney disorders, cardiovascular diseases, osteoporosis and rheumatoid arthritis, also the bioflavonoid is considered to be a potenti
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br Conflict of interest br Acknowledgements This
2020-07-31

Conflict of interest Acknowledgements This work was supported by the National Natural Science Foundation of China (81673837), the Natural Science Foundation of Guangdong Province (S2012040007531) and Science and Technology Planning Project of Guangdong Province (2016A020226039). We also thank
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It was thus found that E
2020-07-31

It was thus found that E1 plays an important role in G. intestinalis biology. Inhibiting E1 expression by RNA antisense in trophozoites was lethal while E1 overexpression induced a five-fold increase in cyst formation during encystation. The changes in E1 location during this process and its localiz
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br Radioligands for the D receptor One
2020-07-31

Radioligands for the D1-receptor One of the first D1-R selective compounds to described was SCH 23390 [22], with in vitro values of between 0.14–0.8 nM in rats [23], and 0.35 nM in the human AZ 10606120 dihydrochloride australia [24]. The compound was radiolabelled with 11C in 1986 [25], shortl
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A strong support for a dual role
2020-07-31

A strong support for a dual role of microglia may be due to distinct microglial phenotypes, which have been broadly categorized into classical pro-inflammatory M1 phenotype and alternative anti-inflammatory M2 phenotype [70,71]. In consistent with these findings, we observed that MPA significantly i
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The biological activity of Hypericum extracts should not
2020-07-31

The biological activity of Hypericum extracts should not be exclusively explained based on the effects of the major compound because it may also include the response to other bioactive compounds present in smaller concentrations. Interaction between compounds (synergistic effect) present in the extr
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The FPGA software development is fully automated
2020-07-31

The FPGA software development is fully automated by FPGA logic synthesis tools and commercial EDAs of FPGA vendors. After programming an RTL (Register-Transfer Level) design with HDLs, the design is transformed into a gate-level design (i.e., netlist) by synthesis software such as ‘Synopsys Synplify
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The GH family includes also xylanases which are
2020-07-30

The GH30 family includes also xylanases which are not MeGlcA-dependent. Most of them are grouped to GH30_7 subfamily that includes XynIV from Trichoderma reesei showing exo- and endo-xylanase activity [11] and XYLD from Bispora sp. MEY-1 [12] having activity towards glucuronoxylan and arabinoxylan,
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br Introduction br Sphingolipid metabolism Sphingolipids are
2020-07-30

Introduction Sphingolipid metabolism Sphingolipids, are fundamental constituents of all eukaryotic membranes and their metabolism is carried out by a broad array of anabolic and JNJ-26854165 mg with ceramide as their hub (for a review, (Hannun and Obeid, 2018)). Ceramide can be formed by multi
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Mutations that alter ligand binding and affinity
2020-07-30

Mutations that alter ligand binding and affinity have been reported. We have shown that a mutation in the C-tail of the BLT1 receptor increased the number of LY2409881 and cellular signalling [47]. In the β2-adrenergic receptor, mutations in the amino-acid structure alter the dynamics and conformat
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br Conclusion CSF R may contribute to limitation of targeted
2020-07-30

Conclusion CSF-1R may contribute to limitation of targeted therapies by providing EGFR-bypassing signals that support proliferation. Multi-kinase inhibitors such as cabozantinib are available, and agents targeting CSF-1R are in clinical trials, however, at present, as inhibitors of tumor-associat
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Results obtained with the CRF
2020-07-30

Results obtained with the CRF receptor antagonists provided evidence that physiological release of CRF and CRF-related peptides within the BNST during restraint modulates the tachycardia through activation of local CRF1 receptors while CRF2 receptors mediates the tail skin temperature responses. Mor
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