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The discovery of proteases that are active in organic solven
2019-07-15
The discovery of proteases that are active in organic solvent media has greatly extended their ability in the synthesis of useful products. Microbial proteases which are able be catalyse in non-aqueous solvents present new expectation in enzyme applications. This kind of enzymes gives a major contri
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In the present study we used linagliptin one of
2019-07-15
In the present study, we used linagliptin, one of the commercially available DPP-4 inhibitors, because it has more long-lasting inhibition of DPP-4 activity than other drugs of this class. We hypothesized that linagliptin may interact with intercellular components, not only with DPP-4 on the plasma
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HA activates its receptor channels to cause an
2019-07-13
HA activates its receptor channels to cause an inward chloride flux in the insect nervous system (Hardie, 1989).
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For reductive amination by L AmDH the term related to
2019-07-12
For reductive amination by L-AmDH, the term related to the enzyme-ammonia complex is excluded rather than the enzyme-pentanone term (Table 1).
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Finally this study described that the lead compound acted
2019-07-11
Finally, this study described that the lead CEP-32496 (1) acted as an efficient alkylating agent for the G4 structure in addition to the previously reported T-T mismatch structure.
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Zoledronic Acid The contribution of Interference
2019-07-10
The contribution of Interference RNA and epigenetic in OA attenuation Interference RNA, a cellular mechanism for post-transcriptional gene silencing that is associated with mRNA.
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Adding more pieces to the puzzle using a
2019-07-09
Adding more pieces to the puzzle, using a human-to-animal crossover study, blood taken from healthy volunteers that underwent exercise was used as a dialysate to perfuse a rabbit heart in a Langendorff model of MI [62].
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The crystal structure of full length CHK is still
2019-07-08
The crystal structure of full-length CHK is still unsolved. However, the close homology between CHK and Csk suggests that these kinases share a similar structure.
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Materials and methods Results
2019-07-05
Materials and methods Results Discussion We initially found that ISL, a natural product with a linear scaffold (2-propenone), is able to inhibit CK2 (IC50 = 17.3 μM). Then we have investigated the inhibitory potential of a novel series of compounds with linear scaffolds by combining fragment-hybrid computational design with in vitro assays.
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As described above when EGCG was orally administered
2019-07-04
As described above, when EGCG was orally administered, CYP3A expression in the liver decreased; however, the CYP3A expression level in the intestine was unchanged (Fig. 3).
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In general terms PLA s participate in the
2019-07-03
In general terms, PLA2s participate in the Lands cycle of phospholipid fatty immunoglobulin light chain variable region fragment [Homo sapiens] recycling [1,15,25], whereby the fatty acid composition at the sn-2 position of phospholipids is tightly controlled by a balance between hydrolytic reactions mediated by PLA2s versus activation of the free fatty acid by acyl-CoA synthetases and subsequent incorporation into phospholipids by lysophospholipid:acyl-CoA acyltransferases.
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Despite robust translation of GA only small amounts of
2019-07-02
Despite robust translation of GA, only small amounts of GR and GP were translated in cultured amyloid A protein fragment [Homo sapiens] and chick embryo spinal cord neural cells from the 75 copies of G4C2 in monocistronic constructs.
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CYP A is involved in the metabolism of approximately
2019-07-01
CYP3A is involved in the metabolism of approximately 50% of all drugs that are currently prescribed to patients [1], [15], [16].
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A key component of the Emergency
2019-06-29
A key component of the Emergency Nutrition Response was the implementation of a Child Nutrition Week to deliver a package of essential nutrition services for children younger than 5 years and their mothers before the onset of the monsoon rains.
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Conflict of interest br Introduction Nifekalant
2019-06-28
Conflict of interest
Introduction Nifekalant hydrochloride was first approved by the Japanese Ministry of Health, Labour and Welfare in 1999 and is now used as a first-line antiarrhythmic drug for refractory ventricular tachyarrhythmias in the country [1].
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