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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]. -
br Antimicrobial drugs are the most
2019-06-27
Antimicrobial drugs are the most counterfeit or substandard drugs worldwide.
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