Search alternatives:
na decrease » pa decreased (Expand Search), la decreased (Expand Search), _ decrease (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
we decrease » _ decrease (Expand Search), mean decrease (Expand Search), teer decrease (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
na decrease » pa decreased (Expand Search), la decreased (Expand Search), _ decrease (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
we decrease » _ decrease (Expand Search), mean decrease (Expand Search), teer decrease (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
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721
Current Monitoring in a Microchannel with Repeated Constrictions for Accurate Detection of Sample Location in Isotachophoresis
Published 2015“…We demonstrate the use of the technique to deliver sample to a designated location in the channel with an accuracy as low as 50 μm. …”
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722
Current Monitoring in a Microchannel with Repeated Constrictions for Accurate Detection of Sample Location in Isotachophoresis
Published 2015“…We demonstrate the use of the technique to deliver sample to a designated location in the channel with an accuracy as low as 50 μm. …”
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723
Current Monitoring in a Microchannel with Repeated Constrictions for Accurate Detection of Sample Location in Isotachophoresis
Published 2015“…We demonstrate the use of the technique to deliver sample to a designated location in the channel with an accuracy as low as 50 μm. …”
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724
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725
Generation and characterization of an antagonistic monoclonal antibody against an extracellular domain of mouse DP2 (CRTH2/GPR44) receptors for prostaglandin D<sub>2</sub>
Published 2017“…After cell ELISA, immunocytochemical, and Western blot analyses, we successfully obtained a novel monoclonal antibody, MAb-1D8, that specifically recognized native mouse DP2, but neither human DP2 nor denatured mouse DP2, by binding to a particular 3D receptor conformation formed by the N-terminus and extracellular loop 1, 2, and 3 of DP2. …”
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726
Controlling the Temperature and Speed of the Phase Transition of VO<sub>2</sub> Microcrystals
Published 2016“…The phase transition speed increases from 4.6 × 10<sup>2</sup> to 1.7 × 10<sup>4</sup> μm/s as the width decreases from ∼50 to ∼2 μm. While the statistical description for a heterogeneous nucleation process explains the size dependence on phase transition temperature of VO<sub>2</sub>, the increase of effective thermal exchange process is responsible for the enhancement of phase transition speed of small VO<sub>2</sub> microcrystals. …”
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727
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728
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729
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730
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731
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732
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733
Identification of Candidate Genes for Reactivity in Guzerat (<i>Bos indicus</i>) Cattle: A Genome-Wide Association Study
Published 2017“…Genotyping was performed using a 50k SNP chip and a two-step mixed model approach (Grammar-Gamma) with a one-by-one marker regression was used to identify QTLs. …”
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734
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735
3‑Hydroxyquinolin-2-Ones Act as Dual Inhibitors of Ferroptosis and Monoamine Oxidase B: Reducing Alzheimer’s Disease-Related Amyloid Precursor Protein and Hyperphosphorylated Tau I...
Published 2025“…Compound <b>21d</b> emerged as a promising candidate, exhibiting potent and selective MAO-B inhibitory activity (IC<sub>50</sub> = 87.47 nM, SI > 229), as well as excellent antiferroptosis activity through modulation of the iron metabolic pathway and GSH-GPX4 axis in vitro<i>.…”
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736
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737
S1 Data -
Published 2024“…Country-specific differences in abortion rates have remained stable over the 50 years of liberalized abortion laws.</p></div>…”
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738
Discovery of New Inhibitors of Hepatitis C Virus NS3/4A Protease and Its D168A Mutant
Published 2019“…Several drugs targeting the protease have been developed, but drug-resistant mutant strains emerged. Here, we screened a library and synthesized a novel class of small molecules based on a tryptophan derivative scaffold identified as HCV NS3/4A protease inhibitors that are active against both wild type and mutant form of the protease. …”
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739
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740