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step decrease » sizes decrease (Expand Search), we decrease (Expand Search)
teer decrease » mean decrease (Expand Search), greater decrease (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
step decrease » sizes decrease (Expand Search), we decrease (Expand Search)
teer decrease » mean decrease (Expand Search), greater decrease (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
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821
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822
Reduced skin lipid content in obese Japanese women mediated by decreased expression of rate-limiting lipogenic enzymes
Published 2018“…Both skin cholesterol and fatty acid levels exhibited an “inverted-U” relationship with BMI, suggesting that there is an optimal BMI for peak lipid content and barrier function. Decreased lipid levels at higher BMI were accompanied by downregulated expression of <i>PPARδ</i> and other genes related to lipid metabolism, including those encoding acetyl-CoA carboxylase and HMG-CoA reductase, the rate-limiting enzymes for fatty acid and cholesterol synthesis, respectively. …”
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823
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824
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825
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826
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827
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828
DataSheet1.docx
Published 2018“…Interestingly, host contact increased the expression and secretion of V. vulnificus RtxA1 toxin, which was decreased and delayed by the rpoS mutation. …”
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829
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830
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831
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832
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833
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834
GNE-781, A Highly Advanced Potent and Selective Bromodomain Inhibitor of Cyclic Adenosine Monophosphate Response Element Binding Protein, Binding Protein (CBP)
Published 2017“…Compound <b>19</b> displays antitumor activity in an AML tumor model and was also shown to decrease Foxp3 transcript levels in a dose dependent manner.…”
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835
<i>Otx</i> knockdown causes a decrease in <i>dct</i> expression in the developing RPE.
Published 2012“…<i>dct</i> expression was reduced only in the ventral most region of the optic cup in single morphants (B–D, white arrows) compared to controls (A). <i>dct</i> expression was significantly decreased in the ventral RPE of <i>otx1a</i>/<i>otx2</i> morphants and to an even greater degree in <i>otx1a</i>/<i>otx1b</i>/<i>otx2</i> morphants (E–F, white arrows). …”
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836
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837
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
Published 2007“…The barriers for the three processes were found to be successively 14.4, 14.5−17.5, and 13.1−15.8 kcal mol<sup>-1</sup>. Within the limitations of the small dataset investigated, emergent trends in the barrier heights can be recognized: the values decrease with the increasing size of the π-electron-donating macrocycle and tend to be lower in the sterically less encumbered series of [2]catenanes containing the 1,3-butadiyne moiety.…”
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838
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
Published 2007“…The barriers for the three processes were found to be successively 14.4, 14.5−17.5, and 13.1−15.8 kcal mol<sup>-1</sup>. Within the limitations of the small dataset investigated, emergent trends in the barrier heights can be recognized: the values decrease with the increasing size of the π-electron-donating macrocycle and tend to be lower in the sterically less encumbered series of [2]catenanes containing the 1,3-butadiyne moiety.…”
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839
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
Published 2007“…The barriers for the three processes were found to be successively 14.4, 14.5−17.5, and 13.1−15.8 kcal mol<sup>-1</sup>. Within the limitations of the small dataset investigated, emergent trends in the barrier heights can be recognized: the values decrease with the increasing size of the π-electron-donating macrocycle and tend to be lower in the sterically less encumbered series of [2]catenanes containing the 1,3-butadiyne moiety.…”
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840
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
Published 2007“…The barriers for the three processes were found to be successively 14.4, 14.5−17.5, and 13.1−15.8 kcal mol<sup>-1</sup>. Within the limitations of the small dataset investigated, emergent trends in the barrier heights can be recognized: the values decrease with the increasing size of the π-electron-donating macrocycle and tend to be lower in the sterically less encumbered series of [2]catenanes containing the 1,3-butadiyne moiety.…”