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Showing 26,601 - 26,620 results of 103,867 for search '(( 5 ((nn decrease) OR (a decrease)) ) OR ( e ((fold decrease) OR (point decrease)) ))', query time: 1.76s Refine Results
  1. 26601
    Bidirectional Optical Control of Proton Motive Force in Escherichia coli Using Microbial Rhodopsins

    Bidirectional Optical Control of Proton Motive Force in Escherichia coli Using Microbial Rhodopsins by Kotaro Nakanishi (3389300)

    Published 2024
    “…These alterations in PMF correspond to +146 mV (<i>Rm</i>XeR) and −140 mV (AR3), respectively. …”
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  2. 26602
    Bidirectional Optical Control of Proton Motive Force in Escherichia coli Using Microbial Rhodopsins

    Bidirectional Optical Control of Proton Motive Force in Escherichia coli Using Microbial Rhodopsins by Kotaro Nakanishi (3389300)

    Published 2024
    “…These alterations in PMF correspond to +146 mV (<i>Rm</i>XeR) and −140 mV (AR3), respectively. …”
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  3. 26603
    Bidirectional Optical Control of Proton Motive Force in Escherichia coli Using Microbial Rhodopsins

    Bidirectional Optical Control of Proton Motive Force in Escherichia coli Using Microbial Rhodopsins by Kotaro Nakanishi (3389300)

    Published 2024
    “…These alterations in PMF correspond to +146 mV (<i>Rm</i>XeR) and −140 mV (AR3), respectively. …”
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  4. 26604
    Bidirectional Optical Control of Proton Motive Force in Escherichia coli Using Microbial Rhodopsins

    Bidirectional Optical Control of Proton Motive Force in Escherichia coli Using Microbial Rhodopsins by Kotaro Nakanishi (3389300)

    Published 2024
    “…These alterations in PMF correspond to +146 mV (<i>Rm</i>XeR) and −140 mV (AR3), respectively. …”
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  5. 26605
    All indicator plants’ mean EC<sub>50</sub> values for seed germination, radicle, and hypocotyl length are represented in a dendrogram (C<sub>1</sub>- Bambara groundnut, C<sub>2</sub>- Radish, C<sub>3</sub>- Sweet gourd, C<sub>4</sub>- Cucumber, C<sub>5</sub>- Tomato, C<sub>6</sub>- pepper, C<sub>7</sub>- Maize, C<sub>8</sub>- Okra, C<sub>9</sub>- Carrot, C<sub>10</sub>- Crabgrass, C<sub>11</sub>- Goosegrass) treated with the leaf, stem and flower extracts of <i>P</i>. <i>hysterophorus</i> with methanol revealed by non-overlapping (SAHN) UPGMA method.

    All indicator plants’ mean EC<sub>50</sub> values for seed germination, radicle, and hypocotyl length are represented in a dendrogram (C<sub>1</sub>- Bambara groundnut, C<sub>2</su... by H. M. Khairul Bashar (14341613)

    Published 2023
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  6. 26606
    SEM Samples of FSW Joints: (i) ABS (800 rpm,10 mm/min) [(a) Cross-sectional View, (b) 250X, (c)1000X} (ii) ABS (1200 rpm,10 mm/min) [(d) Cross-sectional View, (e) 250X, (f)1000X} (iii) ABS (1200 rpm,20 mm/min) [(g) Cross-sectional View, (h) 250X, (i)1000X} (iv) PC (800 rpm,40 mm/min) [(j) Cross-sectional View, (k) 250X, (l)1000X} (v) PC (1200 rpm,20 mm/min) [(m) Cross-sectional View, (n) 250X, (o)1000X}.

    SEM Samples of FSW Joints: (i) ABS (800 rpm,10 mm/min) [(a) Cross-sectional View, (b) 250X, (c)1000X} (ii) ABS (1200 rpm,10 mm/min) [(d) Cross-sectional View, (e) 250X, (f)1000X} (... by Shaheer Ahmed Khan (17797647)

    Published 2025
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  7. 26607
    The detailed risk of bias assessment.

    The detailed risk of bias assessment. by Fatemeh Shahbazi (2271025)

    Published 2025
    “…Therefore, the existence of a dose-response relationship can indicate a causal relationship between music therapy and the improvement of neonatal outcomes.…”
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  8. 26608
    Table_2_PE_PGRS31-S100A9 Interaction Promotes Mycobacterial Survival in Macrophages Through the Regulation of NF-κB-TNF-α Signaling and Arachidonic Acid Metabolism.docx

    Table_2_PE_PGRS31-S100A9 Interaction Promotes Mycobacterial Survival in Macrophages Through the Regulation of NF-κB-TNF-α Signaling and Arachidonic Acid Metabolism.docx by Sheng Liu (279488)

    Published 2020
    “…Interestingly, Rv1768 binding to S100A9 also disturbs the metabolism of arachidonic acid by activating 5-lipoxygenase, increasing lipotoxin A4, and down-regulating cyclooxygenase-2 and prostaglandin E2 expression, thus, promoting mycobacterial survival. …”
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  9. 26609
    Image_4_PE_PGRS31-S100A9 Interaction Promotes Mycobacterial Survival in Macrophages Through the Regulation of NF-κB-TNF-α Signaling and Arachidonic Acid Metabolism.TIF

    Image_4_PE_PGRS31-S100A9 Interaction Promotes Mycobacterial Survival in Macrophages Through the Regulation of NF-κB-TNF-α Signaling and Arachidonic Acid Metabolism.TIF by Sheng Liu (279488)

    Published 2020
    “…Interestingly, Rv1768 binding to S100A9 also disturbs the metabolism of arachidonic acid by activating 5-lipoxygenase, increasing lipotoxin A4, and down-regulating cyclooxygenase-2 and prostaglandin E2 expression, thus, promoting mycobacterial survival. …”
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  10. 26610
    Table_1_PE_PGRS31-S100A9 Interaction Promotes Mycobacterial Survival in Macrophages Through the Regulation of NF-κB-TNF-α Signaling and Arachidonic Acid Metabolism.docx

    Table_1_PE_PGRS31-S100A9 Interaction Promotes Mycobacterial Survival in Macrophages Through the Regulation of NF-κB-TNF-α Signaling and Arachidonic Acid Metabolism.docx by Sheng Liu (279488)

    Published 2020
    “…Interestingly, Rv1768 binding to S100A9 also disturbs the metabolism of arachidonic acid by activating 5-lipoxygenase, increasing lipotoxin A4, and down-regulating cyclooxygenase-2 and prostaglandin E2 expression, thus, promoting mycobacterial survival. …”
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  11. 26611
    Image_2_PE_PGRS31-S100A9 Interaction Promotes Mycobacterial Survival in Macrophages Through the Regulation of NF-κB-TNF-α Signaling and Arachidonic Acid Metabolism.TIF

    Image_2_PE_PGRS31-S100A9 Interaction Promotes Mycobacterial Survival in Macrophages Through the Regulation of NF-κB-TNF-α Signaling and Arachidonic Acid Metabolism.TIF by Sheng Liu (279488)

    Published 2020
    “…Interestingly, Rv1768 binding to S100A9 also disturbs the metabolism of arachidonic acid by activating 5-lipoxygenase, increasing lipotoxin A4, and down-regulating cyclooxygenase-2 and prostaglandin E2 expression, thus, promoting mycobacterial survival. …”
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  12. 26612
    Image_3_PE_PGRS31-S100A9 Interaction Promotes Mycobacterial Survival in Macrophages Through the Regulation of NF-κB-TNF-α Signaling and Arachidonic Acid Metabolism.TIF

    Image_3_PE_PGRS31-S100A9 Interaction Promotes Mycobacterial Survival in Macrophages Through the Regulation of NF-κB-TNF-α Signaling and Arachidonic Acid Metabolism.TIF by Sheng Liu (279488)

    Published 2020
    “…Interestingly, Rv1768 binding to S100A9 also disturbs the metabolism of arachidonic acid by activating 5-lipoxygenase, increasing lipotoxin A4, and down-regulating cyclooxygenase-2 and prostaglandin E2 expression, thus, promoting mycobacterial survival. …”
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  13. 26613
    Image_1_PE_PGRS31-S100A9 Interaction Promotes Mycobacterial Survival in Macrophages Through the Regulation of NF-κB-TNF-α Signaling and Arachidonic Acid Metabolism.TIF

    Image_1_PE_PGRS31-S100A9 Interaction Promotes Mycobacterial Survival in Macrophages Through the Regulation of NF-κB-TNF-α Signaling and Arachidonic Acid Metabolism.TIF by Sheng Liu (279488)

    Published 2020
    “…Interestingly, Rv1768 binding to S100A9 also disturbs the metabolism of arachidonic acid by activating 5-lipoxygenase, increasing lipotoxin A4, and down-regulating cyclooxygenase-2 and prostaglandin E2 expression, thus, promoting mycobacterial survival. …”
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  14. 26614
    SIRT1-mediated CRIF1 deletion-induced inflammatory cytokine and VCAM-1 expression.

    SIRT1-mediated CRIF1 deletion-induced inflammatory cytokine and VCAM-1 expression. by Shuyu Piao (4731327)

    Published 2018
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  15. 26615
    Why Only the 2,6-Bis(o-Carborano)Pyridine-Stabilized Phosphenium Cation Has Succeeded in Splitting H<sub>2</sub>?: Key Design Insights for Next-Gen Phosphenium Pincer Catalysts

    Why Only the 2,6-Bis(o-Carborano)Pyridine-Stabilized Phosphenium Cation Has Succeeded in Splitting H<sub>2</sub>?: Key Design Insights for Next-Gen Phosphenium Pincer Catalysts by Mohmmad Faizan (14122382)

    Published 2025
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  16. 26616
    Why Only the 2,6-Bis(o-Carborano)Pyridine-Stabilized Phosphenium Cation Has Succeeded in Splitting H<sub>2</sub>?: Key Design Insights for Next-Gen Phosphenium Pincer Catalysts

    Why Only the 2,6-Bis(o-Carborano)Pyridine-Stabilized Phosphenium Cation Has Succeeded in Splitting H<sub>2</sub>?: Key Design Insights for Next-Gen Phosphenium Pincer Catalysts by Mohmmad Faizan (14122382)

    Published 2025
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  17. 26617
    Why Only the 2,6-Bis(o-Carborano)Pyridine-Stabilized Phosphenium Cation Has Succeeded in Splitting H<sub>2</sub>?: Key Design Insights for Next-Gen Phosphenium Pincer Catalysts

    Why Only the 2,6-Bis(o-Carborano)Pyridine-Stabilized Phosphenium Cation Has Succeeded in Splitting H<sub>2</sub>?: Key Design Insights for Next-Gen Phosphenium Pincer Catalysts by Mohmmad Faizan (14122382)

    Published 2025
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  18. 26618
    Why Only the 2,6-Bis(o-Carborano)Pyridine-Stabilized Phosphenium Cation Has Succeeded in Splitting H<sub>2</sub>?: Key Design Insights for Next-Gen Phosphenium Pincer Catalysts

    Why Only the 2,6-Bis(o-Carborano)Pyridine-Stabilized Phosphenium Cation Has Succeeded in Splitting H<sub>2</sub>?: Key Design Insights for Next-Gen Phosphenium Pincer Catalysts by Mohmmad Faizan (14122382)

    Published 2025
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  19. 26619
    Why Only the 2,6-Bis(o-Carborano)Pyridine-Stabilized Phosphenium Cation Has Succeeded in Splitting H<sub>2</sub>?: Key Design Insights for Next-Gen Phosphenium Pincer Catalysts

    Why Only the 2,6-Bis(o-Carborano)Pyridine-Stabilized Phosphenium Cation Has Succeeded in Splitting H<sub>2</sub>?: Key Design Insights for Next-Gen Phosphenium Pincer Catalysts by Mohmmad Faizan (14122382)

    Published 2025
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  20. 26620
    Why Only the 2,6-Bis(o-Carborano)Pyridine-Stabilized Phosphenium Cation Has Succeeded in Splitting H<sub>2</sub>?: Key Design Insights for Next-Gen Phosphenium Pincer Catalysts

    Why Only the 2,6-Bis(o-Carborano)Pyridine-Stabilized Phosphenium Cation Has Succeeded in Splitting H<sub>2</sub>?: Key Design Insights for Next-Gen Phosphenium Pincer Catalysts by Mohmmad Faizan (14122382)

    Published 2025
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