Showing 12,981 - 13,000 results of 107,116 for search '(( 50 ((we decrease) OR (mean decrease)) ) OR ( 5 ((point decrease) OR (a decrease)) ))', query time: 1.78s Refine Results
  1. 12981
  2. 12982

    Tunable Electrical Properties of Embossed, Cellulose-Based Paper for Skin-like Sensing by Tongfen Liang (9601461)

    Published 2020
    “…The largest increase in conductivity from 8.38 × 10<sup>–6</sup> to 2.5 × 10<sup>–3</sup> S/m by a factor of ∼300 occurred at a percolation threshold of 3.8 wt % (or 0.36 vol %) with the composite paper plastically compressed by 410 MPa, which caused a decrease of porosity from 88% to 42% on average. …”
  3. 12983

    Tunable Electrical Properties of Embossed, Cellulose-Based Paper for Skin-like Sensing by Tongfen Liang (9601461)

    Published 2020
    “…The largest increase in conductivity from 8.38 × 10<sup>–6</sup> to 2.5 × 10<sup>–3</sup> S/m by a factor of ∼300 occurred at a percolation threshold of 3.8 wt % (or 0.36 vol %) with the composite paper plastically compressed by 410 MPa, which caused a decrease of porosity from 88% to 42% on average. …”
  4. 12984
  5. 12985
  6. 12986
  7. 12987
  8. 12988
  9. 12989
  10. 12990

    Role of <i>inhbaa</i> in the partial rescue of vitellogenic growth in <i>bmp15-/-</i> by <i>inha-/-</i>. by Yue Zhai (3141960)

    Published 2023
    “…The values are expressed as mean ± SEM (n ≥ 5) and analyzed by ANOVA followed by the Tukey HSD for multiple comparisons. …”
  11. 12991

    pone.0331193.t003 - by Carol Kotliar (22351525)

    Published 2025
    “…The global cognitive score increased by 4.6 points (5%) in the intervention group compared to a decrease of 0.5 points in the control group (p < 0.001). …”
  12. 12992

    Baseline characteristics by group. by Carol Kotliar (22351525)

    Published 2025
    “…The global cognitive score increased by 4.6 points (5%) in the intervention group compared to a decrease of 0.5 points in the control group (p < 0.001). …”
  13. 12993
  14. 12994

    Synthesis and Reactivity of Heptamethylcyclohexadienyl Rhodium(III) Complexes by Roman A. Pototskiy (8082911)

    Published 2019
    “…Accordingly, the catalytic reaction of 2-phenylpyridine with 3-hexyne in the presence of <b>4</b> (5 mol %) gave the 9,10-diethyl-8a-azaphenanthrene cation in 61% yield. …”
  15. 12995

    Molecular Origin of Photovoltaic Performance in Donor-<i>block</i>-Acceptor All-Conjugated Block Copolymers by Kendall A. Smith (1477033)

    Published 2015
    “…All-conjugated block copolymers may be an effective route to self-assembled photovoltaic devices, but we lack basic information on the relationship between molecular characteristics and photovoltaic performance. Here, we synthesize a library of poly­(3-hexyl­thiophene) (P3HT) <i>block</i> poly­((9,9-dialkyl­fluorene)-2,7-diyl-<i>alt</i>-[4,7-bis­(alkyl­thiophen-5-yl)-2,1,3-benzo­thiadiazole]-2′,2″-diyl) (PFTBT) donor-<i>block</i>-acceptor all-conjugated block copolymers and carry out a comprehensive study of processing conditions, crystallinity, domain sizes, and side-chain structure on photovoltaic device performance. …”
  16. 12996

    Molecular Origin of Photovoltaic Performance in Donor-<i>block</i>-Acceptor All-Conjugated Block Copolymers by Kendall A. Smith (1477033)

    Published 2015
    “…All-conjugated block copolymers may be an effective route to self-assembled photovoltaic devices, but we lack basic information on the relationship between molecular characteristics and photovoltaic performance. Here, we synthesize a library of poly­(3-hexyl­thiophene) (P3HT) <i>block</i> poly­((9,9-dialkyl­fluorene)-2,7-diyl-<i>alt</i>-[4,7-bis­(alkyl­thiophen-5-yl)-2,1,3-benzo­thiadiazole]-2′,2″-diyl) (PFTBT) donor-<i>block</i>-acceptor all-conjugated block copolymers and carry out a comprehensive study of processing conditions, crystallinity, domain sizes, and side-chain structure on photovoltaic device performance. …”
  17. 12997

    Molecular Origin of Photovoltaic Performance in Donor-<i>block</i>-Acceptor All-Conjugated Block Copolymers by Kendall A. Smith (1477033)

    Published 2015
    “…All-conjugated block copolymers may be an effective route to self-assembled photovoltaic devices, but we lack basic information on the relationship between molecular characteristics and photovoltaic performance. Here, we synthesize a library of poly­(3-hexyl­thiophene) (P3HT) <i>block</i> poly­((9,9-dialkyl­fluorene)-2,7-diyl-<i>alt</i>-[4,7-bis­(alkyl­thiophen-5-yl)-2,1,3-benzo­thiadiazole]-2′,2″-diyl) (PFTBT) donor-<i>block</i>-acceptor all-conjugated block copolymers and carry out a comprehensive study of processing conditions, crystallinity, domain sizes, and side-chain structure on photovoltaic device performance. …”
  18. 12998

    Molecular Origin of Photovoltaic Performance in Donor-<i>block</i>-Acceptor All-Conjugated Block Copolymers by Kendall A. Smith (1477033)

    Published 2015
    “…All-conjugated block copolymers may be an effective route to self-assembled photovoltaic devices, but we lack basic information on the relationship between molecular characteristics and photovoltaic performance. Here, we synthesize a library of poly­(3-hexyl­thiophene) (P3HT) <i>block</i> poly­((9,9-dialkyl­fluorene)-2,7-diyl-<i>alt</i>-[4,7-bis­(alkyl­thiophen-5-yl)-2,1,3-benzo­thiadiazole]-2′,2″-diyl) (PFTBT) donor-<i>block</i>-acceptor all-conjugated block copolymers and carry out a comprehensive study of processing conditions, crystallinity, domain sizes, and side-chain structure on photovoltaic device performance. …”
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