Showing 721 - 740 results of 100,619 for search '(( 5 ((((nn decrease) OR (teer decrease))) OR (a decrease)) ) OR ( 2 step decrease ))', query time: 1.56s Refine Results
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    Decreased activity of FASII favors the cold growth of the <i>ΔcshA</i> strain. by Vanessa Khemici (814639)

    Published 2020
    “…<i>fapR</i> mRNA levels were quantified by RT-qPCR using 16S rRNA as reference gene on total RNAs extracted from <i>wt</i> strain (PR01), <i>ΔcshA</i> strain (PR01-ΔcshA), and suppressor strains <i>ΔcshA/accC</i><sup><i>M385V</i></sup> (C51), <i>ΔcshA/accC</i><sup><i>T183I</i></sup> (sup30), <i>ΔcshA/accD</i><sup><i>F253V</i></sup> (sup17), <i>ΔcshA/accD</i><sup><i>A164V</i></sup> (sup16), <i>ΔcshA/birA</i><sup><i>D320F-FsX28</i></sup> (C58), <i>ΔcshA/birA</i><sup><i>R280stop</i></sup> (sup1) and <i>ΔcshA/bioY</i><sup><i>P123R-FsX1</i></sup> (C66), all at exponential growth phase in MH medium at 25°C. n = 5 for <i>ΔcshA</i>, <i>4 for wt</i> and 3 for all others. …”
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    Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes by Ognjen Š. Miljanić (2485972)

    Published 2007
    “…Four donor−acceptor [2]catenanes with cyclobis(paraquat-<i>p</i>-phenylene) (CBPQT<sup>4+</sup>) as the π-electron-accepting cyclophane and 1,5-dioxynaphthalene (DNP)-containing macrocyclic polyethers as π-electron donor rings have been synthesized under mild conditions, employing Cu<sup>+</sup>-catalyzed Huisgen 1,3-dipolar cycloaddition and Cu<sup>2+</sup>-mediated Eglinton coupling in the final steps of their syntheses. …”
  14. 734

    Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes by Ognjen Š. Miljanić (2485972)

    Published 2007
    “…Four donor−acceptor [2]catenanes with cyclobis(paraquat-<i>p</i>-phenylene) (CBPQT<sup>4+</sup>) as the π-electron-accepting cyclophane and 1,5-dioxynaphthalene (DNP)-containing macrocyclic polyethers as π-electron donor rings have been synthesized under mild conditions, employing Cu<sup>+</sup>-catalyzed Huisgen 1,3-dipolar cycloaddition and Cu<sup>2+</sup>-mediated Eglinton coupling in the final steps of their syntheses. …”
  15. 735

    Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes by Ognjen Š. Miljanić (2485972)

    Published 2007
    “…Four donor−acceptor [2]catenanes with cyclobis(paraquat-<i>p</i>-phenylene) (CBPQT<sup>4+</sup>) as the π-electron-accepting cyclophane and 1,5-dioxynaphthalene (DNP)-containing macrocyclic polyethers as π-electron donor rings have been synthesized under mild conditions, employing Cu<sup>+</sup>-catalyzed Huisgen 1,3-dipolar cycloaddition and Cu<sup>2+</sup>-mediated Eglinton coupling in the final steps of their syntheses. …”
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    Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes by Ognjen Š. Miljanić (2485972)

    Published 2007
    “…Four donor−acceptor [2]catenanes with cyclobis(paraquat-<i>p</i>-phenylene) (CBPQT<sup>4+</sup>) as the π-electron-accepting cyclophane and 1,5-dioxynaphthalene (DNP)-containing macrocyclic polyethers as π-electron donor rings have been synthesized under mild conditions, employing Cu<sup>+</sup>-catalyzed Huisgen 1,3-dipolar cycloaddition and Cu<sup>2+</sup>-mediated Eglinton coupling in the final steps of their syntheses. …”
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