Search alternatives:
teer decrease » mean decrease (Expand Search), greater decrease (Expand Search)
step decrease » sizes decrease (Expand Search), we 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)
2 step » _ step (Expand Search), a step (Expand Search)
teer decrease » mean decrease (Expand Search), greater decrease (Expand Search)
step decrease » sizes decrease (Expand Search), we 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)
2 step » _ step (Expand Search), a step (Expand Search)
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721
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722
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723
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724
Decreased activity of FASII favors the cold growth of the <i>ΔcshA</i> strain.
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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725
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726
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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
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
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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734
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
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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735
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
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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736
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
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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737
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738
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739
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740