Search alternatives:
step decrease » sizes decrease (Expand Search), teer decrease (Expand Search), we decrease (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
c decrease » c decreased (Expand Search), _ decrease (Expand Search), rc decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
step decrease » sizes decrease (Expand Search), teer decrease (Expand Search), we decrease (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
c decrease » c decreased (Expand Search), _ decrease (Expand Search), rc decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
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1761
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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1762
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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1763
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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1764
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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1765
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1766
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1767
rAd-p53 induces apoptosis in HCC cell lines with increased Fbxw7 and decreased c-Myc and Cyclin E.
Published 2013“…Quantification of RT-PCR for p53 and Fbxw7 indicated elevated mRNA levels for rAd-p53 infected Hep3B cells, whereas c-Myc and Cyclin E levels were not significantly decreased. …”
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1768
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1769
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1770
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1771
TNFα significantly decreases PRLR immunoreactivity in the outer root sheath of hair follicles.
Published 2013“…<p>(A) PRLR IR in the outer root sheath of control hair follicles (black arrows) was reduced in comparison PRLR IR after treatment with TNFα at concentrations of (B) 0.5 ng/ml and (C) 5 ng/ml. …”
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1772
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1773
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1774
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1775
A Peptide Mimetic of 5-Acetylneuraminic Acid-Galactose Binds with High Avidity to Siglecs and NKG2D
Published 2015“…In addition, the peptide bound the receptor NKG2D, which contains a lectin-like domain that binds Neu5Ac(α2,3)Gal. …”
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1776
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1777
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1778
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1779
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1780