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5 step » _ step (Expand Search), a step (Expand Search), 2 step (Expand Search)
step decrease » sizes decrease (Expand Search), teer decrease (Expand Search), we decrease (Expand Search)
ng decrease » nn decrease (Expand Search), _ decrease (Expand Search), we decrease (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
5 step » _ step (Expand Search), a step (Expand Search), 2 step (Expand Search)
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1941
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1942
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1943
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1944
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1945
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1946
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1947
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1948
<i>Otx</i> knockdown causes a decrease in <i>dct</i> expression in the developing RPE.
Published 2012“…<i>dct</i> expression was reduced only in the ventral most region of the optic cup in single morphants (B–D, white arrows) compared to controls (A). <i>dct</i> expression was significantly decreased in the ventral RPE of <i>otx1a</i>/<i>otx2</i> morphants and to an even greater degree in <i>otx1a</i>/<i>otx1b</i>/<i>otx2</i> morphants (E–F, white arrows). …”
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1949
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1950
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1951
Early surface PSA-NCAM reduction induced by glutamate exposure.
Published 2014“…(B) Quantification of PSA-NCAM immunoreactive area showed decreased levels at neuronal surface 3 h after glutamate exposure, which remained low for the rest of the studied period (3–6 h). …”
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1952
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1953
Time-course of changes induced on NCAM and SYN synaptic patterns and levels by glutamate exposure.
Published 2014“…<p>Hippocampal neurons in culture (DIV 12–13) were briefly exposed to 5 µM glutamate and evaluated 1, 3, 6 and 12 h later. (A) Microphotographs of hippocampal neurons in culture doubled stained for NCAM and SYN. …”
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1954
GNE-781, A Highly Advanced Potent and Selective Bromodomain Inhibitor of Cyclic Adenosine Monophosphate Response Element Binding Protein, Binding Protein (CBP)
Published 2017“…Compound <b>19</b> displays antitumor activity in an AML tumor model and was also shown to decrease Foxp3 transcript levels in a dose dependent manner.…”
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1955
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1956
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
Published 2007“…The barriers for the three processes were found to be successively 14.4, 14.5−17.5, and 13.1−15.8 kcal mol<sup>-1</sup>. Within the limitations of the small dataset investigated, emergent trends in the barrier heights can be recognized: the values decrease with the increasing size of the π-electron-donating macrocycle and tend to be lower in the sterically less encumbered series of [2]catenanes containing the 1,3-butadiyne moiety.…”
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1957
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
Published 2007“…The barriers for the three processes were found to be successively 14.4, 14.5−17.5, and 13.1−15.8 kcal mol<sup>-1</sup>. Within the limitations of the small dataset investigated, emergent trends in the barrier heights can be recognized: the values decrease with the increasing size of the π-electron-donating macrocycle and tend to be lower in the sterically less encumbered series of [2]catenanes containing the 1,3-butadiyne moiety.…”
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1958
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
Published 2007“…The barriers for the three processes were found to be successively 14.4, 14.5−17.5, and 13.1−15.8 kcal mol<sup>-1</sup>. Within the limitations of the small dataset investigated, emergent trends in the barrier heights can be recognized: the values decrease with the increasing size of the π-electron-donating macrocycle and tend to be lower in the sterically less encumbered series of [2]catenanes containing the 1,3-butadiyne moiety.…”
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1959
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
Published 2007“…The barriers for the three processes were found to be successively 14.4, 14.5−17.5, and 13.1−15.8 kcal mol<sup>-1</sup>. Within the limitations of the small dataset investigated, emergent trends in the barrier heights can be recognized: the values decrease with the increasing size of the π-electron-donating macrocycle and tend to be lower in the sterically less encumbered series of [2]catenanes containing the 1,3-butadiyne moiety.…”
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1960