Search alternatives:
ng decrease » nn decrease (Expand Search), _ decrease (Expand Search), we decrease (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (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)
-
12561
DataSheet1_Population pharmacokinetic study of pemetrexed in chinese primary advanced non-small cell lung carcinoma patients.docx
Published 2022“…Creatinine clearance (CrCl) was identified as a covariate to CL, and ERCC1 (rs3212986) and CYP3A5 (rs776746) gene polymorphisms as covariates to Q. …”
-
12562
Image3_miR-146a is a critical target associated with multiple biological pathways of skin aging.jpg
Published 2024“…Skin function and barrier integrity are actively regulated through circadian rhythm–associated genes and epigenetic mechanisms including DNA methylation/demethylation, histone acetylation/deacetylation, and microRNAs. MicroRNA-146a-5p (miR-146a) has been associated with immune activation and skin inflammation; however, the role of miR-146a in regulating skin aging is an open question. …”
-
12563
Image1_miR-146a is a critical target associated with multiple biological pathways of skin aging.jpg
Published 2024“…Skin function and barrier integrity are actively regulated through circadian rhythm–associated genes and epigenetic mechanisms including DNA methylation/demethylation, histone acetylation/deacetylation, and microRNAs. MicroRNA-146a-5p (miR-146a) has been associated with immune activation and skin inflammation; however, the role of miR-146a in regulating skin aging is an open question. …”
-
12564
Image2_miR-146a is a critical target associated with multiple biological pathways of skin aging.jpg
Published 2024“…Skin function and barrier integrity are actively regulated through circadian rhythm–associated genes and epigenetic mechanisms including DNA methylation/demethylation, histone acetylation/deacetylation, and microRNAs. MicroRNA-146a-5p (miR-146a) has been associated with immune activation and skin inflammation; however, the role of miR-146a in regulating skin aging is an open question. …”
-
12565
-
12566
Investigation of solar PV performance under Doha weather using a customized measurement and monitoring system
Published 2016“…Results predict that the maximum power output from a Poly-crystalline panel decreases by around 30% for a dust exposure of five months. …”
Get full text
Get full text
-
12567
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”
-
12568
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”
-
12569
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”
-
12570
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”
-
12571
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”
-
12572
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”
-
12573
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”
-
12574
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”
-
12575
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”
-
12576
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”
-
12577
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”
-
12578
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”
-
12579
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”
-
12580
Chloro Half-Sandwich Osmium(II) Complexes: Influence of Chelated N,N-Ligands on Hydrolysis, Guanine Binding, and Cytotoxicity
Published 2007“…The Os<sup>II</sup> complexes hydrolyze up to 100 times more slowly than their Ru<sup>II</sup> analogues. The p<i>K</i>*<sub>a</sub> of the aqua adducts decreased with a similar trend (p<i>K</i>*<sub>a</sub> = 6.3 and 5.8 for en and phen adducts, respectively). …”