RNA-sequencing data screening for miR-1247-3p target genes. by Dequan Wang (6007007)

Red and green fluorescence of <i>M</i>. <i>aeruginosa</i> after exposure to different wavelength light and H₂O₂ at 72 hours. by Emma T. Brentjens (17295999)

The observed MRM reactions. by Ewa Paszkowska (21246702)

“…<div><p>Purpose</p><p>Statins are the most commonly used drugs worldwide. Besides a significant decrease in cardiovascular diseases (CVDs) risk, the use of statins is also connected with a broad beneficial pleiotropic effect. …”

Intra- and inter-day precision and accuracy. by Ewa Paszkowska (21246702)

“…<div><p>Purpose</p><p>Statins are the most commonly used drugs worldwide. Besides a significant decrease in cardiovascular diseases (CVDs) risk, the use of statins is also connected with a broad beneficial pleiotropic effect. …”

DA-dip detectable region in the competitive model. by Hidetoshi Urakubo (578508)

“…<p>(A) <i>AC</i>_primed is observed under the stepwise decreasing signal of DA. …”

Side-Chain Engineering for Modulating the Mechanical and Thermosalient Behavior of Elastic Crystals of Triple-Helix Coordination Polymers by Shu-Wen An (7450172)

“…In this work, starting from a previously reported mechanically responsive CP material (<b>U-CF</b>_<b>3</b><b>-phen</b>) with a spine of triple-helix polymeric chains decorated by side-chain organic base ligands (1,10-phenanthroline, <b>phen</b>), two other new triple-helix CPs, <b>U-CF</b>_<b>3</b><b>-bpy</b> and <b>U-CF</b>_<b>3</b><b>-dmbpy</b>, that are isomorphic to <b>U-CF</b>_<b>3</b><b>-phen</b> were synthesized through side-chain engineering, i.e., replacing <b>phen</b> with two other organic base ligands, 2,2′-bipyridine (<b>bpy</b>) or 5,5′-dimethyl-2,2′-bipyridine (<b>dmbpy</b>). …”

Side-Chain Engineering for Modulating the Mechanical and Thermosalient Behavior of Elastic Crystals of Triple-Helix Coordination Polymers by Shu-Wen An (7450172)

“…In this work, starting from a previously reported mechanically responsive CP material (<b>U-CF</b>_<b>3</b><b>-phen</b>) with a spine of triple-helix polymeric chains decorated by side-chain organic base ligands (1,10-phenanthroline, <b>phen</b>), two other new triple-helix CPs, <b>U-CF</b>_<b>3</b><b>-bpy</b> and <b>U-CF</b>_<b>3</b><b>-dmbpy</b>, that are isomorphic to <b>U-CF</b>_<b>3</b><b>-phen</b> were synthesized through side-chain engineering, i.e., replacing <b>phen</b> with two other organic base ligands, 2,2′-bipyridine (<b>bpy</b>) or 5,5′-dimethyl-2,2′-bipyridine (<b>dmbpy</b>). …”

Side-Chain Engineering for Modulating the Mechanical and Thermosalient Behavior of Elastic Crystals of Triple-Helix Coordination Polymers by Shu-Wen An (7450172)

“…In this work, starting from a previously reported mechanically responsive CP material (<b>U-CF</b>_<b>3</b><b>-phen</b>) with a spine of triple-helix polymeric chains decorated by side-chain organic base ligands (1,10-phenanthroline, <b>phen</b>), two other new triple-helix CPs, <b>U-CF</b>_<b>3</b><b>-bpy</b> and <b>U-CF</b>_<b>3</b><b>-dmbpy</b>, that are isomorphic to <b>U-CF</b>_<b>3</b><b>-phen</b> were synthesized through side-chain engineering, i.e., replacing <b>phen</b> with two other organic base ligands, 2,2′-bipyridine (<b>bpy</b>) or 5,5′-dimethyl-2,2′-bipyridine (<b>dmbpy</b>). …”

Side-Chain Engineering for Modulating the Mechanical and Thermosalient Behavior of Elastic Crystals of Triple-Helix Coordination Polymers by Shu-Wen An (7450172)

“…In this work, starting from a previously reported mechanically responsive CP material (<b>U-CF</b>_<b>3</b><b>-phen</b>) with a spine of triple-helix polymeric chains decorated by side-chain organic base ligands (1,10-phenanthroline, <b>phen</b>), two other new triple-helix CPs, <b>U-CF</b>_<b>3</b><b>-bpy</b> and <b>U-CF</b>_<b>3</b><b>-dmbpy</b>, that are isomorphic to <b>U-CF</b>_<b>3</b><b>-phen</b> were synthesized through side-chain engineering, i.e., replacing <b>phen</b> with two other organic base ligands, 2,2′-bipyridine (<b>bpy</b>) or 5,5′-dimethyl-2,2′-bipyridine (<b>dmbpy</b>). …”

The <i>unc-29</i> mutant is sensitive to organic solvent toxicity. by Masahiro Tomioka (430683)

Syntheses of Pentanuclear Group 6 Iridium Clusters by Core Expansion of Tetranuclear Clusters with Ir(CO)₂(η⁵‑C₅Me₄R) (R = H, Me) by Michael D. Randles (1902586)

“…Single-crystal X-ray diffraction studies of <b>1a</b>–<b>1d</b>, <b>2</b>, <b>3a</b>–<b>3d</b>, and <b>4</b> confirmed their molecular structures, including the μ-η¹:η⁵-CH₂C₅Me₄ ligand at hydrido cluster <b>2</b>, derived from a C–H bond activation of one of the methyl groups. …”

Comparison of the effects of several 5-HT receptor antagonists on the plasma concentrations of metabolites and insulin, following 5-HT injection in sheep and mice. by Hitoshi Watanabe (519631)

“…</p>b<p>5-HT: serotonin; Me: methysergide; Ke: ketanserin; SB-26: SB-269970; SB-20: SB-204070; Ro: Ro 04-6790; I: increase; D: decrease; N: no change; +: effective in blocking the effect of 5-HT; −: ineffective in blocking the effect of 5-HT.…”

Schematic of the D2 model (Competitive model). by Hidetoshi Urakubo (578508)

Negative (Prednisone) and basal (ATP) control compounds binding to ALK protein. by Richard Junior Zapata Dongo (17912565)

Functional impact and genomic distribution of A-to-I RNA editing candidate events. by Xinxin Peng (219357)

Dose dependent changes in fluorescence and forward scatter from cyanobacteria treated with H₂O₂. by Emma T. Brentjens (17295999)

Red and green fluorescence of <i>M</i>. <i>aeruginosa</i> cells exposed to H₂O₂ over time relative to control. by Emma T. Brentjens (17295999)

Average green and red fluorescence for three separate experiments at 48 and 72 hours after H₂O₂ exposure. by Emma T. Brentjens (17295999)

RT-qPCR Primer. by Dequan Wang (6007007)

“…The findings of the current study revealed a significant decrease in miR-1247-3p expression in CRC cells, especially those resistant to drugs. …”

The detection of red (652–669 nm) and green (533–550 nm) fluorescence from yellow-green and violet laser excitation in control and H₂O₂-treated <i>M</i>. <i>a... by Emma T. Brentjens (17295999)