IL-1Ra ASO treatment effect on adipose tissue. by Niclas Franck (632562)

High levels of IFNγ partially restores <i>C</i>. <i>trachomatis</i> development in HeLa cells. by Shardulendra P. Sherchand (3133677)

Hatchability and heart rate between two groups. by Yali Ge (417371)

Nakasone. AJP supple Table1, 2, 3 by Toru Aizawa (9001298)

“…<em>Hazard ratio and 95%CI of HGI and HbA1c to incident CKD</em></p> <p>  </p> <p>The data was obtained in Aizawa cohort, in which QR of HGI and HbA1c was almost the same as 0.48 and 0.50 (Table 1) so that scaling was omitted. …”

Supplemental data about the effect of M₄N on energy metabolism. by Kotohiko Kimura (1888807)

<i>C</i>. <i>sinensis</i> promoted the expressions of cytokines in liver and BECs through TLR2 pathway. by Yuru Wang (846969)

Evaluating competitive inhibition by gcn5-F221A using a synthetic pPHO5-yECitrine construct. by Amanda M. Lanza (168454)

“…Increasing expression of <i>gcn5-F221A</i> resulted in decreased mean fluorescence. …”

TLR2 deficiency alleviated liver fibrosis in <i>C</i>. <i>sinensis-</i>infected mice. by Yuru Wang (846969)

<i>C</i>. <i>sinensis</i> ESPs increased the production of IL-6 via TLR2-mediated AKT and p38 pathways. by Yuru Wang (846969)

Image_1_Exploring the potential of pheophorbide A, a chlorophyll-derived compound in modulating GLUT for maintaining glucose homeostasis.pdf by Saptadipa Paul (18132904)

“…To assess how pheophorbide A mechanistically acts on GLUT1 in pancreatic β cell, we transfected INS-1 cells with GLUT1–enhanced green fluorescent protein and checked how the treatment of pheophorbide A (0.50 µM) modulates GLUT1 trafficking using live-cell imaging. …”

Impact of age on sharing of top 5000 TCRβ clones. by Sarah A. Johnson (11355817)

KS1 and KS2 combined RNA-seq experiment differentially expressed genes: <i>Kmt2d</i>^<i>-/-</i> vs <i>Kmt2d</i>^<i>+/+</i>, Day 7. by Christine W. Gao (18794576)

Serum cholesterol concentrations in hyperthyroid cats and euthyroid controls. by Molly A. Bechtold (18794251)

Developmental toxicity induced by 2 μg/ml propofol. by Yali Ge (417371)

Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

“…Among them, <b>14k</b> exhibited most potent activity, with IC₅₀ values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”

Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

“…Among them, <b>14k</b> exhibited most potent activity, with IC₅₀ values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”

Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

“…Among them, <b>14k</b> exhibited most potent activity, with IC₅₀ values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”

Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

“…Among them, <b>14k</b> exhibited most potent activity, with IC₅₀ values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”

Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

“…Among them, <b>14k</b> exhibited most potent activity, with IC₅₀ values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”

Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo by Jun Yan (28467)

“…Among them, <b>14k</b> exhibited most potent activity, with IC₅₀ values of 3–9 nM against six cancer cells, which displayed a 3.8–8.7-fold increase in activity when compare with compound <b>2</b>. …”