DDX5 and DDX17 are required for KSHV lytic reactivation. by Praneet Kaur Sandhu (21156149)

DataSheet_1_Pharmacological Profile of the Sodium Current in Human Stem Cell-Derived Cardiomyocytes Compares to Heterologous Nav1.5+β1 Model.pdf by Dieter V. Van de Sande (8112149)

“…For class Ib drugs phenytoin and lidocaine, which are inactivated state blockers, the affinity decreased more than a twofold when β1 was present. …”

Receiver-operating characteristic curves of % PCT decrease for predicting survival (A) and recovery from dialysis (B) within 28 days after CRRT initiation in patients with SIAKI re... by Il Young Kim (10757390)

Corresponding abundances of pfu/mL were quantified by plaque assay over a 12 h period of incubation in <i>V</i>. <i>splendidus</i> cultures in the presence of phage vB_VspM_VS2 at... by Xuemei Duan (6901601)

Table_1_Elevated hypertriglyceridemia and decreased gallstones in the etiological composition ratio of acute pancreatitis as affected by seasons and festivals: A two-center real-wo... by Wenhua He (5721077)

“…The composition ratio of gallstone AP in the south center was higher than that in the north center (59.5% vs. 49%), especially in summer (62.9% vs. 44.0%) and autumn (61.5% vs. 45.7%, all P<0.001).…”

Transgenic FAR expression significantly decreases fly survival and increases bacterial load 24-hours post-injection. by Sophia C. Parks (11624976)

There is decreased fluorescence from the <i>in planta</i> interaction between sYFPn-2b and sYFPc-AGO1 in the presence of the cucumber mosaic virus 1a protein. by Lewis G. Watt (9728094)

A Bifunctional Three-Dimensional Zn(II) Metal–Organic Framework with Strong Luminescence and Adsorption Cr(VI) Properties by Yufeng Chen (560054)

“…This <b>3D-Zn-MOF</b> has two different types of pores (4.5 × 4.5 Ų, 5.7 × 5.7 Ų). …”

DDX5 and DDX17 are required for EBV lytic reactivation. by Praneet Kaur Sandhu (21156149)

Data_Sheet_1_A20/TNFAIP3 Increases ENOS Expression in an ERK5/KLF2-Dependent Manner to Support Endothelial Cell Health in the Face of Inflammation.docx by Cleide Angolano (10762497)

“…Conversely, siRNA-induced A20 knockdown decreased eNOS mRNA levels, identifying A20 as a physiologic regulator of eNOS expression. …”

Evidence for a bronchoscopic training effect from live viewing of colleagues’ sharp instrument errors. by Caterina Zagona-Prizio (14833699)

High-frequency ultrasound B-mode images of the central 5.7 mm of the cornea from a normal subject (left) and a grade-4 KC patient (right), along with their corresponding thickness... by Sunny Kwok (13124155)

Intravital 2-photon microscopy imaging of acute <i>C</i>. <i>albicans</i> infections of the kidney in real time in a living host. by Fitz Gerald S. Silao (9384713)

Functional antagonism of S1P signaling inhibits cell-to-cell transmission of R5-tropic HIV-1. by Rachel S. Resop (9238645)

Image_1_Neuroplastin 65 deficiency reduces amyloid plaque formation and cognitive deficits in an Alzheimer’s disease mouse model.TIF by Dan-Dan Wu (1449316)

“…Finally, protein levels of 5-hydroxytryptamin (serotonin) receptor 3A and synaptic proteins and neurons were measured.…”

Image_2_Neuroplastin 65 deficiency reduces amyloid plaque formation and cognitive deficits in an Alzheimer’s disease mouse model.TIF by Dan-Dan Wu (1449316)

“…Finally, protein levels of 5-hydroxytryptamin (serotonin) receptor 3A and synaptic proteins and neurons were measured.…”

Image_5_Spliceostatin C, a component of a microbial bioherbicide, is a potent phytotoxin that inhibits the spliceosome.jpg by Joanna Bajsa-Hirschel (3902302)

“…In silico binding studies showed that SPC binds to a pocket between the SF3B3 and PF5A of the spliceosome.…”

Table_5_Spliceostatin C, a component of a microbial bioherbicide, is a potent phytotoxin that inhibits the spliceosome.docx by Joanna Bajsa-Hirschel (3902302)

“…In silico binding studies showed that SPC binds to a pocket between the SF3B3 and PF5A of the spliceosome.…”

Discovery of <i>N</i>‑((3<i>S</i>,4<i>S</i>)‑4-(3,4-Difluorophenyl)piperidin-3-yl)-2-fluoro-4-(1-methyl‑1<i>H</i>‑pyrazol-5-yl)benzamide (Hu7691), a Potent and Selective Akt Inhibitor That Enables Decrease of Cutaneous Toxicity by Jinxin Che (791250)

Discovery of <i>N</i>‑((3<i>S</i>,4<i>S</i>)‑4-(3,4-Difluorophenyl)piperidin-3-yl)-2-fluoro-4-(1-methyl‑1<i>H</i>‑pyrazol-5-yl)benzamide (Hu7691), a Potent and Selective Akt Inhibitor That Enables Decrease of Cutaneous Toxicity by Jinxin Che (791250)