Summary of methodology and data analysis. by Peter A. Pahapill (8468607)

Functional connectivity and structural analysis of trial spinal cord stimulation responders in failed back surgery syndrome by Peter A. Pahapill (8468607)

Effect of carabrone on mitochondrial respiratory chain complex V (ATP synthase). by Xingyu Ren (7358867)

“…<b>(B)</b> Measurement of mitochondrial membrane potential (MMP, Δ<i>Ψ</i>m) in <i><i>G. tritici</i></i>, treatment by carabrone (50 and 100 μM), FCCP (250 nM) and oligomycin A (5 nM), JC-1 monomers (green) indicate decreased MMP, JC-1 aggregates (red) indicate increased MMP, Bar = 100 μm. …”

Image_5_Mechanisms of FH Protection Against Neovascular AMD.TIFF by Céline Borras (3551978)

Table_5_Comparison of the Vaginal Microbiomes of Premenopausal and Postmenopausal Women.PDF by Karol Gliniewicz (3538301)

Dynamic Distribution of Linker Histone H1.5 in Cellular Differentiation by Jing-Yu Li (139513)

“…Depletion of H1.5 results in loss of SIRT1 and H3K9me2, increased chromatin accessibility, deregulation of gene expression, and decreased cell growth. …”

Presenilins are required for maintenance of neural stem cells in the developing brain-5 by Woo-Young Kim (86243)

“…(C, D) was expressed weakly in the control but decreased in the cDKO. (E, F) The expression was strong in the control but decreased in the cDKO. …”

Ras Tyrosine 4 is required for Rabex-5-mediated Ras ubiquitination. by Chalita Washington (8997378)

“…<p>(A) Flag-His6-GFP tagged Ras (Ras^WT) or FLAG-His6-GFP tagged Ras N-terminal fragments tagged with C-terminal localization signal CKML (1–10 CKML, 1–20 CKML) were co-transfected into Schneider S2 cells with HA-Ub with or without Rabex-5 and purified on nickel beads as done previously [<a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1008715#pgen.1008715.ref013" target="_blank">13</a>, <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1008715#pgen.1008715.ref016" target="_blank">16</a>]. …”

Evaluation of the potential of Rejuveinix plus dexamethasone against sepsis - Fig S5 by Fatih M Uckun (13809802)

Silencing of the reporter gene <i>URA5-miRs</i>. by Nan Jiang (21252)

“…<p>(A) The upper panels show a slower growth rate of the transformants of <i>URA5-miR1</i> (two transformants was picked in each case, namely, miR1-1 and miR1-2), and <i>URA5-miR2</i> (miR2-1 and miR2-2), than the wild type B4500, and the transformants of miR1-m (<i>i.e.…”

Altered regulation of Prox1-gene-expression in liver tumors-5 by Jozsef Dudas (46097)

“…When the nuclear extracts were reacted with the same radiolabelled consensus double-stranded oligo in the presence of a 100-fold excess of an unlabeled MAZ-consensus oligo (published in ref. [23]) the intensity of mobility shift significantly decreased (right panel); sample 1: negative control, without nuclear extract. …”

OTUD4 deficiency impairs MHV68 replication <i>in vivo.</i> by Shaowei Wang (490684)

Increased 5-hmC occurs in osteoblast and chondrocyte gene promoters. by Richard C. Lindsey (7148168)

“…(B) Inhibition of PHD2 with Iox2 significantly decreased 5-hmC levels in the promoters of chondrocyte genes HIF1α and VEGF. …”

UHRF2 regulates local 5-methylcytosine and suppresses spontaneous seizures by Yidan Liu (3876598)

“…Therefore, our study has revealed a unique role of UHRF2 in the maintenance of local 5mC levels in brain that is distinct from that of its paralog UHRF1.…”

Figure S1-S21 from miR-196b-5p Regulates Colorectal Cancer Cell Migration and Metastases through Interaction with HOXB7 and GALNT5 by Verena Stiegelbauer (4582930)

“…<p>Supplementary Figure S1 Expression levels of miR-196b-5p in different tumor stages and tumor grade. (A-B) In cohort 1, miR-196b-5p expression decreased with (A) higher tumor stage, whereas no difference could be observed for (B) tumor grade. …”

Reduced control model M5: No accumulation of information across trials. by Veith Weilnhammer (2909060)

“…<p>When simulating data for the <i>no-evidence-accumulation model</i>, we removed the accumulation of information across trials by setting the hazard rate <i>H</i> to 0.5. Simulated data thus depended only on the participant-wise estimates for the amplitudes <i>a</i>_{<i>LLR</i>/<i>ψ</i>}, frequency <i>f</i>, phase <i>p</i>, and inverse decision temperature <i>ζ</i>. …”

Image_5_Climatic and Resource Determinants of Forest Elephant Movements.pdf by Christopher Beirne (636588)

Table_5_Clostridium cellulovorans Proteomic Responses to Butanol Stress.XLSX by Paolo Costa (1396552)

“…Several additional metabolic adaptations were triggered by butanol exposure such as the up-regulation of V- and F-type ATPases (involved in ATP synthesis/generation of proton motive force), enzymes involved in amino acid (e.g., arginine, lysine, methionine, and branched chain amino acids) biosynthesis and proteins involved in cell envelope re-arrangement (e.g., the products of Clocel_4136, Clocel_4137, Clocel_4144, Clocel_4162 and Clocel_4352, involved in the biosynthesis of saturated fatty acids) and a redistribution of carbon flux through fermentative pathways (acetate and formate yields were increased and decreased, respectively). …”

Influenza-induced loss of claudin-5 is due to cleavage by matrix metalloproteases. by Susan M. Armstrong (301641)

“…<p>(A) The reduction in claudin-5 levels is not due to decreased transcription. …”

Receptors mediated changes in ERK1/2 and ERK5 phosphorylation. by Rishi K. Somvanshi (506704)

“…Note that the combined agonist treatment had pronounced effect on ERK5 phosphorylation. Densitometric analysis for the blots (in Panels A-D) was performed by using β-actin or total as loading control and data analysis was done by using ANOVA and <i>post hoc</i> Dunnett’s to compare against basal level (*, <i>p</i><0.05).…”