Nuclear Srebp1 and Srebp2 protein levels and Srebp-dependent lipogenic gene expression are elevated in obese <i>mMgat2</i> and <i>HuMgat2</i> mice. by J. Jose Corbalan (22439198)

Dynamics of PIF4 protein accumulation and autoinhibition in response to temperature. by Sreya Das (20531295)

Box-whisker plots of the relative abundances (%) of coccolithophore species characteristic for the “pseudo-stadial” (PS; 1854.6–1852.8 cm), the interstadial before the YTT eruption... by Jose Dominick Guballa (19739909)

Relative abundance (%) of the main coccolithophore species between 1854.6–1820.4 cm (74.353–73.505 ka) of core SO130-289KL. by Jose Dominick Guballa (19739909)

Comparison of the coccolithophore assemblage to paleo-proxy records between 74.40 to 73.40 ka. by Jose Dominick Guballa (19739909)

qPCR LL-37 gene expression. by Parisa Afzal Haghjoo (22453647)

The expression profile of lipogenic genes, oxidative stress mediators as well as UPR^ER and mitochondrial stress markers. by Summan Thahiem (20988319)

Evaluation of chronic <i>in vivo</i> efficacy in 21 days rat MCT model in prevention mode. by Tobias G. Schips (21799838)

Determination of bladder blood flow in LETO and OLETF rats. by Takafumi Kabuto (14797727)

<i>hdc</i> silencing causes cell death and cell cycle arrest in the PSC. by Bayan Kharrat (19959505)

Targeting of Vps34 or Atg14, but not Uvrag, in Tregs reduces tumor growth in mouse models. by Erienne G. Norton (9612079)

Vps34 supports Treg maintenance in lymphoid and non-lymphoid tissues. by Erienne G. Norton (9612079)

“…GSEA enrichment plots showing increased cTreg signature (left; i.e., top 200 upregulated genes [log₂FC > 0.5, FDR < 0.05] in cTregs versus eTregs) and decreased eTreg signature (right; i.e., top 200 upregulated genes [log₂FC > 0.5, FDR < 0.05] in eTregs versus cTregs) in CD45.2⁺ Tregs from <i>Foxp3</i>^Cre<i>Pik3c3</i>^fl/fl mixed BM chimera mice compared to control mixed BM chimera mice. …”

pI7L suppresses the IFN-<i>γ</i>-triggered JAK-STAT signaling pathway. by Meilin Li (1832905)

Atg14 does not contribute to terminal eTreg generation during perinatal life. by Erienne G. Norton (9612079)

Chromatin accessibility analysis of perinatal Vps34-deficient Tregs. by Erienne G. Norton (9612079)

“…Relative (normalized to average control in each experiment) fold-change comparisons between genotypes in each cell type are shown in bold (<b>A</b>, <b>B</b>). Data are shown as mean ±  s.e.m. (<b>A</b>, <b>B</b>). Two-tailed Student <i>t</i> test (<b>A</b>, <b>B</b>, <b>I</b>), Benjamini–Hochberg test (<b>C</b>), Wilcoxon rank-sum test (<b>G</b>), Fisher’s exact tes<i>t</i> (<b>H</b>), or binomial test (<b>J</b>); NS, not significant. …”

Vps34 orchestrates transcriptional and epigenetic remodeling events corresponding to terminal eTreg differentiation during perinatal life. by Erienne G. Norton (9612079)

“…See also <a href="http://www.plosbiology.org/article/info:doi/10.1371/journal.pbio.3003074#pbio.3003074.s017" target="_blank">S9 Table</a>. Data are shown as mean ± s.e.m. (<b>D</b>). Wilcoxon rank-sum test (<b>A</b>, <b>B</b>; <b>J</b>, right), Benjamini–Hochbert test (<b>C</b>), two-tailed Student <i>t</i> test (<b>D</b>, <b>I</b>), Fisher’s exact test (<b>F</b>–<b>H</b>), or bionomial test (<b>J</b>, left); NS, not significant. …”

Disruption of <i>shk-1</i> increases susceptibility to bacterial pathogens. by Longjun Pu (20685717)

Effects of head motion parameters on developmental changes of nodal entropy. by Tianyuan Lei (19683861)

Prediction of individual spatial patterns of nodal module overlap from structural brain features in children. by Tianyuan Lei (19683861)

The effect of the supernatants of <i>E</i>. <i>coli</i> 25922 in different conditions on MRSA and MSSA and their self-production of EDF. by Shahriar Bakhti (20391188)