Data underlying Figs 1B, 1C, 1E, 1J, 1K, 2B, 2C, 2E, 2F, 2H, 2I, 3B, 3C, 3D, 3E, 3F, 4B, 4D, 4E, 4F, 4G, 5A, 5B, 6E and 6G. by Xinxin Li (281237)

Fig 5 - by Thiago Bezerra Wanderley e Lima (14232350)

Conditional ablation of <i>Ybx1</i> leads to a reduction in cortical progenitor cell pool and a decrease in cortical thickness. by Jian Zhang (1682)

Deletion of <i>Kdm5b</i> in DCs leads to increased cytokine production and decreased Th2 pathology <i>in vivo</i>. by Catherine Ptaschinski (756139)

Increased accumulation of mutant huntingtin aggregates and decreased mobility of autophagosomes in the axon of AP-4 ε KO hippocampal neurons. by Raffaella De Pace (5147120)

CSE decreased epithelial markers in lung epithelial cells. by Irene M. J. Eurlings (645586)

Differential expression analysis of nuclear transcripts after siAPOBEC3A depletion reveals induction of TP53 targets and decreases in cell cycle and cell growth regulator transcrip... by Mason A. McCool (11889842)

Supplementary Material for: Blood Outgrowth Endothelial Cells Reduce Hypoxia-Mediated Fibroblast to Myofibroblast Conversion by Decreasing Proangiogenic Cytokines by Nieves Torres E.C. (3643015)

“…This is associated with a decrease in several proangiogenic genes including vascular endothelial growth factor A, platelet-derived growth factor, fibroblast growth factor and matrix metalloproteinase 2 in fibroblasts in contact with BOEC when compared to fibroblasts alone. …”

Supplementary Figure 2 from Decreased eIF3e Expression Can Mediate Epithelial-to-Mesenchymal Transition through Activation of the TGFβ Signaling Pathway by Guillaume Desnoyers (232704)

“…<p>Supplementary Figure 2- Phosphorylation of eIF4E is decreased in A549 and MCF-10A cells that have decreased eIF3e expression. …”

Excel spreadsheet containing, in separate sheets, the numerical data and statistical analysis for Figure panels 1A, 1B, 1C, 1E, 2A, 2B, 2C, 2D, 2E, 2F, 3B, 3D, 3E, 3G, 4A, 4B, 4C,... by Huizi Li (6241586)

Cytosolic mitochondrial DNA release upon MeV and MeV-ΔV infection in culture and in mice. by Pierre Khalfi (7868252)

Subjects:

MCM-BP can decrease phosphorylation by DDK but is not a substrate. by Tin Nguyen (231591)

Repetitive stress induces a decrease in sound-evoked activity. by Ghattas Bisharat (20706928)

“…(d) Noise-evoked activity rates at different noise intensities for chronically tracked PV cells in baseline and repeated stress conditions (<i>N</i> = 5 mice, <i>n</i> = 31 neurons, mean ± SE). Activity rates decreased during repeated stress compared to baseline (2-way ANOVA, condition F = 49.6, <i>p</i> = 2.6 × 10⁻¹², condition: intensity interaction F = 1.94, <i>p</i> = 0.02, nested ANOVA (mouse nested within session), F = 56.5, <i>p</i> = 8.8 × 10⁻¹⁴, condition: intensity interaction F = 3.5, <i>p</i> = 3.5 × 10⁻⁰⁵). …”

Increasing and decreasing trend in IgG levels among patients during different visits. by Ashraf Hassan Alzaabi (10960548)

NSC population and proliferation decrease drastically during the second postnatal week of DG development. by Cristina Medina-Menéndez (21800157)

A decrease in cellular RNA increases the insolubility of TDP-43. by Shinnosuke Takagi (428655)

“…<p>(A) Electrophoresis of total RNA immunoprecipitated with wild-type TDP-43 or mtRNP2. …”

SNX5 phosphorylation sites. by Nao Itai (5954666)

Subjects:

Inhibition of serine proteases decreases EndMTs and vascular calcification. by Pierre J. Guihard (3391721)

Decrease in GABA_A immunoreactivity in APP mice. by Ksenia V. Kastanenka (3692380)

“…(<b>E</b>) Slow oscillation power (normalized to wildtype) and (<b>F</b>) mean slow oscillation frequency before (WT baseline) and after picrotoxin (PTX) application to brains of 2–4 month old wildtype mice (n = 4 mice). …”

Inhibition of ATM kinase activity decreases H3K36me3 on the HPV31 genome and alters processing of late viral RNAs. by Dipendra Gautam (3215988)