GPC and PCA analysis of loosely-bound sugars in OE control compared to XTH43 samples and RNAi control compared to XTH43-RNAi samples. by Prakash M. Niraula (6816713)

Direct GPC and PCA analysis of loosely-bound sugars in OE control compared to RNAi control and XTH43-OE compared to XTH43-RNAi samples. by Prakash M. Niraula (6816713)

Direct GPC and PCA analysis of tightly-bound sugars in OE control compared to RNAi controls and XTH43-OE compared to XTH43-RNAi samples. by Prakash M. Niraula (6816713)

Direct counterpart GPC analysis of loosely-bound sugars in OE control and XTH43-RNAi samples and RNAi control and XTH43-RNAi samples. by Prakash M. Niraula (6816713)

Direct counterpart comparisons made between the OE control and XTH43-RNAi. by Prakash M. Niraula (6816713)

Direct counterpart comparisons made between the RNAi control and XTH43-OE. by Prakash M. Niraula (6816713)

GPC and PCA analysis of tightly-bound sugars in RNAi control compared to XTH43 samples and RNAi control compared to XTH43-RNAi samples. by Prakash M. Niraula (6816713)

Model showing cellulose microfibrils with bound XyG chains presented only for diagrammatic purposes. by Prakash M. Niraula (6816713)

“…<i>glycines</i>-susceptible outcome as shown in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0244305#pone.0244305.g002" target="_blank">Fig 2B</a> as compared to the OE control in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0244305#pone.0244305.g002" target="_blank">Fig 2A</a>. *** XTH43-OE showing an decrease in XyG chain length and more of those chains. …”

Inhibition of Neuroblastoma Tumor Growth by Targeted Delivery of MicroRNA-34a Using Anti-Disialoganglioside GD₂ Coated Nanoparticles by Amanda Tivnan (163017)

DNA microarray analysis of long-term stationary phase-induced gene expression in <i>E. coli</i> grown in LB broth. by Kotakonda Arunasri (385358)

“…The X-axis represents the log2 fold change and the dark vertical lines represent cut-offs at 2.0 fold decrease and increase. The y-axis represents the p-values and the dark horizontal line indicates a –log10 p value cut-off of 0.05.…”

Gene expression profile of <i>Pcgf5</i>-deficient HSPCs. by Sha Si (2635147)

“…<p>(A) Snapshots of RNA-sequence signals at the <i>Pcgf5</i> gene locus in WT and <i>Pcgf5</i>^<i>Δ/Δ</i> LSK cells isolated from recipient mice repopulated with <i>Pcgf5</i>^<i>Δ/Δ</i> hematopoietic cells. …”

Inhibition of gastric cancer cell SGC-7901 viability by VES. by Liying Hou (769063)

Data_Sheet_2_Nutrient Inputs Stimulate Mercury Methylation by Syntrophs in a Subarctic Peatland.docx by Spencer Roth (11518552)

Table_1_Nutrient Inputs Stimulate Mercury Methylation by Syntrophs in a Subarctic Peatland.XLSX by Spencer Roth (11518552)

Data_Sheet_1_Nutrient Inputs Stimulate Mercury Methylation by Syntrophs in a Subarctic Peatland.DOCX by Spencer Roth (11518552)

The amount (in percent) of total sugars and XyG in Soxhlet-extracted total sugars from <i>G</i>. <i>max</i> root total root tissue dry mass from XTH43-RNAi as compared to the RNAi... by Prakash M. Niraula (6816713)

The amount (in percent) of total sugars and XyG in Soxhlet-extracted total sugars from <i>G</i>. <i>max</i> root total root tissue dry mass of XTH43-OE roots as compared to the OE... by Prakash M. Niraula (6816713)

Effects of K0 and K63only ubiquitin mutants on stalled translation. by Kazuki Saito (86281)

Data_Sheet_1_Mechanistic and biophysical characterization of polymyxin resistance response regulator PmrA in Acinetobacter baumannii.pdf by Zhenlin Ouyang (10175531)

“…This impact resulted in an enhanced cell surface smoothness with fewer modifications, ultimately contributing to a decrease in colistin (polymyxin E) and polymyxin B resistance. …”

Data Sheet 1_Epigallocatechin-3-gallate protects against osteoarthritis-induced chondrocytes dysfunction by regulating PLa2g2a.pdf by Mengyuan Dai (9747317)

“…Notably, epigallocatechin-3-gallate (EGCG), a polyphenolic compound derived from green tea, is a known pan-assay interference compound (PAINS), which may produce non-specific in vitro effects (e.g., protein binding, redox interference) that challenge the interpretation of its pharmacological relevance. …”