The regulatory relationships between the top 5 TFs and their target genes.

<p>The red nodes represent transcription factors and the green nodes represent their target genes.</p

The regulatory relationships between the top 5 TFs and their target genes.

*<p>TF represents the transcription factor. Target gene represents the target gene of transcription factor. cor.1 and cor.2 represent the coexpression correlation between the TF and the target gene in conditions 1 and 2, respectively. DCG indicates the differentially co-expressed gene of a pair of TF and target gene.</p

The top 5 ranked TFs.

*<p>TF represents the transcription factor. RIF represents regulatory impact factor of TF. Rank represents the impact rank of TF.</p

RecN focus is close to the center of the cell treated with MMC.

<p>(A) Most RecN-GFP foci are colocalized with nucleoid at the center area of cells when treated with 2 μg/mL MMC. (B, C) RecN-GFP foci and nucleoids were colocalized at the position of cell plate between two daughter cells in dividing cell pairs. (D) RecN-GFP focus was localized in one of the daughter cells when the chromosome was segregated at the later period of cell cycle after MMC treatment. (E) The white arrows indicated that in a few cells, RecN–GFP foci were not colocalized with the chromosome at the central areas (5% in total, n = 196). (F) Nucleoids were more compacted and the number of RecN-GFP foci increased in some cells (white arrows) (21% of cell in a total, n = 213) after the treatment with 4 μg/mL MMC. Photographs were taken by using an Olympus FV1000 confocal microscope. Cells were stained with DAPI (blue). Each photograph involved 3 different channels for DAPI (in blue) GFP (in green) fluorescence and bright field. Scale bars correspond to 1 μm.</p

Data and analysis code for "Rapid Assessment of Landslide and Rockslide Scale using an Enhanced Probabilistic Neural Network”

The file includes all codes, landslide and rockslide seismic signal datasets for the establishment of ENPP method and case analysis in paper "Rapid Assessment of Landslide and Rockslide Scale using an Enhanced Probabilistic Neural Network"  </p

Movement of RecN in vegetative cells displayed by time-lapse imaging.

<p>The dynamic localization of RecN focus is demonstrated by time-lapse microscopy from the RG-W. Cells were photographed at 3–4 h intervals. Images on the right were taken in bright field and those on the left were taken in fluorescence respectively in 0, 3, 6, and 10 h. The newborn foci were also marked. Images were taken using a Nikon Eclipse 80i microscope. Scale bars correspond to 1 μm.</p

Local Rearrangement in Adsorption Layers of Nanoconfined Ethane

Fluids under nanoconfinement control many environmental and engineering processes. In particular, nanoconfined ethane commonly occurs in hydrocarbon production and gas separation applications. While previous research has measured the pore critical properties and self-diffusivity of nanoconfined ethane, the relationship between molecular organization and phase behavior in nanoporous media persists as a knowledge gap. Through experimental adsorption measurements and molecular dynamics simulations, we report the impact of pore wall proximity, pore size, and temperature on the structure of nanoconfined ethane. We offer evidence for an energetically favorable rearrangement of ethane molecules in the adsorption layer that may contribute to more accurate gas-in-place estimates and more efficient design of gas separation membranes

RecN appears as a single discrete globular focus in newly formed heterocyst and disappears in mature ones.

<p>(A) RecN-GFP focus in heterocyst (white arrow). (B) Rates (in percentage) of heterocysts with RecN–GFP foci after the starvation of combined nitrogen. (C) Western blotting analysis of protein extracts from vegetative cells or enriched heterocysts using anti-RecN antiserum. Lanes 1 and 2: extracts from vegetative cell in 0 and 12 h after nitrogen deprivation; Lanes 3, 4 and 5: extracts from heterocyst in 24, 48 and 72 h after nitrogen deprivation. (D) High concentration of MMC did not lead to the reformation of RecN-GFP foci in mature heterocysts. After 24 h deprivation of combined nitrogen, 4 μg/mL MMC was added into the medium for 3-day cultivation and then the photographs were captured. The white arrows indicate heterocysts. Photographs were taken by using an Olympus FV1000 confocal microscope. Cells were stained with DAPI (blue). The red fluorescence is the fluorescence of photosynthetic pigment. Scale bars correspond to 1 μm.</p

Experimental protocols.

<p><i>A</i>ll groups were subjected to 5-min left main coronary artery occlusion followed by 20-min reperfusion except for the sham-operated group. Remote liver ischemia preconditioning (RLIPC) was induced by four cycles of 5 min of liver ischemia with 5 min intermittent reperfusions. Pharmacological inhibitors (SB216763 and U0126) were administered as a bolus 30 min prior to myocardial ischemia. Two baseline values were recorded: Baseline 1, ten minutes stabilization after instrumentation, and Baseline 2, twenty-five minutes post liver I/R stimulus.</p

RecN forms a single discrete globular focus in vegetative cells.

<p>(A) The three types of vegetative cells divided according to the cell division stages. (B) Localization of RecN-GFP was determined according to its relative position along the x axis and y axis. (C). The locations of the foci in the three types of vegetative cells. The coordinate 0 is the center of the cell. (D) The distributions (in percentage) of the three types of vegetative cells at the relative position of the X-axis. The dynamic localization of RecN-GFP foci was observed with an Olympus FV1000 confocal microscope. Cells were stained with DAPI (blue). Scale bars correspond to 1 μm.</p