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Image Search Results
Journal: Nature Communications
Article Title: SPACEL: deep learning-based characterization of spatial transcriptome architectures
doi: 10.1038/s41467-023-43220-3
Figure Lengend Snippet: a Spatial domains identified by Splane in slice S2 and S5 from Wu et al. dataset, slice S10 from Zhao et al. dataset, and slice S11 released by 10X Genomics. b , c Spatial distribution of chromosome 1q&8q copy number gains ( b ) and 1p copy number losses ( c ) of ST spots in slices S11, calculated by inferCNV. Dashed lines represent the tumor domain. d , e CNVs of chromosome 1q & 8q ( d ) and chromosome 1p ( e ) in each spatial domain calculated by inferCNV. CNVs, copy number variations; center line, median value; box limits, upper and lower quartiles; whiskers, 1.5× interquartile range; n = 11 slices. f From left to right: Splane predicted spatial domains in slice S5, distribution of Splane predicted immune domains D7/D8/D9, distribution of Spoint predicted immune cells, and distribution of H&E staining marked immune spots. g Percentage of H&E staining marked immune spots in each domain of slice S1, S2, S5, and S6. The four slices were H&E stained in the original study. Bar height, mean value; whiskers, mean values ± 95% confidence intervals; n = 4 slices. h From left to right: Splane predicted spatial domains in slice S10, distribution of Splane predicted immune domains D7, D8, and D9, distribution of Spoint predicted immune cells, and distribution of CD3 + immunofluorescence (IF) staining marked immune spots. i Percentage of CD3 + IF staining marked immune spots in each domain of slice S10. Source data are provided as a Source Data file.
Article Snippet: The raw data of 11 ST datasets and five paired single-cell/nucleus RNA sequence datasets are available from the following studies: (1) 12 slices of human DLPFC 10X Visium data at http://research.libd.org/spatialLIBD/ ; (2) six slices of
Techniques: Staining, Immunofluorescence
Journal: PloS one
Article Title: Reduced selenium-binding protein 1 in breast cancer correlates with poor survival and resistance to the anti-proliferative effects of selenium.
doi: 10.1371/journal.pone.0063702
Figure Lengend Snippet: Figure 1. The Expression of SELENBP1 in Normal and Tumor Breast Tissues. Breast cancer tissue arrays were stained by immunohistochemistry using anti-human SELENBP1 antibody at 1:100 dilution. Positive stained cells are shown in dark brown color. (A) Strong positive staining of SELENBP1 in normal breast tissue under low power view (200X). (B–C) Weak positive to negative staining of SELENBP1 in breast cancer tissues under high power view (400X). (D) The Allred scoring distributions of SELENBP1 expression in normal and tumor tissue groups. Inside lines represent means and standard deviations. *p,0.05. (E) Statistical results for the difference between normal and tumor tissues as analyzed by Kruskal-Wallis test. doi:10.1371/journal.pone.0063702.g001
Article Snippet:
Techniques: Expressing, Staining, Immunohistochemistry, Negative Staining
Journal: PloS one
Article Title: Reduced selenium-binding protein 1 in breast cancer correlates with poor survival and resistance to the anti-proliferative effects of selenium.
doi: 10.1371/journal.pone.0063702
Figure Lengend Snippet: Figure 2. SELENBP1 Expression is Progressively Reduced in Advancing Clinical Stages in Breast Cancer Tissues. (A) The scoring distributions of SELENBP1 expression in normal tissues and tumor tissues at stage II and stage III. Inside lines represent means and standard deviations. **p,0.01. (B) Statistical results for the difference between normal and tumor tissues as analyzed by Kruskal-Wallis test. (C) Survival curves of breast cancer patients with respect to different SELENBP1 expression levels are shown at stage II and (D) stage III. Blue and red lines represent the SELENBP1-high and SELENBP1-low groups, respectively. doi:10.1371/journal.pone.0063702.g002
Article Snippet:
Techniques: Expressing
Journal: PloS one
Article Title: Reduced selenium-binding protein 1 in breast cancer correlates with poor survival and resistance to the anti-proliferative effects of selenium.
doi: 10.1371/journal.pone.0063702
Figure Lengend Snippet: Figure 3. The Correlation of SELENBP1 Expression with ER, PR, and TP53 in Breast Cancer Tissues. (A) The scoring distributions of SELENBP1 expression in normal tissues and tumor tissues with ER+ and ER– status. The inside lines represent means and standard deviations. **p,0.01. The difference between normal and ER+ and ER– tumor tissues was analyzed by Kruskal-Wallis test and statistical results are shown (B). Survival curves of breast cancer patients with respect to different SELENBP1 expression are shown in ER+ group in (C). The blue line is the SELENBP1- high group and the red line is the SELENBP1-low group. The scoring distributions of SELENBP1 expression in normal and tumor tissues with PR+/PR–
Article Snippet:
Techniques: Expressing
Journal: Scientific reports
Article Title: IL-17A and its homologs IL-25/IL-17E recruit the c-RAF/S6 kinase pathway and the generation of pro-oncogenic LMW-E in breast cancer cells.
doi: 10.1038/srep11874
Figure Lengend Snippet: Figure 1. Expression of IL-17 cytokines and receptors in clinical samples. The TissueScan Breast Tissue qPCR array was used to determine transcript levels of the IL-17 cytokines (IL-17A and IL-17E) and their receptors (IL-17 RA, IL-17 RB and IL-17 RC). The breast tissue scan contains 48 tissues covering 4 diseases stages and normal tissues. The target transcript levels were normalized to β -Actin and calibrated to the mean mRNA level (arbitrary value of 1) in normal tissue. Data were compared using student’s t test (*P < 0.05, **P < 0.01, ***P < 0.001).
Article Snippet: The target genes expression was also analyzed in normal and tumoral breast tissues using the
Techniques: Expressing