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OriginLab corp
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COMSOL Inc
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Verlag GmbH
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OriginLab corp
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RStudio
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CH Instruments
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Rsoft Inc
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ONTOP PHARMACEUTICALS LIMITED
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Accelrys
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Verlag GmbH
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OriginLab corp
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Image Search Results
Journal: PLoS ONE
Article Title: Transcriptomic Profiling of Gametogenesis in Triploid Pacific Oysters Crassostrea gigas : Towards an Understanding of Partial Sterility Associated with Triploidy
doi: 10.1371/journal.pone.0112094
Figure Lengend Snippet: 2D score plots (A, B and C) obtained by the principal components analysis using GeneANOVA with default/standard parameters and XLStat (Addinsoft) of all 31,918 transcripts in the 32 diploid oyster gonads and the 35 triploid oyster gonads (A: Mitosis (PC1) vs Gonad stages (PC2); B: Gonad stages (PC2) vs Ploidy (PC3); C: Gonad stages (PC2) vs Sex (PC4); PC: principal component).
Article Snippet: The four components with the highest proportion of variance were used to draw
Techniques:
Journal: EMBO Reports
Article Title: PLETHORA‐WOX5 interaction and subnuclear localization control Arabidopsis root stem cell maintenance
doi: 10.15252/embr.202154105
Figure Lengend Snippet: A–G The combined results of the SCN staining in Fig are shown as 2D plots to visualize the correlation of the CSC layer and QC division phenotypes. Number of CSC layers are shown on the y axis and the QC division phenotype is shown on the x‐axis. The darker the color, the more roots show the respective phenotype (see color gradient top right indicating the frequencies in percent). Col wild‐type roots show one layer of CSCs and no EdU stained cells (no QC division) after 24 h EdU staining. Number of analyzed roots ( n ) (biological replicates) is indicated for each genotype and results from 2 to 5 technical replicates per genotype. Source data are available online for this figure.
Article Snippet:
Techniques: Staining
Journal: EMBO Reports
Article Title: PLETHORA‐WOX5 interaction and subnuclear localization control Arabidopsis root stem cell maintenance
doi: 10.15252/embr.202154105
Figure Lengend Snippet: SCN stainings were performed in Arabidopsis thaliana seedlings in the indicated single and double mutant backgrounds expressing either WOX5‐mV, PLT3‐mV or PLT3ΔPrD‐mV driven by their endogenous promoters as well as in Col wild type. A–I The combined results of the SCN staining are shown as 2D plots. Number of CSC layers is shown on the y axis and the QC division phenotype is shown on the x‐axis. The darker the color, the more roots show the respective phenotype (see color gradient on the right indicating the frequencies). J, K Analyses of the SCN staining for CSC layer (J) or QC division (K) phenotypes. The frequencies of roots showing 0–3 CSC layers, or 0–4 dividing QC cells are plotted as bar graphs. Number of analyzed roots ( n ) (biological replicates) is indicated for each genotype and results from 2 to 4 technical replicates. EdU = 5‐ethynyl‐2′‐deoxyuridine; CSC = columella stem cell; QC = quiescent center; W5 = WOX5, P3 = PLT3. Source data are available online for this figure.
Article Snippet:
Techniques: Mutagenesis, Expressing, Staining