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European Collection of Authenticated Cell Cultures
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China Center for Type Culture Collection
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iCell Bioscience Inc
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National Centre for Cell Science
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Johns Hopkins HealthCare
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Rochen Pharma Co Ltd
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Marburg GmbH
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Viromer Transfection
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SAS institute
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MediHerb Pty Ltd
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CC Pro GmbH
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Korean Cell Line Bank
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Image Search Results
Journal: Scientific Reports
Article Title: Medium-chain fatty acids modify macrophage expression of metabolic and inflammatory genes in a PPAR β/δ-dependent manner
doi: 10.1038/s41598-023-38700-x
Figure Lengend Snippet: Expression of Ppard by murine macrophages after siRNA, and after exposure to the study treatments. ( A ) There was an average 97% reduction in the expression of Ppard with the use of the siRNA. ( B ) P = 0.043 for the overall difference in Ppard expression with versus without the siRNA. *Significant difference in effect versus the control group.
Article Snippet:
Techniques: Expressing, Control
Journal: Scientific Reports
Article Title: Medium-chain fatty acids modify macrophage expression of metabolic and inflammatory genes in a PPAR β/δ-dependent manner
doi: 10.1038/s41598-023-38700-x
Figure Lengend Snippet: Expression of genes related to cellular uptake, storage, and efflux of lipids, under the study treatments, in the presence (dark bars) or knockdown (light bars) of Ppard, in resting or LPS-stimulated murine macrophages. C8: Octanoate, C10: Decanoate, C16: Palmitate, Agonist: GW501516. Bars represent fold-change relative to the control group without Ppard knockdown, and without LPS stimulation. Error bars represent the standard error of the mean. *Significant difference in treatment effect versus the control group. P -value for the siRNA*treatment interaction term: 0.009 for Scarb1 , 0.001 for Plin2 and 0.008 for Npc1 .
Article Snippet:
Techniques: Expressing, Knockdown, Control
Journal: Scientific Reports
Article Title: Medium-chain fatty acids modify macrophage expression of metabolic and inflammatory genes in a PPAR β/δ-dependent manner
doi: 10.1038/s41598-023-38700-x
Figure Lengend Snippet: Expression of genes related to lipoprotein-mediated cholesterol transport under the study treatments, in the presence (dark bars) or knockdown (light bars) of Ppard, in resting or LPS-stimulated murine macrophages. C8: Octanoate, C10: Decanoate, C16: Palmitate, Agonist: GW501516. Bars represent fold-change relative to the control group without Ppard knockdown, and without LPS stimulation. Error bars represent the standard error of the mean. *Significant difference in treatment effect versus the control group. P-value for the siRNA*treatment interaction term: < 0.001 for Abca1 , 0.10 for Abcg1 and 0.65 for Pltp .
Article Snippet:
Techniques: Expressing, Knockdown, Control
Journal: Scientific Reports
Article Title: Medium-chain fatty acids modify macrophage expression of metabolic and inflammatory genes in a PPAR β/δ-dependent manner
doi: 10.1038/s41598-023-38700-x
Figure Lengend Snippet: Expression of Cpt1 under the study treatments, in the presence (dark bars) or knockdown (light bars) of Ppard, in resting or LPS-stimulated murine macrophages. C8: Octanoate, C10: Decanoate, C16: Palmitate, Agonist: GW501516. Bars represent fold-change relative to the control group without Ppard knockdown, and without LPS stimulation. *Significant difference in treatment effect versus the control group. P -value for the siRNA*treatment interaction term: 0.15.
Article Snippet:
Techniques: Expressing, Knockdown, Control
Journal: Scientific Reports
Article Title: Medium-chain fatty acids modify macrophage expression of metabolic and inflammatory genes in a PPAR β/δ-dependent manner
doi: 10.1038/s41598-023-38700-x
Figure Lengend Snippet: Expression of the genes for proinflammatory cytokines under the study treatments, in the presence (dark bars) or knockdown (light bars) of Ppard, in resting or LPS-stimulated murine macrophages. C8: Octanoate, C10: Decanoate, C16: Palmitate, Agonist: GW501516. Bars represent fold-change relative to the control group without Ppard knockdown, and without LPS stimulation. Error bars represent the standard error of the mean. *Significant difference in treatment effect versus the control group. P-value for the siRNA*treatment interaction term: < 0.001 for Il6 , 0.23 for Tnf and 0.89 for Ifng .
Article Snippet:
Techniques: Expressing, Knockdown, Control
Journal: Scientific Reports
Article Title: Medium-chain fatty acids modify macrophage expression of metabolic and inflammatory genes in a PPAR β/δ-dependent manner
doi: 10.1038/s41598-023-38700-x
Figure Lengend Snippet: Expression of genes involved in macrophage activation under the study treatments, in the presence (dark bars) or knockdown (light bars) of Ppard, in resting or LPS-stimulated murine macrophages. C8: Octanoate, C10: Decanoate, C16: Palmitate, Agonist: GW501516. Bars represent fold-change relative to the control group without Ppard knockdown, and without LPS stimulation. Error bars represent the standard error of the mean. *Significant difference in treatment effect versus the control group. P -value for the siRNA*treatment interaction term: 0.02 for Nos2 , 0.33 for Ptgs2 and 0.30 for Mmp9 .
Article Snippet:
Techniques: Expressing, Activation Assay, Knockdown, Control
Journal: Scientific Reports
Article Title: Medium-chain fatty acids modify macrophage expression of metabolic and inflammatory genes in a PPAR β/δ-dependent manner
doi: 10.1038/s41598-023-38700-x
Figure Lengend Snippet: Uptake of labelled VLDL and LDL by murine macrophages under the study treatments, in resting ( A ) or LPS-stimulated ( B ) murine macrophages. C8: Octanoate, C10: Decanoate, C16: Palmitate, Agonist: GW501516. Bars represent the proportion of total labeled VLDL + LDL that was taken up by the cells. Error bars represent the standard error of the mean.
Article Snippet:
Techniques: Labeling
Journal: Metabolism Open
Article Title: A systematic review on the effects of Echinacea supplementation on cytokine levels: Is there a role in COVID-19?
doi: 10.1016/j.metop.2021.100115
Figure Lengend Snippet: Characteristics of the in vitro and ex vivo studies included.
Article Snippet: Matthias, 2007 [ ] ,
Techniques: In Vitro, Ex Vivo, Infection, Control, Negative Control, Positive Control, Expressing, Solvent, Isolation, Concentration Assay, High Performance Liquid Chromatography, Gene Expression, Size-exclusion Chromatography, Synthesized, Extraction, Saline, Virus, Mouse Assay, Clinical Proteomics, Cell Culture, Derivative Assay, Purification, Chromatography, Colony-forming Unit Assay, Cytokine Assay, Irradiation