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Inscopix Inc
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Proteintech
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Abbexa Ltd
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Tsang MD Inc
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Siemens AG
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Rauscher GmbH
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SAS institute
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Johns Hopkins HealthCare
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VMware Inc
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Siemens AG
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Cell Signaling Technology Inc
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CEITEC laboratories
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Image Search Results
Journal: Journal of Inflammation Research
Article Title: Histone Deacetylase 6 Regulates the Activation of M1 Macrophages by the Glycolytic Pathway During Acute Liver Failure
doi: 10.2147/JIR.S302391
Figure Lengend Snippet: ( A ) Characteristics of energy metabolism for ALF patients. ( B ) The expression levels of L-Lactate, L-Malate, Isocitrate, Succinate, 3-phosphoglycerate, ADP, α-Ketoglutarate, ATP, Citrate, Oxaloacetate, NAD, NADPH, Phosphoenolpyruvate, and UDPglucose were significantly different between ALF patients and normal volunteers. ( C ) Based on the Pearson correlation analysis method, the correlation coefficient between different metabolites was calculated. The correlation between the different metabolites was displayed in the form of a correlation coefficient matrix heat map, and the expression of each metabolite was replaced by the ratio of the relative expression of the ALF group to the relative expression of the normal group. This matrix chart shows the correlation between significantly different metabolites. The Pearson correlation coefficient value R was between −1 and +1. The correlation coefficient R between metabolites was represented by color and circle, where R > 0 represents a positive correlation, and it was represented by red. R < 0 indicates a negative correlation, which was represented by blue. The larger and darker the circles, the more relevant they were. It was found that the expression for α-Ketoglutarate, Citrate, and Oxaloacetate was positively correlated with ATP. The expression for L-Malate, Isocitrate, and Succinate was negatively correlated with ATP. ( D ) Hypothesis diagram of M1 macrophage energy metabolism during ALF process.
Article Snippet:
Techniques: Expressing
Journal: Journal of Inflammation Research
Article Title: Histone Deacetylase 6 Regulates the Activation of M1 Macrophages by the Glycolytic Pathway During Acute Liver Failure
doi: 10.2147/JIR.S302391
Figure Lengend Snippet: The effect of ACY-1215 on LPS/D-Gal induced ALF mice. ( A ) HE staining was used to detect histopathological changes in liver. TUNEL staining was used to detect the cell apoptosis level. The serum levels of ALT, AST, and TBIL were detected. ( B ) Venn diagram showing the protein quantitative sequencing. ( A ) ACY-1215 intervention group. M: Model group. N: Control group. M/N (up/down) represented the protein whose expression level was increased (decreased) in the model group compared with the normal group. A/M (up/down) represented the protein whose expression level was increased (decreased) in the ACY-1215 intervention group compared with the model group. The table showed different expression levels of MDH1, IDH1 and DNMT1 in different mice groups. ( C ) The substrate and product of MDH1 were L-Malate and Oxaloacetate. The substrate and product of IDH1 were Isocitrate and α-Ketoglutarate. ( D ) The levels of ATP, Oxaloacetate, MDH1, α-Ketoglutarate, Citrate, MDH1, L-Malate, Isocitrate and Succinate in liver were tested. Data are shown as mean ± SD. # P < 0.05, compared with the control group. * P < 0.05, compared with the LPS/D-Gal group.
Article Snippet:
Techniques: Staining, TUNEL Assay, Sequencing, Expressing
Journal: Journal of Inflammation Research
Article Title: Histone Deacetylase 6 Regulates the Activation of M1 Macrophages by the Glycolytic Pathway During Acute Liver Failure
doi: 10.2147/JIR.S302391
Figure Lengend Snippet: The effect of ACY-1215 on energy metabolite in LPS induced RAW264.7 cells. ( A ) The levels of ATP, Oxaloacetate, MDH1, α-Ketoglutarate, Citrate, MDH1, L-Malate, Isocitrate, and Succinate in RAW264.7 cells was tested. ( B – D ) The levels of DDX3X, NLRP3, and DNMT1 were detected by immunofluorescence. ( E ) A histogram was used to show the protein level of DDX3X, NLRP3 and DNMT1. ( F ) Cell apoptosis was detected by flow cytometry. ( G ) The levels of HIF1α, TNF-α, IL-6, and IL-1β in cell were tested by ELISA kits. Data are shown as mean ± SD. # P < 0.05, compared with the control group. * P < 0.05, compared with the LPS group.
Article Snippet:
Techniques: Immunofluorescence, Flow Cytometry, Enzyme-linked Immunosorbent Assay
Journal: PLoS ONE
Article Title: Reliability of multi-site UK Biobank MRI brain phenotypes for the assessment of neuropsychiatric complications of SARS-CoV-2 infection: The COVID-CNS travelling heads study
doi: 10.1371/journal.pone.0273704
Figure Lengend Snippet: In the top two panels, each column represents results for a different class of IDP, from left to right: regional and tissue volumes, cortical area, cortical thickness, regional and tissue intensity, and cortical grey-white contrast. A) Distribution of log-transformed P -values from repeated measures ANOVA testing for a site effect on the mean value of individual IDPs in each class; the solid horizontal line represents the P -value equivalent to FDR = 5%. Green dots represent IDPs fitted to the ANOVA model including data from all four sites; orange dots represent P -values for each IDP fitted to the ANOVA including only data from the three Siemens sites (Cambridge, Oxford, Liverpool). There are more significant between-site differences in mean IDPs, across all 5 classes, when the GE data from KCL are included in the analysis B) Swarm plots showing distribution of intra-class correlation coefficients (ICCs) for the same IDPs, estimated for each pair of all 4 sites (green points), for each pair of the three Siemens sites (orange points), and for comparable test-retest data drawn from the UKB cohort (blue points). Between-site reliability was generally high for all IDP classes compared to the UKB benchmark, whether or not GE data were included in the analysis. C) Each column represents finer-grained results for representative IDPs from each class of IDP: from left to right, left olfactory bulb volume, left precuneus area, left inferior temporal cortical thickness, left caudate intensity and left fusiform CNR. Top row , plots of each IDP for 8 subjects (coloured lines) scanned at each of 4 sites (x-axis labels); the grey violin plots indicate the distributions of the corresponding IDP in the UK Biobank reference datase, using matched random sampling of N = 8 participants. Box and whiskers represent inter-quartile range and 95% confidence intervals respectively. Bottom row , correlations between each pair of sites for each IDP: upper triangle, Pearson’s correlations; lower triangle, Spearman’s correlations.
Article Snippet:
Techniques: Transformation Assay, Sampling
Journal: PLoS ONE
Article Title: Reliability of multi-site UK Biobank MRI brain phenotypes for the assessment of neuropsychiatric complications of SARS-CoV-2 infection: The COVID-CNS travelling heads study
doi: 10.1371/journal.pone.0273704
Figure Lengend Snippet: A) Representative T2 FLAIR images of the same subject scanned at each of 4 sites in the travelling heads study. B) left panel , peri-ventricular white matter hyperintensity volume for 8 subjects (coloured lines) scanned at each of 4 sites (x-axis labels); right panel , correlations between each pair of sites. C) left panel , deep white matter hyperintensity volume for 8 subjects (coloured lines) scanned at each of 4 sites (x-axis labels); right panel , correlations between each pair of sites. In both B) and C) , the upper triangle of the matrix shows Pearson’s correlations and the lower triangle shows Spearman’s correlations; and both IDPs were estimated using BIANCA.
Article Snippet:
Techniques:
Journal: PLoS ONE
Article Title: Reliability of multi-site UK Biobank MRI brain phenotypes for the assessment of neuropsychiatric complications of SARS-CoV-2 infection: The COVID-CNS travelling heads study
doi: 10.1371/journal.pone.0273704
Figure Lengend Snippet: In the top two panels, the left column shows data for 14 IDPs derived from T2* data and the right column shows data for 14 IDPs derived from QSM data. A) Distribution of log-transformed P -values from repeated measures ANOVA testing for a site effect on the mean value of individual IDPs in each class; the solid horizontal line represents the P-value equivalent to FDR = 5%. Green dots represent IDPs fitted to the ANOVA model including data from all four sites; orange dots represent P -values for each IDP fitted to the ANOVA including only data from the three Siemens sites (Cambridge, Oxford, Liverpool). There were more significant between-site differences in mean IDPs when the GE data from KCL were included in the analysis B) Swarm plots showing distribution of intra-class correlation coefficients (ICCs) for the same IDPs, estimated for each pair of all 4 sites (green points), and for each pair of the three Siemens sites (orange points). C) Each column represents finer-grained results for representative IDPs from each class of IDP: from left to right, T2* right pallidum, QSM right pallidum. Top row , plots of each IDP for 8 subjects (coloured lines) scanned at each of 4 sites (x-axis labels). Bottom row , correlations between each pair of sites for each IDP: upper triangle, Pearson’s correlations; lower triangle, Spearman’s correlations.
Article Snippet:
Techniques: Derivative Assay, Transformation Assay
Journal: PLoS ONE
Article Title: Reliability of multi-site UK Biobank MRI brain phenotypes for the assessment of neuropsychiatric complications of SARS-CoV-2 infection: The COVID-CNS travelling heads study
doi: 10.1371/journal.pone.0273704
Figure Lengend Snippet: In the top two panels, each column represents results for a different class of IDP, from left to right: white matter (WM) tract FA, WM tract MO, WM tract diffusivity, WM tract ICVF, WM tract OD and WM tract ISOVF. A) Distribution of log-transformed P -values from repeated measures ANOVA testing for a site effect on the mean value of individual IDPs in each class; the solid horizontal line represents the P -value equivalent to FDR = 5%. Green dots represent IDPs fitted to the ANOVA model including data from all four sites; orange dots represent P -values for each IDP fitted to the ANOVA including only data from the three Siemens sites (Cambridge, Oxford, Liverpool). There were more significant between-site differences in mean IDPs, across all 5 classes, when the GE data from KCL were included in the analysis. B) Swarm plots showing distribution of intra-class correlation coefficients (ICCs) for the same IDPs, estimated for each pair of all 4 sites (green points), for each pair of the three Siemens sites (orange points) and for comparable test-retest data drawn from the UKB cohort (blue points). Between-site reliability was generally high for all IDP classes compared to the UKB benchmark when only Siemens sites were included in the analysis. C) Each column represents finer-grained results for representative IDPs from each class of IDP: from left to right, FA right anterior thalamic radiation. MO left corona radiata, L3 left cingulate gyrus, ICVF left cingulate gyrus, OD superior cerebellar peduncle, and ISOVF superior longitudinal fasciculus. Top row , plots of each IDP for 8 subjects (coloured lines) scanned at each of 4 sites (x-axis labels); the grey violin plots indicate the distributions of the corresponding IDP in the UK Biobank reference dataset, using matched random sampling of N = 8 participants. Box and whiskers represent inter-quartile range and 95% confidence intervals respectively. Bottom row , correlations between each pair of sites for each IDP: upper triangle, Pearson’s correlations; lower triangle, Spearman’s correlations.
Article Snippet:
Techniques: Transformation Assay, Sampling
Journal: PLoS ONE
Article Title: Reliability of multi-site UK Biobank MRI brain phenotypes for the assessment of neuropsychiatric complications of SARS-CoV-2 infection: The COVID-CNS travelling heads study
doi: 10.1371/journal.pone.0273704
Figure Lengend Snippet: The two columns show data on fMRI node amplitude and fMRI connectivity IDPs. Both represent IDPs derived from 25- and 100-node ICA-based parcellations. The fMRI connectivity IDPs represent 6 modes of variation across the functional connectivity network matrices derived from both parcellations. A ) Distribution of log-transformed P -values from repeated measures ANOVA testing for a site effect on the mean value of individual IDPs in each class; the solid horizontal line represents the P -value equivalent to FDR = 5%. Green dots represent IDPs fitted to the ANOVA model including data from all four sites; orange dots represent P -values for each IDP fitted to the ANOVA including only data from the three Siemens sites (Cambridge, Oxford, Liverpool). B) Swarm plots showing distribution of intra-class correlation coefficients (ICCs) for the same IDPs, estimated for each pair of all 4 sites (green points), for each pair of the three Siemens sites (orange points) and for comparable test-retest data drawn from the UKB cohort (blue points). Between-site reliability was generally high for all IDP classes compared to the UKB benchmark, whether or not GE data were included in the analysis. C) Each column represents finer-grained results for representative IDPs from each class of IDP: from left to right, fMRI node 4/25 (medial visual RSN) and summary connectivity mode #3 . Top row , plots of each IDP for 8 subjects (coloured lines) scanned at each of 4 sites (x-axis labels); the grey violin plot indicates the distribution of the corresponding IDP in the UK Biobank reference dataset. Bottom row , correlations between each pair of sites for each IDP: upper triangle, Pearson’s correlations; lower triangle, Spearman’s correlations.
Article Snippet:
Techniques: Derivative Assay, Functional Assay, Transformation Assay