data preprocessing software (idps Search Results


86
Inscopix Inc data processing software idps
Data Processing Software Idps, supplied by Inscopix Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/data processing software idps/product/Inscopix Inc
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data processing software idps - by Bioz Stars, 2026-06
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92
Proteintech idh1 protein
Idh1 Protein, supplied by Proteintech, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 92 stars, based on 1 article reviews
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90
Abbexa Ltd mouse isocitrate dehydrogenase [nadp] cytoplasmic (idh1) elisa kit
( A ) Characteristics of energy metabolism for ALF patients. ( B ) The expression levels of L-Lactate, L-Malate, <t>Isocitrate,</t> 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.
Mouse Isocitrate Dehydrogenase [Nadp] Cytoplasmic (Idh1) Elisa Kit, supplied by Abbexa Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mouse isocitrate dehydrogenase [nadp] cytoplasmic (idh1) elisa kit/product/Abbexa Ltd
Average 90 stars, based on 1 article reviews
mouse isocitrate dehydrogenase [nadp] cytoplasmic (idh1) elisa kit - by Bioz Stars, 2026-06
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90
Tsang MD Inc idps
( A ) Characteristics of energy metabolism for ALF patients. ( B ) The expression levels of L-Lactate, L-Malate, <t>Isocitrate,</t> 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.
Idps, supplied by Tsang MD Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
idps - by Bioz Stars, 2026-06
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90
Siemens AG qsmderived idps
( A ) Characteristics of energy metabolism for ALF patients. ( B ) The expression levels of L-Lactate, L-Malate, <t>Isocitrate,</t> 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.
Qsmderived Idps, supplied by Siemens AG, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/qsmderived idps/product/Siemens AG
Average 90 stars, based on 1 article reviews
qsmderived idps - by Bioz Stars, 2026-06
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90
Rauscher GmbH idps
( A ) Characteristics of energy metabolism for ALF patients. ( B ) The expression levels of L-Lactate, L-Malate, <t>Isocitrate,</t> 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.
Idps, supplied by Rauscher GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/idps/product/Rauscher GmbH
Average 90 stars, based on 1 article reviews
idps - by Bioz Stars, 2026-06
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90
SAS institute small-angle scattering (sas) data
( A ) Characteristics of energy metabolism for ALF patients. ( B ) The expression levels of L-Lactate, L-Malate, <t>Isocitrate,</t> 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.
Small Angle Scattering (Sas) Data, supplied by SAS institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/small-angle scattering (sas) data/product/SAS institute
Average 90 stars, based on 1 article reviews
small-angle scattering (sas) data - by Bioz Stars, 2026-06
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90
Johns Hopkins HealthCare md idps
( A ) Characteristics of energy metabolism for ALF patients. ( B ) The expression levels of L-Lactate, L-Malate, <t>Isocitrate,</t> 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.
Md Idps, supplied by Johns Hopkins HealthCare, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/md idps/product/Johns Hopkins HealthCare
Average 90 stars, based on 1 article reviews
md idps - by Bioz Stars, 2026-06
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90
VMware Inc nsx-idps
( A ) Characteristics of energy metabolism for ALF patients. ( B ) The expression levels of L-Lactate, L-Malate, <t>Isocitrate,</t> 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.
Nsx Idps, supplied by VMware Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/nsx-idps/product/VMware Inc
Average 90 stars, based on 1 article reviews
nsx-idps - by Bioz Stars, 2026-06
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90
Siemens AG qsm-derived idps
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 <t>IDPs</t> 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.
Qsm Derived Idps, supplied by Siemens AG, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/qsm-derived idps/product/Siemens AG
Average 90 stars, based on 1 article reviews
qsm-derived idps - by Bioz Stars, 2026-06
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86
Cell Signaling Technology Inc disordered proteins idps
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 <t>IDPs</t> 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.
Disordered Proteins Idps, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/disordered proteins idps/product/Cell Signaling Technology Inc
Average 86 stars, based on 1 article reviews
disordered proteins idps - by Bioz Stars, 2026-06
86/100 stars
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90
CEITEC laboratories intrinsically disordered proteins
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 <t>IDPs</t> 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.
Intrinsically Disordered Proteins, supplied by CEITEC laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/intrinsically disordered proteins/product/CEITEC laboratories
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( 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.

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: Mouse isocitrate dehydrogenase [NADP] cytoplasmic (IDH1) ELISA kit was purchased from Abbexa (Cambridge, UK, Cat. No. abx515558).

Techniques: Expressing

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.

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: Mouse isocitrate dehydrogenase [NADP] cytoplasmic (IDH1) ELISA kit was purchased from Abbexa (Cambridge, UK, Cat. No. abx515558).

Techniques: Staining, TUNEL Assay, Sequencing, Expressing

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.

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: Mouse isocitrate dehydrogenase [NADP] cytoplasmic (IDH1) ELISA kit was purchased from Abbexa (Cambridge, UK, Cat. No. abx515558).

Techniques: Immunofluorescence, Flow Cytometry, Enzyme-linked Immunosorbent Assay

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.

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: QSM-derived IDPs had generally better between-site reliability (all sites: ICC = 0.67, SD = 0.13; Siemens only sites: ICC = 0.76, SD = 0.14), comparable to good ctest-retest reliability in the UKB data (ICC = 0.66).

Techniques: Transformation Assay, Sampling

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.

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: QSM-derived IDPs had generally better between-site reliability (all sites: ICC = 0.67, SD = 0.13; Siemens only sites: ICC = 0.76, SD = 0.14), comparable to good ctest-retest reliability in the UKB data (ICC = 0.66).

Techniques:

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.

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: QSM-derived IDPs had generally better between-site reliability (all sites: ICC = 0.67, SD = 0.13; Siemens only sites: ICC = 0.76, SD = 0.14), comparable to good ctest-retest reliability in the UKB data (ICC = 0.66).

Techniques: Derivative Assay, Transformation Assay

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.

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: QSM-derived IDPs had generally better between-site reliability (all sites: ICC = 0.67, SD = 0.13; Siemens only sites: ICC = 0.76, SD = 0.14), comparable to good ctest-retest reliability in the UKB data (ICC = 0.66).

Techniques: Transformation Assay, Sampling

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.

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: QSM-derived IDPs had generally better between-site reliability (all sites: ICC = 0.67, SD = 0.13; Siemens only sites: ICC = 0.76, SD = 0.14), comparable to good ctest-retest reliability in the UKB data (ICC = 0.66).

Techniques: Derivative Assay, Functional Assay, Transformation Assay