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Image Search Results


Biomarkers serum concentration variations among targeted time points in comparison to the non-traumatic group and admission: (0 h) time point of (A) VEGF, (B) TNF-α, and (C) PCT.

Journal: Journal of Circulating Biomarkers

Article Title: VEGF, TNF-α, and PCT efficiency for traumatic brain injury prognosis evaluation in the first 72 h

doi: 10.33393/jcb.2026.3633

Figure Lengend Snippet: Biomarkers serum concentration variations among targeted time points in comparison to the non-traumatic group and admission: (0 h) time point of (A) VEGF, (B) TNF-α, and (C) PCT.

Article Snippet: PCT (human procalcitonin ELISA Kit, ABclonal), TNF-α (human TNF-α ELISA Kit, ABclonal), VEGF (human VEGF ELISA Kit, ABclonal).

Techniques: Concentration Assay, Comparison

Receiver operating characteristic curve (ROC) for serum biomarkers measured at two time points post-trauma. The ROC curves in each panel demonstrate the diagnostic performance of each biomarker in distinguishing between control (without trauma) and trauma patients. ( A ) PCT at 24 h, ( B ) PCT at 72 h, ( C ) TNF-α at 24 h, ( D ) TNF-α at 72 h, ( E ) VEGF at 24 h, and ( F ) VEGF at 72 h. Areas under the curve (AUC) reflect the accuracy of each biomarker in differentiating between the two groups.

Journal: Journal of Circulating Biomarkers

Article Title: VEGF, TNF-α, and PCT efficiency for traumatic brain injury prognosis evaluation in the first 72 h

doi: 10.33393/jcb.2026.3633

Figure Lengend Snippet: Receiver operating characteristic curve (ROC) for serum biomarkers measured at two time points post-trauma. The ROC curves in each panel demonstrate the diagnostic performance of each biomarker in distinguishing between control (without trauma) and trauma patients. ( A ) PCT at 24 h, ( B ) PCT at 72 h, ( C ) TNF-α at 24 h, ( D ) TNF-α at 72 h, ( E ) VEGF at 24 h, and ( F ) VEGF at 72 h. Areas under the curve (AUC) reflect the accuracy of each biomarker in differentiating between the two groups.

Article Snippet: PCT (human procalcitonin ELISA Kit, ABclonal), TNF-α (human TNF-α ELISA Kit, ABclonal), VEGF (human VEGF ELISA Kit, ABclonal).

Techniques: Diagnostic Assay, Biomarker Discovery, Control

Heat maps showing the correlation of PCT, TNF-α, and VEGF in the control and trauma patient groups over time. Panel A represents the control group, whereas panels B , C , and D illustrate the correlations in trauma patients at baseline (0 h), 24 h, and 72 h, respectively.

Journal: Journal of Circulating Biomarkers

Article Title: VEGF, TNF-α, and PCT efficiency for traumatic brain injury prognosis evaluation in the first 72 h

doi: 10.33393/jcb.2026.3633

Figure Lengend Snippet: Heat maps showing the correlation of PCT, TNF-α, and VEGF in the control and trauma patient groups over time. Panel A represents the control group, whereas panels B , C , and D illustrate the correlations in trauma patients at baseline (0 h), 24 h, and 72 h, respectively.

Article Snippet: PCT (human procalcitonin ELISA Kit, ABclonal), TNF-α (human TNF-α ELISA Kit, ABclonal), VEGF (human VEGF ELISA Kit, ABclonal).

Techniques: Control

Hyperoxia‐induced senescent fASM secrete higher levels of SASP. Cells cultured till day 7 in normoxic (21% O 2 ) or hyperoxic (50% O 2 ) environment were incubated with fresh growth media in normoxia for 24 h, and the supernatants were collected. Samples were then analyzed for SASP secretion by Eve Technologies Corporation (Calgary, Alberta, Canada) using Luminex xMAP and the Human Cytokine/Chemokine 96‐Plex Discovery Assay Array (HD96) panel. (A) Out of the 96 proteins, 80 were detected and visualized using a heatmap. (B) A detailed analysis of each detected marker is shown as fold‐change normalized to control. For statistical analysis, 2‐way ANOVA with a two‐stage linear step‐up procedure of Benjamini, Krieger and Yekutieli test, with individual variances computed for each comparison was applied. False discovery rate < 0.05 was considered significant. Data are presented as box plot of n = 7 cell lines per group.

Journal: Aging Cell

Article Title: Targeting Hyperoxia‐Induced Cellular Senescence in Developing Human Airway Cells: Senomorphics Versus Senolytics Versus Antioxidants

doi: 10.1111/acel.70538

Figure Lengend Snippet: Hyperoxia‐induced senescent fASM secrete higher levels of SASP. Cells cultured till day 7 in normoxic (21% O 2 ) or hyperoxic (50% O 2 ) environment were incubated with fresh growth media in normoxia for 24 h, and the supernatants were collected. Samples were then analyzed for SASP secretion by Eve Technologies Corporation (Calgary, Alberta, Canada) using Luminex xMAP and the Human Cytokine/Chemokine 96‐Plex Discovery Assay Array (HD96) panel. (A) Out of the 96 proteins, 80 were detected and visualized using a heatmap. (B) A detailed analysis of each detected marker is shown as fold‐change normalized to control. For statistical analysis, 2‐way ANOVA with a two‐stage linear step‐up procedure of Benjamini, Krieger and Yekutieli test, with individual variances computed for each comparison was applied. False discovery rate < 0.05 was considered significant. Data are presented as box plot of n = 7 cell lines per group.

Article Snippet: Supernatants collected at day 8 from normoxia and hyperoxia‐exposed fASM were analyzed for SASP secretion by Eve Technologies Corporation (Calgary, Alberta, Canada) using the Human Cytokine/Chemokine 96‐Plex Discovery Assay Array (HD96) panel.

Techniques: Cell Culture, Incubation, Luminex, Marker, Control, Comparison