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A dietary flavone confers communicable protection against colitis through NLRP6 signaling independently of inflammasome activation.

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The regulatory dendritic cell marker C1q is a potent inhibitor of allergic inflammation.

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Comparative pathology of recombinant murine interferon-gamma in mice and recombinant human interferon-gamma in cynomolgus monkeys.

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Pathophysiologic alterations induced by tumor necrosis factor.

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Pathology induced by leukemia inhibitory factor.

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Correction: Interleukin-22-deficiency and microbiota contribute to the exacerbation of Toxoplasma gondii-induced intestinal inflammation.

Interleukin-22-deficiency and microbiota contribute to the exacerbation of Toxoplasma gondii-induced intestinal inflammation.

A dietary flavone confers communicable protection against colitis through NLRP6 signaling independently of inflammasome activation.

Unravelling the roles of innate lymphoid cells in cerebral malaria pathogenesis.

Neutrophilic NLRP3 inflammasome-dependent IL-1β secretion regulates the γδT17 cell response in respiratory bacterial infections.

The regulatory dendritic cell marker C1q is a potent inhibitor of allergic inflammation.

Ultrasonic imaging of microscopic structures in living organs.

In situ studies of renal arteriolar function using the in vitro-perfused hydronephrotic rat kidney.

Morphometric analysis of vascular smooth muscle cells by scanning electron microscopy.

Comparative pathology of recombinant murine interferon-gamma in mice and recombinant human interferon-gamma in cynomolgus monkeys.

Pathophysiologic alterations induced by tumor necrosis factor.

Pathology induced by leukemia inhibitory factor.

Dabrafenib-Induced Cutaneous Eruptions in a Patient With Langerhans Cell Histiocytosis.

Type 1 diabetes mellitus induced by sintilimab: a case report and related case literature analysis.

Lipocalin-2 Emerges as a Core Pathogenic Mediator and Biomarker in Autosomal Dominant Tubulointerstitial Kidney Disease-UMOD via Transcriptomic Profiling.

Diffuse Large B-cell Lymphoma Initially Managed As Secondary Immune Thrombocytopenia: A Case Report.

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