International journal of molecular sciences

international immunopharmacology

gesundheitswesen (bundesverband der arzte des offentlichen gesundheitsdienstes (germany))

brain, behavior, and immunity

[1] Saikosaponin-d attenuated lipopolysaccharide-induced depressive-like behaviors via inhibiting microglia activation and neuroinflammation.

[2] Glycyrrhizin Inhibits PEDV Infection and Proinflammatory Cytokine Secretion via the HMGB1/TLR4-MAPK p38 Pathway.

[3] sterile inflammation

[4] new prognostic biomarkers and therapeutic effect of bevacizumab for patients with non-small-cell lung cancer

[5] single nucleotide polymorphisms in hmgb1 correlate with lung cancer risk in the northeast chinese han population

[6] fbxw7 suppresses hmgb1-mediated innate immune signaling to attenuate hepatic inflammation and insulin resistance in a mouse model of nonalcoholic fatty liver disease

[7] CXCR7: A key neuroprotective molecule against alarmin HMGB1 mediated CNS pathophysiology and subsequent memory impairment.

[8] HMGB1: an overview of its versatile roles in the pathogenesis of colorectal cancer.

[9] Corrigendum to “HMGB1 contributes to adriamycin-induced cardiotoxicity via up-regulating autophagy” (Toxicology Letters (2018) 292 (115–122), (S0378427418301735), (10.1016/j.toxlet.2018.04.034))

[10] Glycyrrhizin Inhibits PEDV Infection and Proinflammatory Cytokine Secretion via the HMGB1/TLR4-MAPK p38 Pathway.

[11] HMGB1: A Possible Crucial Therapeutic Target for COVID-19?

[12] single nucleotide polymorphisms in hmgb1 correlate with lung cancer risk in the northeast chinese han population

[13] impact of hmgb1/tlr ligand complexes on hiv-1 replication: possible role for flagellin during hiv-1 infection

[14] hmgb1 protects the heart against ischemia–reperfusion injury via pi3k/akt pathway-mediated upregulation of vegf expression

[15] fbxw7 suppresses hmgb1-mediated innate immune signaling to attenuate hepatic inflammation and insulin resistance in a mouse model of nonalcoholic fatty liver disease

[16] elevated levels of von willebrand factor and high mobility group box 1 (hmgb1) are associated with disease severity and clinical outcome of scrub typhus

[17] hmgb1/anti-hmgb1 antibodies define a molecular signature of early stages of hiv-associated neurocognitive disorders (hand)

[18] protective effects of berberine on isoproterenol-induced acute myocardial ischemia in rats through regulating hmgb1-tlr4 axis

[19] hmgb1 in severe soft tissue infections caused by streptococcus pyogenes

[20] novel mechanisms of herbal therapies for inhibiting hmgb1 secretion or action

[21] salidroside inhibits hmgb1 acetylation and release through upregulation of sirt1 during inflammation

[22] Decreased Expression of the High Mobility Group Box 1 (<i>HMGB1</i>) Gene in Peripheral Blood in Patients with Mild or Moderate <i>Clostridioides difficile</i> Infection