HMGB1 protein
Emerging roles for HMGB1 protein in immunity, inflammation, and cancer
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HMGB1 Protein Binds to Influenza Virus Nucleoprotein and Promotes Viral Replication
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High Mobility Group box-1 (HMGB1) Protein As a Biomarker for Acute Cholecystitis
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HMGB1 is negatively correlated with the development of endometrial carcinoma and prevents cancer cell invasion and metastasis by inhibiting the process of epithelial-to-mesenchymal transition
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Investigations into the interactions of the high mobility group box 1 protein and their toxicological relevance
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High mobility group box-1 and its clinical value in breast cancer
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Mechanistic regulation of HMGB1 function in drug-induced liver injury
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HMGB1 Promotes Prostate Cancer Development and Metastasis by Interacting with Brahma-Related Gene 1 and Activating the Akt Signaling Pathway
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Neutrophil extracellular trap induced by HMGB1 exacerbates damages in the ischemic brain
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<p>Inhibition of HMGB1 Overcomes Resistance to Radiation and Chemotherapy in Nasopharyngeal Carcinoma</p>
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Encapsulation of pancreatic islet with HMGB1 fragment for attenuating inflammation
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Radiotherapy-induced cell death activates paracrine HMGB1-TLR2 signaling and accelerates pancreatic carcinoma metastasis
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Aspirin’s Active Metabolite Salicylic Acid Targets High Mobility Group Box 1 to Modulate Inflammatory Responses
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Extracellular High-Mobility Group Box 1 Protein (HMGB1) as a Mediator of Persistent Pain
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Co-transfection of plasmid DNA and laser-generated gold nanoparticles does not disturb the bioactivity of GFP-HMGB1 fusion protein
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Original Article Expression of HMGB1/RAGE protein in renal carcinoma and its clinical significance
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The Role of HMGB1 in the Pathogenesis of Inflammatory and Autoimmune Diseases
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Original Article High mobility group protein B1 (HMGB1) interacts with receptor for advanced glycation end products (RAGE) to promote airway smooth muscle cell proliferation through ERK and NF- B pathways
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Original Article Blocking HMGB1 signal pathway protects early radiation-induced lung injury
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HMGB1 mediates lipopolysaccharide-induced inflammation via interacting with GPX4 in colon cancer cells
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