BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

293 related articles for article (PubMed ID: 37477229)

  • 1. A two-decade journey in identifying high mobility group box 1 (HMGB1) and procathepsin L (pCTS-L) as potential therapeutic targets for sepsis.
    Li J; Zhu CS; He L; Qiang X; Chen W; Wang H
    Expert Opin Ther Targets; 2023; 27(7):575-591. PubMed ID: 37477229
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Endogenous Regulation and Pharmacological Modulation of Sepsis-Induced HMGB1 Release and Action: An Updated Review.
    Zhu CS; Wang W; Qiang X; Chen W; Lan X; Li J; Wang H
    Cells; 2021 Aug; 10(9):. PubMed ID: 34571869
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Targeting HMGB1 in the treatment of sepsis.
    Wang H; Ward MF; Sama AE
    Expert Opin Ther Targets; 2014 Mar; 18(3):257-68. PubMed ID: 24392842
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Therapeutic potential of HMGB1-targeting agents in sepsis.
    Wang H; Zhu S; Zhou R; Li W; Sama AE
    Expert Rev Mol Med; 2008 Nov; 10():e32. PubMed ID: 18980707
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Development of Procathepsin L (pCTS-L)-Inhibiting Lanosterol-Carrying Liposome Nanoparticles to Treat Lethal Sepsis.
    Chen W; Zhu CS; Qiang X; Chen S; Li J; Wang P; Tracey KJ; Wang H
    Int J Mol Sci; 2023 May; 24(10):. PubMed ID: 37239992
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel HMGB1-inhibiting therapeutic agents for experimental sepsis.
    Wang H; Ward MF; Sama AE
    Shock; 2009 Oct; 32(4):348-57. PubMed ID: 19333143
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Therapeutic potential of procathepsin L-inhibiting and progesterone-entrapping dimethyl-β-cyclodextrin nanoparticles in treating experimental sepsis.
    Qiang X; Chen W; Zhu CS; Li J; Qi T; Lou L; Wang P; Tracey KJ; Wang H
    Front Immunol; 2024; 15():1368448. PubMed ID: 38550581
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of procathepsin L (pCTS-L)-neutralizing monoclonal antibodies to treat potentially lethal sepsis.
    Zhu CS; Qiang X; Chen W; Li J; Lan X; Yang H; Gong J; Becker L; Wang P; Tracey KJ; Wang H
    Sci Adv; 2023 Feb; 9(5):eadf4313. PubMed ID: 36735789
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An ongoing search for potential targets and therapies for lethal sepsis.
    Bao GQ; He L; Lee D; D'Angelo J; Wang HC
    Mil Med Res; 2015; 2():20. PubMed ID: 26257917
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The role of high mobility group box 1 in innate immunity.
    Lee SA; Kwak MS; Kim S; Shin JS
    Yonsei Med J; 2014 Sep; 55(5):1165-76. PubMed ID: 25048472
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Targeting HMGB1 for the treatment of sepsis and sepsis-induced organ injury.
    Deng C; Zhao L; Yang Z; Shang JJ; Wang CY; Shen MZ; Jiang S; Li T; Di WC; Chen Y; Li H; Cheng YD; Yang Y
    Acta Pharmacol Sin; 2022 Mar; 43(3):520-528. PubMed ID: 34040166
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A cardiovascular drug rescues mice from lethal sepsis by selectively attenuating a late-acting proinflammatory mediator, high mobility group box 1.
    Li W; Li J; Ashok M; Wu R; Chen D; Yang L; Yang H; Tracey KJ; Wang P; Sama AE; Wang H
    J Immunol; 2007 Mar; 178(6):3856-64. PubMed ID: 17339485
    [TBL] [Abstract][Full Text] [Related]  

  • 13. HMGB1 as a potential therapeutic target.
    Wang H; Li W; Goldstein R; Tracey KJ; Sama AE
    Novartis Found Symp; 2007; 280():73-85; discussion 85-91, 160-4. PubMed ID: 17380789
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neuropeptides rescue mice from lethal sepsis by down-regulating secretion of the late-acting inflammatory mediator high mobility group box 1.
    Chorny A; Delgado M
    Am J Pathol; 2008 May; 172(5):1297-307. PubMed ID: 18385521
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Targeting high mobility group box 1 as a late-acting mediator of inflammation.
    Czura CJ; Tracey KJ
    Crit Care Med; 2003 Jan; 31(1 Suppl):S46-50. PubMed ID: 12544976
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Regulatory Role of High-Mobility Group Protein 1 in Sepsis-Related Immunity.
    Li L; Lu YQ
    Front Immunol; 2020; 11():601815. PubMed ID: 33552058
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Glycyrrhizin attenuates caspase-11-dependent immune responses and coagulopathy by targeting high mobility group box 1.
    Wang Z; Yang X; Wang X; Liang F; Tang Y
    Int Immunopharmacol; 2022 Jun; 107():108713. PubMed ID: 35339905
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Inflammatory response and immune regulation of high mobility group box-1 protein in treatment of sepsis.
    Liu QY; Yao YM
    World J Emerg Med; 2010; 1(2):93-8. PubMed ID: 25214948
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inhibition of high-mobility group box 1 as therapeutic option in autoimmune disease: lessons from animal models.
    Schaper F; Heeringa P; Bijl M; Westra J
    Curr Opin Rheumatol; 2013 Mar; 25(2):254-9. PubMed ID: 23249831
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High-mobility group box-1 isoforms as potential therapeutic targets in sepsis.
    Parrish W; Ulloa L
    Methods Mol Biol; 2007; 361():145-62. PubMed ID: 17172710
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.