about
HMGB1 promotes recruitment of inflammatory cells to damaged tissues by forming a complex with CXCL12 and signaling via CXCR4High mobility group B2 is secreted by myeloid cells and has mitogenic and chemoattractant activities similar to high mobility group B1Extracellular HMGB1, a signal of tissue damage, induces mesoangioblast migration and proliferationAspirin's Active Metabolite Salicylic Acid Targets High Mobility Group Box 1 to Modulate Inflammatory ResponsesCells migrating to sites of tissue damage in response to the danger signal HMGB1 require NF-kappaB activationInduction of inflammatory and immune responses by HMGB1-nucleosome complexes: implications for the pathogenesis of SLEMutually exclusive redox forms of HMGB1 promote cell recruitment or proinflammatory cytokine release.Src family kinases are necessary for cell migration induced by extracellular HMGB1.Glycyrrhizin binds to high-mobility group box 1 protein and inhibits its cytokine activities.High mobility group box 1 orchestrates tissue regeneration via CXCR4.Non-oxidizable HMGB1 induces cardiac fibroblasts migration via CXCR4 in a CXCL12-independent manner and worsens tissue remodeling after myocardial infarction.The chemotactic and mitogenic effects of platelet-derived growth factor-BB on rat aorta smooth muscle cells are inhibited by basic fibroblast growth factorPlatelet-derived growth factor inhibits basic fibroblast growth factor angiogenic properties in vitro and in vivo through its alpha receptor
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Francesco De Marchis
@ast
Francesco De Marchis
@en
Francesco De Marchis
@es
Francesco De Marchis
@nl
type
label
Francesco De Marchis
@ast
Francesco De Marchis
@en
Francesco De Marchis
@es
Francesco De Marchis
@nl
prefLabel
Francesco De Marchis
@ast
Francesco De Marchis
@en
Francesco De Marchis
@es
Francesco De Marchis
@nl
P106
P21
P31
P496
0000-0003-1275-5470