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論文 - 一覧

  • 12 Hits
  • 検索条件 : 絞込み (MeSH = Receptors, Tumor Necrosis Factor / genetics)
生物種 リソース名 タイトル
ヒト・動物細胞 ST2(RCB0224) Protein expression and functional difference of membrane-bound and soluble receptor activator of NF-kappaB ligand: modulation of the expression by osteotropic factors and cytokines.
ヒト・動物細胞 MC3T3-E1(RCB1126) , ST2(RCB0224) Transforming growth factor-beta1 increases mRNA levels of osteoclastogenesis inhibitory factor in osteoblastic/stromal cells and inhibits the survival of murine osteoclast-like cells.
ヒト・動物細胞 HL60(RCB0041) , MC3T3-E1(RCB1126) , MC3T3-G2/PA6(RCB1127) , ST2(RCB0224) Reciprocal gene expression of osteoclastogenesis inhibitory factor and osteoclast differentiation factor regulates osteoclast formation.
ヒト・動物細胞 MC3T3-E1(RCB1126) , ATDC5(RCB0565) Novel function of TWEAK in inducing intervertebral disc degeneration.
ヒト・動物細胞 MC3T3-E1(RCB1126) , RAW 264(RCB0535) , ATDC5(RCB0565) , EL4(RCB1641) TWEAK/Fn14 interaction regulates RANTES production, BMP-2-induced differentiation, and RANKL expression in mouse osteoblastic MC3T3-E1 cells.
ヒト・動物細胞 ST2(RCB0224) Soluble glucocorticoid-induced tumor necrosis factor receptor stimulates osteoclastogenesis by down-regulation of osteoprotegerin in bone marrow stromal cells.
ヒト・動物細胞 Nicotine and lipopolysaccharide stimulate the formation of osteoclast-like cells by increasing macrophage colony-stimulating factor and prostaglandin E2 production by osteoblasts.
ヒト・動物細胞 ST2(RCB0224) Cytokines synergistically induce osteoclast differentiation: support by immortalized or normal calvarial cells.
ヒト・動物細胞 OP9(RCB1124) Signal via lymphotoxin-beta R on bone marrow stromal cells is required for an early checkpoint of NK cell development.
ヒト・動物細胞 ST2(RCB0224) Characterization of structural domains of human osteoclastogenesis inhibitory factor.
ヒト・動物細胞 MC3T3-E1(RCB1126) , ST2(RCB0224) Identity of osteoclastogenesis inhibitory factor (OCIF) and osteoprotegerin (OPG): a mechanism by which OPG/OCIF inhibits osteoclastogenesis in vitro.
ヒト・動物細胞 MC3T3-E1(RCB1126) Prostate cancer mediates osteoclastogenesis through two different pathways.