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Gene Information
Gene symbol: GADD45B
Gene name: growth arrest and DNA-damage-inducible, beta
HGNC ID: 4096
Synonyms: GADD45BETA, DKFZP566B133
Related Genes
Related Sentences
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PMID |
Sentence |
1 |
22986450
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Specific targets in this category included genes asso-ciated with the intrinsic and extrinsic apoptotic pathways (CFLAR, TNFAIP3, TNFRSF10D, SOD2, BCL2A1, BIRC4, PIM2, TNFSF10, TNFRSF10C, CASP2 and CASP8) and genes that act via the NFĸB pathway and other mechanisms to prolong cell viability (NFKB1, NFKB2 and RELA, IL1B, CAST, CDK2,GADD45B, BCL3, BIRC3, CDK2, IL1A, PBEF1, IL6, CXCL1, CCL4 and VEGF).
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2 |
22986450
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Moreover, we demonstrate that the X-linked inhibitor of apoptosis protein remained abundant in polymorphonuclear leukocytes over 48 h of LVS infection, whereas BAX mRNA and protein were progressively downregulated.
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3 |
25479797
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Modulation of the NAS process represents a path toward the development of novel vaccines or drugs, through targets such as myeloid differentiation primary-response protein 88 (MyD88) and tumor necrosis factor (TNF) receptor-associated factor (TRAF) 3 and 6 in Toll-like receptor (TLR)-mediated signaling pathways.
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4 |
25540284
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Secretion of IL-6, RANTES (CCL5) and IP-10 (CXCL10) were assessed by ELISA.
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5 |
25540284
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MPLA alone was a weak stimulator of myeloid differentiation primary response protein 88-dependent IL-6 and did not induce TIR-domain-containing adapter-inducing IFN-β (TRIF)-dependent chemokine responses.
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6 |
25540284
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MPLA significantly reduced LPS-mediated IL-6 production.
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7 |
25540284
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This inhibitory effect was also conferred for the TRIF-dependent chemokines RANTES and IP-10.
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8 |
26090808
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Moreover, in vivo administration of GB promoted up-regulation of CD86, MHC class I and MHC class II and production of IL-6, IL-12 and TNF-α in spleen DCs.
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9 |
26090808
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Furthermore, Toll like receptor 4 (TLR4) and myeloid differentiation primary response 88 (MyD88) signaling pathway were essential for DC activation induced by GB.
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10 |
26090808
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In addition, GB strongly prompted the proliferation of ovalbumin (OVA)-specific CD4 and CD8 T cells.
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