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Interferon-gamma induced protein IFI16 is a unique host factor protein involved in the EBV lifecycle. Reduction of IFI16 protein levels following lytic cycle induction, as well as reactivation from latency after IFI16 mRNA knockdown suggests that IFI16 is crucial for the maintenance of EBV latency.
This study found IFI16 and AIM2 (show AIM2 Proteins) SNPs associated with higher levels of periodontal microorganisms and an increased percentage of periodontal disease clinical parameters.
Importantly, knocking down p204, which is reported as the mouse orthologous of human IFI16, inhibited epidermal hyperplasia in mice with imiquimod-induced psoriasiform dermatitis. These findings indicate that IFI16 plays a critical role in the pathogenesis of psoriasis and may be a potential therapeutic target
IFI16 is a tumour suppressor in HCC (show FAM126A Proteins) via activation of p53 (show TP53 Proteins) signals and inflammasome
in a cohort of patients with genital herpes and healthy controls, the minor G allele of the IFI16 single nucleotide polymorphism rs2276404 was associated with resistance to infection
study identifies the AIM2 (show AIM2 Proteins) inflammasome and cGAS/IFI16-STING-type I IFN pathway as a novel mechanism for host innate immunity to the ALVAC vaccine vector.
this study shows that IFI16 is not essential for the IFN response to human cytomegalovirus infection
findings show that IFI16 rapidly oligomerizes at incoming herpesvirus genomes at the nuclear periphery to transcriptionally repress viral gene expression and limit viral replicative capacity; further demonstrate that IFI16 does not initiate upstream activation of the canonical STING/TBK-1 (show TBK1 Proteins)/IRF3 (show IRF3 Proteins) signaling pathway but is required for downstream antiviral cytokine expression.
The authors observed that a reduced IFI16 expression was associated with a very poor survival in chronic lymphocytic leukemia, but only in cases with ZAP70/CD38 expression.
Findings indicate that expression of the scleroderma autoantigens IFI-16 and CENPs (show APITD1 Proteins), which are associated with severe vascular disease, is increased in vascular progenitors and mature endothelial cells. High level, lineage-enriched expression of autoantigens may explain the striking association between clinical phenotypes and the immune targeting of specific autoantigens.
p204 is a critical component of canonical LPS-TLR4 (show TLR4 Proteins) signaling pathway, and these studies also suggest that p204 could be a potential target to prevent and treat inflammatory and infectious diseases.
Ifi204 is required for EPC (show TCF21 Proteins) differentiation.
p204 initiated innate antiviral responses in adipose cells, thereby modulating adipocyte function.
cGAS and Ifi204 cooperate to produce type I IFNs in response to Francisella infection.
The present study demonstrated that mouse Leydig cells had innate antiviral activities in response to viral DNA challenge through p204 activation.
Data indicate that the transient expression of p204 in the early stage is indispensable for adipocyte differentiation. Disruption of p204 expression patterns at this stage leads to irreversible damage in fat formation.
IFI16 exerts in vivo anti-tumoral activity by promoting apoptosis of tumor cells.
This gene product interacts with the Tpr protein, a component of the nuclear pore complex.
This gene encodes a member of the HIN-200 (hematopoietic interferon-inducible nuclear antigens with 200 amino acid repeats) family of cytokines. The encoded protein contains domains involved in DNA binding, transcriptional regulation, and protein-protein interactions. The protein localizes to the nucleoplasm and nucleoli, and interacts with p53 and retinoblastoma-1. It modulates p53 function, and inhibits cell growth in the Ras/Raf signaling pathway. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
gamma-interferon-inducible protein 16
, interferon-gamma induced protein IFI 16
, interferon-inducible myeloid differentiation transcriptional activator
, interferon, gamma-inducible gene 204
, interferon, gamma-inducible protein 16
, interferon-activable protein 204
, interferon-inducible protein p204
, Gamma-interferon-inducible protein Ifi-16
, interferon induced transmembrane protein 2 (1-8D)
, interferon induced transmembrane protein, like
, interferon-induced transmembrane protein 2
, interferon-inducible protein 16
, interferon activated gene 203
, interferon-activable protein 203
, pyrin and HIN domain-containing protein 1