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These results show that significantly increased levels of FOXO3 (zeige FOXO3 ELISA Kits), IRF4, and xIAP (zeige XIAP ELISA Kits) mRNA in Chinese HIV-1-infected patients.
Mechanistically, we found that BETi-mediated inhibition of cMYC (zeige MYC ELISA Kits) correlates with the upregulation of miR (zeige MLXIP ELISA Kits)-125b-5p and the downregulation of the cMYC (zeige MYC ELISA Kits)/miR (zeige MLXIP ELISA Kits)-125b-5p target gene IRF4, a transcriptional repressor of MICA (zeige MICA ELISA Kits).
BCL7A (zeige BCL7A ELISA Kits), BRWD3 (zeige BRWD3 ELISA Kits), and AUTS2 demonstrate significantly higher mutation frequencies among AA cases. These genes are all involved in translocations in B-cell malignancies. Moreover, we detected a significant difference in mutation frequency of TP53 (zeige TP53 ELISA Kits) and IRF4 with frequencies higher among CA cases. Our study provides rationale for interrogating diverse tumor cohorts to best understand tumor genomics across populations.
IRF4 protects arteries against neointima formation by promoting the expression of KLF4 (zeige KLF4 ELISA Kits) by directly binding to its promoter.
We propose that the Irf4 locus functions as the "reader" of TCR signal strength, and in turn, concentration-dependent activity of Irf4 "writes" T helper fate choice.
PU.1-induced apoptosis in myeloma cells is associated with IRF4 downregulation and subsequent IRF7 (zeige IRF7 ELISA Kits) upregulation.
GM-CSF (zeige CSF2 ELISA Kits) can mediate inflammation and pain by regulating IRF4-induced CCL17 (zeige CCL17 ELISA Kits) production
expression of CARMA1 (zeige CARD11 ELISA Kits) mRNA is likely associated with the expression of MUM1 and shows male predominance in diffuse large B cell lymphoma.
Data show that BCL-6 (zeige BCL6 ELISA Kits) (64%) and MUM1 (45%) were expressed in patients with primary mediastinal large B-cell lymphoma.
The study demonstrated differential MUM-1 expression between PEComas and other true melanocytic tumors
RHS6 is a critical regulatory element for allergic airway inflammation and for coordinate regulation of Th2 cytokine genes by recruiting GATA3 (zeige GATA3 ELISA Kits), SATB1 (zeige SATB1 ELISA Kits), and IRF4.
this study shows that epicutaneous sensitization to house dust mite allergen requires interferon regulatory factor 4-dependent dermal dendritic cells
Cell fate and metabolic state are linked by transcriptional regulators, such as IRF4 and FoxO1 (zeige FOXO1 ELISA Kits), with dual roles in lineage and metabolic choice. Instructing some cells to utilize nutrients for anabolism and differentiation while other cells catabolically self-digest and self-renew may enable growth and repair in metazoa.
Here the authors show that concomitant loss of Tet2 (zeige TET2 ELISA Kits) and Tet3 (zeige TET3 ELISA Kits) in mice at early B cell stage blocked the pro- to pre-B cell transition in the bone marrow, decreased Irf4 expression and impaired the germline transcription and rearrangement of the Igkappa locus.
Data show that Fos-Related Antigen-2 (Fra-2 (zeige FOSL2 ELISA Kits)) is a key upstream regulator of forkhead box O1 (Foxo1 (zeige FOXO1 ELISA Kits)) and interferon regulatory factor 4 (Irf4) expression and influences proliferation and differentiation of B cells at multiple stages.
MTORC2 (zeige CRTC2 ELISA Kits) operated in parallel with the IL-4Ralpha-Stat6 (zeige STAT6 ELISA Kits) pathway.
IRF4 mRNA and protein expression was remarkably suppressed during the development of myeloid-derived suppressor cells in the tumor microenvironment. IRF4 expression in MDSCs can modulate their activity to inhibit T cell proliferation through IL-10 (zeige IL10 ELISA Kits) production and ROS (zeige ROS1 ELISA Kits) generation, and myeloid-specific deletion of IRF4 leads to the increase of MDSC differentiation. IRF4 reduction induced by tumors can increase MDSC numbers.
propose that Irf4 is imperative for thymic Treg homeostasis because it regulates thymic epithelial cell-specific expression of several chemokines and costimulatory molecules indicated in thymocyte development and Treg induction
IRF4a and IRF4b displayed a distinct tissue expression pattern, embryonic stages expression and inducible expression in vivo and in vitro, suggesting that IRF4 paralogues might play different roles in immune system.
The protein encoded by this gene belongs to the IRF (interferon regulatory factor) family of transcription factors, characterized by an unique tryptophan pentad repeat DNA-binding domain. The IRFs are important in the regulation of interferons in response to infection by virus, and in the regulation of interferon-inducible genes. This family member is lymphocyte specific and negatively regulates Toll-like-receptor (TLR) signaling that is central to the activation of innate and adaptive immune systems. A chromosomal translocation involving this gene and the IgH locus, t(6\;14)(p25\;q32), may be a cause of multiple myeloma. Alternatively spliced transcript variants have been found for this gene.
interferon regulatory factor 4
, Interferon regulatory factor 4
, lymphocyte-specific interferon regulatory factor
, multiple myeloma oncogene 1
, PU.1 interaction partner
, Sfpi1/PU.1 interaction partner
, transcriptional activator PIP
, PWWP domain-containing protein MUM1
, mutated melanoma-associated antigen 1