Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Alle Spezies anzeigen
Weitere Synonyme anzeigen
Select your species
nMet accelerated HCC (zeige FAM126A ELISA Kits) tumorigenesis and metastasis via the activation of TAK1/NF-kappaB (zeige NFKB1 ELISA Kits) pathway.
TAK1 protein expression increased in cartilage tissue from spinal tuberculosis patients.
TAK1 regulates Nrf2 (zeige GABPA ELISA Kits) through modulation of Keap-p62/SQSTM1 (zeige SQSTM1 ELISA Kits) interaction. This regulation is important for homeostatic antioxidant protection in the intestinal epithelium.
Overexpression of TAK1 was strongly associated with positive lymph node metastasis in pancreatic ductal adenocarcinoma.
dysregulation of the TAK1 complex produces a close phenocopy of Frontometaphyseal Dysplasia caused by FLNA (zeige FLNA ELISA Kits) mutations; furthermore, the pathogenesis of some of the filaminopathies caused by FLNA (zeige FLNA ELISA Kits) mutations might be mediated by misregulation of signaling coordinated through the TAK1 signaling complex
although TAK1 is located at the crossroad of inflammation, immunity, and cancer, this study reports MAP3K7 mutations in a developmental disorder affecting mainly cartilage, bone, and heart
This study suggests that aberrant activity of TAK1 impairs autophagy and subsequently leads to alterations in the vitality of retinal pigment epithelial cells.
TAK1 may be an important factor involved in the pathogenesis of thyroid cancer, and targeted down-regulation of TAK1 may improve the prognosis of patients with thyroid cancer.
Loss of MAP3K7 are associated with esophageal squamous cell carcinoma.
This paper highlights that targeting the BMP and TGFbeta (zeige TGFB1 ELISA Kits) type I and type II receptors causes a downregulation of XIAP (zeige XIAP ELISA Kits), TAK1, and Id1 (zeige ID1 ELISA Kits) leading to cell death of lung cancer cells.
These results present a novel in vivo function, the negative role of TAK1 (zeige NR2C2 ELISA Kits) in marginal zone B-cell development that is likely associated with NF-kappaB2 activation.
Tnfr1 (zeige TNFRSF1A ELISA Kits) deletion partially restored thymic and lung macrophages.
TAK1 (zeige NR2C2 ELISA Kits) is required for PPARgamma (zeige PPARG ELISA Kits) transactivation and promotes PPARgamma (zeige PPARG ELISA Kits) transcriptional activity synergistically with TAK1 binding protein 1 (TAB1 (zeige TAB1 ELISA Kits)).
inhibition of TAK1 (zeige NR2C2 ELISA Kits) triggered two caspase 8 (zeige CASP8 ELISA Kits) activation pathways through the induction of RIP1 (zeige RALBP1 ELISA Kits)-FADD (zeige FADD ELISA Kits)-caspase 8 (zeige CASP8 ELISA Kits) complex as well as FLIP cleavage/degradation.
Transforming growth factor-beta activated kinase 1 (TAK1) regulation of sterol-regulatory element-binding proteins (SREBPs) critically contributes to the maintenance of liver homeostasis to prevent steatosis, which is a potentially important mechanism to prevent hepatocellular carcinoma (HCC (zeige FAM126A ELISA Kits)) development.
TAK1 (zeige NR2C2 ELISA Kits) regulates Nrf2 (zeige NFE2L2 ELISA Kits) through modulation of Keap-p62/SQSTM1 (zeige SQSTM1 ELISA Kits) interaction. This regulation is important for homeostatic antioxidant protection in the intestinal epithelium.
Mekk1 (zeige MAP2K1 ELISA Kits) (encoded by Map3k1 (zeige MAP3K1 ELISA Kits)) signaling activates Mapks to regulate Cdkn1b (zeige CDKN1B ELISA Kits) (encoding p27(Kip1 (zeige CDKN1B ELISA Kits))) expression and p27(Kip1 (zeige CDKN1B ELISA Kits))-dependent proliferative expansion in response to antigen.
TRADD (zeige TRADD ELISA Kits) knockout blunts pressure overload-induced cardiac hypertrophy through mediating TAK1 (zeige NR2C2 ELISA Kits)/p38 MAPK (zeige MAPK14 ELISA Kits) but not AKT (zeige AKT1 ELISA Kits) phosphorylation
this study demonstrates a pivotal role of TAK1 (zeige NR2C2 ELISA Kits) in dendritic cells in controlling trichloroethylene-induced contact hypersensitivity response and suggests that targeting TAK1 (zeige NR2C2 ELISA Kits) function in DCs may be a viable approach to preventing and treating TCE-related occupational health hazards
The E3 ligase TRIM8 (zeige TRIM8 ELISA Kits) is a potent regulator that exacerbates steatohepatitis and metabolic disorders dependent on its binding and ubiquitinating capacity on transforming growth factor-beta-activated kinase 1.
The protein encoded by this gene is a member of the serine/threonine protein kinase family. This kinase mediates the signaling transduction induced by TGF beta and morphogenetic protein (BMP), and controls a variety of cell functions including transcription regulation and apoptosis. In response to IL-1, this protein forms a kinase complex including TRAF6, MAP3K7P1/TAB1 and MAP3K7P2/TAB2\; this complex is required for the activation of nuclear factor kappa B. This kinase can also activate MAPK8/JNK, MAP2K4/MKK4, and thus plays a role in the cell response to environmental stresses. Four alternatively spliced transcript variants encoding distinct isoforms have been reported.
mitogen-activated protein kinase kinase kinase 7
, TGF-beta-activated kinase TAK1
, TGF-beta activated kinase 1
, TGF-beta-activated kinase 1
, transforming growth factor-beta-activated kinase 1
, mitogen activated protein kinase kinase kinase 7
, transforming growth factor beta-activated kinase 1