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TWEAK (zeige TNFSF12 ELISA Kits) upregulated the expression of Fn14.
Fn14.TRAIL can be converted into a highly effective TRAIL oligomer upon binding to TWEAK (zeige TNFSF12 ELISA Kits) which induces lymphoblast apoptosis.
Data show that aurintricarboxylic acid (ATA) targets the TNF-related WEAK inducer of apoptosis (TWEAK (zeige TNFSF12 ELISA Kits))-fibroblast growth factor-inducible 14 (zeige DDX3X ELISA Kits) (Fn14) signaling axis, which could potentially be developed as a new therapeutic agent for treatment of glioblastoma (GBM) patients.
TNFRSF12A was knocked down in the SMMC7721 cell line through siRNA. This demonstrated that cells exhibited reduced reproductive and metastatic capacity ex vivo.
In this review article, we summarize studies indicating that (i) Fn14 gene expression is low in normal brain tissue but is upregulated in advanced brain cancers and, in particular, in GB tumors ; TWEAK (zeige TNFSF12 ELISA Kits): Fn14 engagement as well as Fn14 overexpression can stimulate glioma cell migration, invasion and resistance to chemotherapeutic agents in vitro.
Fn14 is a receptor of mitogen TWEAK (zeige TNFSF12 ELISA Kits) (tumor necrosis factor (zeige TNF ELISA Kits)-like weak inducer of apoptosis), expressed on the membranes of HPCs and promoting their proliferation.
EGFR (zeige EGFR ELISA Kits) Del 19 may promote Fn14 and JAK1 (zeige JAK1 ELISA Kits)/STAT1 (zeige STAT1 ELISA Kits) expression in NSCLC.
TWEAK (zeige TNFSF12 ELISA Kits)/Fn14 activation induces keratinocyte proliferation under psoriatic inflammation
The results demonstrated that vitreous fluid from patients with PDR had higher levels of TWEAK and Fn14 than that from T2DM patients without PDR, thus suggesting an important regulatory role of TWEAK/Fn14 signaling in the pathogenesis of PDR.
Results indicate that FN14 and GRP94 (zeige HSP90B1 ELISA Kits) are prediction/prognosis markers which open up new possibilities for preventing/treating brain metastasis in breast cancer patients.
TWEAK (zeige TNFSF12 ELISA Kits)/Fn14 interactions play an important role in the pathogenesis of neuropsychiatric lupus by increasing the accumulation of inflammatory cells in the choroid plexus, disrupting blood brain barrier integrity, and increasing neuronal damage
TWEAK (zeige TNFSF12 ELISA Kits)/Fn14 signaling is strongly implicated in the pathogenesis of the cutaneous manifestations in the MRL/lpr (zeige FAS ELISA Kits) model of spontaneous lupus in mice.
In SOD1 (zeige SOD1 ELISA Kits) and Neurotomized mice the results of this studysuggest LC3 (zeige MAP1LC3A ELISA Kits), Fn14, Bcl3 (zeige BCL3 ELISA Kits) and Gadd45a (zeige GADD45A ELISA Kits) as candidate genes involved in the maintenance of the severe atrophic state.
Fn14 mediates wound-healing responses that are necessary to survive acute liver injury during alcohol exposure.
Overexpression of Dnmt3a (zeige DNMT3A ELISA Kits) inhibits the gene expression of Fn14 and attenuates skeletal muscle atrophy upon denervation. Denervation also causes the activation of ERK1/2 (zeige MAPK1/3 ELISA Kits), JNK1 (zeige MAPK8 ELISA Kits)/2, and ERK5 (zeige MAPK7 ELISA Kits) MAPKs and AP1 (zeige JUN ELISA Kits) and SP1 (zeige SP1 ELISA Kits).
TWEAK (zeige TNFSF12 ELISA Kits)-FN14 signaling is necessary for the healthy adult liver to regenerate normally after acute partial hepatectomy.
The levels of TWEAK receptor Fn14 are increased in skeletal muscle during aging. Deletion of Fn14 attenuates age-associated skeletal muscle fiber atrophy.
this study showed that the apoptosis signal-regulating kinase 1 (ASK1 (zeige MAP3K5 ELISA Kits))-JNK1 (zeige MAPK8 ELISA Kits)/2 pathway, which was activated by large magnitude mechanical stretch induced expression of Fn14 gene in osteoblasts.
a model in which constitutive down-regulation of Fn14 facilitates dynamic regulation of Fn14 protein levels and prevents spontaneous or inappropriate receptor signaling.
study demonstrates that TWEAK (zeige TNFSF12 ELISA Kits) induces muscle atrophy through repressing the levels of PGC-1alpha (zeige PPARGC1A ELISA Kits)
Receptor for TNFSF12/TWEAK. Weak inducer of apoptosis in some cell types. Promotes angiogenesis and the proliferation of endothelial cells. May modulate cellular adhesion to matrix proteins.
, fibroblast growth factor-inducible immediate-early response protein 14
, tumor necrosis factor receptor superfamily member 12A
, type I transmembrane protein Fn14
, fibroblast growth factor regulated protein 2
, fibroblast growth factor-regulated protein 2
, fibroblast growth factor-inducible 14