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miRNA-708 acts as a tumor suppressor because it negatively regulates the anti-apoptotic protein c (zeige PROC ELISA Kits)-FLIPL and regulates the sensitivity of renal cancer cells to various apoptotic stimuli.
The (fli:GFP) Casper zebrafish embryo can be used as an efficient animal model to study metastatic behavior of human CM cells and warrants further testing of drug efficacy to aid care of CM patients.
Inhibition of BET bromodomain-dependent XIAP and FLIP expression sensitizes KRAS-mutated non-small cell lung cancer to pro-apoptotic agents.
the c-FLIP and NOXA (zeige PMAIP1 ELISA Kits)/Mcl-1 (zeige MCL1 ELISA Kits) axis participated in the synergistic effect of pemetrexed plus cisplatin in human choroidal melanoma cells
The strongest interaction result in relation to overall breast cancer risk was found between CFLAR-rs7558475 and current smoking (ORint = 0.77, 95% CI: 0.67-0.88, pint = 1.8 x 10(-4) ). The interaction with the strongest statistical evidence was found between 5q14-rs7707921 and alcohol consumption (ORint =1.36, 95% CI: 1.16-1.59, pint = 1.9 x 10(-5) ) in relation to ER- disease risk
findings suggest that expression of cFLIPL regulates the basal interaction of Bcl-2 (zeige BCL2 ELISA Kits) with Beclin-1 (zeige BECN1 ELISA Kits) and substantiates p53 (zeige TP53 ELISA Kits) dependent ubiquitination of Beclin-1 (zeige BECN1 ELISA Kits) during autophagic stress to determine the fate of cell death or survival.
Using the tDED filament structure as a template, structural analyses reveal the interaction surfaces between FADD (zeige FADD ELISA Kits) and caspase-8 (zeige CASP8 ELISA Kits) and the distinct mechanisms of regulation by cFLIP and MC159 through comingling and capping, respectively.
Data in this study show that cFLIPL inhibits IFN regulatory factor 3 (IRF3 (zeige IRF3 ELISA Kits)), a transcription factor central for IFN-beta (zeige IFNB1 ELISA Kits) and IFN-stimulated gene expression.
CFLAR levels were substantially decreased in the livers of subjects with NAFLD and NASH, as compared to that in nonsteatotic controls.
association of c-FLIPL and TIP49 provided an additional mechanism involved in c-FLIPL-mediated functions, including Wnt (zeige WNT2 ELISA Kits) activation
c-FLIP modulation of AKT activity is crucial in controlling PERK signalling and sensitivity to endoplasmic reticulum stress.
Regulatory T cells have a high apoptosis rate ex vivo correlating with low c-FLIP expression.
In conclusion, our data indicated that miR (zeige MLXIP ELISA Kits)-150 potentially contributes to the hepatic steatosis and insulin (zeige INS ELISA Kits) resistance in NAFLD (zeige TSC2 ELISA Kits). miR (zeige MLXIP ELISA Kits)-150/CFLAR pathway may be a new therapeutic strategy against NAFLD (zeige TSC2 ELISA Kits).
Findings establish CFLAR as a key suppressor of steatohepatitis and indicate that the development of CFLAR-peptide-mimicking drugs and the screening of small-molecular inhibitors that specifically block ASK1 (zeige MAP3K5 ELISA Kits) dimerization are new and feasible approaches for NASH (zeige SAMSN1 ELISA Kits) treatment.
knockdown of cFLIPL and induced expression of FADD (zeige FADD ELISA Kits) rapidly accumulate intracellular ROS (zeige ROS1 ELISA Kits) accompanied by JNK1 (zeige MAPK8 ELISA Kits) activation to substantiate apoptosis.
CASP8 (zeige CASP8 ELISA Kits) is present exclusively as its cleaved p43 (zeige AIMP1 ELISA Kits) product, bound to cFLIPL.
The generation of mouse line with Flip deficiency in cells that express cre under the CD11c (zeige ITGAX ELISA Kits) promoter is reported.
c-FLIPL deficiency induces the caspase (zeige CASP3 ELISA Kits)-mediated processing of RTN4 (zeige RTN4 ELISA Kits), thus affecting endoplasmic reticulum (ER) shape and coupling to mitochondria. Thus, it was concluded that c-FLIPL is a novel regulator of ER morphology and ER-mitochondria crosstalk.
Acute organ failure following the loss of anti-apoptotic cellular FLICE-inhibitory protein involves activation of innate immune receptors.
The results reveal a novel inhibitory role of c-FLIP in myeloid cell activation and demonstrate the unexpected anti-inflammatory activity of c-FLIP.
results indicate downregulation of cFLIP during structural luteal regression, suggesting that cFLIP plays a survival role in the bovine corpus luteum
Conservation of FLIP's ability to inhibit apoptosis and to downregulate NF-kappaB (zeige NFKB1 ELISA Kits) activation across species.
cellular-Flice like inhibitory protein (cFLIP) long form, plays an anti-apoptotic role in the granulosa cells of healthy follicles of pig ovaries [cFLIP]
Intracellular remodeling with overexpression of pig c (zeige PIGC ELISA Kits)-FLIP in xenograft cells may decrease the innate cellular responses against xenografts, facilitating long-term xenograft survival.
Intracellular remodeling with the overexpression of c-FLIP(S/L) in xenograft cells may avoid innate cellular attacks against xenografts and facilitate long-term xenograft survival.
Overexpression of c-FLIP in xenograft cells may prevent innate cellular attacks against xenografts opening the window of opportunity for long-term xenograft survival.
The protein encoded by this gene is a regulator of apoptosis and is structurally similar to caspase-8. However, the encoded protein lacks caspase activity and appears to be itself cleaved into two peptides by caspase-8. Several transcript variants encoding different isoforms have been found for this gene, and partial evidence for several more variants exists.
, CASP8 and FADD-like apoptosis regulator
, flice/caspase-i inhibitory protein
, cellular FLICE-like inhibitory protein
, CASP8 and FADD-like apoptosis regulator-like
, FADD-like anti-apoptotic molecule
, FADD-like antiapoptotic molecule 1
, MACH-related inducer of toxicity
, caspase homolog
, caspase-eight-related protein
, caspase-like apoptosis regulatory protein
, caspase-related inducer of apoptosis
, inhibitor of FLICE
, usurpin beta
, FLICE-like inhibitory protein