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FLASH plays two roles in 3' end processing of histone pre-mRNAs: It interacts with Lsm11 to form a docking platform for the polyadenylation factors, and it cooperates with SLBP (zeige SLBP ELISA Kits) to recruit U7 snRNP (zeige LSM2 ELISA Kits) to histone pre-mRNA.
Our results indicate that the APAF1 (zeige APAF1 ELISA Kits), BAX (zeige BAX ELISA Kits), and FLASH genes not only harbor frameshift mutations but also demonstrate mutational ITH, which together might play a role in the tumorigenesis of CRC (zeige CALR ELISA Kits) with MSI (zeige MSI1 ELISA Kits)-H by affecting the apoptosis of cancer cells.
High-quality solution NMR structures of three homeodomains from human proteins ALX4 (zeige ALX4 ELISA Kits), ZHX1 (zeige ZHX1 ELISA Kits) and CASP8AP2 were solved.
the predictive values regarding low expressions of H2AFZ (zeige H2AFZ ELISA Kits) and CASP8AP2 and high white blood cell count suggest that these features could help to identify more accurately patients at greater risk of relapse.
ARS2 (zeige SRRT ELISA Kits) and CASP8AP2 expressions can precisely predict high-risk of relapse and ALL prognosis.
The conserved C-terminal domain shared by FLASH, YARP, and Mute recognizes the C-terminal sequence of NPAT orthologues, thus acting as a signal targeting proteins to histone locus bodies.
Data suggest that SUMO targets FLASH for proteasome-dependent degradation, which is associated with recruitment of FLASH to PML (zeige PML ELISA Kits) bodies.
Hypermethylation of two CpG sites upstream of CASP8AP2 promoter influences gene expression and treatment outcome in childhood acute lymphoblastic leukemia.
FLASH/Lsm11 complex bind a unique combination of polyadenylation factors
These data demonstrate that methylation within the Casp8AP2 promoter correlates with the development of drug resistance and might serve as a biomarker and treatment target for drug resistance in cancer cells.
the functional interaction of E2A (zeige TCF3 ELISA Kits) and FLASH play an important role in cell proliferation and cellular senescence via regulation of p21 expression in experimental glomerulonephritis.
This protein is highly similar to FLASH, a mouse apoptotic protein identified by its interaction with the death-effector domain (DED) of caspase 8. Studies of FLASH protein suggested that this protein may be a component of the death-inducing signaling complex that includes Fas receptor, Fas-binding adapter FADD, and caspase 8, and plays a regulatory role in Fas-mediated apoptosis. Alternative splicing results in multiple transcript variants encoding the same protein.
CASP8 associated protein 2
, caspase 8 associated protein 2
, CASP8-associated protein 2-like
, CASP8-associated protein 2
, FLASH homolog RIP25
, FLICE associated huge
, FLICE-associated huge protein
, human FLASH