anti-FLASH (CASP8AP2) Antikörper

Human CASP8 Associated Protein 2 (CASP8AP2) Interaktionspartner

1. 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 to recruit U7 snRNP to histone pre-mRNA.

2. FLASH is required for embryogenesis, but not for cell proliferation or differentiation in embryonic stem cells.

3. Our results indicate that the APAF1, BAX, and FLASH genes not only harbor frameshift mutations but also demonstrate mutational ITH, which together might play a role in the tumorigenesis of CRC with MSI-H by affecting the apoptosis of cancer cells.

4. High-quality solution NMR structures of three homeodomains from human proteins ALX4, ZHX1 and CASP8AP2 were solved.

5. the predictive values regarding low expressions of H2AFZ and CASP8AP2 and high white blood cell count suggest that these features could help to identify more accurately patients at greater risk of relapse.

6. ARS2 and CASP8AP2 expressions can precisely predict high-risk of relapse and ALL prognosis.

7. 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.

8. Data suggest that SUMO targets FLASH for proteasome-dependent degradation, which is associated with recruitment of FLASH to PML bodies.

9. Hypermethylation of two CpG sites upstream of CASP8AP2 promoter influences gene expression and treatment outcome in childhood acute lymphoblastic leukemia.

10. FLASH/Lsm11 complex bind a unique combination of polyadenylation factors

11. 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.

12. FLASH knockdown in HT1080 mutant cells defective in p53 did not significantly accelerate Fas mediated apoptosis indicating that the effect was dependent on functional p53.

13. This study further defines the role CASP8AP2/FLASH plays in the regulating expression of the replication-dependent histones and shows that its LOF results in broad and reproducible effects on the transcriptome of colorectal cancer cells

14. Data show that show that the transcription factor p73 binds to Flice-Associated Huge Protein (FLASH) and is part of the complex that regulates histone gene transcription.

15. CASP8AP2 is a promising prognostic indicator in pediatric acute lymphoblastic leukemia.

16. PIAS1 is a common partner for two cancer-related nuclear factors, c-Myb and FLASH.

17. Critical residues in human FLASH and Lsm11 that are involved in the interaction between these two proteins, are identified.

18. investigated the expression of three apoptosis related genes, BCL2L13, CASP8AP2, and Livin, as well as their prognostic significance, in a retrospective study of 90 pediatric ALL patients diagnosed between 1996 and 2007 in Taiwan

19. endogenous caspase-8 mediates tumor necrosis factor-alpha-induced activation of NF-kappaB via FLASH

20. FLASH differentially suppresses steroid hormone receptor-induced transcriptional activity by interfering with their association with steroid hormone receptor coactivator 2 (SRC2)/N-CoA2 and SRC3/N-CoA3

Mouse (Murine) CASP8 Associated Protein 2 (CASP8AP2) Interaktionspartner

1. the functional interaction of E2A and FLASH play an important role in cell proliferation and cellular senescence via regulation of p21 expression in experimental glomerulonephritis.

2. Data suggest that SUMO targets FLASH for proteasome-dependent degradation, which is associated with recruitment of FLASH to PML bodies.

3. Data show that homozygous deletion of FLASH results in early embryonic lethality.

4. This enzyme has an essential role in T-cell homeostasis and T-cell-mediated immunity.