anti-WEE1 (WEE1) Antikörper

Mouse (Murine) WEE1 Homolog (S. Pombe) (WEE1) Interaktionspartner

1. Morphine significantly downregulated the expression of miRNA-219-5p, which targets WEE1 to suppress Tyr15 expressions and activate Cdc2 (zeige CDK1 Antikörper), thus inhibiting the morphine-induced macrophage apoptosis.

2. Results revealed that WEE1 is indispensable for maintaining genomic stability and it functions as a haploinsufficient tumor suppressor.

3. Wee1 is directly or indirectly involved in the mechanism of the circadian rhythm-dependent changes in docetaxel-induced intestinal damage.

4. The induction of Wee1 under hypoxia was confirmed both at the mRNA and protein levels.

5. In this study, we found that the chromosomal wee1 gene is also down-regulated by KLF3 (zeige KLF3 Antikörper).

6. The regulation of Wee1 by SadA (zeige BRSK2 Antikörper) and SadB (zeige BRSK1 Antikörper) kinases is essential for the differentiation of polarized neurons.

7. Mammalian Wee1 plays a critical role in maintaining genome integrity and is essential for embryonic survival at the pre-implantation stage of mouse development.

8. expression of wee1 was directly regulated by the molecular components of the circadian clockwork in the regenerating liver

9. transcription repressive activity of TBP-related factor 2 (zeige TBPL1 Antikörper) to wee1 promoter needs association with the promoter and TFIIA (zeige GTF2A1 Antikörper)

10. the suppression of nuclear import of cyclin B1 (zeige CCNB1 Antikörper), the induction of Wee1 kinase activity, and the transient nuclear accumulation of p21(CIP1/WAF1 (zeige CDKN1A Antikörper)) may play important roles in the transient cell cycle delay in response to ionizing radiation

Human WEE1 Homolog (S. Pombe) (WEE1) Interaktionspartner

1. miR (zeige MLXIP Antikörper)-26b governed temozolomide (TMZ)-resistance-mediate epithelial-mesenchymal transition partly due to governing its target Wee1.

2. the data suggest the importance of WEE1 as an enabler of branching vascularisation in colorectal cancer liver metastases.

3. WEE1 is over-expressed and could enhance gastric cancer cell proliferation and metastasis

4. Wee1 is identified as a novel direct target of miR (zeige MLXIP Antikörper)-194. Ectopic expression of Wee1 at least in part overcomes the suppressive impacts of miR (zeige MLXIP Antikörper)-194 on the malignant phenotypes of human laryngeal squamous cell carcinoma

5. High WEE1 expression is associated with non-small cell lung cancer.

6. miR (zeige MLXIP Antikörper)-503 could function as an enhancer of radiation responses in laryngeal carcinoma cells by inhibiting WEE1

7. Data suggest that SMURF1 (zeige SMURF1 Antikörper) is required for S phase progression; SMURF1 (zeige SMURF1 Antikörper) promotes ubiquitination-dependent degradation of WEE1; these functions of SMURF1 (zeige SMURF1 Antikörper) appear to be linked and may be important in cell proliferation and tumorigenesis. (SMURF1 (zeige SMURF1 Antikörper) = SMAD specific E3 ubiquitin protein ligase 1 (zeige SMURF1 Antikörper); WEE1 = wee 1 homolog [S pombe] protein)

8. Date show that when Wee1 alone is inhibited, Chk1 (zeige CHEK1 Antikörper) suppresses CDC45 (zeige CDC45 Antikörper) loading and thereby limits the extent of unscheduled replication initiation and subsequent S-phase DNA damage, despite very high CDK (zeige CDK4 Antikörper)-activity.

9. we overexpressed CKS1B (zeige CKS1B Antikörper) in multiple cell lines and found increased sensitivity to PLK1 (zeige PLK1 Antikörper) knockdown and PLK1 (zeige PLK1 Antikörper) drug inhibition. Finally, combined inhibition of WEE1 and PLK1 (zeige PLK1 Antikörper) results in less apoptosis than predicted based on an additive model of the individual inhibitors, showing an epistatic interaction and confirming a prediction of the yeast data.

10. Wee1 staining intensity was a predictor of favorable metastasis-free and overall survival compared to strong intensity and no or weak staining

Arabidopsis thaliana WEE1 Homolog (S. Pombe) (WEE1) Interaktionspartner

1. the identification of a second member of the RNase H2 complex, RNase H2B (zeige RNASEH2B Antikörper), being able to complement the root growth phenotype of WEE1(KO) plants, is reported.

2. mutant alleles of the genes encoding subunits of the ribonuclease H2 (RNase H2) complex, known for its role in removing ribonucleotides from DNA-RNA duplexes, were identified as suppressor mutants of WEE1 knockout plants.

3. The plant WEE1 kinase acquired an indirect developmental function that is important for meristem maintenance upon replication stress.

4. The WEE1 gene is not rate-limiting for cell cycle progression under normal growth conditions but is a critical target of the ATR (zeige ATR Antikörper)-ATM (zeige ATM Antikörper) signaling cascades that inhibit the cell cycle upon activation of the DNA integrity checkpoints.