...Top1 in Pol II pausing. Here, we demonstrate that Top1 inhibition favors Pol II escape from a promoter-proximal pausing ...
The aromathecin topoisomerase I (top1) inhibitors offer promising scaffolds for the development of novel cancer chemothe...
A recent study found that variation in camptothecin pharmacodynamic genes (TOP1, PARP1, TDP1 and XRCC1) correlated with ...
...TOP1 catalytic activity by interacting directly with the free enzyme and preventing the formation of the DNA-TOP1 comple...
...Top1)-DNA covalent complexes. TDP1 can also hydrolyze other 3'-end DNA alterations including 3'-phosphoglycolate and 3'-...
DNA topoisomerase I (Top1) is an essential nuclear enzyme and a validated target for anticancer agent screening. In a pr...
...TOP1 inhibitor camptothecin are resected normally, but the loading of the RAD51 recombinase is defective. Therefore, MMS...
...TOP1, APC, CBP, ERK, EGFR, C-myc, Cald, DARPP32, MRE11A, AR, EPS8).,Based on these results, validated colorectal cancer ...
...Top1 and Top2) are used to detect ligand-binding pockets. The results show that the atom-contact-pair method has good ac...
...Top1. Taken together, these data indicate that Top1 prevents replication fork collapse by suppressing the formation of R...
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