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1 , e.g. polynucleotide kinase and tyrosyl-DNA phosphodiesterase 1.
2 her increased by inactivation of tyrosyl-DNA phosphodiesterase 1.
3 lternative pathway from PARP and tyrosyl-DNA phosphodiesterase 1.
4 g ectoenzyme PC-1/nucleotide pyrophosphatase phosphodiesterase 1.
5 slinks which can be processed by tyrosyl-DNA phosphodiesterases 1 and 2, nucleotide excision and homo
8 CD39, CD73, ecto-nucleotide pyrophosphatase/phosphodiesterases 1 and 3, CD157, CD38) for the acceler
10 Proteases like Wss1 and Tdp1 (tyrosyl-DNA phosphodiesterase-1) are known to be involved in DPCR; h
11 y C member 6, ectonucleotide pyrophosphatase/phosphodiesterase 1, CD73, progressive ankylosis protein
12 ein (ANK) and ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) act to increase local extrac
13 AMP to AMP by ectonucleotide pyrophosphatase phosphodiesterase 1 (ENPP1) and an optimized assay for t
15 riants in the ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) gene have shown positive ass
20 lymorphism in ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) is associated with type 2 di
21 e report that ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) is preferentially upregulate
22 iation of the ectonucleotide pyrophosphatase phosphodiesterase 1 (ENPP1) K-->Q missense single nucleo
23 m in the ectoenzyme nucleotide pyrophosphate phosphodiesterase 1 (ENPP1) may confer susceptibility to
24 g mutation in ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) was identified in all patien
25 n (ANKH), and ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1), versus paired pulp tissues.
26 onucleotidase ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1), which hydrolyzes extracellu
27 to show that Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 (ENPP1), which hydrolyzes STING-acti
33 sphatase, the ectonucleotide pyrophosphatase/phosphodiesterase 1 enzyme, sodium-dependent phosphate c
34 se, mammalian ectonucleotide pyrophosphatase/phosphodiesterase 1, Escherichia coli RppH, Legionella p
36 cerebellar ataxias-aprataxin and tyrosyl-DNA phosphodiesterase 1-implicating SSBR in protection again
37 uggesting a significant role for tyrosyl-DNA phosphodiesterase 1 in removing 3'-PG blocking groups fo
38 , stimulation of protein ubiquitylation with phosphodiesterase 1 inhibitors, correction of titin stif
40 ini, and were more persistent in tyrosyl-DNA phosphodiesterase 1-mutant SCAN1 than in normal cells, s
46 break repair factors, including tyrosyl-DNA phosphodiesterase-1 or XRCC1, resulted in increased Top1
47 tive feedback loops, including activation of phosphodiesterase-1 (PDE-1), dampen the rise of cGMP.
48 nd evaluated for their inhibitory effects on phosphodiesterase 1 (PDE1) and phosphodiesterase 4 (PDE4
49 ]pyrimidin-4(3H)-one (5cc), an orally active phosphodiesterase-1 (PDE1) inhibitor aimed at restoring
50 by poly(ADP-ribose) glycohydrolase (PARG) or phosphodiesterase 1 prevents PAR polymer-induced cell de
54 te inhibitory activities against tyrosyl-DNA phosphodiesterase 1 (TDP1) and tyrosyl-DNA phosphodieste
55 ngly, the CRISPR/Cas9 mutants of TYROSYL-DNA PHOSPHODIESTERASE 1 (TDP1) are insensitive to CPT, and o
60 potential anticancer drug target tyrosyl-DNA phosphodiesterase 1 (TDP1) in a very simple, high throug
61 ere, we reveal the importance of tyrosyl-DNA phosphodiesterase 1 (TDP1) in the repair of nuclear and
69 ere, we report that depletion of Tyrosyl DNA phosphodiesterase 1 (TDP1) sensitizes human cells to alk
70 ted to the reduced expression of tyrosyl-DNA-phosphodiesterase 1 (TDP1), a DNA repair enzyme, in ATL
72 viduals containing a mutation in tyrosyl-DNA phosphodiesterase 1 (TDP1), an enzyme that cleaves 3'-ph
73 ement of topoisomerase 1 (TOP1), tyrosyl-DNA phosphodiesterase 1 (TDP1), and single-strand break repa
74 at they can be repaired by human tyrosyl-DNA phosphodiesterase 1 (TDP1), AP endonuclease 1 (APE1) and
75 n the DNA end-processing enzyme, tyrosyl-DNA phosphodiesterase 1 (TDP1), causes progressive neurodege
76 dies now reveal that an ataxia gene, tyrosyl phosphodiesterase 1 (TDP1), repairs single-stranded DNA
77 plementing protein 1 (XRCC1) and tyrosyl-DNA phosphodiesterase 1 (TDP1), using fluorescence- and ligh
78 This is typified by defects in tyrosyl DNA phosphodiesterase 1 (TDP1), which removes stalled topois