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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.
6 CD39, CD73, ecto-nucleotide pyrophosphatase/phosphodiesterases 1 and 3, CD157, CD38) for the acceler
8 riants in the ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) gene have shown positive ass
11 lymorphism in ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) is associated with type 2 di
12 e report that ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) is preferentially upregulate
13 iation of the ectonucleotide pyrophosphatase phosphodiesterase 1 (ENPP1) K-->Q missense single nucleo
14 m in the ectoenzyme nucleotide pyrophosphate phosphodiesterase 1 (ENPP1) may confer susceptibility to
15 g mutation in ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) was identified in all patien
16 n (ANKH), and ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1), versus paired pulp tissues.
21 sphatase, the ectonucleotide pyrophosphatase/phosphodiesterase 1 enzyme, sodium-dependent phosphate c
23 cerebellar ataxias-aprataxin and tyrosyl-DNA phosphodiesterase 1-implicating SSBR in protection again
24 uggesting a significant role for tyrosyl-DNA phosphodiesterase 1 in removing 3'-PG blocking groups fo
26 ini, and were more persistent in tyrosyl-DNA phosphodiesterase 1-mutant SCAN1 than in normal cells, s
32 break repair factors, including tyrosyl-DNA phosphodiesterase-1 or XRCC1, resulted in increased Top1
33 tive feedback loops, including activation of phosphodiesterase-1 (PDE-1), dampen the rise of cGMP.
34 by poly(ADP-ribose) glycohydrolase (PARG) or phosphodiesterase 1 prevents PAR polymer-induced cell de
37 te inhibitory activities against tyrosyl-DNA phosphodiesterase 1 (TDP1) and tyrosyl-DNA phosphodieste
42 potential anticancer drug target tyrosyl-DNA phosphodiesterase 1 (TDP1) in a very simple, high throug
43 ere, we reveal the importance of tyrosyl-DNA phosphodiesterase 1 (TDP1) in the repair of nuclear and
49 ere, we report that depletion of Tyrosyl DNA phosphodiesterase 1 (TDP1) sensitizes human cells to alk
50 ted to the reduced expression of tyrosyl-DNA-phosphodiesterase 1 (TDP1), a DNA repair enzyme, in ATL
52 viduals containing a mutation in tyrosyl-DNA phosphodiesterase 1 (TDP1), an enzyme that cleaves 3'-ph
53 ement of topoisomerase 1 (TOP1), tyrosyl-DNA phosphodiesterase 1 (TDP1), and single-strand break repa
54 dies now reveal that an ataxia gene, tyrosyl phosphodiesterase 1 (TDP1), repairs single-stranded DNA
55 plementing protein 1 (XRCC1) and tyrosyl-DNA phosphodiesterase 1 (TDP1), using fluorescence- and ligh
56 This is typified by defects in tyrosyl DNA phosphodiesterase 1 (TDP1), which removes stalled topois
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