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1 ernary complex of enzyme*gapped DNA*dNTP (2'-deoxynucleotide triphosphate).
2 ed because the reaction lacked the requisite deoxynucleotide triphosphate.
3 orrelated with a rapid decrease in available deoxynucleotide triphosphates.
4 novel checkpoint responsive to low levels of deoxynucleotide triphosphates.
5 lon nor theta influenced the Km of alpha for deoxynucleotide triphosphate and only slightly decreased
6 ginine 67 are functionally equivalent to the deoxynucleotide triphosphate binding residues arginine 5
8 o acid that lies above the nucleobase of the deoxynucleotide triphosphate (dNTP) and is expected to p
9 RNA template-DNA primer duplex and incoming deoxynucleotide triphosphate (dNTP) at 3.0-A resolution.
10 primer, and DNA template in the presence of deoxynucleotide triphosphate (dNTP) complementary to the
12 se controlling the size of the intracellular deoxynucleotide triphosphate (dNTP) pool, a limiting fac
13 -121.6-fold lower binding affinity (K(d)) to deoxynucleotide triphosphate (dNTP) substrates than HIV-
14 n Arg668 and the ring oxygen of the incoming deoxynucleotide triphosphate (dNTP) using a combination
15 he 3'-OH on the sugar moiety of the incoming deoxynucleotide triphosphate (dNTP), we examined how thi
17 ested to play an important role in supplying deoxynucleotide triphosphates (dNTP) for DNA repair duri
18 th protonation of the gamma-phosphate of the deoxynucleotide triphosphate(dNTP) via a solvent water m
20 ductase (RNR) supplies the balanced pools of deoxynucleotide triphosphates (dNTPs) necessary for DNA
21 ctively incorporate Watson-Crick base-paired deoxynucleotide triphosphates (dNTPs) over incorrectly p
22 -limiting enzyme in the de novo synthesis of deoxynucleotide triphosphates (dNTPs), is a potential ta
24 cation blocker alpha-amanitin, NTPs (but not deoxynucleotide triphosphate [dNTPs]) templated at downs
25 ype oligonucleotides were mixed with various deoxynucleotide triphosphates in the presence of Sr(2)(+
26 ent with the high ratio of ribonucleotide to deoxynucleotide triphosphates in tissues, and that riboa
28 whose products supply the mitochondria with deoxynucleotide triphosphate pools needed for DNA replic
29 de reductase and the consequent depletion of deoxynucleotide triphosphate pools result in a cellular
30 r the removal of HAP from purine pools, from deoxynucleotide triphosphate pools, and from DNA, and we
31 lls into S-phase under conditions of altered deoxynucleotide triphosphate pools, particularly an incr
32 bstrate was observed in reactions containing deoxynucleotide triphosphates required to make full-leng
34 nus to the alpha-beta bridging oxygen of the deoxynucleotide triphosphate; this neutralizes the evolv
35 in myeloid cells by hydrolyzing the cellular deoxynucleotide triphosphates to a level below that whic
36 nterococcus faecalis is a distant homolog of deoxynucleotide triphosphate triphosphohydrolases (dNTPa
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