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1 but not by the viral DNA synthesis inhibitor phosphonoacetate, a result which classifies it as an ear
2 not appear necessary for the degradation of phosphonoacetate and 2-phosphonopropionate by either Pse
4 -3-one-1,1-dioxide to produce mixed sequence phosphonoacetate and thiophosphonoacetate oligodeoxynucl
8 riboses and phosphate backbone replacements (phosphonoacetates and amides); however, the range of che
10 ion expressed late in infection, inasmuch as phosphonoacetate blocked the translocation of ICP0 in wi
11 on the latter host the ability to mineralize phosphonoacetate but on the former the ability to utiliz
14 and metal ion specificity tests showed that phosphonoacetate hydrolase is also a two-zinc ion metall
16 ch, we circumscribed the biological range of phosphonoacetate hydrolase to a select group of bacteria
17 he X-ray structure of phosphonoformate-bound phosphonoacetate hydrolase was determined to reveal that
18 hosphonoacetate, which is also an inducer of phosphonoacetate hydrolase, entry of 2-phosphonopropiona
19 ovel carbon-phosphorus bond cleavage enzyme, phosphonoacetate hydrolase, from Pseudomonas fluorescens
24 ide and herpesvirus DNA polymerase inhibitor phosphonoacetate, indicating that vIL-8 is expressed wit
25 w general method for the introduction of the phosphonoacetate moiety into the indole C-2 position, th
26 as been developed for the alpha-arylation of phosphonoacetates utilizing parallel microscale experime
27 ected only in cells grown in the presence of phosphonoacetate, whereas transcripts of phnR were obser
29 s infected and maintained in the presence of phosphonoacetate, which is an inhibitor of viral DNA syn