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1 during the cell cycle in the trypanosomatid Crithidia fasciculata.
2 th the nonspecific nucleoside hydrolase from Crithidia fasciculata.
3 or the nonspecific nucleoside hydrolase from Crithidia fasciculata.
4 s Trypanosoma cruzi, Trypanosoma brucei, and Crithidia fasciculata.
5 mitochondrial fraction of the trypanosomatid Crithidia fasciculata.
6 mulate periodically during the cell cycle in Crithidia fasciculata.
9 tochondrial DNA ligase in the trypanosomatid Crithidia fasciculata, and we show that an epitope-tagge
10 nosomatid species, Leishmania tarentolae and Crithidia fasciculata, at resolutions up to 2.7 angstrom
11 The nonspecific nucleoside hydrolase from Crithidia fasciculata cocrystallized with p-aminophenyli
12 DNA (kinetoplast DNA) of the trypanosomatid Crithidia fasciculata consists of minicircles and maxici
15 DNA (kinetoplast DNA) of the trypanosomatid Crithidia fasciculata has an unusual structure composed
17 A pol beta from the trypanosomatid parasite Crithidia fasciculata, however, is the first example of
18 DNA polymerase beta from the trypanosomatid Crithidia fasciculata, however, was the first mitochondr
19 production of a cysteine-less variant of the Crithidia fasciculata inosine-guanosine permease CfNT2 t
21 Kinetoplast DNA, the mitochondrial DNA of Crithidia fasciculata, is organized into a network conta
23 he 5'- or 3'-untranslated regions of several Crithidia fasciculata messenger RNAs encoding proteins i
24 or mutants of the inosine-guanosine-specific Crithidia fasciculata nucleoside transporter 2 (CfNT2) t
30 s cerevisiae , Schizosaccharomyces pombe and Crithidia fasciculata , unlike the related Escherichia c
31 sion of D-Glc to D-Ara in the trypanosomatid Crithidia fasciculata using positionally labeled [(13)C]
33 prepared from Trypanosoma brucei brucei and Crithidia fasciculata, we have found that aromatic amino
34 ities are present in a cytosolic fraction of Crithidia fasciculata, which is easily grown at room tem