コーパス検索結果 (left1)
通し番号をクリックするとPubMedの該当ページを表示します
1 kDNA decatenation assay indicated that XWL-1-48 signific
2 kDNA synthesis involves release of individual minicircle
3 kDNA, the mitochondrial genome of trypanosomatids, is a
6 binding domain of AEP-1 results in aberrant kDNA structure and reduced cell growth, indicating that
8 poisomerase II interaction (DNA cleavage and kDNA decatenation assays), alongside cytotoxicity tests
10 measured by real-time qPCR: OligoC-TesT and kDNA PCR detected 100% and 99% of positive samples when
11 ries of analogues of the known antiprotozoal kDNA binder 2-((4-(4-((4,5-dihydro-1H-imidazol-3-ium-2-y
14 ins), that neutralize the negatively charged kDNA, thereby affecting the activity of mitochondrial en
16 led assignment of proteins to five classes - kDNA synthesis, site of scission selection, scission, se
17 ecombinant proteins is capable of compacting kDNA networks in vitro and was shown to bind preferentia
18 ciated proteins in organizing and condensing kDNA networks into this disc structure, we have cloned t
19 lear extracts containing Metnase decatenated kDNA more rapidly than those without Metnase, and neutra
20 At later times following TbLOK1 depletion, kDNA was lost and a more drastic alteration in mitochond
24 We compared the decay of kinetoplast DNA (kDNA) and spliced-leader RNA (SL-RNA) in vitro, in vivo,
27 ondrial genome, also called kinetoplast DNA (kDNA) forms an Olympic-ring-like network of interlinked
31 whole linearized minicircle kinetoplast DNA (kDNA) of the Leishmania subgenus Viannia from biopsy lys
32 C-TesT with those of nested kinetoplast DNA (kDNA) PCR, nested internal transcribed spacer 1 (ITS-1)
34 ome of trypanosomes, termed kinetoplast DNA (kDNA), contains thousands of minicircles and dozens of m
36 osome mitochondrial genome, kinetoplast DNA (kDNA), is a massive network of interlocked DNA rings, in
39 ion of RNAi was the loss of kinetoplast DNA (kDNA), the cell's catenated mitochondrial DNA network.
46 library screen for loss of kinetoplast DNA (kDNA), we identified an uncharacterized Trypanosoma bruc
57 the molecular mechanism of compensation for kDNA loss by showing FO-independent generation of the mi
59 ergetically demanding apparatus required for kDNA maintenance and expression serves the production of
63 seven DNA polymerases (pols) are involved in kDNA transactions, including three essential proteins re
65 f type II topoisomerases that participate in kDNA metabolism (we term the T. brucei brucei gene TbTOP
66 sential protein, it plays important roles in kDNA arrangement and replication, as well as in the main
68 intenance and expression of its kinetoplast (kDNA), the mitochondrial genome of this parasite and a p
76 by RNAi there is a striking accumulation of kDNA late theta structure replication intermediates, wit
82 TbPIF8 is positioned on the distal face of kDNA disk and its localization patterns vary with differ
83 cle-dependent changes in the localization of kDNA replication enzymes by combining immunofluorescence
89 their mode of action with diverse methods of kDNA decatenation, DNA-Topo cleavage complex, comet, DNA
95 nterval [CI], 63 to 78%), similar to that of kDNA PCR (72%; 95% CI, 65 to 80%; P = 0.69) but signific
96 ts on replication enzymes, how the timing of kDNA synthesis is controlled during the cell cycle, and
100 In this review, we discuss recent studies on kDNA structure and replication, emphasizing recent devel
102 intricate mitochondrial DNA (kinetoplast or kDNA) in the form of a network of thousands of interlock
103 intricate mitochondrial DNA (kinetoplast or kDNA) of Trypanosoma brucei brucei and related kinetopla
104 ng the mitochondrial genome of the parasite (kDNA), with an accumulation of the protein at or near th
105 To test their validity for quantification, kDNA copy numbers were compared between Leishmania speci
107 degraded more rapidly during treatment than kDNA, and correlated better with microscopic examination
111 TbPOLIB and TbPOLIC localized beside the kDNA where replication occurs, and their knockdown by RN
112 vered p166, a protein localizing between the kDNA and basal body in intact cells and in isolated flag
113 alizes to the region of the cell between the kDNA and the flagellum and purifies with the tripartite
116 localize in two antipodal sites flanking the kDNA during replication, they behave differently at othe
117 e enzyme in two antipodal sites flanking the kDNA, show that a function of this topoisomerase II is t
119 ucture rich in basic proteins that links the kDNA discs during their segregation and is maintained be
122 In Crithidia fasciculata, rotation of the kDNA disk relative to the antipodal attachment sites res
123 nicircles accumulate on opposite ends of the kDNA disk, a pattern that did not suggest kinetoplast mo
125 ent mutants exhibited high compaction of the kDNA network and displayed atypical phenotypes, such as
131 l DNA could be repaired, suggesting that the kDNA in the kinetoplast of trypanosomatids has unique re
133 alizes within the mitochondrion close to the kDNA disk in patterns that vary with the cell cycle.
136 16 shows that p16 is present both within the kDNA disc and in the mitochondrial matrix at opposite ed
138 important when I learned that parasites with kDNA threaten huge populations in underdeveloped tropica