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1 t a time corresponding to duplication of the kinetoplast DNA.
2 oci, and uniparental retention of maxicircle kinetoplast DNA.
3 ce-based genomic library for cells that lose kinetoplast DNA.
4 necropsy material, using probes specific for kinetoplast DNA.
5 mitochondrion, above and below the condensed kinetoplast DNA.
6 c properties that target the minor groove of kinetoplast DNA.
7       One striking phenotype was the loss of kinetoplast DNA after interference with expression of a
8 terference (RNAi) of p38 resulted in loss of kinetoplast DNA and accumulation of a novel free minicir
9 than wild type topo II alpha in decatenating kinetoplast DNA and also exhibits a 2-4-fold decrease in
10 approximately equal distribution of parental kinetoplast DNA between daughter kinetoplasts resulted i
11                        Nae I-43K decatenated kinetoplast DNA containing nicked circles, implying that
12 y ATP-dependent DNA supercoil relaxation and kinetoplast DNA decatenation assays.
13 ocalized in the antipodal sites flanking the kinetoplast DNA disk, as previously shown in C. fascicul
14 xpression of BBP59 inhibited cytokinesis and kinetoplast DNA division, like knockdown of CK1.2.
15  A time-course of DNA synthesis (nuclear and kinetoplast DNA), duplication of organelles (basal body,
16 ctivity as judged by an inability to convert kinetoplast DNA from the catenated to the decatenated fo
17                                              Kinetoplast DNA in African trypanosomes contains a novel
18                                  The loss of kinetoplast DNA in Leishmania tarentolae, which occurs i
19  kinetoplast to photooxidize selectively the kinetoplast DNA is suggested.
20 ondrial genome of Trypanosoma brucei, called kinetoplast DNA, is a network of topologically interlock
21                     We compared the decay of kinetoplast DNA (kDNA) and spliced-leader RNA (SL-RNA) i
22                               By considering kinetoplast DNA (kDNA) as a template for cleavage into t
23 heritance appears uniparental for maxicircle kinetoplast DNA (kDNA) but biparental for minicircle kDN
24 rth: their mitochondrial genome, also called kinetoplast DNA (kDNA) forms an Olympic-ring-like networ
25                                              Kinetoplast DNA (kDNA) is a novel form of mitochondrial
26                                          The kinetoplast DNA (kDNA) is a topologically complex genome
27                                              Kinetoplast DNA (kDNA) is organized into a concatenated
28 ically amplified whole linearized minicircle kinetoplast DNA (kDNA) of the Leishmania subgenus Vianni
29 sitivity of OligoC-TesT with those of nested kinetoplast DNA (kDNA) PCR, nested internal transcribed
30                                The multicopy kinetoplast DNA (kDNA) probes were the most sensitive an
31 mitochondrial genome of trypanosomes, termed kinetoplast DNA (kDNA), contains thousands of minicircle
32                                              Kinetoplast DNA (kDNA), from trypanosomatid mitochondria
33        The trypanosome mitochondrial genome, kinetoplast DNA (kDNA), is a massive network of interloc
34                        This genome, known as kinetoplast DNA (kDNA), is organized as a single, massiv
35 escribed a remarkable DNA structure known as kinetoplast DNA (kDNA), isolated from a parasite.
36 otype upon induction of RNAi was the loss of kinetoplast DNA (kDNA), the cell's catenated mitochondri
37                                              Kinetoplast DNA (kDNA), the form of mitochondrial DNA in
38                                              Kinetoplast DNA (kDNA), the mitochondrial DNA in kinetop
39                                              Kinetoplast DNA (kDNA), the mitochondrial DNA of trypano
40                                              Kinetoplast DNA (kDNA), the trypanosome mitochondrial DN
41                                              Kinetoplast DNA (kDNA), the trypanosome mitochondrial ge
42                                              Kinetoplast DNA (kDNA), the unusual mitochondrial DNA of
43        In an RNAi library screen for loss of kinetoplast DNA (kDNA), we identified an uncharacterized
44 etwork of minicircles and maxicircles called kinetoplast DNA (kDNA).
45 rlocked circular DNA molecules that form the kinetoplast DNA (kDNA).
46 usual features, a mitochondrial DNA known as kinetoplast DNA (kDNA).
47 he ability to unknot (decatenate) and cleave kinetoplast DNA (kDNA).
48 ariable fragments of the Leishmania species' kinetoplast DNA (kDNA).
49                                              Kinetoplast DNAs (kDNAs) are structurally complex circul
50  fit the working hypothesis that the loss of kinetoplast DNA leads to a respiratory defect which then
51       In one cloned cell line with inducible kinetoplast DNA loss, we found that the RNA interference
52  (RNAi) of TbPIF1 causes a growth defect and kinetoplast DNA loss.
53 l genomic complements from both parents, but kinetoplast DNA maxicircles from one parent.
54 mania parasite contains approximately 10,000 kinetoplast DNA minicircles, which are unequally distrib
55 ing the 75 C-terminal amino acids can rescue kinetoplast DNA missegregation but not the lack of ATOM
56  ultimately led to shrinkage and loss of the kinetoplast DNA network and cessation of growth of the c
57 ity found associated with the mitochondrial, kinetoplast DNA network in trypanosomatid protozoa.
58 ed guide RNAs upon segregation of the single kinetoplast DNA network into daughter cells at cell divi
59 tions with respect to the mitochondrial DNA (kinetoplast DNA network) in this organism are strikingly
60 tenation of plasmid DNA, and decatenation of kinetoplast DNA networks.
61     The final disappearance of the stainable kinetoplast DNA occurred at a cell division in which all
62 ween the complex restriction patterns of the kinetoplast DNA of any of the parasites from Timargara c
63                       The mitochondrial DNA (kinetoplast DNA) of the trypanosomatid Crithidia fascicu
64                       The mitochondrial DNA (kinetoplast DNA) of the trypanosomatid Crithidia fascicu
65  of these DNAs has not been possible since a kinetoplast DNA primase has not been available.
66 these results suggest a point of control for kinetoplast DNA replication through the regulation of th
67 tor with genes involved in processes such as kinetoplast DNA replication, mitochondrial mRNA synthesi
68 st and is essential for both cell growth and kinetoplast DNA replication.
69 ial protein, which we term p38, functions in kinetoplast DNA replication.
70 ignificant implications for the mechanism of kinetoplast DNA replication.
71 u were tested with a DNA probe directed at a kinetoplast DNA segment of Trypanosoma cruzi.
72 circles to the network and caused a delay in kinetoplast DNA segregation.
73                                          The kinetoplast DNA sequence of parasitic microorganisms, fo
74                                              Kinetoplast DNA synthesis involves release of minicircle
75                                              Kinetoplast DNA synthesis involves release of minicircle
76                  The selective inhibition of kinetoplast DNA synthesis was caused by a selective loca
77                                       During kinetoplast DNA synthesis, minicircles are released from
78 ed by proteolysis of a helicase; the complex kinetoplast DNA system yields a clear view of how mitoch
79    We evaluated the serum levels of T. cruzi kinetoplast DNA (TckDNA), T. cruzi 18S ribosomal DNA (Tc
80 have an unusual mitochondrial genome, called kinetoplast DNA, that is a giant network containing thou
81                                              Kinetoplast DNA, the mitochondrial DNA of Crithidia fasc
82                                              Kinetoplast DNA, the mitochondrial DNA of trypanosomatid
83                                              Kinetoplast DNA, the trypanosome mitochondrial genome, i
84 reatly enhanced Topo IIalpha decatenation of kinetoplast DNA to relaxed circular forms.
85 g region of the TOP2 gene, which encodes the kinetoplast DNA topoisomerase, and have carried out dele
86  two kinetoplast ribosomal proteins with the kinetoplast DNA was observed by immunofluorescence, sugg
87                                   Leishmania kinetoplast DNA was quantified in whole blood with real-
88  division in which all the remaining visible kinetoplast DNA was retained by one of the daughter cell
89 parasitic heterocyclic dications can have on kinetoplast DNA, we have constructed ligation ladders, w