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1 1 419 bp (plus about 2000 bp of undetermined telomeric sequences).
2  G-quadruplex, and (iii) an i-motif of human telomeric sequence.
3 specificity to the hairpin form of the viral telomeric sequence.
4 e-stranded DNA as well as internal tracts of telomeric sequence.
5  flexibility of a model single-stranded long telomeric sequence.
6 nteractions and DNA repair within the GGTTAC telomeric sequence.
7 les stabilize the G4DNA derived from a human telomeric sequence.
8 brid G-quadruplex structures formed by human telomeric sequence.
9 fic manner, and discriminates against RNA of telomeric sequence.
10 er extent than the quadruplex DNA of a human telomeric sequence.
11  the interface between the duplex and the 3' telomeric sequence.
12 n]pyrrole, the more strongly it binds to the telomeric sequence.
13 ely without polymerase-mediated extension of telomeric sequence.
14  exchanges between often imperfectly matched telomeric sequences.
15 elomerase templating region in vivo with non-telomeric sequences.
16 forms of several oligonucleotides containing telomeric sequences.
17 d DNA damage foci and loss or duplication of telomeric sequences.
18 ation events between different DNAs at their telomeric sequences.
19 ity of telomerase to elongate completely non-telomeric sequences.
20 e non-replicative DNA rings containing yeast telomeric sequences.
21 of labile mRNAs, 5'- and 3'-splice sites and telomeric sequences.
22 vely binds to and protects otherwise exposed telomeric sequences.
23 s), ultimately leading to stochastic loss of telomeric sequences.
24  Sessea (family Solanaceae) lack known plant telomeric sequences.
25  a variety of DNA structures without or with telomeric sequences.
26 r Y. lipolytica telomeres but also for human telomeric sequences.
27 lytica (GGGTTAGTCA)(n) and human (TTAGGG)(n) telomeric sequences.
28 ion nor in vitro DNA replication through non-telomeric sequences.
29 rity of known naturally occurring eukaryotic telomeric sequences.
30 bility by repressing recombination involving telomeric sequences.
31 enome against recombination events involving telomeric sequences.
32 tion fork progression through the repetitive telomeric sequences.
33 a cells that lack telomerase or have altered telomeric sequences.
34 recombination events and accelerated loss of telomeric sequences.
35 ramolecular G-quadruplex formed by the human telomeric sequence 5'-(GGTTAG)(5)-3', and that inhibits
36 quence was removed on addition of Sch. pombe telomeric sequence, a process similar to that described
37 genomic stability in addition to maintaining telomeric sequences above a critical length.
38                      In both structures, the telomeric sequence adopts an intramolecular quadruplex s
39 uplex formed by the 22-mer four-repeat human telomeric sequence AG3(TTAG3)3 and (ii) the intermolecul
40 ic effect on its affinity toward the cognate telomeric sequence, alleviating the need for homodimeriz
41                      How these proteins find telomeric sequences among a genome of billions of base p
42 s that result in an increase in HR between a telomeric sequence and a more internal sequence, which n
43 uctures, including those formed in the human telomeric sequence and in the promoter regions of bcl-2
44 ormation with effective packing in the human telomeric sequence and provide important implications fo
45 replication fork pause was specific to yeast telomeric sequence and was independent of the Sir and Ri
46 demonstrated that TbPolIE is associated with telomeric sequences and here we show that RNAi-mediated
47 MECs emerge from senescence, exhibit eroding telomeric sequences and ultimately enter telomere-based
48 mpassing long tracts of alpha satellite DNA, telomeric sequences, and the human hypoxanthine phosphor
49 d DNA-DNA bridging (trans-interactions) in a telomeric sequence- and length-dependent manner.
50 rom degradation in a CDC13-dependent manner, telomeric sequences are added efficiently, and addition
51  major conformations in K(+) solution, human telomeric sequences are always in equilibrium between Hy
52  have implications for current models of how telomeric sequences are lost in normal somatic cells and
53                                   Repetitive telomeric sequences are maintained by telomerase, a ribo
54                    Short, repetitive, G-rich telomeric sequences are synthesized by telomerase, a rib
55 x known as shelterin prevents recognition of telomeric sequences as sites of DNA damage.
56 uadruplex structures formed within the human telomeric sequence, as well as the effects of sequence a
57 ric DNA primers that carried one repeat of a telomeric sequence at various positions upstream of a no
58 overhangs, blunt ends or 3' termini with non-telomeric sequences at the junction are deficient in loo
59 ded DNA (ssDNA) containing the Chlamydomonas telomeric sequence but not the RNA containing the cognat
60 emplate containing four repeats of the human telomeric sequence by stabilizing the RNA G-quadruplex s
61 enzymes, efficiently extended completely non-telomeric sequences by positioning the 3' terminus at a
62 itically important for the proper capping of telomeric sequences by shelterin.
63            We show that a three-repeat human telomeric sequence can also associate with a single-repe
64   Formation of the G-quadruplex in the human telomeric sequence can inhibit the activity of telomeras
65 ll dividing cells are subject to the loss of telomeric sequences, cells with long proliferative lifes
66 ential lies in overcoming the steady loss of telomeric sequence commonly referred to as the 'end-repl
67  selectively target sequence variants of the telomeric sequences containing adenine-to-thymine mutati
68  exhibited a strong preference for Tg in the telomeric sequence context.
69 d enhanced glycosylase activity on Gh in the telomeric sequence context.
70 ic G-quadruplex formed by the Oxytricha nova telomeric sequence d(G(4)T(4)G(4)) with a peptide nuclei
71 demonstrate by NMR that the two-repeat human telomeric sequence d(TAGGGTTAGGGT) can form both paralle
72 mplate consisting of 10 repeats of the human telomeric sequence d(TTAGGG) and deoxy- and ribonucleosi
73                                    The human telomeric sequence d[T(2)AG(3)](4) has been demonstrated
74  in particular, that produced from the human telomeric sequence d[T(2)AG(3)](4).
75  of a misfolded G-quadruplex in a particular telomeric sequence decreases with an increase in the loo
76 the same assay, we differentiate 4q from 10q telomeric sequences, determine A/B haplotype, identify p
77 didates, we have targeted a 24-nt G4-forming telomeric sequence employing a receptor-based virtual sc
78 short region of the immediately adjacent non-telomeric sequence, exist in two distinct types of chrom
79 al changes are also observed with the duplex telomeric sequence from the Oxytricha species.
80 mobilization; mutant Rap1p binding sites and telomeric sequences from other organisms were not suffic
81 art because the perfect repetitive nature of telomeric sequence hampers in situ detection of telomere
82 ilization of DNA G-quadruplexes in the human telomeric sequence have been shown to inhibit the activi
83                                              Telomeric sequences have been translocated to the centro
84                             The guanine-rich telomeric sequences have the ability to form G-quadruple
85 his suggests that as hTRF2 recruits hRap1 to telomeric sequences, hRap1 alters the affinity of hTRF2
86 ring was diminished by addition of competing telomeric sequences, implicating a role for an as yet un
87 adruplex structure formed by a variant human telomeric sequence in K(+) solution.
88 uplex formed in a native, non-modified human telomeric sequence in K(+) solution.
89 we report the folding structure of the human telomeric sequence in K+ solution determined by NMR.
90  rate constant was 2-fold lower for the same telomeric sequence in the duplex form ((3.0 +/- 1.3) x 1
91  stimulation is dependent on the presence of telomeric sequence in the duplex regions of the substrat
92 d serve to hold the genomic subtelomeric and telomeric sequences in a partially single-stranded confi
93 g that t-loops can also form at interstitial telomeric sequences in a TRF2-dependent manner, forming
94 een confounded by the underrepresentation of telomeric sequences in standard libraries.
95 erase adds telomeric repeats directly to non-telomeric sequences in Tetrahymena, forming de novo telo
96  retention of G.G pairing is specific to the telomeric sequence incorporating the 5' leading sequence
97 when it was adjacent to an internal tract of telomeric sequence, indicating that Cdc13p binding was t
98 nvolved in mismatch repair (MMR), suppresses telomeric sequence insertion (TSI) at intra-chromosomal
99 an also associate with a single-repeat human telomeric sequence into a structure with the same topolo
100                      An insertion of a 49-bp telomeric sequence into the coding region of HIS4 strong
101 umor samples contain somatic integrations of telomeric sequences into non-telomeric DNA.
102 ecombination hotspot created by insertion of telomeric sequences into the region upstream of HIS4.
103                                              Telomeric sequences investigated include the Oxytricha 3
104 ng of HJs with a telomeric center or lacking telomeric sequence is unaffected.
105  hRap1 are in a complex, its affinity for ds telomeric sequences is 2-fold higher than TRF2 alone and
106 rate that TRF2 association with interstitial telomeric sequences is stabilized by co-localization wit
107 cated reverse transcriptase that synthesizes telomeric sequences, is strongly associated with cancer,
108 telomere becomes dysfunctional, the terminal telomeric sequence itself determines the fate of that te
109                                 Interstitial telomeric sequences (ITSs) are present in many eukaryoti
110           Aberrant formation of interstitial telomeric sequences (ITSs) promotes genome instabilities
111 ylation extends 1 to 2 kbp from Interstitial Telomeric Sequences (ITSs) that abut or are very near to
112 ns within chromosomes, known as interstitial telomeric sequences (ITSs).
113 ide, which base-pairs near the 5' end of the telomeric sequence, leaving a telomerase-extendable 3' t
114 ic chromosomes that may arise as a result of telomeric sequence loss.
115                                       Hence, telomeric sequences may have evolved to facilitate their
116 summary of recent research performed on long telomeric sequences, nominally defined as those that can
117 inum drug cisplatin, which targets the human telomeric sequence nonspecifically, the platinum-interca
118 of conventional DNA synthesis, a net loss of telomeric sequences occurs at each cell division.
119  Mb were assembled, including 4 contigs with telomeric sequences on both ends and an additional 8 con
120 n both ends and an additional 8 contigs with telomeric sequences on either the 5' or 3' end.
121 me integrity through synthesis of repetitive telomeric sequences on the ends of eukaryotic chromosome
122 e budding yeast Cdc13p binds single-stranded telomeric sequences, prevents lethal degradation of chro
123                                       G-rich telomeric sequences readily form structures stabilized b
124                                          The telomeric sequence repeats at the ends of eukaryotic chr
125 yme that maintains telomere length by adding telomeric sequence repeats onto chromosome ends.
126 yme that maintains telomere length by adding telomeric sequence repeats onto chromosome ends.
127 rase is a ribonucleoprotein enzyme that adds telomeric sequence repeats to the ends of linear chromos
128 ized DNA and plasmids containing Histoplasma telomeric sequences showed the greatest transformation e
129                                          The telomeric sequence shows intrinsic structure polymorphis
130 erin, fission yeast shelterin is composed of telomeric sequence-specific double- and single-stranded
131 ted reduced activity on a more physiological telomeric-sequence substrate.
132                                       Longer telomeric sequences, such as TTAGGGTT, TTAGGGTTA, and TA
133         Sgs1p efficiently unwinds G-G paired telomeric sequences, suggesting that one function of Sgs
134  single-stranded representative of the yeast telomeric sequence [Tel11, d(GTGTGGGTGTG)] with a 3 pM a
135 dominant conformation for the extended 26 nt telomeric sequence Tel26 in the presence of K+, regardle
136  cancer cells causes incorporation of mutant telomeric sequences, telomere uncapping, and initiation
137                             While all mutant telomeric sequences tested induced heterodicentric chrom
138                                 The pause at telomeric sequence TG(1-3) repeats was stronger at the t
139 h unprecedented transition dynamics in human telomeric sequences that contain four to eight TTAGGG re
140 tory sequences show striking similarities to telomeric sequences that form diverse G-quartet structur
141 iliense and L. carrikeri showed interstitial telomeric sequences that probably resulted from expansio
142 te folds back and hybridizes with downstream telomeric sequence to form a t loop that is stable in th
143             Telomerase adds a hexonucleotide telomeric sequence to the chromosomal ends during replic
144                              Addition of non-telomeric sequences to the distal portion of a 3' overha
145 cer cells to evade cell senescence by adding telomeric sequences to the ends of chromosomes.
146 r containing two tandem repeats of the human telomeric sequence (TTAGGG) into di- and tetrameric G-qu
147 in the GGG triplet found in the G-rich human telomeric sequence (TTAGGG), making telomeres highly sus
148  in cancer and aging has made the repetitive telomeric sequences (TTAGGG repeats) and the G-quadruple
149 nce for the presence of the Arabidopsis-type telomeric sequence (TTTAGGG)n at the chromosome termini
150 nsfer with optical tweezers to measure human telomeric sequences under tension.
151 mposed of a heterogeneous mixture of GT-rich telomeric sequence, unlike in higher eukaryotes which ha
152 icity, we studied five and six repeats human telomeric sequence using a combination of single molecul
153 of a peptide nucleic acid probe specific for telomeric sequence was evaluated.
154                            Much of the human telomeric sequence was removed on addition of Sch. pombe
155                Direct repeats of Arabidopsis telomeric sequence were constructed to test telomere-med
156 trast, chromosomal end fusions that retained telomeric sequence were observed in nontransformed DNA-P
157                Two constructs with 2.6 kb of telomeric sequence were used to transform maize immature
158 A fragments composed solely of mitochondrial telomeric sequences were detected and their properties w
159                                  The loss of telomeric sequences with each cell division eventually i
160 f chromosomes in ALT cells contain canonical telomeric sequences with the same terminus bias (-ATC) o
161 mportantly, WRN's specificity for the G-rich telomeric sequence within this precise structural contex
162 s improved 500-fold by the addition of yeast telomeric sequences within the T-DNA sequence.
163 ly be detected in the specifically truncated telomeric sequences without any 5'-flanking residues, ou
164 ng and both factors bind along their cognate telomeric sequences without showing strong cooperative i

 
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