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1 ribonucleic acid (RNA) backbone catalyzed by ribonuclease H.
2 , plastocyanin, staphylococcal nuclease, and ribonuclease H.
3 ne the folding landscape of Escherichia coli ribonuclease H, a protein well characterized by hydrogen
4                                     Although ribonuclease H activity has long been implicated as a mo
5 ted DNA polymerase activities coupled with a ribonuclease H activity to synthesize a double-stranded
6  DNA 3'-end-directed and RNA 5'-end-directed ribonuclease H activity.
7 to study the stabilities of Escherichia coli ribonuclease H and its variants, both in purified form a
8  cleavage of the RBG mRNA in the presence of ribonuclease H and ODNs of varying association kinetics
9 election by reverse transcriptase-associated ribonuclease H and subsequent removal from nascent (+)-D
10  members of the 5'-3' exonuclease family: T4 ribonuclease H and the N-terminal domain of Thermus aqua
11 ation data collected on the proteins E. coli ribonuclease H and the trimeric E. coli membrane associa
12 nto 4 domains (terminal protein, spacer, rt, ribonuclease H) and each of these can be numbered separa
13 typically uses the S9.6 antibody or inactive ribonuclease H, both requiring a large number of cells w
14  RNA/DNA hybrid could aid in positioning the ribonuclease H catalytic center at the PPT/U3 junction a
15 oligonucleotides and deoxyribonuclease I and ribonuclease H cleavages.
16 all reduction in activity of T. thermophilus ribonuclease H compared to its mesophilic E. coli homolo
17 o F61Y included 3'-PPT insertions suggesting ribonuclease H defect.
18  folding, dimerization and subunit-selective ribonuclease H domain (RH) proteolysis.
19 lambda-Cro repressor, interleukin 8, and the ribonuclease H domain of HIV-1 reverse transcriptase.
20                   Mutations within a cryptic ribonuclease H domain within Argonaute2, as identified b
21 wn how often mutations in the connection and ribonuclease H domains of reverse transcriptase (RT) eme
22 lds, such as Rossmann fold, ferredoxin fold, ribonuclease H fold, and TIM beta/alpha-barrel.
23           TEFM contains two HhH motifs and a Ribonuclease H fold, similar to the nuclear transcriptio
24 ino acid change can convert Escherichia coli ribonuclease H from a three-state folder that populates
25 y essential aspartate to Mg(2+) or Ca(2+) in ribonuclease H from two organisms were computed using um
26                                              Ribonucleases H from organisms that grow at different te
27                                              Ribonucleases H from the thermophilic bacterium Thermus
28 because it is specifically recognized by the ribonuclease H function of HIV reverse transcriptase.
29                                              Ribonucleases H have mostly been implicated in eliminati
30          Our findings demonstrate a role for ribonuclease H in human neurological disease and suggest
31           Mutation analyses and analogies to ribonuclease H indicate that insertion of this glutamate
32 ich act upon DNA.RNA hybrid substrates (e.g. ribonuclease H) is impacted when the hybrids contain pho
33  the native cofactor in many enzymes such as ribonuclease H, its competitor Ca(2+) may also bind to t
34                                              Ribonuclease H-like (RNHL) superfamily, also called the
35 8 candidate gene, and confirmed that loss of Ribonuclease H-Like 1 (RNHL-D1) is responsible for Rht8
36  motif for heterochromatic silencing and for ribonuclease H-like cleavage (slicing) of target message
37 ant, form stable ON/RNA duplexes and support ribonuclease H mediated heteroduplex cleavage, all with
38 strains, and between wild type and different ribonuclease H-mutant genotypes.
39 ence of the free energy of unfolding for two ribonucleases H, one from the mesophile Escherichia coli
40 ificantly larger than derived previously for ribonuclease H or recently, using "meta-analysis" for ub
41                                    Since the ribonuclease H (RH) domain contains an occult cleavage s
42 rse transcriptase (RT) contains a C-terminal ribonuclease H (RH) domain on its p66 subunit that can b
43 ed to allow interaction with residues in the ribonuclease H (RNase H) active site and thumb subdomain
44 e nucleic acid duplex in the vicinity of the ribonuclease H (RNase H) active site.
45  structural elements, the DNA polymerase and ribonuclease H (RNase H) activities of enzymes bearing a
46  (BBNH) inhibits both the DNA polymerase and ribonuclease H (RNase H) activities of the human immunod
47 everse transcriptase (RT) DNA polymerase and ribonuclease H (RNase H) activities reside in spatially
48 tase (RT) coordinates DNA polymerization and ribonuclease H (RNase H) activities using two discrete a
49 he site of T --> F substitution and enhanced ribonuclease H (RNase H) activity approximately 12-13 bp
50 suitable for screening compounds against the ribonuclease H (RNase H) activity of HIV-1 reverse trans
51  of mesoxalic acid, was found to inhibit the ribonuclease H (RNase H) activity of HIV-1 RT under stra
52 7447, was proposed to allosterically inhibit ribonuclease H (RNase H) activity of human immunodeficie
53 e) as potent and selective inhibitors of the ribonuclease H (RNase H) activity of human immunodeficie
54                      RNA degradation via the ribonuclease H (RNase H) activity of human immunodeficie
55 account the possible effects of NNRTI on the ribonuclease H (RNase H) activity of RT, despite recent
56  approach previously used for inhibiting HIV ribonuclease H (RNase H) and integrase strand transfer (
57 se (IN) and reverse transcriptase-associated ribonuclease H (RNase H) are both selective targets for
58 li maltose binding protein (MBP) and E. coli ribonuclease H (RNase H) as our model proteins, we monit
59                                              Ribonuclease H (RNase H) belongs to the nucleotidyl-tran
60                                              Ribonuclease H (RNase H) belongs to the nucleotidyl-tran
61 and approximately 4-9 bp downstream from the ribonuclease H (RNase H) catalytic center.
62                      The PPT is resistant to ribonuclease H (RNase H) cleavage and is used as a prime
63                                              Ribonuclease H (RNase H) cleavages and nucleocapsid prot
64 zing RTs prevents polymerization-independent ribonuclease H (RNase H) cleavages of the donor template
65 DNTP) occupies the interface between the p66 ribonuclease H (RNase H) domain and p51 thumb of human i
66 eolytic attack by HIV-1 protease cleaves the ribonuclease H (RNase H) domain of a single subunit to y
67 (AZT) selected for the Q509L mutation in the ribonuclease H (RNase H) domain of HIV-1 reverse transcr
68 s in the connection subdomain and C-terminal ribonuclease H (RNase H) domain of human immunodeficienc
69 he highly conserved Asp549 of the retroviral ribonuclease H (RNase H) domain were evaluated in the he
70 inant p66 polypeptides containing a modified ribonuclease H (RNase H) domain were purified and evalua
71  associated with both the DNA polymerase and ribonuclease H (RNase H) domains.
72                                 Two types of Ribonuclease H (RNase H) excise ribonucleotides when the
73                                          The ribonuclease H (RNase H) family of enzymes selectively d
74 ng trajectories of ancestral proteins of the ribonuclease H (RNase H) family using ancestral sequence
75 idated reverse transcriptase (RT) associated ribonuclease H (RNase H) for human immunodeficiency viru
76               The well-characterized protein ribonuclease H (RNase H) from Escherichia coli populates
77                                          The ribonuclease H (RNase H) function of the reverse transcr
78 at a site at which the reverse transcriptase ribonuclease H (RNase H) has created a nick or short gap
79 s duplex include the thumb subdomain and the ribonuclease H (RNase H) primer grip, the latter compris
80  (HIV) reverse transcriptase (RT) associated ribonuclease H (RNase H) remains an unvalidated antivira
81        Reverse transcriptase (RT) associated ribonuclease H (RNase H) remains the only virally encode
82  (HIV) reverse transcriptase (RT)-associated ribonuclease H (RNase H) remains the only virally encode
83                                              Ribonuclease H (RNase H) selectively degrades the RNA st
84                          The kinetics of the ribonuclease H (RNase H) surface hydrolysis of RNA-DNA h
85         To remove hybrids, all organisms use ribonuclease H (RNase H) to specifically degrade the RNA
86 -H(epsilon) bond vectors of Escherichia coli ribonuclease H (RNase H) were determined by NMR spin rel
87 ric oligodeoxynucleotide (ODN) libraries and ribonuclease H (RNase H) were used to identify regions o
88  examines a mesophilic phylogenetic clade of ribonuclease H (RNase H), furthering its extensive chara
89 structure of a hybrid duplex in complex with ribonuclease H (RNase H), suggested that this flexibilit
90 INSTIs) that also displayed activity against ribonuclease H (RNase H).
91 associated DNA polymerase, and RT-associated ribonuclease H (RNase H).
92 NA microarrays with either ribonuclease S or ribonuclease H (RNase H).
93                                              Ribonucleases H (RNases H) are endonucleases which cleav
94                                              Ribonucleases H (RNases H) comprise a family of metal-de
95                Previous studies of bacterial ribonucleases H (RNases H) from the thermophile Thermus
96                                     Although ribonucleases H (RNases H) have long been implicated in
97                                          The ribonucleases H (RNases H) of HIV and hepatitis B virus
98                    In general, cells evolved ribonucleases H (RNases H) specialized in the removal of
99 mains and the acquisition of an Archaea-like ribonuclease H (RNH) domain.
100         The reverse transcriptase-associated ribonuclease H (RT/RNase H) domains from the gypsy group
101                Loss-of-function mutations in ribonuclease H, senataxin, and topoisomerase I that reso
102 ed by five alpha-helices that belongs to the ribonuclease H superfamily.
103 synthesis causes an increase in the ratio of ribonuclease H to polymerase activity thereby promoting
104 integrity, and the relative contributions of ribonucleases H to mitigating the negative effects of hy
105 t constitutively express an Escherichia coli ribonuclease H transgene show a marked reduction in RNA/
106      These RNA.DNA hybrids are eliminated by ribonuclease H treatment.
107  the folding process of Thermus thermophilus ribonuclease H using circular dichroism, fluorescence, a
108                       The kinetic folding of ribonuclease H was studied by hydrogen exchange (HX) pul
109 ing intermediate of the Thermus thermophilus ribonuclease H, which forms before the rate-limiting tra
110 s of 6 randomly chosen internal positions in ribonuclease H with Lys and Glu suggest that the ability
111 n (named for the protein piwi) is similar to ribonuclease H, with a conserved active site aspartate-a

 
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