戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

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 ulting from rapid binding of the promoter to T7 RNA polymerase.
2 vitro run-off RNA synthesis is bacteriophage T7 RNA polymerase.
3 (Gly) to glyQS leader RNA generated by phage T7 RNA polymerase.
4 stream of -17 in transcription regulation of T7 RNA polymerase.
5 tochondria that we had engineered to contain T7 RNA polymerase.
6 h transcription by Escherichia coli and then T7 RNA polymerase.
7  siRNAs are siRNAs produced by bacteriophage T7 RNA polymerase.
8 the second resembles the specificity loop of T7 RNA polymerase.
9 nscription under the T7 class II promoter by T7 RNA polymerase.
10 anscription by both RNA polymerase II and by T7 RNA polymerase.
11 cultivated with human cells transfected with T7 RNA polymerase.
12  range of temperature and salinity than does T7 RNA polymerase.
13 ressed in the cytoplasm of cultured cells by T7 RNA polymerase.
14 or transcription of nucleosomal templates by T7 RNA polymerase.
15  in baby hamster kidney cells that expressed T7 RNA polymerase.
16 a new part for this function: a split intein T7 RNA polymerase.
17 ed antibody raised against the C-terminus of T7 RNA polymerase.
18 ngent for Syn5 RNA polymerase as compared to T7 RNA polymerase.
19 us locations within the promoter element for T7 RNA polymerase.
20 increase in fluorescence upon binding to the T7 RNA polymerase.
21 g low concentrations of ribonucleotides than T7 RNA polymerase.
22  in which we repositioned gene 1, coding for T7 RNA polymerase.
23 inant vaccinia virus (MVA-T7) that expressed T7 RNA polymerase.
24  understand the interaction of promoter with T7 RNA polymerase.
25 se is 24 degrees C, much lower than that for T7 RNA polymerase.
26 scherichia coli using pTara as the source of T7 RNA polymerase.
27 y kidney cells that constitutively expressed T7 RNA polymerase.
28 with a vaccinia virus recombinant expressing T7 RNA polymerase.
29 hymena group I intron using a mutant form of T7 RNA polymerase.
30 with a vaccinia virus recombinant expressing T7 RNA polymerase.
31 ro transcription of linearized plasmids with T7 RNA polymerase.
32 in the cytoplasm of mouse OST7-1 cells using T7 RNA polymerase.
33 rmediates during transcription initiation by T7 RNA polymerase.
34  of the mtRNAP closely resembles that of the T7 RNA polymerase.
35  BSRT7-5 cells, which constitutively express T7 RNA polymerase.
36 ducing RNA transcripts of various lengths by T7 RNA polymerase.
37 es by in vitro transcription reactions using T7 RNA polymerase.
38 initially transcribing abortive complexes in T7 RNA polymerase.
39                          We demonstrate that T7 RNA polymerase accepts this fluorescent ribonucleosid
40 placing the template strand correctly in the T7 RNA polymerase active site upon promoter melting for
41 nucleic acid scaffolds that, when mixed with T7 RNA polymerase, allow the formation of functional tra
42 thesis using in vitro transcription by phage T7 RNA polymerase allows preparation of milligram quanti
43 protein expression 5- to 10-fold compared to T7 RNA polymerase alone while enhancing reovirus rescue
44 wnian motion and transcription elongation of T7 RNA polymerase along aligned DNA molecules bound to s
45 T7 gene 3.5 that affect its interaction with T7 RNA polymerase, also reduce the interference with T7
46                             Transcription by T7 RNA polymerase alters the folding pathway of both RNA
47  5' end of the RNA transcript or SMART) with T7 RNA polymerase amplification.
48 l by combining exponential (PCR) and linear (T7 RNA polymerase) amplification.
49              These catalytic properties make T7 RNA polymerase an ideal tool for synthesizing large f
50                                        Using T7 RNA polymerase and a cloned template containing the r
51  and RNA-primed DNA "bubble" constructs with T7 RNA polymerase and by initiating transcription at pro
52 ould be generated following transcription by T7 RNA polymerase and cleavage by hepatitis delta virus
53 ned protein systems that minimally contained T7 RNA polymerase and DNA gyrase.
54 cs between single molecules of bacteriophage T7 RNA polymerase and DNA, as a function of tension.
55 rminator protein (Reb1p) was unable to block T7 RNA polymerase and E. coli DnaB helicase.
56 ugates inhibited transcription elongation by T7 RNA polymerase and eukaryotic RNA polymerase II from
57                                  Here we use T7 RNA polymerase and exonuclease III as probes to obtai
58 ese data show that O(6)-meG partially blocks T7 RNA polymerase and human RNA polymerase II elongation
59 ified O(6)-meG DNA template by bacteriophage T7 RNA polymerase and human RNA polymerase II.
60           Bacteriophage T7 lysozyme binds to T7 RNA polymerase and inhibits transcription initiation
61 an layer of the cell wall, but it also binds T7 RNA polymerase and inhibits transcription, and it sti
62        8azaGTP is an efficient substrate for T7 RNA polymerase and is incorporated specifically oppos
63                            The bacteriophage T7 RNA polymerase and its promoters were used in a model
64  of DNA templates, in vitro transcription by T7 RNA polymerase and kit-based purification provides a
65 d cross-links on transcription elongation by T7 RNA polymerase and mammalian RNA polymerase II.
66  their effect on transcription elongation by T7 RNA polymerase and mammalian RNA polymerase II.
67            C3P3, a fusion protein containing T7 RNA polymerase and NP868R, was found to increase prot
68 was due to a combination of mutations in the T7 RNA polymerase and other genes expressed at the same
69  of the analogues is readily incorporated by T7 RNA polymerase and produces fully active transcripts
70 control the expression of both bacteriophage T7 RNA polymerase and recombinant gene(s) of interest.
71 hymine glycol on transcription elongation by T7 RNA polymerase and RNA polymerase II from rat liver.
72                                              T7 RNA polymerase and site-specifically platinated DNA t
73 scription system was applied, which utilizes T7 RNA polymerase and template DNAs that are either mode
74 d d5SICS:dNaM are selectively transcribed by T7 RNA polymerase and that the efficiency of d5SICS:dNaM
75 e (nA) and 2-thiouracil (sU) are taken up by T7 RNA polymerase and that the resulting RNA possesses r
76 atch and dialysis mode) under the control of T7 RNA polymerase and to other environments where transc
77              Transcription of RNA pools with T7 RNA polymerase and UNH(2) or USH occurred with effici
78 xtracted from these cells was amplified with T7 RNA polymerase and used to hybridize a microarray con
79 tude larger binding constant between DNA and T7 RNA polymerase, and five to six times larger rate con
80  cap analogue was an efficient substrate for T7 RNA polymerase, and the mRNA transcribed, with a poly
81 scription substrate for Escherichia coli and T7 RNA polymerases, and yeast RNA polymerase III.
82 d strand blocked transcription elongation by T7 RNA polymerase approximately 50% of the time but did
83 ter linkages; both Klenow DNA polymerase and T7 RNA polymerase are found to synthesize complementary
84 ng in vitro transcription of longer repeats, T7 RNA polymerase arrests in the promoter distal end of
85  experimental system that uses bacteriophage T7 RNA polymerase as a probe for aspects of nucleosome t
86 he case for phage polymerases, as used here (T7 RNA polymerase), as well as RNA polymerases in bacter
87 etic studies, we propose that a fast form of T7 RNA polymerase binds promoter double-stranded DNA by
88 y shown to increase the thermal tolerance of T7 RNA polymerase can increase the activity of mutants w
89  with a biotin tag, have been prepared using T7 RNA polymerase-catalyzed transcription of synthetic D
90      We determined the crystal structures of T7 RNA polymerase complexes captured during the de novo
91     Transcription initiation as catalyzed by T7 RNA polymerase consists primarily of promoter binding
92                                        Phage T7 RNA polymerase contains within its single polypeptide
93 rated a fusion protein of the mouse CTD with T7 RNA polymerase (CTD-T7 RNAP).
94 in the thumb subdomain (residues 335-408) of T7 RNA polymerase decrease elongation complex stability
95  from the initial, promoter-bound complex of T7 RNA polymerase describes the very beginning of the in
96 hypernegative supercoiling of plasmid DNA by T7 RNA polymerase did not require anchoring of DNA to th
97 nst a d(tC-A) base pair only by factors <10, T7 RNA polymerase discriminates against tC-A base pair f
98 Based on the recent crystal structure of the T7 RNA polymerase-DNA complex, we propose that the large
99                                  Remarkably, T7 RNA polymerase does not incorporate tCTP with the sam
100                       We established an RVFV T7 RNA polymerase-driven minigenome system in which T7 R
101 M1 was expressed by using the vaccinia virus T7 RNA polymerase-driven overexpression system, in our n
102                             We established a T7 RNA polymerase-driven reverse genetics system to resc
103 also made in vivo in uninfected cells when a T7 RNA polymerase-driven transient-transfection system w
104 ady-state conditions and also transcribed by T7 RNA polymerase efficiently in either direction.
105                                              T7 RNA polymerase elongates RNA at a relatively high rat
106  slippage synthesis, this study reveals that T7 RNA polymerase elongation complexes containing only a
107               Furthermore, NEP and the phage T7 RNA polymerase exhibit similar sensitivity to inhibit
108               Viral RNAs were transcribed by T7 RNA polymerase expressed from recombinant vaccinia vi
109 d in molecular biology applications that use T7 RNA polymerase for in vitro transcription.
110 cription, T7 lysozyme, does not compete with T7 RNA polymerase for RNA cross-linking, implying that t
111 initiation by affecting both the affinity of T7 RNA polymerase for the promoter and the efficiency of
112    During the early stages of transcription, T7 RNA polymerase forms an unstable initiation complex t
113 polymerase-driven minigenome system in which T7 RNA polymerase from an expression plasmid drove expre
114 e sliding and transcription by bacteriophage T7 RNA polymerase from the nucleosomal template, but not
115 tion of the nontemplate strand on release of T7 RNA polymerase from the T7 promoter.
116 e constructed in which the ecdysone promoter-T7 RNA polymerase gene had been integrated intact, as de
117 here that the pET system, in which the phage T7 RNA polymerase gene is expressed via lac operon contr
118 ible and glucose-repressible expression of a T7 RNA polymerase gene that has been integrated with an
119 , in which a lambdaDE3 prophage containing a T7 RNA polymerase gene under the control of lacUV5 promo
120           To assay late gene expression, the T7 RNA polymerase gene was inserted into the genome of t
121                   Independent populations of T7 RNA polymerase genes were subjected to one of two sel
122                In transcription studies with T7 RNA polymerase, H3 and H4 were transferred to the nas
123 n alternative and facile delivery system for T7 RNA polymerase has been devised and constructed.
124 hat the high-resolution crystal structure of T7 RNA polymerase has been solved.
125              This biotin-PC GMP, accepted by T7 RNA polymerase, has been used to transcribe RNAs rang
126         Recent studies in the single subunit T7 RNA polymerase have argued against scrunching as the
127 lve non-equivalent mechanisms, as mutants of T7 RNA polymerase have been identified that fail to reco
128                   Over the years, a panel of T7 RNA polymerases have been designed or evolved to acce
129 hnique, termed immuno-detection amplified by T7 RNA polymerase (IDAT) that is capable of monitoring p
130     With the linear amplification ability of T7 RNA polymerase, IDAT represents a significant improve
131 the present study the gene for bacteriophage T7 RNA polymerase, implanted with a eukaryotic nuclear l
132                      The structures of phage T7 RNA polymerase in an elongation phase substrate compl
133 As of PaV RNAs 1 and 2 were cotranscribed by T7 RNA polymerase in baby hamster kidney cells that expr
134 a single protein having the expected size of T7 RNA polymerase in immunoblots of cell extracts probed
135 rigins contain T7 promoters, but the role of T7 RNA polymerase in initiating replication is not under
136  These results highlight the malleability of T7 RNA polymerase in recognizing its promoter element an
137 nstrates that halted elongation complexes of T7 RNA polymerase in the absence of termination signals
138 nucleosomes, and transcription was done with T7 RNA polymerase in the presence of a negatively coiled
139                  Transcription was done with T7 RNA polymerase in the presence of E. coli topoisomera
140 sphate (tCTP) and tested it as substrate for T7 RNA polymerase in transcription reactions, a convenie
141 a coli DNA replication and DnaB helicase and T7 RNA polymerase in vitro in both orientations.
142  the polyprotein and transfected the derived T7 RNA polymerase in vitro transcripts into FRhK-4 cells
143 oncentration, Hlp represses transcription by T7 RNA polymerase in vitro whereas the individual N- and
144 ffects of this structure on transcription by T7 RNA polymerase in vitro.
145 ient, completely inhibiting transcription by T7 RNA polymerase in vitro.
146 this (CG)(14) sequence on transcription with T7 RNA polymerase in vitro.
147  as in defined transcription reactions using T7 RNA polymerase in vitro.
148  be exclusively transcribed by bacteriophage T7 RNA polymerase in vivo.
149  current study strongly supports a model for T7 RNA polymerase in which initial bubble collapse from
150                                            A T7 RNA polymerase in which Tyr639 is mutated to Phe read
151                 When transcribing a guanine, T7 RNA polymerase incorporates tCTP with 2-fold higher c
152                                     Further, T7 RNA polymerase incorporates ZTP opposite its Watson-C
153 here that transcription by the bacteriophage T7 RNA polymerase increases the deamination of cytosine
154 ce with similar kinetics upon binding to the T7 RNA polymerase, indicating that the TATA sequence bec
155                        Crystal structures of T7 RNA polymerase initiation and elongation complexes ha
156                          It is proposed that T7 RNA polymerase interacts directly with the Hoogsteen
157                                    We divide T7 RNA polymerase into two expression domains and fuse e
158                                              T7 RNA polymerase is an excellent candidate for studying
159                                              T7 RNA polymerase is known to induce bending of its prom
160                                              T7 RNA polymerase is one of the simplest RNA polymerases
161 In contrast, nascent pre-mRNA synthesized by T7 RNA polymerase is quantitatively assembled into the n
162                                Bacteriophage T7 RNA polymerase is the best-characterized member of a
163                                        Phage T7 RNA polymerase is the only DNA-dependent RNA polymera
164  is conjugated to an antibody (Ab), and then T7 RNA polymerase is used to amplify RNA from the double
165                   The fastidious behavior of T7 RNA polymerase limits the incorporation of synthetic
166                        Here we show by using T7 RNA polymerase-mediated production of PV genomic RNA,
167                                              T7 RNA polymerase mutants that exhibit reduced elongatio
168 ng a modified vaccinia virus which expresses T7 RNA polymerase (MVA-T7).
169 accinia virus MVA encoding the bacteriophage T7 RNA polymerase (MVA/T7).
170 wing expression in a modified vaccinia virus/T7 RNA polymerase (MVA/T7RP) system.
171 We also observe binding and transcription by T7 RNA polymerases on single combed T7 DNA molecules wit
172 removed from RNA substrates transcribed from T7 RNA polymerase or delivered directly to the cytoplasm
173 ally inhibited DNA transcription mediated by T7 RNA polymerase or human RNA polymerase II in vitro an
174 DNA transcription mediated by single-subunit T7 RNA polymerase or multisubunit human RNA polymerase I
175 ing transcription mediated by single-subunit T7 RNA polymerase or multisubunit human RNA polymerase I
176  to examine the fidelity of transcription by T7 RNA polymerase past an adenine residue adducted at th
177            Time-resolved characterization of T7 RNA polymerase pausing and terminating at a class II
178                             The structure of T7 RNA polymerase presented here differs significantly f
179                                              T7 RNA polymerase presents a very simple model system fo
180  reverse transcription with oligo(dT) with a T7 RNA polymerase promoter (T7dT) on the 5' end, and sub
181 y assembling five cDNA fragments between the T7 RNA polymerase promoter and the autocatalytic hepatit
182 st, capsid did not inhibit expression from a T7 RNA polymerase promoter construct, suggesting that th
183 ntrinsic and polymerase-induced bends in the T7 RNA polymerase promoter DNA.
184                                          The T7 RNA polymerase promoter has been proposed to contain
185 l) contains a non-functional single-stranded T7 RNA polymerase promoter sequence.
186  PLP-1 domain in Escherichia coli by using a T7 RNA polymerase promoter system or as a maltose-bindin
187  plasmid vector directly downstream from the T7 RNA polymerase promoter, and capped RNA transcripts d
188 s NP, P, and L proteins under control of the T7 RNA polymerase promoter, were transfected into A549 c
189         These results suggested that, in the T7 RNA polymerase-promoter complex, the polymerase molec
190 ase of the T7 promoter is inhibited when the T7 RNA polymerase-promoter interaction is strengthened.
191 that open complex formation in bacteriophage T7 RNA polymerase:promoter binary complexes is thermodyn
192 specific stabilizing interactions, of the 17 T7 RNA polymerase promoters in the phage genome, 15 begi
193 translated in HeLa cells when transcribed by T7 RNA polymerase provided by a recombinant vaccinia vir
194 ed from cotransfected plasmids driven by the T7 RNA polymerase provided by the recombinant vaccinia v
195 e synthesized by in vitro transcription with T7 RNA polymerase, providing an economical alternative t
196                                              T7 RNA polymerase recognizes a small promoter, binds DNA
197                                We found that T7 RNA polymerase recognizes NTPalphaSe Sp diastereomers
198 mid with pTara provides a low-cost method of T7 RNA polymerase-regulated expression that can be fine-
199 o I, bcTopo IIIalpha), have been cloned into T7 RNA polymerase-regulated plasmid expression vectors a
200                                              T7 RNA polymerase requires a double-stranded DNA promote
201 ins of AMPV/CO, into cells stably expressing T7 RNA polymerase resulted in the recovery of infectious
202 nscription complexes formed by bacteriophage T7 RNA polymerase reveal a nucleotide-addition cycle dri
203             Transcription footprinting using T7 RNA polymerase revealed major single-base damage site
204           Bacteriophage T7 lysozyme binds to T7 RNA polymerase (RNAP) and regulates its transcription
205             We have examined the behavior of T7 RNA polymerase (RNAP) at a set of promoter variants h
206 orm a functional open complex, bacteriophage T7 RNA polymerase (RNAP) binds to its promoter DNA and i
207   Recent work showed that the single-subunit T7 RNA polymerase (RNAP) can generate misincorporation e
208                  The region in bacteriophage T7 RNA polymerase (RNAP) comprising residues 421-425 con
209                      The high specificity of T7 RNA polymerase (RNAP) for its promoter sequence is me
210                   To initiate transcription, T7 RNA polymerase (RNAP) forms a specific complex with i
211 n vitro transcription of the kan gene by the T7 RNA polymerase (RNAP) in the presence of AID and a ge
212                                              T7 RNA polymerase (RNAP) is able to traverse a variety o
213                      Transcription errors by T7 RNA polymerase (RNAP) may occur as the result of a me
214 We have characterized the roles of the phage T7 RNA polymerase (RNAP) thumb subdomain and the RNA bin
215 stability is a kinetic mechanism that allows T7 RNA polymerase (RNAP) to achieve promoter specificity
216 ted a series of plasmid templates that allow T7 RNA polymerase (RNAP) to be halted at defined interva
217 mplex (EC), the single-subunit bacteriophage T7 RNA polymerase (RNAP) undergoes dramatic conformation
218                       Using PACE, we evolved T7 RNA polymerase (RNAP) variants that recognize a disti
219 omplex (IC) to an elongation complex (EC) in T7 RNA polymerase (RNAP), we used nucleic acid-protein c
220 acts as a partial block to the bacteriophage T7 RNA polymerase (RNAP), which allows nucleotide incorp
221  pausing and/or termination by bacteriophage T7 RNA polymerase (RNAP).
222 leic acid scaffolds of defined sequence with T7 RNA polymerase (RNAP).
223          Yeast mitochondrial (YMt) and phage T7 RNA polymerases (RNAPs) are two divergent representat
224  template that contains promoters for T3 and T7 RNA polymerases (RNAPs) in opposing orientations, and
225  of bound target by quantifying DNA tails by T7 RNA polymerase runoff transcription and real-time pol
226                                              T7 RNA polymerase selectively transcribes T7 genes durin
227  this system, we found that transcription by T7 RNA polymerase strikingly induced the formation of hy
228                            Comparison of the T7 RNA polymerase structure with that of the homologous
229 reted in the context of our revised model of T7 RNA polymerase, suggest a conserved fold.
230 s in mammalian cells were investigated using T7 RNA polymerase-synthesized small interfering RNA and
231                                              T7 RNA polymerase synthesizes, in addition to run-off pr
232    We found that siRNAs synthesized from the T7 RNA polymerase system can trigger a potent induction
233  of transcription in the model bacteriophage T7 RNA polymerase system, the simplest possible reaction
234 n transfer RNAPhe (tRNAPhe) transcribed in a T7 RNA polymerase system.
235                            The structures of T7 RNA polymerase (T7 RNAP) captured in the initiation a
236 nd single guide RNAs (sgRNAs) produced using T7 RNA polymerase (T7 RNAP) efficiently edit the Plasmod
237                           The structure of a T7 RNA polymerase (T7 RNAP) initiation complex captured
238                  Transcription initiation by T7 RNA polymerase (T7 RNAP) is regulated by the specific
239             During transcription initiation, T7 RNA polymerase (T7 RNAP) melts specifically the -4 to
240  in vitro transcription system with purified T7 RNA polymerase (T7 RNAP) or rat liver RNAP II, we cha
241   To address this, we modified bacteriophage T7 RNA polymerase (T7 RNAP) to create a library of trans
242  amide linkage were tested as substrates for T7 RNA polymerase (T7 RNAP) transcription.
243 ake messenger RNA transcripts, bacteriophage T7 RNA polymerase (T7 RNAP) undergoes a transition from
244 sed on co-delivery of mRNA(A64) encoding for T7 RNA polymerase (T7 RNAP) with a T7-driven plasmid, pr
245 l interest, T7 RNA polymerase (T7RP) and the T7 RNA polymerase-T7 lysozyme complex (T7RPL) in forms s
246                                          The T7 RNA polymerase-T7 lysozyme complex regulates phage ge
247     On the basis of their recently described T7 RNA polymerase-T7 promoter crystal structure, Cheetha
248                            Studies of halted T7 RNA polymerase (T7RNAP) elongation complexes (ECs) or
249                   We have used bacteriophage T7 RNA polymerase (T7RNAP) to study the transcriptional
250 al4, (ii) transcription by the bacteriophage T7 RNA polymerase (T7RNAP), and (iii) FLP-mediated site-
251  approaches that may be of general interest, T7 RNA polymerase (T7RP) and the T7 RNA polymerase-T7 ly
252 ubstitute was a more effective substrate for T7 RNA polymerase than 5-(2-mercaptoethyl)uridine tripho
253 otein trans-splicing, yielding a full-length T7 RNA polymerase that can transcribe genes via a T7 pro
254                                  Variants of T7 RNA polymerase that reduce toxicity were constructed
255 ed an unusual type of termination signal for T7 RNA polymerase that requires a conserved 7-base pair
256 re by providing examples of (i) selection of T7 RNA polymerases that recognize orthogonal promoters a
257                                           In T7 RNA polymerase these changes involve refolding and re
258      Unlike the salt-sensitive bacteriophage T7 RNA polymerase, this marine RNA polymerase requires 1
259                                        Using T7 RNA polymerase to explore the transcriptional accessi
260 nt translation of viral transcripts, we used T7 RNA polymerase to express constructs engineered with
261 ence functional) by DNA polymerase, allowing T7 RNA polymerase to generate a target-dependent RNA sig
262      The PCRcDNA was in vitro transcribed by T7 RNA polymerase to generate complementary RNA (cRNA),
263                          Using bacteriophage T7 RNA polymerase to install poly(G) tails on mRNAs tran
264 rt of the upstream binding energy is used by T7 RNA polymerase to melt the downstream initiation regi
265                                 Inability of T7 RNA polymerase to processively transcribe higher euka
266                       We have used the model T7 RNA polymerase to transcribe reconstituted nucleosome
267                           As observed during T7 RNA polymerase transcript elongation, substrate loadi
268 ast 100-fold more efficient than that from a T7 RNA polymerase transcript with the same sequence.
269 ed by these genes were overexpressed using a T7 RNA polymerase transcription (pET102/D-TOPO) system i
270 ese stereoisomers on RNA synthesis, in vitro T7 RNA polymerase transcription assays were performed us
271 the non-template strand reduces the yield of T7 RNA polymerase transcription by more than an order of
272     Here, we photo-cross-linked the RNA in a T7 RNA polymerase transcription complex and mapped a maj
273 aracterize the transitions that occur in the T7 RNA polymerase transcription complex during initiatio
274 ur picture of the functional architecture of T7 RNA polymerase transcription complexes remains incomp
275 e sequences on transcription we have studied T7 RNA polymerase transcription of G-rich sequences in v
276 anslated in vivo after transcription using a T7 RNA polymerase transcription system.
277                              We have studied T7 RNA polymerase transcription through the sequence fro
278                            For bacteriophage T7 RNA polymerase, transcription begins with a marked pr
279                                              T7 RNA polymerase undergoes dramatic structural rearrang
280                     The N-terminal domain of T7 RNA polymerase undergoes large conformational changes
281 ation complex to an elongation complex (EC), T7 RNA polymerase undergoes major conformational changes
282                                Bacteriophage T7 RNA polymerase undergoes major conformational changes
283 ity in a simplified model system, by using a T7 RNA polymerase variant capable of transcribing nuclei
284                     We apply CPR to evolve a T7 RNA polymerase variant that recognizes an orthogonal
285 tem also enables the continuous evolution of T7 RNA polymerase variants capable of initiating transcr
286                                              T7 RNA polymerase was able to bypass all the photoproduc
287                                  The induced T7 RNA polymerase was exclusively localized in the nucle
288                                      A caged T7 RNA polymerase was expressed in cells with an expande
289 quence preference in start site selection by T7 RNA polymerase was investigated by using a series of
290  and open complex formation in bacteriophage T7 RNA polymerase was investigated using 2-aminopurine (
291                Transcription driven by phage T7 RNA polymerase was not regulated by cobalamins, altho
292                                  The induced T7 RNA polymerase was present at numerous punctate foci
293  Here, using a purified in vitro system with T7 RNA polymerase, we show that increased distance betwe
294                                        Using T7 RNA polymerase, we synthesized the hantavirus S segme
295      Both RNA polymerases I and III, but not T7 RNA polymerase, were inhibited by juglone.
296 strate here that the P266L point mutation in T7 RNA polymerase, which shows dramatically reduced abor
297 lular synthesis of the LCMV MG was driven by T7 RNA polymerase whose expression was also mediated by
298 emplate encoding the initial sequence GGGA., T7 RNA polymerase will synthesize a 'ladder' of poly-G R
299              Further, we found that a mutant T7 RNA polymerase with a slower rate of elongation cause
300                       We fluorescently label T7 RNA polymerase with antibodies and use flow to convec

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top