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1 ript found in vegetative cells appears to be monocistronic.
2 icated that each flagellar filament gene was monocistronic.
3  part of a four-gene operon, whereas hvnB is monocistronic.
4 lso indicated that each of the p28 genes was monocistronic.
5         The erpG and erpH genes appear to be monocistronic.
6 n analyses revealed that S. gordonii luxS is monocistronic.
7 alysis revealed that oxyR was expressed as a monocistronic 1-kb mRNA and that dps mRNA was approximat
8                         Transcription of the monocistronic 1.3-kb xylF mRNA is inducible by xylose an
9 that includes both mga and emm12 genes and a monocistronic 1.6-kb mga message.
10 tions revealed that xynB is transcribed as a monocistronic 1.9-kb mRNA.
11 ealed that the engO gene is transcribed as a monocistronic 2.6-kb mRNA.
12 ibited PV UTR-mediated translation from both monocistronic and bicistronic RNAs.
13 a normal 5'-UTR with 16 CGG repeats for both monocistronic and dicistronic (luciferase) reporter cons
14 ocin resistance gene sh-ble as a reporter in monocistronic and dicistronic constructs, and consistent
15                      We designed a series of monocistronic and dicistronic GluR2 cDNA constructs that
16  strain A2 were analyzed in helper-dependent monocistronic and dicistronic minireplicons which were c
17 enetic data, one of the fused transcripts is monocistronic and encodes a bifunctional fusion protein.
18  two classes of mRNA are accumulated, one is monocistronic and encodes Adh alone, the other is dicist
19                   The pycB gene was probably monocistronic and followed by a putative gene of a DNA-b
20 anscriptional analysis showed that PG0352 is monocistronic and is regulated by a sigma70-like promote
21          Thus, it was concluded that gntT is monocistronic and is regulated by two promoters.
22                        The gene, instead, is monocistronic and located within the tra-trb-rep gene cl
23 1 min on the E. coli chromosome; the gene is monocistronic and non-essential for growth.
24 tern of transcription, including alternative monocistronic and polycistronic messages.
25 thermore, the M2-1 protein was shown to bind monocistronic and polycistronic RS virus mRNAs during in
26 ot analysis suggested that the hmuO mRNA was monocistronic and that transcription was heme inducible.
27 oding a thermosensitive gluconate kinase, is monocistronic and transcribed divergently from the idnD-
28                    Most eukaryotic mRNAs are monocistronic and translated by cap-dependent initiation
29                They are translated from nine monocistronic and two bicistronic transcripts whose nati
30 ssentially all eukaryotic cellular mRNAs are monocistronic, and are usually transcribed individually.
31 ct RNA synthetic processes: transcription of monocistronic, capped, and polyadenylated subgenomic mes
32                                Low levels of monocistronic clpP mRNA and accumulation of intron-conta
33 aled that cobB is primarily expressed as two monocistronic cobB mRNAs from two transcription start si
34 ly detected in bacteria transformed with the monocistronic construct RDRP:GFP; expression of the down
35 luding N. europaea, also possess a divergent monocistronic copy of amoC (amoC(3)) of unknown function
36 nents of tonB-exbB-exbD operons and one as a monocistronic copy; all are actively transcribed in ATCC
37 only reduced 2-fold relative to a comparable monocistronic cre gene.
38 similarly as compared to currently available monocistronic CRISPR/Cas9 libraries, with only one vecto
39 entified the transcription start site of the monocistronic dmcA mRNA.
40 tudies, such as promoterless dicistronic and monocistronic DNA and dicistronic RNA tests, are require
41 stronic RNA and promoterless dicistronic and monocistronic DNA assays.
42                                          The monocistronic ES containing the MVAT4 vsg does not inclu
43 t nucleotide sequence changes, although this monocistronic ES undergoes a pattern of base J modificat
44         Some of the rare VSG mRNAs come from monocistronic ESs in which the promoters are situated ab
45 d any significant effect on the synthesis of monocistronic F mRNA or F protein, virus replication, vi
46 n in M-F readthrough mRNA and an increase in monocistronic F mRNA.
47 e transcription from readthrough M-F mRNA to monocistronic F mRNA.
48 on of M-F readthrough mRNA at the expense of monocistronic F mRNA.
49                 Efficient translation of the monocistronic GBV-CAT RNAs required the inclusion of GBV
50                       Extensive searches for monocistronic GCR mRNAs using nuclease mapping and rever
51                       Except for the latter, monocistronic gene annotation was expanded using the abo
52 cate that the S-layer gene is a single-copy, monocistronic gene in C. rectus.
53             Cot alpha, which is encoded by a monocistronic gene, was first detected late in sporulati
54 ed notion that speB is transcribed only as a monocistronic gene.
55 anistic logic of clustering of nonhomologous monocistronic genes in eukaryotes is not immediately obv
56 of the decay of mRNA encoded by seven small, monocistronic genes showed that PNPase was the major enz
57 are duplicated less often in the genome than monocistronic genes.
58 lated parallel evolution from dicistronic to monocistronic genomic form within the family Dicistrovir
59 omosomes in local clusters that also contain monocistronic germline-expressed genes.
60      Proline recognition is conferred by the monocistronic gerVB gene, the presence of which also imp
61 sion was not coupled to the stabilization of monocistronic gfp transcripts in dicistronic reporter li
62 filtrate at the site of inoculation than the monocistronic gp120 DNA vaccine.
63 te proliferative responses compared with the monocistronic gp120 DNA vaccine.
64 equence in the halocin H4 preprotein and the monocistronic halH4 gene have some unusual features.
65 amino acid residues) in both bicistronic and monocistronic HCV cell culture-based (HCVcc) genomes rev
66                                            A monocistronic letE RNA is abundant during the exponentia
67 ed to remove v-cyclin sequences and generate monocistronic LUC transcripts.
68 tion of test sequences containing 3' ss into monocistronic luciferase reporter vectors widely used in
69  the Rep22 virus produced very low levels of monocistronic M and F mRNA, consistent with the M-F read
70         The ccp gene was expressed only as a monocistronic message and induction was only observed af
71 he luxS gene was maximally transcribed, as a monocistronic message, in the early mid-log phase of gro
72 ding frame (ORF) was transcribed as a 7.8 kb monocistronic message.
73 tion indicated that pepO is transcribed as a monocistronic message.
74 on by selectively assembling and translating monocistronic messages derived from different chromosome
75  potential in polycistronic messages than in monocistronic messages in Escherichia coli.
76 indicating that the genes are transcribed as monocistronic messages.
77 the 5' ends of downstream genes, to generate monocistronic messages.
78 ced, during transcription, to produce mature monocistronic messengers.
79 iously undetected due to the short length of monocistronic minigenomes and which is due at least part
80 ription of the inserted downstream gene as a monocistronic mRNA and resulted instead in polymerase re
81 ossibilities could result in expression of a monocistronic mRNA encoding the downstream cistron and f
82 showed that tpx and rbpA were transcribed as monocistronic mRNA species or as a bicistronic operon.
83                           rpsO mRNA, a small monocistronic mRNA that encodes ribosomal protein S15, w
84 psO gene specifies a small (388-nucleotide), monocistronic mRNA that encodes ribosomal protein S15.
85 tion, expression of the additional gene as a monocistronic mRNA was suppressed by mutations at the en
86  more than one polypeptide from an otherwise monocistronic mRNA, and can restore expression of polype
87 A and that ahpC also was present as a 0.6-kb monocistronic mRNA.
88 B was transcribed as an approximately 1.6-kb monocistronic mRNA.
89 so enhance translation in the 5' leader of a monocistronic mRNA.
90 tated by intracellular metabolic labeling of monocistronic mRNAs and the dicistronic readthrough RNAs
91 g polycistronic pre-mRNAs are processed into monocistronic mRNAs by conventional 3' end formation, cl
92                   Using both bicistronic and monocistronic mRNAs containing the c- myc 5' UTR, we dem
93  acid starvation also induced translation of monocistronic mRNAs containing the cat-1 5'-leader, in a
94 NA regulons ensure coordinated expression of monocistronic mRNAs encoding functionally related protei
95                            The expression of monocistronic mRNAs for the five genes examined (NS1, NS
96 istronic transcripts produces polyadenylated monocistronic mRNAs modified to form the 5' cap4 structu
97 tern of transcription--forcing production of monocistronic mRNAs--and the pattern of translation of e
98 processing of the operon transcript into two monocistronic mRNAs.
99 -end sequences to yield a series of discrete monocistronic mRNAs.
100  than did the synthesis of the corresponding monocistronic mRNAs.
101 ts and then often are processed further into monocistronic mRNAs.
102  increased, compensating for the loss of the monocistronic mRNAs.
103 oding for multiple peptides) is processed to monocistronic mRNAs.
104 through mRNAs concomitant with a decrease of monocistronic NS1 and NS2 mRNA levels.
105 mpanied by a small increase in the levels of monocistronic NS1 and NS2 mRNAs.
106 entation patterns, clpP was found to be in a monocistronic operon, whose transcription was induced ab
107       The gene appeared to be expressed as a monocistronic operon.
108 sequence suggest that this gene is part of a monocistronic operon.
109 ned and found in a single genomic copy, in a monocistronic operon.
110  15 genes from up to 60 parts (or mixtures); monocistronic, operon-based or hybrid configurations; an
111 pendent translation of globin mRNA in either monocistronic or bicistronic RNAs.
112         The TEV IRES enhanced translation of monocistronic or dicistronic mRNAs in vitro under compet
113 , eIF4F stimulated translation from uncapped monocistronic or dicistronic mRNAs to a greater extent t
114 n plasmids or on the chromosome, they can be monocistronic or part of a polycistronic operon.
115                                              Monocistronic ORF1 and ORF2 transcripts were identified
116               The vast sequence diversity of monocistronic ORF2 mRNAs could underlie functional diffe
117 supporting endogenous functional capacity of monocistronic ORF2 variants in the human brain.
118 e p28 genes were not detected by RT-PCR, but monocistronic p28 mRNA transcripts were detected by Nort
119 loid leukemia cell lines transduced with the monocistronic pHR-CD80 vector or the bicistronic pHR-GM/
120 ted with its promoter and transcribed into a monocistronic precursor RNA.
121                  A novel 3'-end is formed in monocistronic psbI transcripts, and this is the only ter
122 nscript was disrupted in the revertants, but monocistronic psbM mRNA accumulated normally.
123  gp120-specific immune response than did the monocistronic pV1J-gp120 plasmid.
124                                          The monocistronic rca gene was inactivated in vivo and resul
125  a tricistronic receptor operon, gerU, and a monocistronic receptor component, gerVB.
126 n was encapsidated more efficiently than the monocistronic replicon with the EMCV IRES but less effic
127 ation of EMCV-Luc-PV was compared to that of monocistronic replicons encoding luciferase with either
128 ern blot, ribonuclease protection assay, and monocistronic reporter assay, demonstrated that the hTPH
129 hen tested in the 5' untranslated regions of monocistronic reporter genes, both leader sequences enha
130 anslation in the 5' untranslated region of a monocistronic reporter mRNA.
131  Moreover, uncapped GATA-4 5'-UTR containing monocistronic reporter mRNAs continue to be well transla
132 initiation, confers efficient translation to monocistronic reporter mRNAs in cell-free extracts.
133 e 5' end is blocked by a strong hairpin in a monocistronic reporter.
134  rhodesiense expresses a metacyclic vsg as a monocistronic RNA from a promoter located 2 kilobases (k
135 n cold, are messenger-active single-stranded monocistronic RNA viruses that have evolved a highly com
136 duce false-positive results if unanticipated monocistronic RNAs arise from the dicistronic construct
137 osoma brucei, steady-state levels of mature, monocistronic RNAs change throughout the parasitic life
138  Rabbit reticulocyte lysates programmed with monocistronic RNAs containing 5' ends of GBV-A or GBV-C
139                                          The monocistronic RSV-CAT minigenome consists of the chloram
140 ith a multipartite genome consisting of four monocistronic segments (segments 1 to 4).
141 hough most sigE transcription appeared to be monocistronic, sigE was also transcribed as part of a la
142 cting protein (P6) which is expressed from a monocistronic subgenomic RNA.
143 ycistronic operons and those predicted to be monocistronic, then classified by basal expression level
144 ng frame of 200 codons and is expressed as a monocistronic transcript (of approximately 750 bases) fr
145                                            A monocistronic transcript of sodC accumulates only in sta
146 a bicistronic transcript or was present as a monocistronic transcript that was also highly induced un
147                The dual functionality of the monocistronic transcript was confirmed by complementing
148                                     A single monocistronic transcript was found for mtbA that initiat
149              The etrB gene is expressed as a monocistronic transcript, and EtrB autoregulates express
150 lotting revealed that bmpD is expressed as a monocistronic transcript, which indicates that it is not
151    ORF58 was expressed in low abundance as a monocistronic transcript, with a long 5' untranslated re
152 d rpsM polycistronic transcripts and the lpp monocistronic transcript.
153 espore-specific sigmaG and appears to give a monocistronic transcript.
154 7 kb for xynA, and 4 kb for pelA, indicating monocistronic transcription of these genes.
155 ctor in which the Oct3/4 promoter drives the monocistronic transcription of Venus and a puromycin-res
156            This approach predicted about 864 monocistronic transcripts and 533 polycistronic operons
157  function and which resulted in formation of monocistronic transcripts by splicing.
158  be sensitive enough to detect low levels of monocistronic transcripts derived via a cryptic promoter
159 for the production of both polycistronic and monocistronic transcripts from A. carterae minicircles,
160 additionally characterised polycistronic and monocistronic transcripts from two plastid loci, psbD-tR
161 reading frames and expression of full-length monocistronic transcripts in both isolates, Western blot
162 sT valT lysW valZ lysY lysZ lysQ, as well as monocistronic transcripts like pheU, pheV, asnT, asnU, a
163                                Two different monocistronic transcripts originate from UL34 at early a
164 Rs of human Sno and mouse Bad mRNAs although monocistronic transcripts were not detectable on Norther
165                     The gene is expressed as monocistronic transcripts with multiple 5' termini, and
166 ated in-frame open reading frames (ORFs), 14 monocistronic transcripts, 99 polygenic RNAs, 101 non-co
167 Whereas the N and P ORFs are translated from monocistronic transcripts, the M, G, and pol ORFs are tr
168  that is independent of its stabilization of monocistronic transcripts.
169 re-mRNAs produced by eukaryotic operons into monocistronic transcripts.
170   Acam and the 5'-most gene (gene1) generate monocistronic transcripts.
171 ron, nor is it due to translation of cryptic monocistronic transcripts.
172 gently transcribed operons inserted into the monocistronic tRNA gene, pheV.
173 resulting virus expresses readily detectable monocistronic v-FLIP mRNAs that are undetectable in wild
174             Similar splicing events produced monocistronic v-FLIP transcripts in KSHV-infected primar
175  and propose this influences the choice of a monocistronic variant surface glycoprotein expression si
176 ia cell lines transduced with the pHR-GM-CSF monocistronic vector was 2182.9 pg/10(6) cells per 24 ho
177 regulatory elements and the apportionment of monocistronic versus dicistronic transcription of both g
178                  The sspH and sspL genes are monocistronic, whereas tlp is the second gene in an oper
179            The sspI, sspK and sspM genes are monocistronic, while sspO is the first gene in a likely
180    Studies demonstrate that the gntR gene is monocistronic, while the gntU and gntK genes, which are

 
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