ライフサイエンスコーパス: transcribe

1 rgical procedures were directly observed and transcribed.

2 Interviews were audio recorded and transcribed.

3 All interviews were audio-recorded and transcribed.

4 depending on whether they are independently transcribed.

5 l divisions in the same cells in which it is transcribed.

6 al regions, centromeres are instead actively transcribed.

7 ted binding sites to determine how a gene is transcribed?

8 es with two priming techniques to faithfully transcribe 16S rRNA and amoA transcripts from marine sed

9 d for bacterial RNA polymerase to accurately transcribe a promoter in vitro.

10 journey of RNA polymerase II (Pol II) as it transcribes a gene is anything but a smooth ride.

11 posi's sarcoma-associated herpesvirus (KSHV) transcribes a long noncoding polyadenylated nuclear (PAN

12 e (RNAP) molecules engaged in the process of transcribing a gene of interest.

13 itochondrial genes in Lophophytum are highly transcribed, accurately spliced, and efficiently RNA edi

14 These results indicate that mlonRNAs are transcribed across the fbp1 promoter as a short-range in

15 with a high-throughput enhancer screen (self-transcribing active regulatory region sequencing (STARR-

16 Here, we adapted self-transcribing active regulatory region sequencing (STARR-

17 F-associated loci for RE activity using self-transcribing active regulatory region sequencing and a r

18 ubsequently, using an adaptation of the self-transcribing active regulatory region sequencing approac

19 RNA polymerase II (Pol II) transcribes all protein-coding genes and many noncoding

20 rough direct binding of TET3 to the paternal transcribed allele of the imprinted gene Small nuclear r

21 ber sensory neurons; report that muscle mSCs transcribe an array of genes encoding neuropeptides, neu

22 of similar magnitude to the time required to transcribe an average length yeast gene.

23 Enriched mRNAs were nascently transcribed and accumulated in the nucleus due to a chan

24 ally in the case of AT-rich DNA sequences-be transcribed and initiate MAVS-dependent RNA sensing and

25 d around transcription start sites of highly transcribed and paused genes and that Pol II promoter-pr

26 hat much of the non-protein-coding genome is transcribed and plays a diverse functional role in funda

27 hod for massively parallel analysis of newly transcribed and pre-existing mRNAs from the same cell.

28 CRISPR arrays are transcribed and processed into individual CRISPR RNAs th

29 negative-sense segmented RNA genome that is transcribed and replicated by the viral heterotrimeric R

30 We found that copBL are co-transcribed and that their transcription is increased du

31 es reveal that the majority of the genome is transcribed and that there are more long non-coding RNAs

32 Spacers are transcribed and the resulting CRISPR (cr)RNAs assemble w

33 scanning," wherein the majority of genes are transcribed and therefore subject to transcription-coupl

34 olymerase (FluPol), which is responsible for transcribing and replicating the negative-sense viral RN

35 irus is its polymerase, a complex capable of transcribing and replicating the viral genome.

36 major additional contributions from reverse-transcribing and single-stranded (ss) DNA viruses.

37 ng to determine an in-cell architecture of a transcribing and translating expressome at subnanometer

38 ll suspensions, cells isolated, mRNA reverse transcribed, and barcoded before high-throughput sequenc

39 on gene is evolutionarily conserved, broadly transcribed, and capable of expressing protein.IMPORTANC

40 find that ~15% of the mouse pseudogenes are transcribed, and that highly transcribed parent genes te

41 Determining whether and how a gene is transcribed are two of the central processes of life.

42 rs, while genes within the latter are likely transcribed as a consequence of their proximity to upstr

43 The uncharacterized locus scfCDE was transcribed as an operon and is predicted to encode an A

44 Bacterial ribosomal RNAs (rRNAs) are transcribed as precursors and require processing by Ribo

45 We further identified a long-non coding RNA transcribed at CHPT1 enhancer (also known as enhancer RN

46 s CRISPR technology to generate up to 44,000 transcribed barcodes in an inducible fashion at any poin

47 er RNAs (eRNA) are unstable non-coding RNAs, transcribed bidirectionally from active regulatory seque

48 NA) molecules that were successfully reverse transcribed but to which a second oligonucleotide handle

49 Herpes simplex virus 1 (HSV-1) genes are transcribed by cellular RNA polymerase II (Pol II).

50 Genes are often transcribed by multiple RNA polymerases (RNAPs) at densi

51 s and controls the fate of many nascent RNAs transcribed by RNA polymerase II (RNAPII).

52 U6 snRNA is transcribed by RNA polymerase III (Pol III) and has an e

53 The vast majority of the genome is transcribed by RNA polymerases.

54 The interview recordings were transcribed by the research team and entered into a qual

55 The SARS-CoV-2 genome is replicated and transcribed by the RNA-dependent RNA polymerase holoenzy

56 and of interspersed genes, and all genes are transcribed by the same DNA strand, suggesting that part

57 Cas9 are devoid of the expected 5' overhangs transcribed by the virus.

58 n improved transfection protocol of in vitro transcribed Cas9 mRNA and crRNA:tracrRNA duplex that can

59 RNA polymerase transcribes certain genomic loci with higher errors rate

60 ct genomic locations, which include actively transcribed chromatin and heterochromatin, and cause wid

61 y the distribution of TFIIH and Spt4/Spt5 in transcribed chromatin and Rad26 mainly functions downstr

62 Interviews were transcribed, coded, and analyzed thematically.

63 Interviews were transcribed, coded, and evaluated with thematic analysis

64 M structures of E. coli sigma(28) -dependent transcribing complexes on a complete flagella-specific p

65 erogeneity across the population of actively transcribing complexes.

66 hen plasmid target sequences are efficiently transcribed, Csm6 is dispensable and DNA degradation by

67 al to the gene (cis-regulatory factors), and transcribed distal genes (trans-regulatory factors).

68 lysis was performed on lncRNA-CCL2, which is transcribed divergently to the gene, CCL2, encoding a pr

69 tact virions ("triple-layer particles"), non-transcribing DLPs and transcribing DLPs.

70 layer particles"), non-transcribing DLPs and transcribing DLPs.

71 We then show that interrupting the transcribed DNA strand with an internal desthiobiotin-tr

72 erminate (readthrough genes), are aberrantly transcribed due to upstream termination failure (read-in

73 Thus, repetitive elements transcribed during development drive RLR-mediated inflam

74 Evidence suggests that BHLF1 is also transcribed during latent infection, which prompted us t

75 PHO mRNAs are transcribed during phosphate starvation when lncRNA synt

76 Plant seeds contain many mRNAs that are transcribed during seed development.

77 These mRNAs are transcribed during seed maturation, suggesting a role fo

78 although GAMYB-like genes are constitutively transcribed during vegetative growth, their effects are

79 o the host cell along with the phage DNA and transcribes early phage genes.

80 system, called Zombie, phage RNA polymerases transcribe engineered barcodes in fixed cells.

81 Only about 6% of transcribed enhancers defined by CAGE-tag analysis are a

82 Our findings show that CGI-associated transcribed enhancers display a series of characteristic

83 We show that transcribed enhancers share a number of CGI-dependent ch

84 super-enhancers, including bi-directionally transcribed enhancers, which are often restricted to imm

85 The interviews were orally translated, transcribed, entered into Dedoose software for coding, a

86 f the window of time over which each nucleus transcribes even-skipped plays a critical role in stripe

87 In C. elegans, piRNAs are transcribed from > 15,000 discrete genomic loci by RNA p

88 multi-exonic non-coding RNA (mencRNA) genes transcribed from 1.5-Mb intervals surrounding 139 breast

89 ir own promoter (bona fide) and TEs that are transcribed from a neighboring gene promoter such as wit

90 SWINGN is transcribed from an enhancer and modulates the activatio

91 timulated genes (ISGs) on hepadnaviral mRNAs transcribed from cccDNA, we found that downregulating th

92 e miRNAs are antisense to each other and are transcribed from divergent noncoding RNAs in the latency

93 17beta-estradiol via estrogen-receptor (ER, transcribed from ESR1) dependent mechanisms, but is not

94 erR, including P (mer) , is removed, merA is transcribed from P (oah) independently of Hg(II).

95 n of novel functions the pools are typically transcribed from random-sequence DNA templates, yielding

96 the presence of an endogenous antisense RNA, transcribed from the 3'-end of the human CD39/ENTPD1 gen

97 hancer RNA (eRNA) is a type of noncoding RNA transcribed from the enhancer.

98 RNA transcribed from the full-genome cDNA was highly infecti

99 own cartilage associated microRNAs and those transcribed from the Hox complexes, and the downregulati

100 nin (HN), a small bioactive peptide normally transcribed from the Mt genome.

101 , which overlap protein coding genes and are transcribed from the opposite DNA strand, constitute an

102 A 1 (INCR1) as a long noncoding RNA (lncRNA) transcribed from the PD-L1 locus and show that INCR1 con

103 he choline kinase beta (CHKB) gene, which is transcribed from the same DNA strand and terminates just

104 s, while methylation turnover is elevated in transcribed gene bodies.

105 Much of the mammalian genome is transcribed, generating long non-coding RNAs (lncRNAs) t

106 RNA polymerases (RNAPs) transcribe genes through a cycle of recruitment to promo

107 lation and the known distribution of 5hmC at transcribed genes and active enhancers.

108 encoded by Set1/COMPASS on certain actively transcribed genes and that this protective role is most

109 Most metazoan polymerase II-transcribed genes carry canonical initiation with pyrimi

110 cp2-L10a-Egfp) TRAP mice to profile actively transcribed genes in developing postnatal mouse PCs and

111 Actively transcribed genes in mammals are decorated by H3K79 meth

112 r RNA (tRNA) genes are among the most highly transcribed genes in the genome owing to their central r

113 position occurs in a directed fashion on all transcribed genes regardless of their overall transcript

114 on of histone H3K4 is a hallmark of actively transcribed genes that depends on mono-ubiquitination of

115 , EloA localizes to both thousands of Pol II transcribed genes with preference for transcription star

116 P1 level, more abundant strand-breaks in the transcribed genes, and degradation of RNAP II relative t

117 ly decreased global transcription, repair of transcribed genes, and error-free double-strand break re

118 In contrast to transcribed genes, centromere regions retain transcripti

119 3 up-regulated and 148 down-regulated or not transcribed genes, were simultaneously impacted by intro

120 Y of D. miranda still contains many actively transcribed genes, which compromise the formation of sil

121 ins (ACDs) that enclose active chromatin and transcribed genes.

122 ically marks the promoter region of actively transcribed genes.

123 over LINE-1 repeats and repetitive exons in transcribed genes.

124 an epigenetic mark associated with actively transcribed genes.

125 R-loop accumulation genome-wide at actively transcribed genes.

126 amental function in defining the fate of the transcribed genome.

127 enerated by SaCas9 nickase to mimic actively transcribed genomic loci that are more susceptible to cy

128 s not simply due to genetic variation in the transcribed genomic regions.

129 Transcribed genomic repetitive sequences, including simp

130 RNA cleavage factor components from actively transcribing genomic loci, providing a mechanism for hyp

131 ications are a common by-product of in vitro transcribed gRNA.

132 elements in myeloid malignancies by mapping transcribed HERV genes and generating a library of 1169

133 ion, whereas homozygous animals consistently transcribed higher levels of KLRA, regardless of the all

134 r replication-competent and intact provirus, transcribed HIV, and displayed clonal expansion.

135 elicase directly in front of the replicating-transcribing holo-RdRp, constraining models for nsp13 fu

136 RNA polymerase II (Pol II) transcribes hundreds of thousands of transcription units

137 1(lo) NKT cells were found to constitutively transcribe IL-10 mRNA and, accordingly, produced IL-10 u

138 ch continued transcription would necessarily transcribe immediately adjacent genes and result in conf

139 Some of these A3G retrocopies are transcribed in a variety of tissues and able to restrict

140 nting evidence indicates that TEs are highly transcribed in early embryo development and contribute t

141 reover, P. stutzeri dinitrogen reductase was transcribed in JGTA-S1 even under adequate N.

142 coding genes, many lncRNAs were specifically transcribed in one ecotype and/or differentially express

143 hat the HoxC gene cluster was co-opted to be transcribed in the distal limb ectoderm, where it is act

144 In eukaryotes, tRNAs are transcribed in the nucleus and subsequently exported to

145 eats are normally silent but can be actively transcribed in tumor cells, where increased HSATII copy

146 mplex analytes, such mRNA vaccines and mRNAs transcribed in vivo.

147 ter enables repeatable information access by transcribing information from DNA without destroying it.

148 st of Group IV sigmas, numbers of genes they transcribe, insight into the diverse suite of processes

149 Coders conducted qualitative analysis of transcribed interviews using Grounded Theory.

150 Transcribed interviews were analyzed in NVivo, computer-

151 The expansion is transcribed into a long repetitive RNA, which negatively

152 The telomere downstream of the active VSG is transcribed into a long-noncoding RNA (TERRA), which for

153 ned for purity and quality, and then reverse transcribed into cDNA before being subjected to real-tim

154 ngle-cell RNA-seq (sequencing of RNA reverse transcribed into cDNA) and found that neurogenesis and h

155 unnatural nucleotides is efficiently reverse transcribed into cDNA, and we develop an assay to measur

156 rdr6 mutants in which genomic RNA is reverse transcribed into complementary DNA.

157 A was extracted from all samples and reverse transcribed into complementary DNA; V1-V2 regions of 16S

158 ext, during the targeting phase, spacers are transcribed into CRISPR RNAs (crRNAs) that guide CRISPR-

159 uman immunodeficiency virus (HIV) is reverse-transcribed into DNA and integrated into the host genome

160 Spacers are transcribed into guide RNAs that direct the Cas9 nucleas

161 s of regulatory elements functions only when transcribed into RNA, as they serve as the binding sites

162 al DNA sequences known as spacers, which are transcribed into short RNA guides to specify the targets

163 vader, integrated into the CRISPR locus, and transcribed into short RNAs that direct RNA-guided Cas n

164 ncode a multifunctional protein that reverse transcribes its mRNA into DNA at the site of insertion b

165 half of the viral life cycle, HIV-1 reverse transcribes its RNA genome and integrates the double-str

166 njectable nanocarrier that delivers in vitro-transcribed (IVT) CAR or TCR mRNA for transiently reprog

167 e stability required of TECs to processively transcribe large genomic regions necessitates robust mec

168 rised of a TAD boundary overlapping a highly transcribed large gene with APH-induced RT-delay.

169 activity depends on ComW, as DeltacomW cells transcribe late genes and transform at levels 10- and 10

170 red more HIV DNA than did CD103(-) cells but transcribed less HIV RNA per provirus.

171 After initiation, RNAPII enzymes pause after transcribing less than 100 bases; precisely how RNAPII p

172 s during DNA repair is accelerated 2-fold at transcribed loci relative to non-transcribed loci.

173 d 2-fold at transcribed loci relative to non-transcribed loci.

174 er in yeast to systematically decode, at one transcribed locus, the chromatin binding changes of hund

175 hed relative to other classes for active and transcribed marks, that TEs encompass a higher proportio

176 ide also prevents translation of these newly transcribed messages, leading to an apparent drop in TE

177 In eukaryotes, RNA polymerase II (RNApII) transcribes messenger RNA from template DNA.

178 ast, makes use of poly-dT primers to reverse transcribe mRNA, followed by linear amplification throug

179 Therapeutic strategies based on in vitro-transcribed mRNA (IVT) are attractive because they avoid

180 at promotes the release of exosomes carrying transcribed mRNAs and targeting peptides.

181 on barcoded beads, efficiently marking newly transcribed mRNAs with T-to-C substitutions.

182 detect the capping level on several in vitro transcribed mRNAs.

183 Because Pol II transcribes multiple gene types, its termination occurs

184 thereby delivering the m(6)A MTC to actively transcribed nascent RNAs to deposit m(6)A co-transcripti

185 which were robust and associated with long, transcribed neural genes that were also robust RDC-genes

186 ve proviruses are not silent, are capable of transcribing novel unspliced forms of HIV-RNA transcript

187 ied Pol I and Pol III, but not Pol II, could transcribe nucleosomal templates.

188 ch methylates adenosine when it is the first transcribed nucleotide.

189 d operons are gene blocks whose genes are co-transcribed on a single mRNA molecule.

190 early half of the human genome and are often transcribed or exhibit cis-regulatory properties with un

191 pseudogenes are transcribed, and that highly transcribed parent genes tend to give rise to many proce

192 oordinates chromatin-based regulation in the transcribed part of the genome.

193 nucleic acid was extracted from DBS, reverse transcribed, PCR amplified, and analyzed by population-b

194 The amount of pgRNA transcribed per cccDNA also decreased from HB1 to HB5 (P

195 DENDRO utilizes transcribed point mutations and accounts for technical n

196 ease and its relationship to the activity of transcribing Pol II is not understood.

197 are arranged in directional arrays that are transcribed polycistronically, and individual mRNAs are

198 ces and extrinsic obstacles, including other transcribing polymerases, the replication machinery and

199 e (Pol) I is a 14-subunit enzyme that solely transcribes pre-ribosomal RNA.

200 viral late transcripts that are prematurely transcribed, presumably due to cryptic transcription ear

201 ynamic ribonucleoparticles as they are being transcribed, processed, and exported.

202 re length of the chromosome from which it is transcribed, recruiting factors to modify underlying chr

203 ce and expression conservation of intergenic transcribed regions (ITRs) in four Poaceae species.

204 Transcribed regions and exons in RTR account for ~42% an

205 suggest that Elongin A localizes to actively transcribed regions and potential enhancers, and the lev

206 These networks are enriched for novel transcribed regions and target genes in heterochromatin

207 while the association of Spt6 and Set2 with transcribed regions is partially dependent on Spn1.

208 d redistribution of elongating RNAPII within transcribed regions toward the transcriptional start sit

209 s and recruits BRD2 to the rDNA promoter and transcribed regions via association with upstream bindin

210 der replication stress, especially in highly transcribed regions where the presence of H3K4me is high

211 To achieve high-resolution profiles of transcribed regions, an RNA fragmentation step before bi

212 plication forks through DNA damage, actively transcribed regions, structured DNA and compact chromati

213 tative trait loci for annotated genes, novel transcribed regions, transposable elements, and microbia

214 e conclude that EloA broadly associates with transcribed regions, tunes RNA Pol II transcription leve

215 o occur near active promoters, enhancers and transcribed regions.

216 tin and less so in the promoter and actively transcribed regions.

217 eading of H3K9me and silencing into actively transcribed regions.

218 how that total RNA is sufficient to identify transcribed regulatory elements and capture the dynamics

219 veals that cis effects are widespread across transcribed regulatory elements, and the strongest cis e

220 plex enzymes is critical for life, including transcribing, replicating and repairing DNA.

221 nts (SINEs) are RNA polymerase III (RNAPIII)-transcribed, retrotransposable noncoding RNA (ncRNA) ele

222 rarchy based on the differential capacity to transcribe ribosomal DNA and synthesize proteins.

223 lture, 16S bacterial PCR and/or 28S-internal transcribed ribosomal gene spacer (28S-ITS) fungal PCR.

224 Hmo1 is enriched at highly transcribed ribosomal genes, known to be depleted of his

225 ucleoli and associates with RNA polymerase I transcribed ribosomal RNA gene, Rn45s.

226 rexpressed BC200 by transfection of in vitro transcribed RNA and transient expression from transfecte

227 An in vitro-transcribed RNA aptamer (trans-RA16) that targets non-sm

228 ingly, Mex67 is essential to stabilize newly transcribed RNA before Xpo1-mediated nuclear export.

229 Long noncoding RNAs (lncRNAs) are a class of transcribed RNA molecules greater than 200 nucleotides i

230 of in vitrotranscription (SPRINT), in vitro transcribed RNA sequence-specifically triggers the RNase

231 th other detection techniques using in vitro-transcribed RNA.

232 ion of negatively supercoiled DNA behind the transcribing RNA polymerase.

233 on incorporates a feedback mechanism whereby transcribed RNAs initially stimulate but then ultimately

234 quintessential feature of RNA polymerase II-transcribed RNAs, and a textbook aspect of co-transcript

235 s where SMARCB1 differentially binds locally transcribed RNAs.

236 he simple modification of both synthetic and transcribed RNAs.

237 ure to H(2)O(2), A. baumannii differentially transcribes several hundred genes.

238 lls, splicing occurs after RNA polymerase II transcribes several kilobases of pre-mRNA, suggesting th

239 ate anti-sigma protein RsfG, encoded by a co-transcribed sigG1-neighbouring gene.

240 Other inbred lines are known to transcribe significantly different sets of genes, indica

241 maturation of all regular RNA polymerase II transcribed snRNAs of the major and minor spliceosomes b

242 3 at promoters marked by H3K4me3 in actively transcribing somatic cells(7).

243 of by-products derived from the 5'-external transcribed spacer (ETS) of 45S pre-rRNA, as MTR4 does.

244 biome studies rely on sequencing of internal transcribed spacer (ITS) amplicons.

245 ofile, and Sanger sequencing of the internal transcribed spacer (ITS) and D1/D2 regions of the riboso

246 ing tool with great accuracy, while internal transcribed spacer (ITS) and D1/D2 sequencing were succe

247 Fungi were isolated, and a fungal internal transcribed spacer (ITS) clone library survey was perfor

248 nt using Illumina sequencing of the internal transcribed spacer (ITS) gene.

249 ochrome b as well as in the nuclear internal transcribed spacer (ITS) region and 28 S rRNA.

250 ungal barcode-the nuclear ribosomal internal transcribed spacer (ITS) region-and offers all ~1 000 00

251 ndidate genera encountered in prior internal transcribed spacer 1 (ITS1)-based surveys.

252 d to recognise FAWs on the basis of internal transcribed spacer 1 (ITS1).

253 this cross-sectional study, we use internal transcribed spacer 1 amplicon sequencing to evaluate the

254 olic controls using fungal-specific internal transcribed spacer amplicon sequencing of fecal samples.

255 work analysis based on 16S rDNA and internal transcribed spacer deep sequencing.

256 We amplified the internal transcribed spacer region 2 of the nuclear ribosomal ope

257 6S amplicon sequencing) and fungal (internal transcribed spacer region amplicon sequencing) communiti

258 alysis based on the sequence of the internal transcribed spacer region of fungal ribosomal RNA encodi

259 con sequencing of the ribosomal RNA internal transcribed spacer region to examine the microdiversity

260 g, respectively, atpE genes and the internal transcribed spacer region.

261 nomic assertions based on ribosomal internal transcribed spacer regions (ITS1/2) and expanded protein

262 rmatitidis; for 5, we sequenced the internal transcribed spacer regions, and for 4 others the whole g

263 specific sequence, belonging to the Internal Transcribed Spacers region, was used to design the real-

264 lymerase (RNAP)-stalling DNA damage from the transcribed strand (TS) of active genes.

265 ogenesis display lower mutation rates on the transcribed strand and have low diversity in the populat

266 etween mutation types predominant on the non-transcribed strand and on the strand lagging during repl

267 ion-coupled repair (TCR) complex on actively transcribed strands.

268 Amazon, Apple, Google, IBM, and Microsoft-to transcribe structured interviews conducted with 42 white

269 The transcribed switch regions can recombine, leading to a c

270 as effects on tail lengths peak for recently transcribed target mRNAs and then subside.

271 ed to effects on mRNA levels, even for newly transcribed target mRNAs.

272 , T. brucei uses RNA polymerase I (Pol I) to transcribe the active ES, which is unprecedented among e

273 linker-sequence, and the RNA polymerase that transcribes the hairpins.

274 pendent RNA polymerase, which replicates and transcribes the vRNA genome.

275 ntron that is generated by RNA polymerase II transcribing the circular viral genome more than once.

276 RNA-polymerase II (RNAPII) can successfully transcribe them.

277 itiate transcription and cannot consistently transcribe through long DNA sequences.

278 n whether Pol I has an intrinsic capacity to transcribe through nucleosomes.

279 ta to identify both uni- and bidirectionally transcribed TIRs with 70% improvement in accuracy, three

280 Recent studies have shown that enhancers are transcribed to produce enhancer RNAs (eRNAs).

281 els of gene expression and the activities of transcribed/translated proteins, we introduce nucleic ac

282 the ONs from an RNase T1 digest of in vitro transcribed tRNA, which are purified after ribozyme-fusi

283 tronic gene cluster, emtABCD, differentially transcribed under estrogen-fed conditions and predicted

284 Some ERVs have been shown to be transcribed under physiological and pathological conditi

285 An operon's genes are co-transcribed under the control of a single promoter to a

286 nd fourth clusters grouped genes differently transcribed upon exposure to diazepam and propranolol, r

287 cient tool to rapidly screen for the role of transcribed variants on gene expression.

288 Interviews were transcribed verbatim and analysed using Haase's adaptati

289 Data were transcribed verbatim and analysed using thematic analysi

290 Interviews were transcribed verbatim and coded in an iterative process u

291 Qualitative interviews were audio-recorded, transcribed verbatim, and coded.

292 erases to replicate entire viral genomes and transcribe viral mRNAs from individual viral genes as we

293 s that cross-link the head domain uncoat and transcribe viral positive-sense RNA with kinetics simila

294 Integration of the reverse-transcribed viral DNA into host chromosomes is a critica

295 5' methylated cap and 3' poly(A) tail of the transcribed viral mRNAs.

296 This polymerase transcribes viral genomes to produce RNAs that lead to i

297 otein of RSV replicates the viral genome and transcribes viral mRNAs.

298 FluPol transcribes vRNA using a host-capped mRNA primer and rep

299 During in vitro latency, VLT is transcribed, whereas VLT-ORF63 expression is induced by

300 Mammalian genomes are extensively transcribed, which produces a large number of both codin