ライフサイエンスコーパス: ribosomal RNA

1 4-subunit enzyme that solely transcribes pre-ribosomal RNA.

2 es to pseudouridine in small nuclear RNA and ribosomal RNA.

3 pulation with the G2376C mutation in the 23S ribosomal RNA.

4 ablishes idiosyncratic interactions with the ribosomal RNA.

5 -generation sequencing targeting 16S and 18S ribosomal RNA.

6 atalyse the site-specific 2-O-methylation of ribosomal RNA.

7 s measured by metagenomic sequencing and 16s ribosomal RNA.

8 such as the structure and maturation of its ribosomal RNA.

9 ansport chain and a full set of transfer and ribosomal RNAs.

10 ins, and defective processing of chloroplast ribosomal RNAs.

11 ient enzyme specialized in synthesizing most ribosomal RNAs.

12 -term ART (HIV+ LTART) from Mexico using 16S ribosomal RNA (16sRNA) targeted sequencing.

13 , DNA-directed RNA polymerase II (RPB2), 18S ribosomal RNA (18S), 28S ribosomal RNA (28S) across diff

14 Here, we link ribosomal RNA 2'-O-methylation (2'-O-Me) to the etiology

15 rase II (RPB2), 18S ribosomal RNA (18S), 28S ribosomal RNA (28S) across different developmental stage

16 l richness, we analyzed over 1.7 billion 16S ribosomal RNA amplicon sequences in the V4 hypervariable

17 sition and functions were assessed using 16S ribosomal RNA amplicon sequencing and metagenomic shotgu

18 16S ribosomal RNA amplicon sequencing was used for identific

19 Shotgun and 16S ribosomal RNA amplicon sequencing were performed on fece

20 Bacterial 16S ribosomal RNA analyses were performed on stool samples f

21 16s ribosomal RNA analysis of keystone pathogen Porphyromona

22 ogenome contained 13 protein coding genes, 2 ribosomal RNA and 22 transfer RNA genes, and a control r

23 partments-nucleoli, where it associates with ribosomal RNA and is required for efficient separation o

24 stilled water, extracted total RNA, depleted ribosomal RNA and performed whole-transcriptome RT-seque

25 y analyses demonstrated the role of USP36 in ribosomal RNA and protein synthesis.

26 Virgin Islands, amplifying the large-subunit ribosomal RNA and psbA protein D1 marker genes, revealed

27 synthesize the proteins of a cell, comprise ribosomal RNA and ribosomal proteins, which coassemble h

28 ize the upper airway microbiome, we used 16S ribosomal RNA and shotgun metagenomic sequencing.

29 N1-regulated genes, including those encoding ribosomal RNA and the cytokine IL1B.

30 nomic units were pyrosequenced targeting 16S ribosomal RNA and volatile organic compounds determined

31 tains 114 genes, coding for 81 protein, four ribosomal RNAs and 29 transfer RNAs.

32 Processing of chloroplast ribosomal RNAs and assembly of ribosomal subunits were d

33 y recently the role of its basic components, ribosomal RNAs and proteins, in translational control ha

34 Then, by analyzing the ribosomal RNAs and proteins, we explain the observed geo

35 s that are peculiar to specific positions in ribosomal RNAs and that are stabilized by tertiary inter

36 occus were assessed by DNA sequencing of 16S ribosomal RNA, and absolute S. aureus abundance was meas

37 n a eukaryotic-specific pocket formed by 28S ribosomal RNA, and alters the path of the nascent polype

38 narily widespread regulatory function beyond ribosomal RNA, and that they are often autoregulatory.

39 cted database growth, submission wizards for ribosomal RNA, and the transfer of Expressed Sequence Ta

40 t, an exuberant fraction of reads mapping to ribosomal RNA, and the unstranded nature of the sequenci

41 uence families in that database (16S and 23S Ribosomal RNAs), as well as improved accuracies for long

42 s is initiated with the transcription of pre-ribosomal RNA at the 5' external transcribed spacer, whi

43 habitual low dietary fiber intake using 16S ribosomal RNA-based approaches.

44 nities in fecal samples were profiled by 16S ribosomal RNA-based polymerase chain reaction-temporal t

45 faceted transcription factor in enhancer and ribosomal RNA biology.

46 Based on 18 S ribosomal RNA, but not ITS2 sequence data due to inconsi

47 Cell growth requires synthesis of ribosomal RNA by RNA polymerase I (Pol I).

48 tic analyses of sequences of the partial 18S ribosomal RNA, D2-D3 of 28S rRNA, internal transcribed s

49 ical technique, allowed us to reduce the 16S ribosomal RNA data complexity into a microbial signature

50 The probe incorporated into the bacterial ribosomal RNA decoding site, fluorescently reports antib

51 complete nuclear transcriptome, including a ribosomal RNA degradation procedure that minimizes pre-r

52 cRNA expression from both simulated and real ribosomal RNA-depleted (rRNA-depleted) RNA-seq datasets.

53 We conclude that use of a standard ribosomal RNA depletion method for library preparation c

54 nd function by suppressing the biogenesis of ribosomal RNA-derived siRNAs (risiRNAs).

55 (such as tRNA-derived small RNAs, microRNAs, ribosomal RNA-derived small RNAs and long non-coding RNA

56 The ribosomal RNA distribution inside the cells hints to spa

57 e 5' external transcribed spacer RNA and all ribosomal RNA domains.

58 internal transcribed spacer region of fungal ribosomal RNA encoding genes demonstrated consistent and

59 U-alpha is also needed for clustering of 6/7 ribosomal RNA-encoding loci.

60 was closely associated with sharply reduced ribosomal RNA expression.

61 to the most-likely IDs, (iii) comprehensive ribosomal RNA filtering for accurate mapping of exogenou

62 emistry to detect mucin 2, as well as by 16S ribosomal RNA fluorescence in situ hybridization, transc

63 roviding a thermodynamic basis for vectorial ribosomal RNA flux out of the nucleolus.

64 Like depletion of ribosomal RNA for mRNA-seq and mitochondrial DNA for ATA

65 tly tethered subunits where core 16S and 23S ribosomal RNAs form a single chimeric molecule.

66 sic sites in nascent RNA, messenger RNA, and ribosomal RNA from yeast and human cells.

67 o evaluate the diagnostic performance of 16S ribosomal RNA gene (rRNA) polymerase chain reaction (PCR

68 We used 16S ribosomal RNA gene (V1-V3) analysis to characterize the

69 12 and laboratory tests were performed; 16S ribosomal RNA gene (V4V5) sequencing was performed on st

70 We used 16S ribosomal RNA gene amplicon sequencing to profile microb

71 n of fecal microbiota were determined by 16S ribosomal RNA gene amplicon sequencing, and metabolite p

72 Fecal microbiota were analyzed by V3-V4 16S ribosomal RNA gene amplicon sequencing.

73 ion of the cervico-vaginal microbiota by 16S ribosomal RNA gene amplicon sequencing.

74 nile meatal swab through high-throughput 16s ribosomal RNA gene amplicon sequencing.

75 By sequencing microbial 16S ribosomal RNA gene amplicons, we found that changing cli

76 Faecal 16S ribosomal RNA gene analysis was undertaken.

77 ed by sequencing the V3/V4 region of the 16S ribosomal RNA gene and by hierarchical clustering.

78 and fecal samples were analyzed by both 16S ribosomal RNA gene and transcript amplicon sequencing; 2

79 By applying metabolomic and metagenomic (16S ribosomal RNA gene and whole-genome shotgun sequencing)

80 on was identified with sequencing of the 16S ribosomal RNA gene in breast milk, areolar skin, and inf

81 oughput sequencing after construction of 16S ribosomal RNA gene libraries.

82 lysis, have been developed to detect the 23S ribosomal RNA gene mutations that confer resistance to a

83 ing profiles from COI, cytochrome b, and 16S ribosomal RNA gene PCR products.

84 using droplet digital PCR and bacterial 16S ribosomal RNA gene quantification and sequencing.

85 Using faecal 16S ribosomal RNA gene sequences and host genotype data from

86 Bacterial 16S ribosomal RNA gene sequences from each sample were ampli

87 global-sampling effort, we analysed the 16S ribosomal RNA gene sequences from ~1,200 activated sludg

88 xonomic units, enable bacterial and archaeal ribosomal RNA gene sequences to be followed across multi

89 We performed 16S ribosomal RNA gene sequencing analysis of stool samples

90 Using 16S ribosomal RNA gene sequencing and a clustering approach,

91 Feces were collected and analyzed by 16S ribosomal RNA gene sequencing and bacterial community an

92 iota composition was characterized using 16S ribosomal RNA gene sequencing and culture.

93 lysis of fecal microbiota composition by 16S ribosomal RNA gene sequencing and fecal/urinary metaboli

94 Various approaches, including bacterial 16S ribosomal RNA gene sequencing and metagenomic shotgun se

95 The HMP used both 16S ribosomal RNA gene sequencing and whole-genome metagenom

96 tool sub-Operational Taxonomic Units from16S ribosomal RNA gene sequencing data.

97 16S ribosomal RNA gene sequencing detected diverse bacterial

98 We conducted 16S ribosomal RNA gene sequencing of an ICU admission swab a

99 Analysis of 16S ribosomal RNA gene sequencing of cervicovaginal lavage c

100 We conducted 16S ribosomal RNA gene sequencing to characterize intestinal

101 The predictive value of 16S ribosomal RNA gene sequencing was not superior to the si

102 16S ribosomal RNA gene sequencing was performed on DNA extra

103 16S ribosomal RNA gene sequencing was performed on sputum fr

104 We applied 16S ribosomal RNA gene sequencing, shotgun metagenomic seque

105 Feces were collected and analyzed by 16S ribosomal RNA gene sequencing.

106 the intestinal microbiota by culture and 16S ribosomal RNA gene sequencing.Among the 3161 enrolled pr

107 on day 1 and week 12 and profiled using 16S ribosomal RNA gene sequencing; 122 patients had paired s

108 ntitative polymerase chain reaction, and 16S ribosomal RNA gene sequencing; lamina propria and mesent

109 position was evaluated by sequencing the 16S ribosomal RNA gene V1-V3 region.

110 Bacterial DNA was isolated, and the 16S ribosomal RNA gene was amplified and sequenced.

111 ranscribed spacer 2 and the D2 region of 28S ribosomal RNA gene were sequenced and fungi identified.

112 ere sequenced using the V4 region of the 16S ribosomal RNA gene with clustering of Gardnerella vagina

113 associates with RNA polymerase I transcribed ribosomal RNA gene, Rn45s.

114 Using amplicon sequencing of the 16S ribosomal RNA gene, we found that when seagrass meadows

115 -cell diversity of the usually conserved 16S ribosomal RNA gene, we suggest that gene conversion occu

116 atform targeting the V3-V4 region of the 16S ribosomal RNA gene.

117 d taxon-specific quantitative PCR of the 16S ribosomal RNA gene.

118 eq sequencing amplicons of the bacterial 16S ribosomal RNA gene.

119 n, and infant stool by sequencing of the 16S ribosomal RNA gene.

120 hain reaction (PCR) assays targeting the 16S ribosomal RNA gene.

121 focused on the MPa adhesion gene and the 16S ribosomal RNA gene.

122 n and sequencing of the V4 region of the 16S ribosomal RNA gene.

123 d by 454-pyrosequencing of the bacterial 16S ribosomal RNA gene.

124 on was confirmed using sequencing of the 16S ribosomal RNA gene.

125 obacteria (WMD: 1.16 log10 copies of the 16S ribosomal RNA gene; 95% CI: 0.06, 2.26; P = 0.04).

126 Telomeres and ribosomal RNA genes (rDNA) are essential for cell surviv

127 hibitor of RNA polymerase I transcription of ribosomal RNA genes (rDNA), induces replication stress a

128 cox1-3, nad1-6, nad4L, atp6 and cob) and two ribosomal RNA genes (rrnL and rrnS), but the atp8 gene w

129 ng nested polymerase chain reaction (PCR) of ribosomal RNA genes and a novel assay that amplifies a c

130 Ribosomal RNA genes are arranged in large arrays with hu

131 rearrangements among the protein-coding and ribosomal RNA genes could be inferred across the phyloge

132 Here, by sequencing 16S ribosomal RNA genes in 40 soils sampled from along a 1,6

133 Ribosomal RNA genes in sequenced DNA of natural ferns, t

134 into complementary DNA; V1-V2 regions of 16S ribosomal RNA genes were amplified and sequenced on an I

135 allo-HSCT at engraftment were analyzed; 16S ribosomal RNA genes were sequenced and analyzed from eac

136 d includes 13 protein-coding genes (PCGs), 2 ribosomal RNA genes, 22 transfer RNA genes and an 834 bp

137 sponding to active transposons, CRISPR loci, ribosomal RNA genes, rolling circle origins of replicati

138 ne expression, including upregulation of the ribosomal RNA genes.

139 ut microbiome composition sequenced from 16S ribosomal RNA genes.

140 enes such as that encoding the small subunit ribosomal RNA has revealed the extensive diversity of ba

141 ultiple genes impacting protein synthesis: a ribosomal RNA helicase gene, tRNA biosynthesis genes, an

142 mbled NPET, including an aberrantly flexible ribosomal RNA helix 74, resulting in at least three diff

143 and Nog1 work together in the maturation of ribosomal RNA helix 74, which is required to ensure prop

144 abundance, and rich phylogenetic content of ribosomal RNA in a rapid fluorescent hybridization assay

145 NSP1 binds to 18S ribosomal RNA in the mRNA entry channel of the ribosome

146 Here we used amplicon sequencing of the ribosomal RNA internal transcribed spacer region to exam

147 tructured tethers that integrate 16S and 23S ribosomal RNAs into single-chain ribosomal RNAs that rem

148 to most eukaryotes, the large subunit (LSU) ribosomal RNA is fragmented into two large and four smal

149 the nascent chain and the negatively charged ribosomal-RNA lining the exit tunnel, and for quickly ej

150 een upon complete deletion of the multi-copy ribosomal RNA locus.

151 ient feature of classical DBA is a defect in ribosomal RNA maturation that generates nucleolar stress

152 that U3 snoRNA, a non-coding RNA involved in ribosomal RNA maturation, is critical for chondrocyte pr

153 antitative polymerase chain reaction and 16S ribosomal RNA metagenomic sequencing.

154 Longitudinal analyses of 16S ribosomal RNA, metagenomic, metatranscriptomic and cytok

155 binding and Mtb ribosome inhibition requires ribosomal RNA methylation in both ribosome subunits by T

156 de resistance determinants including a novel ribosomal RNA methyltransferase situated in a CRISPR (cl

157 de resistance determinants including a novel ribosomal RNA methyltransferase situated in a CRISPR arr

158 g, and liver inflammation and intestinal 16s ribosomal RNA microbiota sequencing were performed.

159 Our knowledge about the repertoire of ribosomal RNA modifications and the enzymes responsible

160 n break' has been described in which the 28S ribosomal RNA molecule is cleaved into two subparts.

161 The 16S ribosomal RNA molecules and the associated gene were seq

162 cale features of ribosomes-such as why a few ribosomal RNA molecules dominate the mass and why the ri

163 2 domains of the large subunit (LSU) nuclear ribosomal RNA (nrRNA) gene and by morphological characte

164 physically tied to the transcription of pre-ribosomal RNA (pre-rRNA) and to large ribosomal subunit

165 orders, yet its role in processing precursor ribosomal RNA (pre-rRNA) is largely unclear.

166 e in ribosome biogenesis, functioning in pre-ribosomal RNA (pre-rRNA) processing as a component of th

167 RNA degradation procedure that minimizes pre-ribosomal RNA (pre-rRNA) transcripts.

168 olus, involves coordinated expression of pre-ribosomal RNAs (pre-rRNAs) and ribosomal proteins, pre-r

169 e cells and in muscles of mice without NO66, ribosomal RNA, pre-rRNA, and protein synthesis all incre

170 ach shows predominant binding of the 45S pre-ribosomal RNA precursor molecules.

171 ing affected transcription and processing of ribosomal RNA precursors, as well as the translation of

172 modulation factor (PA3049), is required for ribosomal RNA preservation during prolonged nutrient sta

173 ON LIMIT2 (ISE2) is required for chloroplast ribosomal RNA processing and chloro-ribosome assembly.

174 nd organism viability because of its role in ribosomal RNA processing and protein synthesis, which is

175 ent classes, enables identification of novel ribosomal RNA processing factors and sites, and suggests

176 identified a 3' to 5' exoribonuclease, RRP6 (ribosomal RNA processing protein 6), as a CELF1-interact

177 in translation of RPS28 mRNA blocks pre-18S ribosomal RNA processing, resulting in a reduction in th

178 n particle assembly and thus possibly to pre-ribosomal RNA processing.

179 th ribosomes and that EBP1 silencing hinders ribosomal RNA processing.

180 eotide kinase activities with known roles in ribosomal RNA processing.

181 exosome component 2 (EXOSC2), also known as ribosomal RNA-processing protein 4 (RRP4), were recently

182 ts derived from healthy individuals and that ribosomal RNA production increases with age, indicating

183 egrated with analysis of fecal bacterial 16S ribosomal RNA profiles and clinical disease severity ind

184 that host-derived RNAs, most prominently 5S ribosomal RNA pseudogene 141 (RNA5SP141), bound to RIG-I

185 it methyltransferase H (RlmH) methylates 23S ribosomal RNA pseudouridine 1915 (Psi1915), which lies n

186 nal transcribed spacer with or without D1/D2 ribosomal RNA regions.

187 iation of ribosome assembly factors with pre-ribosomal RNA results in the formation of the small subu

188 Ribosomal RNA (rRNA) accounts for the majority of the RN

189 Interfering with ribosomal RNA (rRNA) accumulation triggered nucleolar st

190 ite-specific endonucleolytic cleavage in 25S ribosomal RNA (rRNA) adjacent to the c loop of the expan

191 unit has been built de novo and includes 15S ribosomal RNA (rRNA) and 34 proteins, including 14 witho

192 ucturally conserved domain that binds the 5S ribosomal RNA (rRNA) and allows its incorporation into r

193 has an unexpected role in the biogenesis of ribosomal RNA (rRNA) and in haematopoiesis.

194 ding process requiring tight coordination of ribosomal RNA (rRNA) and ribosomal protein (RP) producti

195 nervous system development, a disturbance of ribosomal RNA (rRNA) biogenesis and tp53 activation, whi

196 Ribosomal RNA (rRNA) biogenesis is a multistep process r

197 that directly mediate the expression of the ribosomal RNA (rRNA) components of ribosomes.

198 We use ribosomal RNA (rRNA) encoding gene phylogenies to demons

199 tuberculosis (Mtb) possess species-specific ribosomal RNA (rRNA) expansion segments and ribosomal pr

200 emoval of essentially all eukaryote-specific ribosomal RNA (rRNA) expansion segments, reducing the rR

201 ial ribosomal protein MRPS10 and reduced 12S ribosomal RNA (rRNA) expression, suggesting mitochondria

202 We reanalyzed raw 16S ribosomal RNA (rRNA) gene sequences and metadata from pu

203 gal molecular diversity (small subunit (SSU) ribosomal RNA (rRNA) gene sequences) in field samples.

204 al specimens is commonly performed using 16S ribosomal RNA (rRNA) gene sequences.

205 d-collected Helicoverpa zea larvae using 16S ribosomal RNA (rRNA) gene sequencing and matrix-assisted

206 In the present study, 16S ribosomal RNA (rRNA) gene sequencing was applied to sali

207 on and profiled the gut microbiota using 16S ribosomal RNA (rRNA) gene V4-V5 deep sequencing.

208 quencing of hypervariable regions of the 16s ribosomal RNA (rRNA) gene.

209 Arabidopsis thaliana, a significant loss of ribosomal RNA (rRNA) genes with a past history of a muta

210 ransfer RNA (tRNA) binding region of the 28S ribosomal RNA (rRNA) in the large ribosomal subunit.

211 Ribosomal RNA (rRNA) is co- and post-transcriptionally p

212 Ribosomal RNA (rRNA) is transcribed from rDNA by RNA pol

213 The pathways for ribosomal RNA (rRNA) maturation diverge greatly among th

214 ad, loss of PP7L compromised translation and ribosomal RNA (rRNA) maturation in chloroplasts, pointin

215 Post-transcriptional ribosomal RNA (rRNA) modifications are present in all or

216 : see text] bound to the ribosome reveal 23S ribosomal RNA (rRNA) nucleotide A1913 positional changes

217 side chain of macrolides interacts with 23S ribosomal RNA (rRNA) nucleotides A752 and U2609, that we

218 ng residue networks (sectors) within the 23S ribosomal RNA (rRNA) of the large ribosomal subunit.

219 we found reduced pseudouridine levels in the ribosomal RNA (rRNA) of the patients.

220 The resulting accumulation of ribosomal RNA (rRNA) precursor-analyzed by RNA fluoresce

221 ur data shows that stabilization of aberrant ribosomal RNA (rRNA) precursors in an enp1-1 mutant caus

222 ty of the U2AF1-S34F mutant cells and causes ribosomal RNA (rRNA) processing defects, thus indicating

223 We examined the relationship between ribosomal RNA (rRNA) production and IGF-1-mediated myotu

224 ol gene regulation, but regulatory roles for ribosomal RNA (rRNA) remain largely unexplored.

225 "Omic" methodologies such as 16S ribosomal RNA (rRNA) sequencing and time-of-flight mass

226 lected for 6 wk for microbiota analysis [16S ribosomal RNA (rRNA) sequencing].

227 increased in size, forming a surface-exposed ribosomal RNA (rRNA) shell of unknown function, which ma

228 ng community RNA through its radiocarbon and ribosomal RNA (rRNA) signatures.

229 ach organism has evolved to possess a unique ribosomal RNA (rRNA) species optimal for its physiologic

230 een studied in detail, little is known about ribosomal RNA (rRNA) structural rearrangements that take

231 Activation of ribosomal RNA (rRNA) synthesis is pivotal during cell gr

232 enesis and identified a role for this GEF in ribosomal RNA (rRNA) synthesis that is mediated by Rac1

233 rmation of RNAP clusters is driven by active ribosomal RNA (rRNA) transcription and that RNAP cluster

234 Ribosomal RNA (rRNA) transcription by RNA polymerase I (

235 el factors (SCFs) GreB and DksA both repress ribosomal RNA (rRNA) transcription, but SCF loading and

236 otypes from a ~1.7 x 10(7) member library of ribosomal RNA (rRNA) variants, as well as identifying mu

237 bosomes cleaved at helix 69 (H69) of the 26S ribosomal RNA (rRNA), a key part of ribosome decoding ce

238 duced small RNA (tiRNA) and transcription of ribosomal RNA (rRNA), respectively.

239 A-seq requires efficient physical removal of ribosomal RNA (rRNA), which otherwise dominates transcri

240 tes with Grc3-Rat1-Rai1 to process precursor ribosomal RNA (rRNA), yet its mechanism of action remain

241 tudy, we evaluated two methods for preparing ribosomal RNA (rRNA)-depleted sequencing libraries for R

242 the transcription and processing of nascent ribosomal RNA (rRNA).

243 PNK, to orchestrate processing of precursor ribosomal RNA (rRNA).

244 esidues on other RNA molecules, primarily on ribosomal RNA (rRNA).

245 rects 2'-O-methylation at uridine 116 of 18S ribosomal RNA (rRNA).

246 g, cleavage, and modification of nascent pre-ribosomal RNA (rRNA).

247 r the stepwise assembly of the large-subunit ribosomal RNA (rRNA).

248 rial DNAs of two kinds: maxicircles encoding ribosomal RNAs (rRNAs) and proteins and minicircles bear

249 Ribosomal RNAs (rRNAs) are essential components of the r

250 Ribosomal RNAs (rRNAs) are main effectors of messenger R

251 Bacterial ribosomal RNAs (rRNAs) are transcribed as precursors and

252 by auxiliary factors that process and modify ribosomal RNAs (rRNAs) or are involved in ribosome assem

253 f GLTSCR2 impairs maturation of 18S and 5.8S ribosomal RNAs (rRNAs), and Nop53 is required for matura

254 r certain non-coding RNAs (ncRNAs) including ribosomal RNAs (rRNAs), transfer RNAs (tRNAs), small nuc

255 h the hierarchical addition of proteins to a ribosomal RNA scaffold.

256 These include ribosomal RNA segments that constitute the peptidyl tran

257 d, and the V1-V3 region of the bacterial 16S ribosomal RNA sequences were amplified and sequenced to

258 We performed bacterial 16S ribosomal RNA sequencing and analysis directly from clin

259 Feces from mice were analyzed by 16s ribosomal RNA sequencing and compared to 16s sequencing

260 heral blood mononuclear cells as well as 16S ribosomal RNA sequencing data from bronchoalveolar lavag

261 House dust microbiome analysis using 16S ribosomal RNA sequencing identified 202 and 171 bacteria

262 The 16s ribosomal RNA sequencing identified significant differen

263 By using V4 and full-length 16S ribosomal RNA sequencing of a series of fecal samples, w

264 spectroscopy for metabolic profiling and 16S ribosomal RNA sequencing to assess the gut microbiome.

265 Samples were analyzed by 16S ribosomal RNA sequencing, and diet-related metabolites w

266 esence of collagenolytic colonies and by 16S ribosomal RNA sequencing, which determined the anatomic

267 Fecal samples underwent 16S ribosomal RNA sequencing.

268 erial microbiota was characterized using 16S ribosomal RNA sequencing.

269 on status was established by culture and 16S ribosomal RNA sequencing.

270 r-associated microbiota were assessed by 16s ribosomal RNA sequencing.

271 Microbiota data were obtained using 16S ribosomal RNA sequencing.

272 sition of the microbiota was analyzed by 16S ribosomal RNA sequencing.

273 Fecal samples were analyzed by 16s ribosomal RNA sequencing.

274 is fragmented into two large and four small ribosomal RNAs (srRNAs) pieces, and this additional proc

275 rorhinotermes hosts, including small subunit ribosomal RNA (SSU rRNA) sequences from single cells.

276 in the ribosome's decoding center to adopt a ribosomal RNA-stabilized single-stranded helix.

277 rs the integrity of the nucleolus, impairing ribosomal RNA synthesis and evoking the ribosomal protei

278 associated with ATM-dependent repression of ribosomal RNA synthesis and large-scale reorganization o

279 icase DHX33, which is critically involved in ribosomal RNA synthesis and mRNA translation.

280 n the nucleoli is required for inhibition of ribosomal RNA synthesis and nucleolar segregation in res

281 ARF plays a significant role in regulating ribosomal RNA synthesis and processing, ribosome export

282 creases upstream binding factor recruitment, ribosomal RNA synthesis, ribonucleotide levels, and affe

283 ts in cardiomyocytes, indicative of impaired ribosomal RNA synthesis.

284 16S ribosomal RNA target gene sequencing was performed and t

285 y samples were collected and analyzed by 16S ribosomal RNA targeted pyrosequencing.

286 recognition of its two structurally distinct ribosomal RNA targets.

287 16S and 23S ribosomal RNAs into single-chain ribosomal RNAs that remain uncleaved by ribonucleases an

288 is derived from Salmonella 5'-leader of the ribosomal RNA transcript and has a 'stem' structure-cont

289 F13 1A is a nucleolar protein that represses ribosomal RNA transcription and attenuates protein synth

290 Via this mechanism, HOXB-AS3 regulates ribosomal RNA transcription and de novo protein synthesi

291 MYC mediates ribosomal RNA transcription in 2-cell embryos, supportin

292 tress response associated with inhibition of ribosomal RNA transcription was previously shown to pote

293 Applying EmPC-seq to the ribosomal RNA transcriptome, we show that TEELs of RNA p

294 s were mostly identified on transfer RNA and ribosomal RNA until the last decade, when they have been

295 amplicon-based sequencing targeting the 16S ribosomal RNA V3-V4 region was performed.

296 of sputum microbiota composition (using 16S ribosomal RNA V4 gene region sequencing) with CLD define

297 ata package provides count data for both 16S ribosomal RNA variable regions, integrated with phylogen

298 ata sets from amplicon sequencing of two 16S ribosomal RNA variable regions, with extensive controlle

299 a DNA library of V3 region of bacterial 16S ribosomal RNA was subjected to paired-end Illumina seque

300 Moreover, the direct use of ribosomal RNA without requiring the PCR pre-amplificatio