ライフサイエンスコーパス: ribosomal RNA

1 ablishes idiosyncratic interactions with the ribosomal RNA.

2 essed by sequencing the V4 region of the 16S ribosomal RNA.

3 -binding site and captures the 5' end of pre-ribosomal RNA.

4 on single-locus data, most typically nuclear ribosomal RNA.

5 anscriptase polymerase chain reaction of 16S ribosomal RNA.

6 distance consistent with that inferred from ribosomal RNA.

7 vitro express significantly lower levels of ribosomal RNA.

8 ercent of mycoplasma-mapped reads aligned to ribosomal RNA.

9 in transport, NLSs may facilitate folding of ribosomal RNA.

10 wn as a mediator of antibiotic resistance in ribosomal RNA.

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

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

13 9-nt stem-loop region from the large subunit ribosomal RNA.

14 steps in the 3' major domain of the 20S pre-ribosomal RNA.

15 folate-dependent flavoprotein seen to modify ribosomal RNA.

16 spacer 2 (ITS2) that separates 5.8S and 25S ribosomal RNAs.

17 ins, and defective processing of chloroplast ribosomal RNAs.

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

19 Reconstructing 16S ribosomal RNA, a phylogenetic marker gene, is usually re

20 16S ribosomal RNA amplicon sequencing was used for identific

21 robiota composition was determined using 16S ribosomal RNA analysis, and expression of a set of genes

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 Both ribosomal RNA and messenger RNA sequences were dominated

25 at nucleic acids, particularly extracellular ribosomal RNA and micro-RNAs, significantly contribute t

26 profiled ribosome complexes and analyzed the ribosomal RNA and protein components from these persiste

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

28 ey share an evolutionarily conserved core of ribosomal RNA and proteins.

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 n size and encode 12 protein-coding genes, 2 ribosomal RNAs and 22 transfer RNA genes.

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

33 ely 12 kb, the LIR contained large and small ribosomal RNAs and eight protein coding genes.

34 promotes the transcription of the genes for ribosomal RNAs and many other components involved in rib

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

36 ls for taxonomic identification of expressed ribosomal RNA, and inference of EM function based on pla

37 anied by massive mRNA reduction, cleavage of ribosomal RNA, and phosphorylation of PKR and eIF2alpha

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

39 ulation, including microRNAs, transfer RNAs, ribosomal RNA, and yRNA fragments.

40 ased mechanism may generalize to other tRNA, ribosomal-RNA, and sno-RNA fragments.

41 exes-UtpA and UtpB-interact with nascent pre-ribosomal RNA are poorly understood.

42 or fermentative end-product analysis and 16S ribosomal RNA bacterial gene amplification for bacterial

43 a (BOBCAT) study were evaluated by using 16S ribosomal RNA-based methods.

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

45 icrobiota profiles were characterized by 16S ribosomal RNA-based sequencing.

46 sent here phylogenomic (135 proteins and two ribosomal RNAs), Bayesian relaxed molecular clock (18 pr

47 MRPS7 is a 12S ribosomal RNA-binding subunit of the small mitochondrial

48 nd CPEB4 LCD-expressing animals have altered ribosomal RNA biogenesis, ribosomal protein gene express

49 processing of other non-coding RNAs (mostly ribosomal RNAs), but have also been implicated in proces

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

51 s, enhances the function of transfer RNA and ribosomal RNA by stabilizing the RNA structure.

52 reported urinary cell mRNA signature of 18S ribosomal RNA, CD3epsilon mRNA, and interferon-inducible

53 to cleave pre-ribosomal RNA to yield the 18S ribosomal RNA component of 40S ribosomal subunits.

54 imately 80 ribosomal proteins (RPs) into the ribosomal RNA core.

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

56 ing a machine-learning-based approach to 16S ribosomal RNA data sets generated from monthly faecal sa

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

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

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

60 cations and sequencing strategies, including ribosomal RNA-depleted samples.

61 We also demonstrated that ribosomal RNA depletion does not equally deplete ribosom

62 The ribosomal RNA distribution inside the cells hints to spa

63 ple, distant assembly factors and functional ribosomal RNA elements, manifesting their critical roles

64 e-specific proteins, protein insertions, and ribosomal RNA expansion segments of the 80 proteins and

65 was closely associated with sharply reduced ribosomal RNA expression.

66 es, including the well-studied large subunit ribosomal RNA family, and for the first time includes in

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

68 es we obtained nucleotide-resolution maps of ribosomal RNA flexibility revealing structurally distinc

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

70 assembly of ribosomal proteins and numerous ribosomal RNA folding steps.

71 is considered to be a dedicated regulator of ribosomal RNA folding, and has been shown to prevent Rho

72 ions but not in neocentromere regions, while ribosomal RNAs frequently emerged in neocentromere regio

73 16S ribosomal RNA gene amplicon pyrosequencing and HPV DNA t

74 easured, and microbiota were analyzed by 16S ribosomal RNA gene amplicon pyrosequencing.

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

76 In human beings, 16S ribosomal RNA gene analyses showed an increased proporti

77 16S ribosomal RNA gene analysis demonstrated that dusp6-defi

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

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

80 f the hypervariable regions V1-V3 of the 16S ribosomal RNA gene had greater accuracy than sequencing

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

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

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

84 Archaea, and Eukarya characterized by their ribosomal RNA gene phylogenies and genomic features.

85 protein, localizes in nucleoli and binds to ribosomal RNA gene promoters to help repress rRNA genes.

86 We performed 16S ribosomal RNA gene quantitative polymerase chain reactio

87 new simulation framework for generating 16S ribosomal RNA gene read counts that may be useful in com

88 Next-generation sequencing of 16S ribosomal RNA gene regions was used to characterize the

89 al phyla were identified only from their 16S ribosomal RNA gene sequence.

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

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

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

93 th chronic constipation and evaluated by 16S ribosomal RNA gene sequencing (average, 49,186 reads/sam

94 production data together with small subunit ribosomal RNA gene sequencing and biogeochemical data in

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

96 16S ribosomal RNA gene sequencing characterized the microbio

97 16S ribosomal RNA gene sequencing detected diverse bacterial

98 nciples, study design, and a workflow of 16S ribosomal RNA gene sequencing methodology, primarily for

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

100 n of gut microbiota was determined using 16S ribosomal RNA gene sequencing of stool samples.

101 In particular, the 16S ribosomal RNA gene sequencing technique has played an im

102 16S ribosomal RNA gene sequencing was used to characterize t

103 Samples were analyzed by 16S ribosomal RNA gene sequencing.

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

105 Sequencing of the bacterial 16S ribosomal RNA gene showed decreased bacterial diversity

106 ng of the hypervariable V3 region of the 16S ribosomal RNA gene showed members of the families of Lac

107 Here, we use a 16S ribosomal RNA gene survey in a lake that has chemical gr

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

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

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

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

112 eq sequencing of the V4-V5 region of the 16S ribosomal RNA gene.

113 ag sequencing of the V3-V5 region of the 16S ribosomal RNA gene.

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

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

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

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

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

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

120 en the two proteins could explain the shared ribosomal RNA genes (rDNA) phenotypes.

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

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

123 ith RNA Polymerase I, associates with active ribosomal RNA genes and is required for serum-induced ac

124 e blocks and functional elements such as the ribosomal RNA genes and the centromeres, are largely ina

125 Microbiologists utilize ribosomal RNA genes as molecular markers of taxonomy in

126 e Carl Woese reported in PNAS how sequencing ribosomal RNA genes could be used to distinguish the thr

127 d rRNA assembly tool, REAGO (REconstruct 16S ribosomal RNA Genes from metagenOmic data).

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

129 , we sequenced the mitochondrial 12S and 16S ribosomal RNA genes of males and females from the Arizon

130 We used transcribed portions of ribosomal RNA genes to identify several transcriptionall

131 equences aligning to Balamuthia mandrillaris ribosomal RNA genes were identified in the CSF by MDS.

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

133 By combining pyrosequencing of 18S ribosomal RNA genes with data on multiple environmental

134 F1 prevents antisense transcription over the ribosomal RNA genes, a process which we here show to be

135 inds the promoter and coding regions of most ribosomal RNA genes, facilitating transcription and poss

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

137 other fungi, with substantial reductions of ribosomal RNA genes, transporters, transcription factors

138 ated through the sequencing of small subunit ribosomal RNA genes.

139 olide and fluoroquinolone antibiotics in 23S ribosomal RNA, gyrA, gyrB, and parC genes.

140 Metagenomic analysis of 16S ribosomal RNA has been used to profile microbial communi

141 Conserved M-domain residues contact ribosomal RNA helices 24 and 59.

142 Sequencing of the 16S ribosomal RNA identified Bifidobacterium as associated w

143 equencing were used to analyze bacterial 16S ribosomal RNA in ileal contents from the rats.

144 activity of FGFR2 in BBDS elevates levels of ribosomal RNA in the developing bone, consequently promo

145 to the P site, revealing an active role for ribosomal RNA in the translocation process.

146 stitution at the level of individual protein/ribosomal RNA interactions are developed for two tempera

147 acterial isolates were identified by 16S-23S ribosomal RNA intergenic spacer region sequencing for ge

148 Ribosomal RNA is naturally amplified in bacterial cells,

149 me has been described as a ribozyme in which ribosomal RNA is responsible for peptidyl-transferase re

150 , but whether this involves modifications of ribosomal RNA is unclear.

151 oma and Leishmania, the 26/28S large subunit ribosomal RNA is uniquely composed of 6 rRNA fragments.

152 ic ribosomal RNA (rRNA) and among eukaryotic ribosomal RNAs is focused in expansion segments (ESs).

153 e bulk of the transcribed genome, apart from ribosomal RNAs, is at the level of noncoding RNA genes.

154 s contain 26/28S, 5S, and 5.8S large subunit ribosomal RNAs (LSU rRNAs) in addition to the 18S rRNA o

155 mutation was associated with a defect in pre-ribosomal RNA maturation.

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

157 robustly overexpresses the mitochondrial 12S ribosomal RNA methyltransferase TFB1M (Tg-mtTFB1 mice) e

158 ative stress, independent of their predicted ribosomal RNA modifications.

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

160 hich are specific to mitochondria, and three ribosomal RNA molecules.

161 Ribosomal RNAs must also be exported from the nucleus an

162 2 domains of the large subunit (LSU) nuclear ribosomal RNA (nrRNA) gene and by morphological characte

163 Although m(6)A is present in the ribosomal RNA of bacteria, its occurrence in mRNA still

164 Here we present an update to the ribosomal RNA operon copy number database (rrnDB), a pub

165 Here, we show that the number of ribosomal RNA operons (rrn) in bacterial genomes predict

166 shift site or both, can act by pairing with ribosomal RNA or as stem loops or pseudoknots even with

167 vicida based on sequence analyses of the 16S ribosomal RNA, pgm, and pdpD genes.

168 y more complex evolutionary history than 16S ribosomal RNA phylogenies, suggesting that horizontal ge

169 specimens were cultured and analyzed by 16S ribosomal RNA polymerase chain reaction (PCR) for the pr

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

171 RNA) base-pairs to multiple sites in the pre-ribosomal RNA (pre-rRNA) to promote early cleavage and f

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

173 Pre-ribosomal RNAs (pre-rRNAs) must be processed stepwise an

174 ious studies have shown that copy numbers of ribosomal-RNA precursor (pre-rRNA) of specific pathogen

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

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

177 e in situ hybridization using a specific 16S ribosomal RNA probe and genomic DNA probe.

178 RRP1B (ribosomal RNA processing 1 homolog B) was first identifi

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

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

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

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

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

184 0 hexamer, but some promoters, including the ribosomal RNA promoter rrnB P1, start 9 nt from the -10

185 ound complexes on the M. tuberculosis rrnAP3 ribosomal RNA promoter.

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

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

188 yses were performed on stool samples via 16S ribosomal RNA pyrosequencing and correlations between di

189 ) and controls (n = 15) were analyzed by 16S ribosomal RNA pyrosequencing and culture-based methods.

190 The structure shows how features of ribosomal RNA rearrange to hand off the A-site tRNA to t

191 the pathogenic mechanism of this mutation of ribosomal RNA remains controversial.

192 ed ribosomal protein (r-protein) binding and ribosomal RNA remodelling events in the nucleolus, nucle

193 Although ribosomal RNA represents the majority of cellular RNA, a

194 Ribosomal RNA (rrn) operons, characteristically present

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

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

197 noglycoside antibiotics, which by binding to ribosomal RNA (rRNA) affect bacterial protein synthesis.

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

199 ivergence between prokaryotic and eukaryotic ribosomal RNA (rRNA) and among eukaryotic ribosomal RNAs

200 iota by pyrosequencing the gene encoding 16S ribosomal RNA (rRNA) and measured markers of microbial t

201 hough evidence for a system that coordinates ribosomal RNA (rRNA) and ribosomal protein gene (RPG) tr

202 on of total ncRNA, including 5S, 16S and 23S ribosomal RNA (rRNA) and tRNA, from mycobacteria, using

203 structure of the GTPase center (GAC) of 23S ribosomal RNA (rRNA) as seen in cocrystals is extremely

204 associated with stem cells, neurogenesis and ribosomal RNA (rRNA) biogenesis.

205 Processes of ribosomal RNA (rRNA) expansion can be "observed" by comp

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

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

208 s between ribosomal proteins (rproteins) and ribosomal RNA (rRNA) facilitate the formation of functio

209 mbo 2 assay) for detection of C. trachomatis ribosomal RNA (rRNA) from direct ocular samples.

210 16S ribosomal RNA (rRNA) gene and other environmental sequen

211 dense time-series data, we sequenced the 16S ribosomal RNA (rRNA) gene from DNA isolated from the fec

212 hniques, DNA sequencing of the bacterial 16S ribosomal RNA (rRNA) gene or whole metagenome shotgun (W

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

214 Owing to divergent 16S ribosomal RNA (rRNA) gene sequences, 50-100% of organism

215 Individual isolates were identified by 16S ribosomal RNA (rRNA) gene sequencing and compared with v

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

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

218 In eukaryotes, scores of excess ribosomal RNA (rRNA) genes are silenced by repressive ch

219 hat bind and discriminate the A-tRNA-namely, ribosomal RNA (rRNA) helices H89, H91, and ribosomal pro

220 ding involves both ribosomal protein and 18S ribosomal RNA (rRNA) interactions.

221 orrhagic Escherichia coli and that Howardula ribosomal RNA (rRNA) is depurinated during Spiroplasma-m

222 GTPases) with the sarcin-ricin loop (SRL) of ribosomal RNA (rRNA) is pivotal for hydrolysis.

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

224 p21, confers atheroprotection by controlling ribosomal RNA (rRNA) maturation and modulating pathways

225 During ribosomal RNA (rRNA) maturation, cleavages at defined si

226 Ribosomal RNA (rRNA) modifications are essential for rib

227 le the D1-D2 hypervariable region of the 28S ribosomal RNA (rRNA) of R. glutinis from each of the SSc

228 i, we examined the relative positions of the ribosomal RNA (rRNA) operons in space.

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

230 is an unconventional HSP crucial for correct ribosomal RNA (rRNA) processing and preventing aberrant

231 and with the p.I31F RPS29 mutation had a pre-ribosomal RNA (rRNA) processing defect compared with the

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

233 owing where ribosomal proteins interact with ribosomal RNA (rRNA) provides a strategic platform to in

234 posed of two subunits, each built on its own ribosomal RNA (rRNA) scaffold.

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

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

237 g cell nuclear antigen (PCNA) expression and ribosomal RNA (rRNA) synthesis in T cells during activat

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

239 SAT) system that allows for co-activation of ribosomal RNA (rRNA) transcription and ribosome assembly

240 Female GSCs display high levels of ribosomal RNA (rRNA) transcription, and Udd becomes enri

241 ed production of ribosomal proteins (RP) and ribosomal RNA (rRNA), including the processing of the la

242 dinated production of ribosomal proteins and ribosomal RNA (rRNA), including the processing of the la

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

244 oped combined assays that couple BONCAT with ribosomal RNA (rRNA)-targeted fluorescence in situ hybri

245 g arginine-rich linear motifs (R-motifs) and 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 nd RNase L-independent cleavage sites within ribosomal RNAs (rRNAs) and (iii) 2', 3'-cyclic phosphate

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

250 ional capacity and maturation of chloroplast ribosomal RNAs (rRNAs) are perturbed in mterf6-1 mutants

251 Based on SHAPE probing data alone, ribosomal RNAs (rRNAs) from three diverse organisms--the

252 n eukaryotes contain 79-80 proteins and four ribosomal RNAs (rRNAs) more than 5,400 nucleotides long.

253 cess involving the folding and processing of ribosomal RNAs (rRNAs), concomitant binding of ribosomal

254 scRNAs, respectively), transfer (tRNAs), and ribosomal RNAs (rRNAs).

255 ecific non-coding RNAs, including miRNAs and ribosomal RNAs (rRNAs).

256 e most components of the bacterial ribosome (ribosomal RNAs [rRNAs] and ribosomal proteins) are well

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

258 ogrammatic access to curated, representative ribosomal RNA sequence alignments from bacterial, archae

259 Many molecular recognition methods target ribosomal RNA sequences due to their specificity and abu

260 About 70% of near-full length bacterial 16S ribosomal RNA sequences from dolphins are unique.

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

262 cuss some applications and challenges of 16S ribosomal RNA sequencing as well as directions for futur

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

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

265 re previously enrolled in a protocol for 16S ribosomal RNA sequencing of fecal microbiota.

266 uorescent Pseudomonads in natural soils; 16S ribosomal RNA sequencing revealed that accession-specifi

267 16S ribosomal RNA sequencing was conducted on microbial DNA

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

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

270 uniparental rDNA (encoding 18S, 5.8S and 26S ribosomal RNA) silencing (nucleolar dominance) and rRNA

271 on of ribonucleoprotein complexes, including ribosomal RNA, small nucleolar RNAs (snoRNAs) and 7SK RN

272 inding of eRF1 flips nucleotide A1825 of 18S ribosomal RNA so that it stacks on the second and third

273 on of PCR-based surveys of the small-subunit ribosomal RNA (SSU rRNA) gene.

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

275 How early binding proteins change the ribosomal RNA structure so that later proteins may join

276 ly critical for recognition of both tRNA and ribosomal RNA substrates.

277 Ribosomal RNA surveys have identified four major clades

278 recently reported on an integrated, one-pot ribosomal RNA synthesis (rRNA), ribosome assembly, and t

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

280 Depletion of GTP inhibits ribosomal RNA synthesis in T cells by inhibiting transcr

281 aurin markedly potentiates the inhibition of ribosomal RNA synthesis, PCNA expression, and T-cell act

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

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

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

285 recognition of its two structurally distinct ribosomal RNA targets.

286 To this end, we rationally designed a ribosomal RNA that covalently links the ribosome subunit

287 t and organization encoding 35 proteins, two ribosomal RNAs, three putative open reading frames and 3

288 hich co-transcriptionally associate with pre-ribosomal RNA to form the small subunit processome.

289 ous molecular technologies (ranging from 16S ribosomal RNA to shotgun metagenomic sequencing) in enum

290 x whose only known function is to cleave pre-ribosomal RNA to yield the 18S ribosomal RNA component o

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

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

293 Ribosomal RNA transcription mediated by RNA polymerase I

294 cells, nutrients and growth factors regulate ribosomal RNA transcription through various key factors

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

296 r localization that is dependent upon active ribosomal RNA transcription.

297 After 14 days, 16S ribosomal RNA transcripts/genome declined 96%, indicatin

298 to subserve housekeeping functions in cells-ribosomal RNAs, transfer RNAs, and small nucleolar RNAs.

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

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