ライフサイエンスコーパス: ribosomal RNA gene

1 n analyses of other data sets (e.g., the 18S ribosomal RNA gene).

2 h-throughput sequencing of the bacterial 16S ribosomal RNA gene.

3 terial levels by quantitative PCR of the 16S ribosomal RNA gene.

4 3 hypervariable region of the bacterial 16 s ribosomal RNA gene.

5 mplification and sequencing of bacterial 16S ribosomal RNA gene.

6 abundant in the nontranscribed region of the ribosomal RNA gene.

7 identity was confirmed by sequencing the 16s ribosomal RNA gene.

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

9 ycoplasma-specific primers targeting the 16S ribosomal RNA gene.

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

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

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

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

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

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

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

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

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

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

20 uencing of the V1-V3 region of bacterial 16S ribosomal RNA genes.

21 geting the Rpd3L/Sin3L complex for silencing ribosomal RNA genes.

22 in the H. pylori chromosome but numerous in ribosomal RNA genes.

23 ibosomal DNA to repress the transcription of ribosomal RNA genes.

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

25 unction with phylogenies that track with the ribosomal RNA genes.

26 o the Roche Amplicor PCR assay targeting 16s ribosomal RNA genes.

27 gulated at the level of transcription of the ribosomal RNA genes.

28 nsensus reference sequences of small subunit ribosomal RNA genes.

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

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

31 sequences of the mitochondrial small subunit ribosomal RNA gene (16S rDNA; rns).

32 nd mitochondrial gene, the large-subunit 16S ribosomal RNA gene (16S), showed little deviation from n

33 Complete small subunit ribosomal RNA gene (18S rDNA) sequence analysis was used

34 Acanthamoeba into genotypes based on nuclear ribosomal RNA gene (18S rDNA, Rns) sequences.

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

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

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

38 ealed by the highly fragmented mitochondrial ribosomal RNA genes also appears to have originated at t

39 rated 144 viromes, 84 metagenomes and 84 16S ribosomal RNA gene amplicon datasets to characterize vir

40 16S ribosomal RNA gene amplicon pyrosequencing and HPV DNA t

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

42 onomic units (zOTUs) obtained from V4 of 16S ribosomal RNA gene amplicon sequences.

43 microbiota composition were evaluated by 16S ribosomal RNA gene amplicon sequencing analysis.

44 gut microbial diversity in cicadas using 16S ribosomal RNA gene amplicon sequencing data from 197 wil

45 unctionalized variant of cholesterol and 16S ribosomal RNA gene amplicon sequencing of faecal samples

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

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

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

49 aspirates were collected and examined by 16S ribosomal RNA gene amplicon sequencing.

50 onths of age, and microbiota analyzed by 16S ribosomal RNA gene amplicon sequencing.

51 l swab specimens through high-throughput 16s ribosomal RNA gene amplicon sequencing.

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

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

54 molecular and microscopic analysis using 16S ribosomal RNA gene amplicon-sequencing of colonic biopsi

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

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

57 16S ribosomal RNA gene analysis demonstrated that dusp6-defi

58 Faecal 16S ribosomal RNA gene analysis was undertaken.

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

60 PCR) amplification of the P. jirovecii mtLSU ribosomal RNA gene and immunofluorescence microscopy (IF

61 Methods: We performed 16S ribosomal RNA gene and shotgun metagenomics sequencing o

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

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

64 o genomes, (iv) pairwise identity of the 16S ribosomal RNA genes and (v) pairwise identity of an addi

65 within the 14,100 basepairs (bp) are the two ribosomal RNA genes and 13 protein coding genes typical

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

67 to the internal promoter element of the 5 S ribosomal RNA genes and acts as a positive transcription

68 rn blots probed with chloroplast and nuclear ribosomal RNA genes and end-labeled restriction fragment

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

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

71 ts with data sets of sequenced bacterial 16S ribosomal RNA genes and total-faecal-community DNA.

72 across all seasons, underwent bacterial (16S ribosomal RNA gene) and fungal (internal transcribed spa

73 primers were used to amplify regions of 16S ribosomal RNA genes, and amplicons were sequenced using

74 bosomal DNA, the mating type locus, tRNA, 5S ribosomal RNA genes, and genes that are highly transcrib

75 and tRNA(Ile) located downstream of the two ribosomal RNA genes, and upstream of where they are typi

76 s in the nontranscribed spacer 3' of the 35S ribosomal RNA gene are important to the polar arrest of

77 Ribosomal RNA genes are arranged in large arrays with hu

78 of nucleotide substitution in mitochondrial ribosomal RNA genes are described and applied in a phylo

79 All 13 protein-coding genes and the two ribosomal RNA genes are of similar sizes to those found

80 Ribosomal RNA genes are organized in tandem arrays calle

81 and meiotic recombination between the tandem ribosomal RNA gene array (rDNA).

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

83 ntact animals exposed to 5-HT identified the ribosomal RNA genes as PARP-dependent effector genes.

84 unique sites in the small and large subunit ribosomal RNA genes (as of February 2002).

85 ined the cytosine methylation content of the ribosomal RNA genes at the two nucleolus organizer regio

86 IA-dependent transcription of the Xenopus 5S ribosomal RNA gene but not TFIIIA-independent transcript

87 protein that regulates expression of the 5 S ribosomal RNA gene by binding specifically to the intern

88 We also show that repression of ribosomal RNA genes by JHDM1B is dependent on its JmjC d

89 nded dramatically owing to the sequencing of ribosomal RNA genes cloned from environmental DNA.

90 rial lineage that contains SAR11 and related ribosomal RNA gene clones was among the first groups of

91 h altered frequencies of DSBs (including the ribosomal RNA gene cluster) are known targets of Sir2p d

92 e highly repeated, highly self-similar human ribosomal RNA gene clusters as sentinel biomarkers for d

93 ually all bacteria have the highly expressed ribosomal RNA genes co-directional with replication.

94 quencing of a 284-basepair region of the 16S ribosomal RNA gene confirmed that the sequence is closel

95 multaneous visualization of two sets of four ribosomal RNA genes confirms tetraploidy of this clone.

96 o determine the extent of human variation in ribosomal RNA gene content (rDNA) and patterns of rDNA c

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

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

99 ased procedure, PCR amplification of the 16S ribosomal RNA gene coupled with very deep sequencing of

100 The most abundant class of bacterial ribosomal RNA genes detected in seawater DNA by gene clo

101 Elimination of the nucleolus by removing the ribosomal RNA genes disrupted this process causing incre

102 There are 55 putative genes: three ribosomal RNA genes, eight transfer RNA genes, 22 protei

103 D2 in the methylation-mediated inhibition of ribosomal RNA gene expression.

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

105 e polymerase chain reaction (PCR) of the 16S ribosomal RNA gene followed by Sanger sequencing, multip

106 nd PCR targeting the V1-V3 region of the 16S ribosomal RNA gene, followed by next-generation sequenci

107 r 1alpha and the mitochondrial small subunit ribosomal RNA genes for F. oxysporum strains from banana

108 ties commonly involves the classification of ribosomal RNA gene fragments.

109 (20 out of 36), or PCR amplification of the ribosomal RNA gene from feces with T. foetus-specific pr

110 Culture-independent surveys based on ribosomal RNA genes from deep-sea hydrothermal deposits

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

112 Previous studies indicated that ribosomal RNA genes from one parental origin are epigene

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

114 A 16S ribosomal RNA gene has been sequenced from Heliobacteriu

115 DNA sequencing of the ribosomal RNA genes has been used to identify these para

116 Bichir mitochondrial protein-coding and ribosomal RNA genes have greater sequence similarity to

117 Although Micromonas isolates have high 18S ribosomal RNA gene identity, we found that genomes from

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

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

120 o the intergenic spacer (IGS) of the 18S.25S ribosomal RNA genes in potato.

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

122 lear development the Tetrahymena thermophila ribosomal RNA gene is excised from micronuclear chromoso

123 Regulation of ribosomal RNA genes is a fundamental process that suppor

124 transcriptional initiation of fission yeast ribosomal RNA genes is dependent on the core ribosomal R

125 or allopolyploids, often one parental set of ribosomal RNA genes is transcribed and the other is sile

126 in, we sequenced bacterial 16S small-subunit ribosomal RNA genes isolated from the inner elbow of fiv

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

128 ver, we find that transcribed regions of the ribosomal RNA gene loci exhibit rapid exchange of H3/H4

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

130 tain hundreds of tandemly repeated copies of ribosomal RNA genes needed to support cellular viability

131 Furthermore, in embryos lacking ribosomal RNA genes, nucleolar proteins were redistribut

132 a real-time PCR assay for detecting the 16S ribosomal RNA gene of M. tuberculosis.

133 port the pyrosequencing of the bacterial 16S ribosomal RNA gene of more than 600 Arabidopsis thaliana

134 We sequenced the 18S ribosomal RNA gene of seven isolates of the enigmatic ma

135 The 16S ribosomal RNA gene of the hyperthermophilic nitrogen fix

136 amine genetic variation in the small subunit ribosomal RNA gene of three bipolar planktonic foraminif

137 Small subunit ribosomal RNA genes of Archaea were amplified from soil

138 ibed spacer (ITS) regions separating nuclear ribosomal RNA genes of Chlorophytes has improved the fid

139 lymerase chain reaction assays targeting 16S ribosomal RNA genes of Gardnerella vaginalis, Lactobacil

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

141 Examining the 16S ribosomal RNA genes of Solirubrobacter revealed substant

142 Results of this study also showed the two ribosomal RNA genes of the three species had very limite

143 iption factor TFIIIA, which regulates the 5S ribosomal RNA genes of Xenopus laevis.

144 Oligonucleotide fingerprinting of ribosomal RNA genes (OFRG) is a procedure that sorts rRN

145 Here we show that the ribosomal RNA gene operon (rrn) copy number, a genomic t

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

147 Here, the results of a 16S ribosomal RNA gene PCR/sequencing assay performed on ple

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

149 Phylogenetic analyses using multiple ribosomal RNA genes place this clade with Rozella, the p

150 and dysbiosis index were analyzed using 16S ribosomal RNA gene polymerase chain reaction DNA amplifi

151 position was evaluated using broad-range 16S ribosomal RNA gene polymerase chain reaction with high-t

152 tionship between the number of copies of the ribosomal RNA gene present in its chromosomal array and

153 city, with genes for only three proteins and ribosomal RNA genes present in scrambled fragments origi

154 ribosomal RNA genes is dependent on the core ribosomal RNA gene promoter and is stimulated by an upst

155 SL1, essential for Pol I recruitment to the ribosomal RNA gene promoter, also has an essential postp

156 ntial for preinitiation complex formation at ribosomal RNA gene promoters in vitro.

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

158 Microbiomes were analyzed with 16S ribosomal RNA gene pyrosequencing together with quantita

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

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

161 accharomyces cerevisiae, the tandem array of ribosomal RNA genes (RDN1) is a target for integration o

162 genetic element that maps within an X-linked ribosomal RNA gene (rDNA) array of D. melanogaster.

163 e probes needed for analyzing populations of ribosomal RNA gene (rDNA) clones by hybridization experi

164 y demonstrated that the core promoter of rat ribosomal RNA gene (rDNA) contains an E-box-like sequenc

165 The 45S and 5S ribosomal RNA gene (rDNA) loci were simultaneously visua

166 omic DNA sequences, especially environmental ribosomal RNA gene (rDNA) sequences.

167 community genomic DNA, amplification of 16S ribosomal RNA genes (rDNA) and subsequent examination of

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

169 The 35S ribosomal RNA genes (rDNA) are organized as repeated arr

170 ly demonstrated that the expression of human ribosomal RNA genes (rDNA) in normal and cancer cells is

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

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

173 enesis requires accelerated transcription of ribosomal RNA genes (rDNAs).

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

175 tructed with phylogenetic markers, including ribosomal RNA gene regions and other highly conserved ge

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

177 Sequencing of 16S ribosomal RNA genes revealed a relative abundance of Bac

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

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

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

181 RNA polymerase I of only one parental set of ribosomal RNA genes (rRNA genes).

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

183 Further, the hypothesis that ribosomal RNA gene "satellite association" induced by in

184 Ribosomal RNA gene sequence data indicate the presence o

185 The 16S ribosomal RNA gene sequence of an unknown organism was o

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

187 n and phylogenetic analysis of small-subunit ribosomal RNA gene sequences allow microbes to be identi

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

189 was to provide a reference collection of 16S ribosomal RNA gene sequences collected from sites across

190 sts and animals, but the lack of data beyond ribosomal RNA gene sequences from all but a few describe

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

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

193 We examined 13,355 prokaryotic ribosomal RNA gene sequences from multiple colonic mucos

194 ed a network-based analysis of bacterial 16S ribosomal RNA gene sequences from the fecal microbiota o

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

196 Our analysis of 16S ribosomal RNA gene sequences obtained from 20 distinct s

197 Analysis of bacterial and archaeal 16S ribosomal RNA gene sequences revealed 25 bioindicator am

198 ature analyses of these cloned small subunit ribosomal RNA gene sequences revealed a cluster of Archa

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

200 s of polymerase chain reaction-amplified 16S ribosomal RNA gene sequences.

201 ing of APOL9-binding bacterial taxa with 16S ribosomal RNA gene sequencing (APOL9-seq), we identify t

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

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

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

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

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

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

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

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

210 position and density were measured using 16S ribosomal RNA gene sequencing and quantitative polymeras

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

212 16S ribosomal RNA gene sequencing characterized the microbio

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

214 16S ribosomal RNA gene sequencing detected diverse bacterial

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

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

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

218 16S ribosomal RNA gene sequencing of lung washes and buccal

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

220 Recent 16S ribosomal RNA gene sequencing studies revealed gut dysbi

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

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

223 In this study, we used ribosomal RNA gene sequencing to identify the zooxanthel

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

225 16S ribosomal RNA gene sequencing was performed on DNA extra

226 16S ribosomal RNA gene sequencing was performed on sputum fr

227 On stool samples, 16S ribosomal RNA gene sequencing was performed, and taxonom

228 16S ribosomal RNA gene sequencing was used to characterize t

229 wheezing cohort were characterized using 16S ribosomal RNA gene sequencing, and unsupervised hierarch

230 crobiome measures, characterized through 16S ribosomal RNA gene sequencing, included alpha diversity

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

232 Ribosomal RNA gene sequencing, targeting prokaryotic and

233 etagenomics analysis was performed using 16S ribosomal RNA gene sequencing, whereas host sebocyte gla

234 22 healthy children, ages 7-12 years, by 16S ribosomal RNA gene sequencing, with an average of 54,287

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

236 uated for bacterial composition based on 16S ribosomal RNA gene sequencing.

237 2 groups based on features derived from 16S ribosomal RNA gene sequencing.

238 and descending colons were determined by 16S ribosomal RNA gene sequencing.

239 ecipients of allo-HCT and analyzed using 16S ribosomal RNA gene sequencing.

240 icrobial taxonomic profiling, mostly via 16S ribosomal RNA gene sequencing.

241 from 877 participants was analyzed using 16S ribosomal RNA gene sequencing.

242 Microbiota analysis was performed by 16S ribosomal RNA gene sequencing.

243 rom weekly stool samples was analyzed by 16S ribosomal RNA gene sequencing.

244 VRE on selective media and analyzed via 16S ribosomal RNA gene sequencing.

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

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

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

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

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

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

251 n of genes encoding known virulence factors, ribosomal RNA gene spacer restriction fragment length po

252 relative abundance of archaeal small subunit ribosomal RNA genes (SSU rDNA) in the subgingival crevic

253 with comparable accuracy to the phylogeny of ribosomal RNA genes, substantially improving on a known

254 Sequence comparisons of small-subunit ribosomal RNA genes suggest a deep evolutionary divergen

255 ic analysis of the full-length small subunit ribosomal RNA gene suggests this pathogen's placement in

256 iopsy samples were analyzed by bacterial 16S ribosomal RNA gene survey and classified into types usin

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

258 Recently, cultivation-independent ribosomal RNA gene surveys have indicated a potential im

259 In this study, we used pyrosequencing of 16S ribosomal RNA gene tags to compare the composition of th

260 evolution of their gut microbiota, using 16S ribosomal RNA gene-targeted amplicon sequencing.

261 This group accounts for 26% of all ribosomal RNA genes that have been identified in sea wat

262 ng of a variable region of the bacterial 16S ribosomal RNA gene to characterize the bacterial communi

263 nes, and (5) linking protein coding genes to ribosomal RNA genes to aid metabolic inference in 16S rR

264 DNA and targeted sequencing of bacterial 16S ribosomal RNA genes to gain an understanding of how micr

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

266 Ribosomal RNA gene transcription by RNA polymerase I (Po

267 nscription factor IIIA (TFIIIA) activates 5S ribosomal RNA gene transcription in eukaryotes.

268 Ribosomal RNA gene transcription, co-transcriptional pro

269 lant hybrids is the uniparental silencing of ribosomal RNA gene transcription, or nucleolar dominance

270 omerase IIalpha in RNA polymerase I-directed ribosomal RNA gene transcription, which drives cell grow

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

272 Genome sequence information that would allow ribosomal RNA gene trees to be related to broader patter

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

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

275 12 and laboratory tests were performed; 16S ribosomal RNA gene (V4V5) sequencing was performed on st

276 ng protocol that produces reads spanning 16S ribosomal RNA gene variable regions 1 and 2 ( approximat

277 The V3-V5 region of the bacterial 16S ribosomal RNA gene was amplified and pyrosequenced, resu

278 and the V3 to V4 variable region of the 16S ribosomal RNA gene was amplified and sequenced.

279 Region V3-V5 of the 16S ribosomal RNA gene was amplified and sequenced.

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

281 on sequencing of the V1-V2 region in the 16S ribosomal RNA gene was performed in stool samples of pat

282 containing the Xenopus borealis somatic 5 S ribosomal RNA gene was used as a model system to determi

283 The Xenopus borealis somatic 5S ribosomal RNA gene was used as a model system to determi

284 n vivo topological domain size for the human ribosomal RNA genes was estimated between 30,000 and 45,

285 e nucleolar organizer regions (NORs) and the ribosomal RNA genes was examined by Southern analysis an

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

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

288 By sequencing 16S ribosomal RNA genes, we show that a longitudinal selecti

289 taining clusters of transcriptionally active ribosomal RNA genes, we studied the binding of angiogeni

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

291 -PCR) analysis and pyrosequencing of the 16S ribosomal RNA gene were used to analyze the diversity of

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

293 Fragments of 16S ribosomal RNA genes were detected by polymerase chain re

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

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

296 y sequencing of the V3-V4 regions of the 16S ribosomal RNA gene, were performed.

297 f angiogenin to the intergenic spacer of the ribosomal RNA gene where many of the transcription regul

298 to bind to enhancer regions upstream of the ribosomal RNA genes, which are clustered at NORs.

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

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