ライフサイエンスコーパス: ribonucleic acid

1 glutamine, omega3 fatty acids, arginine, and ribonucleic acid.

2 h a decrease in myosin heavy chain messenger ribonucleic acid.

3 ecretions were tested for shedding of RV-A16 ribonucleic acid.

4 relevant to studies of structure-function in ribonucleic acids.

5 s were reduced by specific small interfering ribonucleic acids.

6 (HIV-1) Tat protein is mediated by specific ribonucleic acids.

7 cose, and expression levels of NPs and micro ribonucleic acid 425 (miR-425), a negative regulator of

8 Depletion of JunB by small interfering ribonucleic acid abrogates TGF-beta-induced disruption o

9 ion protein silencing with small interfering ribonucleic acid also resulted in the worsening of activ

10 sequence-activity relationships in proteins, ribonucleic acid and deoxyribonucleic acid.

11 ranslates genetic information from messenger ribonucleic acid and makes protein accordingly.

12 favour the condensation of monomers to form ribonucleic acid and peptides.

13 Arc messenger ribonucleic acid and protein are localized in activated

14 Messenger ribonucleic acid and protein expression were confirmed i

15 ed suppression (>2 weeks) of PAI-1 messenger ribonucleic acid and protein in rat heart tissues after

16 wed expression changes at both the messenger ribonucleic acid and protein level.

17 ynamics, and rhythms in endogenous messenger ribonucleic acid and protein levels of BMAL1.

18 se subtilisin/kexin type 9 (PCSK9) messenger ribonucleic acid and protein levels were determined by u

19 xpressed functional FLT3, and FLT3 messenger ribonucleic acid and protein were up-regulated under oxi

20 protein (RNP) complexes, composed of a small ribonucleic acid and three proteins of 100, 193, and 240

21 We characterize both unmodified and modified ribonucleic acids and present the first application of a

22 nd anti-oncogenes transcriptional (messenger ribonucleic acid) and translational (protein) products i

23 f ribonucleic acid, species, including micro-ribonucleic acids, and allow for a genome-wide investiga

24 tive delivery of therapeutic antisense micro-ribonucleic acid (antimiR) molecules to the myocardium i

25 on of tissue necrosis factor alpha messenger ribonucleic acid as compared to controls as early as 1-h

26 the structures suggested the location of the ribonucleic acid backbone phosphates in the ribonucleoti

27 We found that the ribonucleic acid-binding protein Arrest (Aret) is expres

28 ogenous CHGA expression by small interfering ribonucleic acid caused approximately two-thirds depleti

29 regenerative capacity of chemically modified ribonucleic acid (cmRNA) (encoding BMP-2) complexed with

30 nterference motif, the specific small CRISPR ribonucleic acid (crRNA) transcribed from expanded CRISP

31 annexin V expression using small interfering ribonucleic acid decreased caspase-3 activity and increa

32 tein, blood and monocyte Lp-PLA(2) messenger ribonucleic acid decreased transiently, and plasma Lp-PL

33 Here, we used (deoxy)ribonucleic acid (DNA)-origami technology to construct s

34 t gene expression, but significant messenger ribonucleic acid downregulation of IKACh-inhibiting RGS

35 uringiensis; next-generation double-stranded ribonucleic acid (dsRNA) PIPs have been recently approve

36 odeoxynucleotides and nucleases as messenger ribonucleic acid, enabled high knockin efficiencies in d

37 with l-arginine and omega-3 (n-3) fatty and ribonucleic acids (experimental arm), or an isocaloric i

38 Ribonucleic acid export 1 (Rae1) and Nup98 are evolution

39 ignal-mediated protein export, and messenger ribonucleic acid export but no apparent mitotic failure.

40 Ribonucleic acid expression analysis identified changes

41 ndothelial TNFalpha-induced VCAM-1 messenger ribonucleic acid expression and promoter activity, and i

42 Studies of messenger ribonucleic acid expression have also shown promise for

43 terase-4D (PDE4D) isoform-specific messenger ribonucleic acid expression in the lung.

44 Maximum messenger ribonucleic acid expression of both cytokines was observ

45 ere collected for determination of messenger ribonucleic acid expression of IL-10 by reverse transcri

46 Adipose messenger ribonucleic acid expression of inflammatory genes includ

47 was not related to changes in the messenger ribonucleic acid expression of Kir6.1, Kir6.2, SUR1A, SU

48 uitment maneuver did not influence messenger ribonucleic acid expression of receptor for advanced gly

49 n humans, the industrialization of messenger ribonucleic acid expression profiling, and the maturatio

50 IKACh) with patch clamp recording, messenger ribonucleic acid expression with quantitative polymerase

51 stinal tumours, we performed mRNA (messenger ribonucleic acid) expression profiling of 16 human and 6

52 In left ventricle at baseline, messenger ribonucleic acid for atrial natriuretic peptide (ANP) an

53 RNAs) are a subclass of regulatory noncoding ribonucleic acids for which expression and function in h

54 We analyzed HCV ribonucleic acid from sequential serum and PBMC samples

55 hese samples were subjected to 16S ribosomal ribonucleic acid gene (V3-V4 region) sequencing.

56 miRNAs, short ribonucleic acid gene regulators, are increasingly popul

57 (ELISA), and the microbiota by 16S ribosomal ribonucleic acid gene sequencing.

58 Enteroviral ribonucleic acids have been identified in heart muscle o

59 ion." Three of these substances (no data for ribonucleic acid) have been evaluated as individual supp

60 s of IL-10 nor expression of IL-10 messenger ribonucleic acid in circulating mononuclear cells differ

61 Immunostaining for KLP68D and ribonucleic acid in situ hybridization for KLP64D demons

62 rion protein gene-specific small interfering ribonucleic acid in vivo and in vitro.

63 nd chemistry to uncover the complex roles of ribonucleic acids in cellular processes.

64 The overall folds of the three ribosomal ribonucleic acids in our model are consistent with those

65 Clathrin depletion by ribonucleic acid interference (RNAi) impairs mitotic spi

66 gene network with high prediction power for ribonucleic acid interference (RNAi) phenotypes in Caeno

67 , we completed a genome-wide (~14,000 genes) ribonucleic acid interference (RNAi) screen that targete

68 Using ribonucleic acid interference (RNAi), we showed that dia

69 re confirmed in vivo, as depletion of NPM by ribonucleic acid interference eliminated phosphorylation

70 endogenous dynamin2 or eNOS expression with ribonucleic acid interference impairs, bacterial invasio

71 Proteomic approaches and ribonucleic acid interference knockdown identified lymph

72 By ribonucleic acid interference screening using a phosphor

73 Using ribonucleic acid interference screens for autophagy-regu

74 Despite the promise of ribonucleic acid interference therapeutics, the delivery

75 In this paper, we use ribonucleic acid interference to deplete Hax1 in the neu

76 Ras V12 or B-Raf V600E but can be rescued by ribonucleic acid interference-mediated depletion of c-my

77 ) were reduced at the protein but not at the ribonucleic acid level.

78 ic patients showed increased ABCA1 messenger ribonucleic acid levels (a marker of LXR activation) and

79 s, addresses 1) using testing for plasma HIV ribonucleic acid levels (i.e., viral load) and CD4+ T ce

80 Type I and IIx myosin heavy chain messenger ribonucleic acid levels in the diaphragm.

81 r, there were significantly higher messenger ribonucleic acid levels of osteogenic differentiation ma

82 lta-aminolevulinic acid synthase 1 messenger ribonucleic acid levels, delta-aminolevulinic acid, and

83 us was associated with lower CXADR messenger ribonucleic acid levels, suggesting that decreased cardi

84 elial nitric oxide synthase (eNOS) messenger ribonucleic acid levels.

85 Long noncoding ribonucleic acids (lncRNAs) are a subclass of regulatory

86 on, local synthesis as a result of messenger ribonucleic acid localization, or F-actin turnover all m

87 Accordingly, small interfering ribonucleic acid-mediated knockdown of Cdh1 stabilized M

88 -containing cultures after short interfering ribonucleic acid-mediated knockdown of epidermal growth

89 In this paper, we show that short hairpin ribonucleic acid-mediated knockdowns (KDs) of LRRTM1, LR

90 Ribonucleic acid-mediated transcriptional gene silencing

91 , more than 35 platelet-associated messenger ribonucleic acid mediators involved in arterial injury a

92 ed to test the hypothesis that cardiac micro-ribonucleic acid (miR) profiling in severe heart failure

93 of this study is to identify cell-free micro ribonucleic acid (miRNA) biomarkers in graft preservatio

94 e expression, monocyte-derived exosome micro-ribonucleic acid (miRNA) expression, plasma inflammation

95 pics in genetics of longevity, such as micro-ribonucleic acid (miRNA) genetics, polygenic risk scores

96 could be associated with differential micro-ribonucleic acid (miRNA) profiles.

97 -of-principle studies of an innovative micro-ribonucleic acid (miRNA) reporter-probe biosensor that d

98 Micro-ribonucleic acids (miRNAs) are in the spotlight as post-

99 Micro-ribonucleic acids (miRNAs) are noncoding small ribonucle

100 gous mutations in the mitochondrial transfer ribonucleic acid modifying factor (TRMU) in a single pat

101 ular complex that consists of at least three ribonucleic acid molecules and a large number of protein

102 This paper concerns the synthetic design of ribonucleic acid molecules, using our recent algorithm,

103 The eNOS messenger ribonucleic acid (mRNA) abundance was measured using rea

104 anogaster midoogenesis, when oskar messenger ribonucleic acid (mRNA) anchoring depends on its own loc

105 en previously shown that TNF-alpha messenger ribonucleic acid (mRNA) and protein are rapidly expresse

106 The SDF-1 messenger ribonucleic acid (mRNA) and protein expression were also

107 uid nitrogen, and analyzed for CaR messenger ribonucleic acid (mRNA) by Northern blot, and were analy

108 ssayed alpha1- and beta-AR subtype messenger ribonucleic acid (mRNA) by quantitative real-time revers

109 ce of the UPR-induced spliced HAC1 messenger ribonucleic acid (mRNA) correlates with the recovery of

110 that miR-34a directly targets the messenger ribonucleic acid (mRNA) encoding E2F3 and significantly

111 o down regulated Dectin-1 receptor messenger ribonucleic acid (mRNA) expression in the macrophages.

112 messenger ribonucleic acid (mRNA) expression of Indian Hh, a ligan

113 Messenger ribonucleic acid (mRNA) expression of platelet-derived g

114 ction and accurate quantitation of messenger ribonucleic acid (mRNA) gene transcripts in single cells

115 microarrays measure the levels of messenger ribonucleic acid (mRNA) in a sample using probe sequence

116 arked increase in NOX5 protein and messenger ribonucleic acid (mRNA) in CAD versus non-CAD vessels.

117 ns of GPR7, NPB, and NPW precursor messenger ribonucleic acid (mRNA) in the rat brain by using in sit

118 rifice will increase oxytocin (OT) messenger ribonucleic acid (mRNA) levels in the paraventricular an

119 We compared LV messenger ribonucleic acid (mRNA) levels of atrial natriuretic fac

120 D-Ser744-748 were reduced, whereas messenger ribonucleic acid (mRNA) levels of NPPA, NPPB, and sarcop

121 The authors measured messenger ribonucleic acid (mRNA) levels of three activity-depende

122 LA PITX2 messenger ribonucleic acid (mRNA) levels were measured in 95 patie

123 investigated the expression of ERK messenger ribonucleic acid (mRNA) of the prefrontal cortex (PFC),

124 NS1 inhibits cellular messenger ribonucleic acid (mRNA) processing and export, down-regu

125 monstrate that hPSCs have a unique messenger ribonucleic acid (mRNA) reserve of CENP-A not found in s

126 We studied the messenger ribonucleic acid (mRNA) structure and the genetic change

127 Regulation of messenger ribonucleic acid (mRNA) subcellular localization, stabil

128 anscription factor (TF) binding to messenger ribonucleic acid (mRNA) synthesis.

129 The use of synthetic messenger ribonucleic acid (mRNA) to express specific proteins is

130 Expression of HDACs 1-11 messenger ribonucleic acid (mRNA) was compared between RASFs and o

131 The levels of AT(1)R and AT(2)R messenger ribonucleic acid (mRNA) were examined in lymphocytes fro

132 eptor 4 (TLR4) and angiotensinogen messenger ribonucleic acid (mRNA) were measured in the heart after

133 anscription rate of nascent NOSIII messenger ribonucleic acid (mRNA).

134 ation, storage, and degradation of messenger ribonucleic acids (mRNAs) are key steps in the posttrans

135 Export of messenger ribonucleic acids (mRNAs) into the cytoplasm is a fundam

136 Proteins and messenger ribonucleic acids (mRNAs) of KATP pore subunits and mRNA

137 Non-coding ribonucleic acids (ncRNA) are functional RNA molecules t

138 ed next generation sequencing on whole blood ribonucleic acid obtained within six hours of birth from

139 Inhibition of LDH activity by small hairpin ribonucleic acid or expression of phospho-deficient LDHA

140 old increase in whole-blood CXCL16 messenger ribonucleic acid (p < 0.001) and a 1.7-fold increase in

141 explants treated with p63 small interfering ribonucleic acid partially restored the epidermal phenot

142 an inactive 7SK.HEXIM1.P-TEFb small nuclear ribonucleic acid particle for inhibition of transcriptio

143 leate the formation of the 7SK small nuclear ribonucleic acid particle.

144 I proteins generate and use PIWI-interacting ribonucleic acid (piRNA) to repress expression of TE gen

145 16S ribosomal-ribonucleic acid polymerase chain reaction (PCR) and tar

146 IKKalpha travels with the elongating form of ribonucleic acid polymerase II together with heterochrom

147 omplex is followed by the recruitment of the ribonucleic acid polymerase resulting in the formation o

148 which genes themselves involved in messenger ribonucleic acid processing and regulation of gene expre

149 nuclear speckles, nuclear bodies enriched in ribonucleic acid-processing factors.

150 th factor and dramatically changed the micro-ribonucleic acid profile of fibroblast-secreted EMVs in

151 gress in deoxyribonucleic acid and messenger ribonucleic acid profiling, advances in basic biology ha

152 CSp-EMVs for 24 h followed by exosomal micro-ribonucleic acid profiling.

153 resonance profiling); deoxyribonucleic acid, ribonucleic acid, protein, and metabolic approaches all

154 L1 adipocytes subjected to small interfering ribonucleic acid reduction of Munc18c as a model of impa

155 rotein transcription factors or by conserved ribonucleic acid regulatory motifs in >250 genomes from

156 ce with prion protein gene-small interfering ribonucleic acid resulted in spontaneous experimental au

157 Mean baseline plasma HCV ribonucleic acid (RNA) = 6.7 log10 IU/mL and changed by

158 (13)C labeling patterns in nucleosides from ribonucleic acid (RNA) and deoxyribonucleic acid (DNA) i

159 lexes composed of rev response element (RRE) ribonucleic acid (RNA) and multiple molecules of rev pro

160 Ribonucleic acid (RNA) aptamers employed in this class o

161 Biosensors built using ribonucleic acid (RNA) aptamers show promise as tools fo

162 ence of base-pairing and tertiary structure, ribonucleic acid (RNA) assumes a random-walk conformatio

163 strengthened the case for the involvement of ribonucleic acid (RNA) at an early stage in the origin o

164 ics simulations to study the cleavage of the ribonucleic acid (RNA) backbone catalyzed by ribonucleas

165 sense mutations in exon 9 of RBM20, encoding ribonucleic acid (RNA) binding motif protein 20.

166 encoding a presumed full-length glycine-rich ribonucleic acid (RNA) binding protein was isolated from

167 n of rapid, selective, and sensitive DNA and ribonucleic acid (RNA) biosensors capable of minimizing

168 r 2A (SUR2A) subunits was performed on total ribonucleic acid (RNA) from rat embryonic heart-derived

169 nvironmental deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) from three size fractions (pico-,

170 CT4, SOX2, KLF4 and c-MYC, and one noncoding ribonucleic acid (RNA) gene, the microRNA (miRNA) miR302

171 The negative-strand ribonucleic acid (RNA) genome of the virus is wrapped ar

172 PB)-related proteins, including AGO2 and the ribonucleic acid (RNA) helicase DDX6.

173 Persistence of Zika virus (ZIKV) ribonucleic acid (RNA) in semen is common after infectio

174 We previously showed that HIV ribonucleic acid (RNA) is enriched in CD30+CD4+ T cells

175 n and quantification were performed on total ribonucleic acid (RNA) isolated from whole blood.

176 who have <350 CD4+ T cells/mm3 or plasma HIV ribonucleic acid (RNA) levels of >55,000 copies/mL (by b

177 The nonenzymatic replication of ribonucleic acid (RNA) may have enabled the propagation

178 newed appreciation for the dynamic nature of ribonucleic acid (RNA) modifications and for the impact

179 Ribonucleic acid (RNA) modifications play an important r

180 When a ribonucleic acid (RNA) molecule folds, it often does not

181 are crucial factors that stabilize a complex ribonucleic acid (RNA) molecule's three-dimensional (3D)

182 As (miRNAs) are short, non-coding regulatory ribonucleic acid (RNA) molecules commonly found in urina

183 Comparison of ribonucleic acid (RNA) molecules is important for reveal

184 le-stranded deoxyribonucleic acid (ssDNA) or ribonucleic acid (RNA) molecules with a high binding aff

185 ipulation of deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) molecules, followed by explanatio

186 ttractive approaches to analyze and simulate ribonucleic acid (RNA) molecules, for example, for struc

187 tional slippage is a class of error in which ribonucleic acid (RNA) polymerase incorporates nucleotid

188 by HO-1, iron has been shown to inhibit HCV ribonucleic acid (RNA) polymerase, but little is known a

189 CV antibody positive (34%), and 108 were HCV-ribonucleic acid (RNA) positive (20%).

190 udies have suggested that Ebola virus (EBOV) ribonucleic acid (RNA) potentially present in the semen

191 The aim of this study was to develop ribonucleic acid (RNA) profiles that could serve as nove

192 Briefly, virus-specific ribonucleic acid (RNA) purification was achieved by a pr

193 We describe a ribonucleic acid (RNA) reporter system for live-cell ima

194 Ribonucleic acid (RNA) secondary structure prediction co

195 Predicting the secondary structure of an ribonucleic acid (RNA) sequence is useful in many applic

196 ascade reaction to induce the degradation of ribonucleic acid (RNA) specifically in tumor microenviro

197 HIV-deoxyribonucleic acid and/or plasma HIV-ribonucleic acid (RNA) testing.

198 ities have been redefining the importance of ribonucleic acid (RNA) through the study of small molecu

199 nscription and inhibition of LMNB1 messenger ribonucleic acid (RNA) translation by miRNA-23a.

200 Baseline CD4 cell counts and plasma HIV ribonucleic acid (RNA) values were 245 cells/mm(3) and 4

201 omplementary deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) which showed the modification to

202 mulation of the viral envelope protein, ZIKV ribonucleic acid (RNA), and infectious viral particles i

203 e amounts of deoxyribonucleic acid (DNA) and ribonucleic acid (RNA), including micro RNAs, can also b

204 Ribosomal ribonucleic acid (RNA), transfer RNA and other biologica

205 srA/RsmA homologs are an extensive family of ribonucleic acid (RNA)-binding proteins that function as

206 The assembly and composition of ribonucleic acid (RNA)-transporting particles for asymme

207 s microRNA (miRNA) binding sites on a target ribonucleic acid (RNA).

208 ompacted into chromatin and transcribed into ribonucleic acid (RNA).

209 odification of normal nucleosides within the ribonucleic acid (RNA).

210 response upon detection and binding to viral ribonucleic acid (RNA).

211 sis identifies CLUH as a cytosolic messenger ribonucleic acid (RNA; mRNA)-binding protein.

212 detected on Northern blots containing total ribonucleic acids (RNA) of S. kunkelii cultures and S. k

213 Interactions of ribonucleic acids (RNA) with basic ligands such as prote

214 The chemical synthesis of ribonucleic acids (RNA) with novel chemical modification

215 A previous limitation in the analysis of ribonucleic acids (RNAs) by mass spectrometry (MS) has b

216 ality control pathways that target defective ribonucleic acids (RNAs) for degradation play key roles

217 Genetically encoded fluorescent ribonucleic acids (RNAs) have diverse applications, incl

218 ading of Argonaute (Ago) proteins with small ribonucleic acids (RNAs) in Drosophila melanogaster cell

219 he purpose of the majority of such noncoding ribonucleic acids (RNAs) remained paradoxical for a long

220 miRNAs-small, noncoding ribonucleic acids (RNAs) that regulate gene expression b

221 lasticity is the targeted delivery of select ribonucleic acids (RNAs) to synaptodendritic sites of pr

222 terize post-transcriptional modifications of ribonucleic acids (RNAs).

223 ibe a method for the comparative analysis of ribonucleic acids (RNAs).

224 al tool for the characterization of modified ribonucleic acids (RNAs).

225 seudouridine is found in almost all cellular ribonucleic acids (RNAs).

226 ystrophia myotonica protein kinase messenger ribonucleic acids (RNAs; mRNAs) with expanded CUG repeat

227 criptional methylation of specific ribosomal ribonucleic acid (rRNA) and transfer RNA (tRNA) nucleoti

228 Mutations in 23S ribosomal ribonucleic acid (rRNA) loci (macrolide resistance-assoc

229 A newer ribosomal ribonucleic acid (rRNA)-based amplification test was com

230 em by partially sequencing the 16s ribosomal ribonucleic acid (rrs), flagellin (flaB), and deoxyribon

231 genesis using a functional small interfering ribonucleic acid screen.

232 , followed by histological analyses and deep ribonucleic acid sequencing (RNA-seq) of the myocardium

233 old (54-70 years) donors were assayed using ribonucleic acid sequencing (RNA-seq).

234 routine analysis of large-scale single-cell ribonucleic acid sequencing (scRNA-seq) data.

235 Ribonucleic acid sequencing analysis indicated that a nu

236 -sensitive human lncRNAs via next-generation ribonucleic acid sequencing and microarray approaches.

237 Ribonucleic acid sequencing and microarray-derived data

238 Ribonucleic acid sequencing and reverse transcriptase po

239 Using ribonucleic acid sequencing on peripheral blood mononucl

240 Ribonucleic acid sequencing, Mtb proteome arrays, and me

241 composition was explored using 16S ribosomal ribonucleic acid sequencing.

242 Longitudinal samples were collected for ribonucleic acid sequencing.

243 alternative splicing events from single-cell ribonucleic acid-sequencing experiments), an R package f

244 TRPC3 channel or nonsilencing short hairpin ribonucleic acid (shRNA) to make the channel knockdown (

245 e cellular effects observed by short hairpin ribonucleic acid (shRNA)-mediated MELK knockdown in cell

246 harmacological inhibition, small interfering ribonucleic acid (siRNA) depletion, and antibody blockin

247 ing either scyphostatin or short interfering ribonucleic acid (siRNA) leads to reversion to the "youn

248 sed nanoparticle-delivered small interfering ribonucleic acid (siRNA) to silence IRF5 in macrophages

249 Small interfering ribonucleic acid (siRNA), 20-25 base pairs in length, ca

250 CEACAM6-specific short interfering ribonucleic acid (siRNA), but not control siRNA, increas

251 igated the hypothesis that small interfering ribonucleic acid (siRNA)-mediated E-selectin blockade in

252 Experiments using small interfering ribonucleic acids (siRNA) to specifically knock down p53

253 Short interfering ribonucleic acids (siRNAs) are important agents for RNA

254 Small interfering ribonucleic acids (siRNAs) form potentially the most imp

255 Short interfering ribonucleic acids (siRNAs) offer a highly specific and s

256 y cytoplasmic enzymes into short interfering Ribonucleic Acids (siRNAs) once inside cells.

257 In yeast, the U2 small nuclear ribonucleic acid (snRNA) component of the spliceosome is

258 ellular contexts, including during messenger ribonucleic acid sorting in Drosophila melanogaster oocy

259 the accurate quantification and analysis of ribonucleic acid, species, including micro-ribonucleic a

260 d after the introduction of small inhibitory ribonucleic acids specific to E2F6.

261 , a model cholinergic synapse, contain small ribonucleic acids (sRNAs), primarily the 5' ends of tran

262 e V1V2 region of the small subunit ribosomal ribonucleic acid (SSU-rRNA) gene recovered from fresh co

263 The C+84A disrupted an A/U-rich messenger ribonucleic acid stability element, and in transfected l

264 f CHGB, which disrupts an A/U-rich messenger ribonucleic acid stability element, associates with not

265 ns (or Single Nucleotide Variants) in folded RiboNucleic Acid structures that cause local or global c

266 A novel universal support for deoxyribo- and ribonucleic acid synthesis has been developed.

267 e, LID/DeltaM2-2/1030s, with deletion of RSV ribonucleic acid synthesis regulatory protein M2-2 and g

268 lisiran, a double-stranded small interfering ribonucleic acid that inhibits PCSK9 synthesis.

269 of antiplatelet drugs and contain messenger ribonucleic acid that is translationally active.

270 zation of activated ribonucleotides leads to ribonucleic acids that contain a mixture of 2',5'- and 3

271 bonucleic acids (miRNAs) are noncoding small ribonucleic acids that play a prominent role in the init

272 (miRNA) is a class of small, single-stranded ribonucleic acids that regulate gene expression post-tra

273 We used lentiviral small hairpin ribonucleic acid to deplete talin in mammary epithelial

274 LA messenger ribonucleic acid transcripts for collagen I, III, transf

275 in reaction assessed atrial tissue messenger ribonucleic acid transcripts involved in the fibrosis pa

276 adrenergic pathway, here shown for messenger ribonucleic acid translational control at the CYB561 ste

277 tored neurite outgrowth to short interfering ribonucleic acid-treated cultures, implying that epiderm

278 In vivo prion protein gene-small interfering ribonucleic acid treatment effects were of limited durat

279 In vivo prion protein gene-small interfering ribonucleic acid treatment promoted T cell differentiati

280 in is mediated by interactions with transfer ribonucleic acid (tRNA) genes and their regulatory facto

281 e, the GsDnmt2 enzyme has a swapped transfer ribonucleic acid (tRNA) specificity.

282 In prokaryotes and archaea transfer ribonucleic acid (tRNA) stability as well as cellular UV

283 00G transition in the mitochondrial transfer ribonucleic acid (tRNA)(Ile) gene, which was shown to be

284 s in vitro from purified ribosomes, transfer ribonucleic acids (tRNAs) and 33 recombinant proteins.

285 Transfer ribonucleic acids (tRNAs) are challenging to identify an

286 Transfer ribonucleic acids (tRNAs) are essential for protein synt

287 tudies of their incorporations from transfer ribonucleic acids (tRNAs) are few.

288 n Sm proteins on uridine-rich, small nuclear ribonucleic acids (U snRNAs).

289 The median age was 36 years, HIV-1 ribonucleic acid was 4.56 log10 copies/mL, and CD4 count

290 Ribonucleic acid was extracted from the adductor muscle,

291 Viral ribonucleic acid was extracted from tissues and amplifie

292 Labeled complementary ribonucleic acid was hybridized to a custom Affymetrix o

293 Ribonucleic acid was isolated using the cesium chloride-

294 situ hybridization for Epstein-Barr-encoded ribonucleic acid was performed on formalin-fixed tissues

295 p of Rpl10 that embraces the P-site transfer ribonucleic acid was required for release of Tif6, 90 A

296 romium(V)-mediated oxidative damage of deoxy-ribonucleic acids was investigated at neutral pH in aque

297 icated sample plates, enzymatic digestion of ribonucleic acids was performed on probe (i.e., on the m

298 rtrophy and AC6 knockdown (small interfering ribonucleic acid), which recapitulated in vivo findings.

299 c) RNAs represent a newly described class of ribonucleic acid whose importance in human disease remai

300 on of the full-length human CYB561 messenger ribonucleic acid with its cognate 3'-UTR.