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 hormone does not act to stabilize tyrosinase ribonucleic acid.

4 s were reduced by specific small interfering ribonucleic acids.

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

6 on both the structure and function of these 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 , p21waf1/cip1, is elevated at the messenger ribonucleic acid and protein levels in all HTLV-I-infect

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

37 Ribonucleic acid expression analysis identified changes

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

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

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

41 Maximum messenger ribonucleic acid expression of both cytokines was observ

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

43 Adipose messenger ribonucleic acid expression of inflammatory genes includ

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

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

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

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

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

49 tor diethylpyrocarbonate was used during the ribonucleic acid extraction procedure.

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

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

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

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

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

55 Enteroviral ribonucleic acids have been identified in heart muscle o

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

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

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

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

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

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

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

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

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

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

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

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

68 Proteomic approaches and ribonucleic acid interference knockdown identified lymph

69 By ribonucleic acid interference screening using a phosphor

70 Using ribonucleic acid interference screens for autophagy-regu

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

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

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

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

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

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

77 one-induced increase in tyrosinase messenger ribonucleic acid levels suggesting that ongoing protein

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

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

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

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

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

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

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

85 Ribonucleic acid-mediated transcriptional gene silencing

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

105 ose in peripheral blood, expressed messenger ribonucleic acid (mRNA) for IL-5, IL-6, and IL-10.

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

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

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

109 r maze had elevated levels of BDNF messenger ribonucleic acid (mRNA) in the hippocampus (p < .05), a

110 ut not arginine vasopressin (AVP), messenger ribonucleic acid (mRNA) in the hypothalamic paraventricu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

129 We found that messenger ribonucleic acids (mRNAs) for MCP-1, MCP-3, RANTES, MIP-

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

165 Individual plasma HIV-1 ribonucleic acid (RNA) loads were stable during observat

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

167 Ribonucleic acid (RNA) modifications play an important r

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

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

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

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

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

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

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

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

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

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

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

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

180 Ribonucleic acid (RNA) secondary structure prediction co

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

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

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

184 The cells were pelleted, and ribonucleic acid (RNA) was extracted by using RNAzol B.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

209 genesis using a functional small interfering ribonucleic acid screen.

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

211 Ribonucleic acid sequencing analysis indicated that a nu

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

213 Ribonucleic acid sequencing and microarray-derived data

214 Ribonucleic acid sequencing and reverse transcriptase po

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

237 In cells treated with the ribonucleic acid synthesis inhibitor, 5,6-dichloro-1-bet

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

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

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

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

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

243 The RAT9/NUP85 (ribonucleic acid trafficking) gene encodes an 84.9-kDa p

244 the strain carrying the rat8-1 allele (RAT = ribonucleic acid trafficking).

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

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

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

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

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

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

251 e substitution of a single-stranded transfer ribonucleic acid (tRNA) fragment serves as the first dim

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

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

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

255 00G transition in the mitochondrial transfer ribonucleic acid (tRNA)(Ile) gene, which was shown to be

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

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

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

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

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

261 Ribonucleic acid was extracted from the adductor muscle,

262 Viral ribonucleic acid was extracted from tissues and amplifie

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

264 Ribonucleic acid was isolated using the cesium chloride-

265 GH-treated rats, myocardial IGF-I messenger ribonucleic acid was not different among the three group

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

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

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

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

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

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

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