ライフサイエンスコーパス: RT

1 RT and choice effects were largely congruent in the visu

2 RT followed by IGF1R neutralization in orthotopic colore

3 RT is facilitated by sequential proton-coupled electron

4 RT is thus a versatile tool that can be used for both co

5 RT plans and cardiac doses were reviewed.

6 RT reduced the rate of death from breast cancer (BCD) fo

7 RT-PCR data also showed that the expression of mature mi

8 RT-PCR demonstrated that 10 microM YC-1 reduced hypoxia-

9 RT-PCR of mature miR-17-92 in cells demonstrated the sel

10 RT-qPCR analysis revealed that TrkC-miR2 is significantl

11 RT-qPCR data revealed that AgNPs induced greater changes

12 RT-qPCR suggests model specific gene expression for nine

13 RT-qPCR verified model specific and nonspecific expressi

14 ociated with the Tyr181Cys mutation in HIV-1 RT has been a key roadblock in the discovery of nonnucle

15 at are critical for its recognition by HIV-1 RT remain unclear.

16 recognized within covalently tethered HIV-1 RT-nucleic acid complexes.

17 These data suggest that HIV-2 RT exhibits higher fidelity during viral replication, an

18 trate that mutant M41L/D67N/K70R/S215Y HIV-2 RT lacks ATP-dependent excision activity, and recombinan

19 ective responses were observed in 4 out of 9 RT patients (44%) and in 0 out of 16 CLL patients (0%).

20 Adapting RT-escalated radiation dose to the FDG-avid tumor detect

21 patients at times before, during, and after RT administration and then correlated to overall surviva

22 molecular subtype on overall survival after RT using a meta-analysis of the METABRIC and TCGA BC pat

23 ng the H-bond between Y731 and Y730 to allow RT to propagate to Y730.

24 lities during development, revealing altered RT of the TP63 gene as an early event in disease progres

25 We found that loss of Scn8a leads to altered RT cell intrinsic excitability and a failure in recurren

26 time loop-mediated isothermal amplification (RT-LAMP) with SYTO-9 as the signal reporter.

27 An RT-RPA assay targeting a recent epidemic human norovirus

28 ecrosis were more likely to have received an RT boost.

29 ng ultrafiltration, gel electrophoresis, and RT-qPCR (quantitative reverse transcription polymerase c

30 ation between corticospinal excitability and RT, such that larger motor-evoked potentials (MEPs) meas

31 Using FACS and RT-PCR, we examined the phenotype of generated IgE(+) ce

32 enes, as confirmed by immunofluorescence and RT-qPCR.

33 and angiogenesis by immunohistochemistry and RT-PCR.

34 water molecules inside the pore, both LT and RT data sets are consistent with the positions observed

35 on (SSH) followed by 454 pyrosequencing, and RT-qPCR methods.

36 ted with HOL1 genotype, as shown by qPCR and RT-qPCR.

37 ary, rostral, and rostrotemporal (AI, R, and RT) core areas on the supratemporal plane, continuing to

38 RNA-seq and RT-qPCR identified potential downstream genes of SPL4.

39 t rely on reverse transcription (RT) such as RT-qPCR and RNA-Seq.

40 +), effectively reductively couples NO(g) at RT in methanol (MeOH), giving a structurally characteriz

41 complexed all (225) Ac (26 kBq) in 5 min at RT.

42 n Outcome and Measures: Correlations between RT-QuIC results and the final diagnosis of recruited pat

43 sed to compare overall survival (OS) between RT dose groups, accounting for age, sex, race, stage, su

44 T) boost to the tumor bed after whole-breast RT (WBRT) for ductal carcinoma in situ (DCIS) is largely

45 glucocorticoid-mediated ST2 was assessed by RT-qPCR, ChIP assay and luciferase reporter assay.

46 rent genotypes and organs, were confirmed by RT-qPCR Corresponding target transcripts, predicted in s

47 cruzi deoxyribonucleic acid was detected by RT-PCR at 30, 60, 90, 120, 150, 180, and 360 days.

48 Arbovirus RNA detection by RT-PCR should be part of the management of GBS cases.

49 ransiently transfected cells was examined by RT-PCR, western blot analysis, and immunohistochemistry.

50 paracrine IGF1/IGF1R signaling initiated by RT-activated CAF worsens colorectal cancer progression,

51 vered once every 2 weeks, followed or not by RT at 40 Gy delivered 4 weeks after the last R-CHOP cycl

52 Gene expression analyses were performed by RT-PCR.

53 ogy; for HMPV, 172 (8.5%) tested positive by RT-PCR and 147 (7.3%) by serology; for the PIVs, 94 (4.6

54 r RSV, 287 (14.2%) patients were positive by RT-PCR and 234 (11.6%) were positive by serology; for HM

55 ; and for AdV, 111 (5.5%) tested positive by RT-PCR and 62 (3.1%) by serology.

56 ; for the PIVs, 94 (4.6%) tested positive by RT-PCR and 92 (4.6%) by serology; and for AdV, 111 (5.5%

57 st GSH, Grx1 and Trx1 levels as reflected by RT-PCR, Western blotting and immunohistochemistry analys

58 M positive, and 27 of the 40 (68%) tested by RT-PCR were positive.

59 cripts, predicted in silico and validated by RT-qPCR, often showed opposite expression profiles than

60 ssimilation were the key genes, validated by RT-qPCR, which expressed in a network manner with tissue

61 sible primers for experimental validation by RT-PCR and displays those, along with the matching prote

62 dorsal root ganglion neurons by single-cell RT-PCR.

63 -quality intact RNA suitable for single-cell RT-qPCR as well as RNA-Seq, enabling the reliable detect

64 Using molecular cloning, RT-PCR, Western blotting, immunolocalization and in vitr

65 By contrast, RT received only approximately 45% from MGv, and an equa

66 this trial was not inferior to conventional RT and was not associated with increased late toxicity.

67 Patients were allocated to conventional RT of 78 Gy in 39 fractions over 8 weeks or to hypofract

68 ion by real-time quaking-induced conversion (RT-QuIC) and tyramide signal amplification immunohistoch

69 ng the real-time quaking-induced conversion (RT-QuIC) seeding assay, which detects minute amounts of

70 tro by real-time quaking-induced conversion (RT-QuIC).

71 vitro real-time quaking-induced conversion (RT-QuIC).

72 ration real-time quaking-induced conversion (RT-QuIC).

73 e diagnostic performance of the improved CSF RT-QuIC is superior to surrogate marker tests for prion

74 ous for codon 129 generated intermediate CSF RT-QuIC patterns, whereas genetic prion diseases reveale

75 ostic specificity and 92% sensitivity of CSF RT-QuIC in a blinded retrospective analysis matched the

76 The CSF RT-QuIC differentiated 94% of cases of sporadic Creutzfe

77 ngineered proviral plasmids encoding diverse RTs within the backbone of HIV-1 strain NL4-3.

78 ionizing radiations are often needed during RT, leading to severe damages to normal tissues adjacent

79 EL_PSSM-RT is evaluated by five-fold cross-validation using PDNA

80 ates and found that lipid extraction enabled RT-QuIC detection of CWD prions in a 2-log10-greater con

81 Of 5,126 patients enrolled, RT-PCR and serology test results were available for 2,02

82 ance status, 0 to 1) received dose-escalated RT to 70 to 90 Gy (median, 74 Gy) in six trials.

83 by the inverse K277R mutation, establishing RT as the genetic locus for aptamer-mediated HIV-1 inhib

84 ence of bleeding, and 5.2-fold higher if EVD RT-PCR cycle threshold value was </=20.

85 measured at rest were associated with faster RTs.

86 ority of involved-field RT to extended-field RT regarding PFS was confirmed (HR, 1.0; 95% CI, 0.8 to

87 53 months), noninferiority of involved-field RT to extended-field RT regarding PFS was confirmed (HR,

88 ia accuracy differences when controlling for RT, bias and sensitivity.

89 priateness of reference genes is crucial for RT-qPCR.

90 3 doses (arm A) vs accelerated-fractionation RT (70 Gy/35 over 6 weeks) plus panitumumab at 9 mg/kg i

91 -dose cisplatin vs accelerated-fractionation RT plus the anti-EGFR antibody panitumumab.

92 f panitumumab plus accelerated-fractionation RT was not superior to cisplatin plus standard-fractiona

93 omized 1:1 to receive standard-fractionation RT (70 Gy/35 over 7 weeks) plus cisplatin at 100 mg/m2 i

94 ior to cisplatin plus standard-fractionation RT in LA-SCCHN and noninferiority was not proven.

95 LA-SCCHN treated with standard-fractionation RT plus high-dose cisplatin vs accelerated-fractionation

96 irus, K103, was found to encode a functional RT among those examined.

97 ity of these ligands, together with a higher RT of the representative compound 11 with respect to our

98 rs and probes for the quantification of HRV, RT-dPCR outperformed RT-qPCR by consistently and accurat

99 Hypofractionated RT is given over a shorter time with larger doses per tr

100 Hypofractionated RT is more convenient for patients and should be conside

101 Conclusion The hypofractionated RT regimen used in this trial was not inferior to conven

102 ractions over 8 weeks or to hypofractionated RT of 60 Gy in 20 fractions over 4 weeks.

103 bazine (ABVD) plus 20 Gy involved-field (IF)-RT to more intensive four cycles of ABVD plus 30 Gy IF-R

104 intensive four cycles of ABVD plus 30 Gy IF-RT was confirmed with 10-year PFS of 87% each (HR, 1.0;

105 After BEACOPPbaseline, 20 Gy IF-RT was noninferior to 30 Gy (10-year PFS, 84% v 84%; HR,

106 in situ hybridization, immunohistochemistry, RT-PCR, northern blot and western blot experiments.

107 rable spectroscopic properties, and improved RT were identified.

108 owever, evidence of an overall difference in RT effect between subtypes was weak ( P = .21).

109 ABAergic signaling may produce excitation in RT neurons.

110 thern blots) were used as reference genes in RT-qPCR experiments, but recent studies in different sys

111 find that [Cl(-)]i remains relatively low in RT neurons.

112 O) systemic activity on clinical outcomes in RT-treated non-small cell lung cancer (NSCLC).

113 ls a host of features not seen previously in RTs that may contribute to distinctive biochemical prope

114 prove local tumor control without increasing RT-induced lung toxicity (RILT), and possibly improve su

115 ng memory-guided saccades, while influencing RTs and errors, did not affect choice behavior.

116 tol, and found all three similarly inhibited RT-QuIC.

117 ve biochemical properties of group II intron RTs, and it provides a prototype for many related bacter

118 ucleoside analogue RTIs (NRTIs) blocked K103 RT activity and consistently inhibited the replication o

119 ofovir (TDF), show efficacy in blocking K103 RT.

120 LiCl@RT-COF-1 exhibits a conductivity value of 6.45 x 10(-3)

121 he concentration of dNTP substrates to limit RT.

122 In a computational model of a local RT network featuring slow Cl(-) extrusion kinetics, simi

123 nd monochloramine with CT values for 2 log10 RT-qPCR reduction between 300 and 360 mg-min/L.

124 mpound 9 on sleep-wake states indicated long RT was translated into sustained inhibition of rapid eye

125 The effects of long RT compound 9 on sleep-wake states indicated long RT was

126 the receptor (2.2 min for 5) and much longer RTs (e.g., 376 min for 27 or 391 min for 31).

127 The identification of LTR-RTs is critical for achieving high-quality gene annotati

128 Long terminal repeat retrotransposons (LTR-RTs) are prevalent in plant genomes.

129 y of young elements; the rarity of young LTR-RTs is a consequence of fewer births rather than access

130 fic for genotype A measles virus (MeV) (MeVA RT-quantitative PCR [RT-qPCR]) that can identify measles

131 e standard real-time RT-PCR method, the MeVA RT-qPCR showed 99.5% specificity for genotype A and 94%

132 ilar to those we found experimentally, model RT neurons are predisposed to an activity-dependent swit

133 able to propagate activity within the model RT nucleus.

134 Molecules RT and accurate mass were recorded in a database for eac

135 Moreover, RT-PCR analysis confirmed that the expression of the RNA

136 In contrast, mRNA RT-PCR had low clinical sensitivity (75%) but high speci

137 syndrome, 6 had positive and 2 had negative RT-QuIC findings for a sensitivity of 75% (95% CI, 36%-9

138 diversity of chromosomal sites harboring new RT insertions.

139 tform for investigating functional sub-50-nm RT skyrmions, pointing towards the development of skyrmi

140 re screened for nucleoside and nonnucleoside RT inhibitor DRM.

141 roadblock in the discovery of nonnucleoside RT inhibitors (NNRTIs).

142 Consistent with this notion, RT-PCR of lymphocyte cell lines from one of the kindreds

143 Interestingly, the immunological activity of RT does not exhibit linear dose-response correlation.

144 eriments also highlight the applicability of RT-QuIC to identify potential therapeutic inhibitors of

145 On the basis of RT-qPCR data, electrostatic interactions and an ion-exch

146 The effect of RT in the presumed low-risk luminal A-like tumors was ex

147 patients did not seem to benefit effects of RT.

148 ) Lu-PPNs greatly enhanced the efficacies of RT and/or PDT.

149 To evaluate the impact of RT-aptamer binding specificity on replication, we engine

150 l to guarantee satisfactory normalization of RT-qPCR data when using DNBS-Model.

151 oid syndromes, we tracked the progression of RT abnormalities during development, revealing altered R

152 ionally, we found an increased dispersion of RTs during MW suggesting that attention during these tim

153 regulatory characteristics of this family of RTs ensure its rapid but stepwise accumulation in plant

154 gorithm for sporadic CJD combines CSF and OM RT-QuIC testing to provide virtually 100% diagnostic sen

155 values for kon but not necessarily optimized RT, which is key to predicting optimal efficacy in vivo.

156 quantification of HRV, RT-dPCR outperformed RT-qPCR by consistently and accurately quantifying HRV R

157 The presence of DR decreased the overall RT by 13.04-16.63 mum.

158 pathy was negatively associated with overall RT (central, S3, T3, I3, and N3 sectors, P = .004-.024)

159 rring around 1:1 stoichiometry with packaged RT.

160 qPCR) and reverse transcription-digital PCR (RT-dPCR) for quantifying HRV RNA using genotype-specific

161 s of reverse transcription-quantitative PCR (RT-qPCR) and reverse transcription-digital PCR (RT-dPCR)

162 time reverse transcription-quantitative PCR (RT-qPCR) assay utilizing Pleiades probe chemistry and an

163 ough reverse transcription-quantitative PCR (RT-qPCR), is a common approach employed to investigate t

164 RNA reverse transcription-quantitative PCR (RT-qPCR)-based assays and from outgrowth assay readout b

165 ymerase chain reaction (PCR), real time PCR (RT-PCR) and dot blot hybridization have also been propos

166 ing both conventional PCR and real-time PCR (RT-PCR).

167 loped a real-time reverse transcription-PCR (RT-PCR) method specific for genotype A measles virus (Me

168 asles virus (MeV) (MeVA RT-quantitative PCR [RT-qPCR]) that can identify measles vaccine strains rapi

169 Unlike conventional PCR, RT-PCR detected pork DNA in nine processed food samples

170 sing the antitumor response of perioperative RT, these agents may even be combined with RT, concurren

171 to predict outcomes and perhaps personalize RT dosage to improve survival.Significance: Radiotherapy

172 gulate SAMHD1 and HIV permissivity at a post-RT step, revealing a mechanism by which the HIV-1 reserv

173 4-20 days using the reverse-toggle protocol (RT-MEF).

174 of the pair-relationships extracted by PSSM-RT and the results validates the usefulness of PSSM-RT f

175 the results validates the usefulness of PSSM-RT for encoding DNA-binding residues.

176 ative real-time polymerase chain reaction (Q-RT-PCR).

177 Quantitative RT-PCR and ELISA were used to determine transcript and s

178 Quantitative RT-PCR revealed significant inverse associations between

179 Microarray analysis, quantitative RT-PCR, and immunoblotting revealed that IRF2 regulated

180 se chain reaction (RT-PCR), and quantitative RT-PCR (qRT-PCR), and the proinflammatory cytokines inte

181 RNA sequencing and quantitative RT-PCR analyses identified reduced transcript levels dur

182 iocyanate-dextran uptake assay, quantitative RT-PCR analysis of tight junction proteins, myosin light

183 Y11, and P2Y13 was confirmed by quantitative RT-PCR and immunocytochemistry.

184 l lung tissue was determined by quantitative RT-PCR.

185 BER genes were assessed by quantitative RT-PCR.

186 istology, immunohistochemistry, quantitative RT-PCR, ELISA, and flow cytometry.

187 xis, apoptosis, ELISA, Luminex, quantitative RT-PCR, and flow cytometric assays.

188 ted in independent LSE samples (quantitative RT-PCR and Western blotting) and in normal and AE skin b

189 1), were confirmed by real-time quantitative RT-PCR, and DNA methylation of their promoter regions wa

190 ution flow cytometry, real-time quantitative RT-PCR, and mass spectrometry were used to characterize

191 Using quantitative RT-PCR, we detected matriptase mRNA in several regions o

192 ormal-weight children) by using quantitative RT-PCR.

193 ort of lung tumor tissues using quantitative RT-PCR.

194 extent of connections between MGN and AI, R, RT, RTp, and STGr using retrograde and anterograde anato

195 The use of a radiotherapy (RT) boost to the tumor bed after whole-breast RT (WBRT)

196 valuate the effect of adjuvant radiotherapy (RT) after breast conservation surgery in different breas

197 Adjuvant radiotherapy (RT) in breast cancer (BC) is often used to eradicate rem

198 ften are treated with external radiotherapy (RT) over 8 to 9 weeks.

199 phy (PET) imaging and internal radiotherapy (RT).

200 unity influences the impact of radiotherapy (RT) in cancer, but mechanistic connections remain obscur

201 local relapse, the addition of radiotherapy (RT) to limb-sparing surgery may result in higher local c

202 Preoperative radiotherapy (RT) is a mainstay in the management of rectal cancer, a

203 th stage III disease receiving radiotherapy (RT) with carboplatin-paclitaxel or cisplatin-etoposide w

204 patients with BC treated with radiotherapy (RT) after breast-conserving surgery.

205 FR) monoclonal antibodies with radiotherapy (RT) to standard chemoradiotherapy in locoregionally adva

206 rse-transcription polymerase chain reaction (RT-PCR) analysis in 17 cases and by serology in 6 cases.

207 rse-transcription polymerase chain reaction (RT-PCR) and in situ hybridization to test if GPR30 is ex

208 rse-transcription polymerase chain reaction (RT-PCR) for laboratory-confirmed influenza virus infecti

209 ured by real time polymerase chain reaction (RT-PCR) in asymptomatic Chagas carriers.

210 rse-transcription polymerase chain reaction (RT-PCR) testing was not performed, resulting in a missed

211 rse transcription-polymerase chain reaction (RT-PCR) to analyse the effects of these treatments on nu

212 rse-transcription polymerase chain reaction (RT-PCR), and quantitative RT-PCR (qRT-PCR), and the proi

213 rs with real-time polymerase chain reaction (RT-PCR)-confirmed EVD were enrolled retrospectively in 5

214 itative real-time polymerase chain reaction (RT-PCR)and in situ hybridization assays, we validated th

215 time quantitative polymerase chain reaction (RT-qPCR) assays in Gabonese children with severe (n = 18

216 rse-transcriptase polymerase-chain-reaction (RT-PCR)-confirmed, protocol-defined, influenza-like illn

217 nsic excitability and a failure in recurrent RT synaptic inhibition.

218 mismatches in primer/probe binding regions, RT-dPCR may be the optimal molecular method for future H

219 The reported RT-RPA method shows promise for sensitive point-of-care

220 Results RT reduced the cumulative incidence of ipsilateral breas

221 acterial and eukaryotic non-LTR retroelement RTs.

222 Retrotransposons (RTs) can rapidly increase in copy number due to periodic

223 retrotransposon, telomerase, and retroviral RTs as well as the spliceosomal protein Prp8 in eukaryot

224 pes by means of immunofluorescence staining, RT-PCR, and qRT-PCR, and qRT-PCR analysis revealed incre

225 ith larger doses per treatment than standard RT.

226 Subsequently, RT-activated CAFs promoted survival of colorectal cancer

227 X-ray structure of Aqy1 at room temperature (RT) at 1.3 A resolution, and by exploring the structural

228 tivities of 10(-2) S/cm at room temperature (RT).

229 pproximately 25 degrees C (room temperature, RT), was studied to evaluate shelf-life comparatively to

230 CMT (P = .032), temporal RT at 1500 mum (P = .03), mean CT (P = .009), and mean n

231 [Cl(-)]i Neurons of the reticular thalamic (RT) nucleus express reduced levels of KCC2, indicating t

232 Our results suggest that RT alters IDO-mediated immune status in NSCLC patients a

233 Among the RT abnormalities, we identified the tumor protein p63 ge

234 onformation of Y731, ostensibly breaking the RT pathway in alpha2.

235 ion that is globally better described by the RT than by the low-temperature (LT) crystal structure.

236 ed without affecting performance; hence, the RT may be modulated by factors other than computation ti

237 Meanwhile, the RT efficacies are limited by different mechanisms, among

238 nvestigate the diagnostic performance of the RT-QuIC prion test in the broad phenotypic spectrum of p

239 Among RIV4 recipients, the RT-PCR-confirmed influenza attack rate was 2.2% (96 case

240 his patient-level analysis suggests that the RT boost confers a statistically significant benefit in

241 rate and early diagnosis of CJD by using the RT-QuIC assay on CSF samples, OM samples, or both.

242 maintaining inhibitory signaling within the RT nucleus and suggest how this important activity choke

243 restricts the spread of activity within the RT nucleus.

244 n [(35)S]GTPgammaS binding assays, and their RTs appeared correlated to their (in)surmountable antago

245 mine the optimal adjuvant radiation therapy (RT) dose following resection of localized MCC of the ext

246 bilitating side effect of radiation therapy (RT) of several cancers including lung and breast cancers

247 Until recently, radiation therapy (RT) was believed to mediate antineoplastic activity most

248 ge I disease treated with radiation therapy (RT), doses >/=30.6 Gy were associated with a significant

249 over, kinematic analyses revealed that these RT biases could occur without changing the underlying co

250 ), as well as the overall retinal thickness (RT) (S3, N3, I3, S6, and T6 sectors), were decreased at

251 ivity, and recombinant virus containing this RT remains susceptible to AZT inhibition.

252 In comparison to the standard real-time RT-PCR method, the MeVA RT-qPCR showed 99.5% specificity

253 cal cortical GABA levels, and reaction time (RT) in a group of 20 healthy human adults.

254 on difficulty, fixations, and reaction time (RT) measures.

255 antagonists with very short residence time (RT) at the receptor (2.2 min for 5) and much longer RTs

256 tic parameters kon, koff and residence time (RT) were determined.

257 d with improved affinity and residence time (RT).

258 The response time (RT), limit of detection (LOD), and linear dynamic range

259 tes with each containing MS, retention time (RT), and MS/MS information.

260 s were measured by prolonged reaction times (RT) in sustained attention to response tasks (SART), whe

261 tive standard deviations of retention times (RT; n = 6) typically between 2 and 5%.

262 ersed therapeutic resistance of GBM cells to RT in hypoxic microenvironments through enhanced activat

263 on Subtype was not predictive of response to RT, although, in our study, human epidermal growth facto

264 exhibited the strongest positive response to RT, increasing in abundance by 124% more than the overal

265 Old male rats were submitted to RT (ladder climbing, progressive load, 3 times a week fo

266 Resistance training (RT) has been indicated to minimize the age-induced muscl

267 amers that bind HIV-1 reverse transcriptase (RT) inhibit HIV-1 replication, but little is known about

268 HIV-1 non-nucleoside reverse transcriptase (RT) inhibitors (NNRTIs) are hindered by their unsatisfac

269 Nucleoside reverse transcriptase (RT) inhibitors (NRTIs) are the backbone of current antir

270 HIV-1 reverse transcriptase (RT) possesses both DNA polymerase activity and RNase H a

271 eep sequencing of HIV reverse transcriptase (RT) was performed (Roche/454), and the sequences were sc

272 l screening using HIV-reverse transcriptase (RT), adenylate/guanylate kinase, and human DNA polymeras

273 eficiency virus (HIV) reverse transcriptase (RT)-associated ribonuclease H (RNase H) remains the only

274 ral polymerase, HIV-1 reverse transcriptase (RT).

275 (SIV) carrying HIV-1 reverse transcriptase (RT-SHIV), compared to uninfected macaques, and interesti

276 ease in nonnucleoside reverse-transcriptase (RT) inhibitor (NNRTI) resistance mutations (from 0.3% to

277 rial group II intron reverse transcriptases (RTs) function in both intron mobility and RNA splicing a

278 ers a block, limiting reverse transcription (RT) of the incoming viral RNA genome.

279 chniques that rely on reverse transcription (RT) such as RT-qPCR and RNA-Seq.

280 MHD1 suppresses viral reverse transcription (RT) through depletion of cellular dNTPs but is naturally

281 in reaction (PCR) and reverse-transcription (RT) PCR were applied to nasopharyngeal swab (NPS) sample

282 sient species generated by radical transfer (RT) from a stable diferric-tyrosyl radical cofactor loca

283 We report covalent inhibitors of Tyr181Cys RT (CRTIs) that can completely knock out activity of the

284 esistance to inhibitors than a commonly used RT-qPCR assay.

285 We used RT-PCR to profile ionotropic glutamate receptor expressi

286 Using RT, we observe enhanced antioxidant capability of activa

287 outbreaks to detect CV-A6 and CV-A10, using RT-PCR.

288 , and tissue biomarkers (determined by using RT-PCR and immunohistochemistry) were evaluated.

289 ted from patients and healthy controls using RT-qPCR and receiver operating characteristic (ROC) anal

290 itute an operon, which we corroborated using RT-PCR.

291 IL-12/23p40 and IL-23p19 were measured using RT-PCR.

292 ll survival of patients receiving CRT versus RT.

293 the reaction speed for RNA amplification via RT-LAMP.

294 f MACE data, candidate genes were tested via RT-qPCR and a strong positive correlation between both d

295 The primary end point was RT-PCR-confirmed, protocol defined, influenza-like illne

296 to investigate survival rate associated with RT.

297 amplicon sequencing and bioinformatics with RT-qPCR and physicochemical investigations.

298 e RT, these agents may even be combined with RT, concurrently and sequentially.

299 mprovement in overall survival compared with RT alone (hazard ratio, 0.90; 95% CI, 0.86 to 0.94; P <

300 Data for patients with RT-associated breast AS evaluated at our institution fro