ライフサイエンスコーパス: R

1 R and Bioconductor were used for data analysis.

2 R code is available at github.com/james-e-barrett.

3 R loops, which are mainly co-transcriptional, abundant R

4 R neurons recruit both GABA and GABA-A receptors to thei

5 R(2) was 0.85 and 0.83, respectively.

6 (R)-2,3-Di-O-benzylglyceraldehyde and N-tosyl homoallylam

7 (R)-BPO-27 fully blocked CFTR chloride conductance in epi

8 R-loops accumulate in nucleoli during RNA polymerase I (

9 R-loops are known to interfere with replication forks, a

10 R-spondin1 is a secreted regulator of WNT signaling, inv

11 ) than did steatosis (beta = -0.5, P < .001, R(2) = 0.33).

12 diffusion coefficient (beta = -0.3, P = .02, R(2) = 0.33) than did steatosis (beta = -0.5, P < .001,

13 let cadmium content and both age (p = 0.048, R(2) = 0.09) and female gender (women: 36.88 +/- 4.11 vs

14 r included nine microRNAs, p=3.63 x 10(-08), R(2)=0.358, permutation-based p=0.039, the gene targets

15 the concentration ranges of 0.8-400mugL(-1) (R(2)=0.998).

16 of P-P bonds to produce silylphosphines (R(1)R(2)P-SiR(3)R(4)R(5)).

17 ently reported the discovery of AT-076 (1), (R)-7-hydroxy-N-((S)-1-(4-(3-hydroxyphenyl)piperidin-1-yl

18 ptide substance P (SP) receptor neurokinin 1-R (NK1-R).

19 phores of the chelating inhibitors (S)-10a, (R)-10a, and 10b were binding within the MMP-13 active si

20 11C-(R)-PK11195 positron emission tomography reveals increase

21 by cadmium doping into the [Au23(SR)16](-) (R = cyclohexyl) nanocluster, in which two neighboring su

22 is analysis is undertaken using the ERA-20CM-R river flow reconstruction for the twentieth century.

23 r a median follow-up of 34 months, with 25% (R-CHOP) and 18% (VR-CHOP) of patients having had PFS eve

24 For the more stable silanone 2b (R = t-Bu), a selective transformation to the first repor

25 to produce silylphosphines (R(1)R(2)P-SiR(3)R(4)R(5)).

26 ured height = 0.838*predicted height + 18.3; R(2) = 0.51) with an average error of 3.3%.

27 utral cluster compounds [Ge9{Si(TMS)3}3PR2] (R: Cy (1), (i)Pr (2)) with discrete Ge-P exo bonds.

28 produce silylphosphines (R(1)R(2)P-SiR(3)R(4)R(5)).

29 d to have a Deming-regression slope of 0.97 (R(2) = 0.960) when compared to the total bilirubin value

30 tor (SSRCalc) SCX model ( approximately 0.99 R(2) value) exceeds all previously reported predictors f

31 of D(+*)-(3)(A(-*)-R(*)) and D(+*)-(1)(A(-*)-R(*)), and subsequent reduction of R(*) only occurs in D

32 ction of R(*) only occurs in D(+*)-(1)(A(-*)-R(*)).

33 a 3:1 statistical mixture of D(+*)-(3)(A(-*)-R(*)) and D(+*)-(1)(A(-*)-R(*)), and subsequent reductio

34 by spin statistics of the uncorrelated A(-*)-R(*) radical pair, where the initial charge separation y

35 transfer within the triradical forms D(+*)-A-R(-), but its yield is controlled by spin statistics of

36 Out of 11 adjuvants, only two, Abisco((R))-100 and CoVaccineHT(TM), enhanced vaccine efficacy a

37 Abraxane(R), the albumin bound PTX, represents a superior replace

38 While Abraxane(R) is now considered a gold standard in chemotherapy, it

39 Yeast lacking SGS1 accumulate R-loops and gamma-H2A at sites of Sgs1 binding, replicat

40 rongly related to soil humus C accumulation (R(2) = 0.94, p < 0.001).

41 Used in combination with the ACE-R, it provided additional value and identified almost al

42 e predictor of the error variance for acute (R(2) = 0.20; P < 0.0001) and daily (R(2) = 0.23; P < 0.0

43 ic toxicity with similar precision; adjusted R(2) and R(2) values ranged from 0.56 to 0.86 and 0.66-0

44 athophysiology of FXS as the GABABR agonist (R)-baclofen rescued the imbalances between excitatory an

45 The TLR7 agonists R-837 and R-848 were used to mimic a viral insult in the

46 age rate of decline was faster in the ALSFRS-R, with less between-patient variability at baseline (p<

47 Although R-loops play important roles in gene expression and reco

48 An R implementation of QUBIC is presented here with two uni

49 An R package for performing number and brightness image ana

50 An R-loop is a DNA:RNA hybrid formed during transcription w

51 s increased, and that of topoisomerase 1, an R-loop preventing factor, is decreased at R-loop-enriche

52 Here, we developed a new method and an R package, to easily infer candidate miRNA-mRNA target i

53 The RDI method has been implemented as an R package, and is available for download through Bitbuck

54 We built both an R package and web server to provide ADAGE signature anal

55 We have developed geneAttribution, an R package that assigns candidate causal gene(s) to a ris

56 ene Network Expression Simulator in R) is an R package that provides an interface to simulate gene ex

57 chet mechanism), the rear foot producing an (R)-stereocenter at its point of attachment to the track.

58 curve with alpha = 0.51 +/- 0.05 Gy(-1) and R(2) = 0.8838.

59 ty with similar precision; adjusted R(2) and R(2) values ranged from 0.56 to 0.86 and 0.66-0.85, resp

60 h had an OH group substituted at the R-6 and R-7 position on the ring A, showed similar antioxidant a

61 The TLR7 agonists R-837 and R-848 were used to mimic a viral insult in the upper air

62 Both AI and R received nearly 90% of their thalamic inputs from the

63 lly verified for R = 2,6-iPr2C6H3 (Dipp) and R = tBu, and the pentasulfide (n = 5) for R = Dipp.

64 rs of the niche factors Wnt2b, Gremlin1, and R-spondin1, and are sufficient to promote maintenance of

65 , or vimentin expression between placebo and R-ketorolac treatment groups.

66 onyl)-1H-indol-3-yl]methylene}succinate and (R)-2,2,5,5-tetramethyl-1,3-dioxolane-4-carbaldehyde, fac

67 The Human antigen R protein (HuR) is an RNA-binding protein that recognize

68 nvolve modulatory regulatory factors such as R-spondin 1 (Rspo1), an extracellular protein that enhan

69 an R-loop preventing factor, is decreased at R-loop-enriched regions of IFNG and TBX21 (TH1 genes) in

70 in learning and memory, such as Creb, GABA B R and Ip3k, indicating extensive involvement of DNA meth

71 unite into mirror-symmetric pentamers (G-R-B-R-G) by adhesion.

72 hree recently published Bayesian LMMs, Bayes R, BSLMM, and BOLT-LMM, we investigate an existing data

73 31, 2013 to assess the associations between R/S and incident all-cause mortality using proportional

74 n between (18)F-FDG uptake and TSPO binding (R = 0.69, P < 0.005).

75 PandaR is provided as a Bioconductor R Package and is available at bioconductor.org/packages/

76 the DNA walking system to Pacific Bioscience(R) Next-generation sequencing technology.

77 lly targeted for optimized PE consumption by R. ruber.

78 re studied using the TSPO radioligand (11)C-(R)-PK11195.

79 It is demonstrated that [(11)C]-(R)-3 readily crosses the blood-brain barrier (BBB) in ro

80 arge variation occurred in the calibrations, R(2) and RPD due to the variability of the samples.

81 rectal swabs directly using the Xpert Carba-R assay is effective for rapid detection and identificat

82 assessed the performance of the Xpert Carba-R test, a rapid real-time quantitative PCR (qPCR) assay

83 chia coli or Saccharomyces cerevisiae caused R-loop accumulation along rDNA.

84 Loss of either RNase H1 or Top1 caused R-loop accumulation, and the accumulation of R-loops was

85 rennets were covalently immobilized on CLEA(R) magnetic supports and the immobilization procedure wa

86 less active, with a correlation coefficient (R(2)) of IC50versus log of autoxidation rate of 0.75.

87 ion (RMSEP) and the correlation coefficient (R).

88 The all-classes comparison (R(2) = 0.86 and Q(2) = 0.83) indicated that OA patients

89 nent of the WPC has the highest correlation (R = -0.6) with NINO3.4.

90 A significant correlation (R(2) 0.85) between the p-PAH and black carbon emissions

91 reactive antibody which was lowest in the D+/R- group.

92 ptor (beta2-AR) and D1 dopamine receptor (D1-R).

93 r acute (R(2) = 0.20; P < 0.0001) and daily (R(2) = 0.23; P < 0.0001) EI.

94 nd deltaGamma; (3) demonstration that deltaR/R after only approximately 200 measurements is substanti

95 gical recordings show that Sema-1a-dependent R axon lamination is required for preventing the spread

96 ese helicases is suppressed by destabilizing R-loops while Pif1 and Rrm3 binding to tDNAs is increase

97 O collisions leading to genome-destabilizing R-loops.

98 ite good with coefficients of determination (R(2)) varying from 0.94 to 0.97.

99 hod is implemented in specifically developed R code, which has been made publicly available.

100 ose who developed other psychotic disorders (R(2) = 9.2%, p = .002).

101 ses in CH4 emission in response to drawdown (R(2) = 0.84, p < 0.01), suggesting that eutrophication m

102 MO), which turns rectification off and drops R to 6.

103 Zn(2+) in opposing directions across the S(E)R membrane in cardiomyocytes and that changes in their a

104 d on RNaseH1-mediated suppression of ectopic R-loops, inversely correlates with disease severity scor

105 From October 12-15th, 2016, EMBOmid R:EMBL held a symposium to bring together those in the s

106 ctivity led to the finding that enantiomers (R,R)-68 and (S,S)-68 have differential effects on the ra

107 zebrafish model, we show that encapsulated (R)-roscovitine can speed up inflammation resolution in v

108 ound that previous cocaine exposure enhanced R-O associations in DLS.

109 Methods 2 and 3 estimate R by fitting a model of the spread of infection to data

110 d CT data of patients with CoreValve, Evolut R, and SAPIEN 3 transcatheter aortic valve replacement e

111 nalytical performances such as, for example, R(2) of the calibration curve of 0.98 and 0.99 for prote

112 given value of the surface roughness factor (R).

113 me-wide association studies by using FarmCPU R package to identify 17 genetic loci associated with co

114 ns that correlated with the natural feeding (R = 0.792; P < .0001).

115 ales (R(2) = 11.1%, P < 0.0001) and females (R(2) = 16.8%, P < 0.0001).

116 us pulposus (R = 0.92) and annulus fibrosus (R = 0.83) regions.

117 n the auditory stimulation and the following R peak was significantly shortened in MCS when the audit

118 nd R = tBu, and the pentasulfide (n = 5) for R = Dipp.

119 hibition points to R-loops as precursors for R-lesions.

120 have been crystallographically verified for R = 2,6-iPr2C6H3 (Dipp) and R = tBu, and the pentasulfid

121 The third approach starting from R-mandelic acid, involving the RCM reaction to install t

122 and unite into mirror-symmetric pentamers (G-R-B-R-G) by adhesion.

123 In intron-containing genes, R-loops are bounded between the transcription start site

124 01) and with CAL change after therapy in GR (R(2) = 0.49, P <0.05).

125 eviewed for demographics, Hanifin & Rajka (H&R) and United Kingdom Working Party (UKWP) criteria.

126 currence of 691.8, 29.9% and 30.8% met the H&R and UKWP criteria, respectively.

127 , 1-I (R(1) =OEt, R(2) =H) and 2-I (R(1) =H, R(2) =NMe2 ).

128 knockdown abolished the protection against H/R-induced myocytes injury by AS-1.

129 w cytometric analysis of lung tissue from H2 R-deficient animals revealed increased numbers of CD1d(+

130 on hepatitis B virus (HBV) reactivation (HBV-R) in patients with HBV-HCV co-infection.

131 29 patients with HBV-R receiving HCV DAAs.

132 in most of the variability in GEP at hourly (R(2 ) = 0.77) to interannual (R(2 ) = 0.80) timescales.

133 had no benefit on the primary outcome (HVLT-R-DR; difference in means -0.43 [95% CI -1.73 to 0.87]).

134 s of two active complexes are reported, 1-I (R(1) =OEt, R(2) =H) and 2-I (R(1) =H, R(2) =NMe2 ).

135 reported, 1-I (R(1) =OEt, R(2) =H) and 2-I (R(1) =H, R(2) =NMe2 ).

136 It affords either the [Co(I)((R)salophen)K] complexes or the [Co(II)2(bis-salophen)M2]

137 , whether CD6 plays any role in intestinal I/R-induced injury and, if so, the underlying mechanisms,

138 actors defining surgical outcomes-that is, I/R, LR, and liver malignancy-is less clear.

139 amma-GRK2 inhibition initiated 1 week post-I/R provided little to no further protection in mice with

140 d myocardial injury in wild type mice post-I/R.

141 of neprilysin in both zones, suggesting r-I/R induced intrinsic remote conditioning.

142 effect of microbiota depletion upon renal I/R injury.

143 mined in mouse focal ischemia/reperfusion (I/R) model.

144 n of ATF6 in cardiac myocytes subjected to I/R increased reactive oxygen species and necrotic cell de

145 The Portrait Staph ID/R BCP results were compared with results from convention

146 We evaluated the Portrait Staph ID/R blood culture panel (BCP) multiplex PCR assay (Great B

147 and S-9-PAHSA, and this approach identified R-9-PAHSA as the predominant stereoisomer that accumulat

148 an samples visualized using the ImageStream((R)) platform (Millipore Sigma, Darmstadt, Germany), and

149 lation with the later functional impairment (R(2) =0.94).

150 ets in ImmPort (immport.org) for analysis in R.

151 The proposed method is implemented as in R and will be available an a Bioconductor package.

152 ed by cytosine deamination of DNA engaged in R-loops and the other by MutLgamma cleavage.

153 tation of the proposed method is provided in R package MWLasso.

154 chastic Gene Network Expression Simulator in R) is an R package that provides an interface to simulat

155 Increased R gnavus was observed before the onset of allergic manif

156 h NADP(H) and the pharmaceutical ingredient (R)-rasagiline are reported.

157 INH-R was found in 86 (26.7%) patients, MDR in 15 (4.7%) pat

158 tment with the small molecule TNFR inhibitor R-7050 partially protected hyperoxaluric mice from nephr

159 8-H4 epigenetic marks by the ACK1 inhibitor (R)-9bMS-sensitized naive and enzalutamide-resistant pros

160 rimido-pyrrolo-oxazine-dione CFTR inhibitor (R)-BPO-27 for antisecretory therapy of diarrheas caused

161 copherol were weakly associated with intake (R(2) < 0.25).

162 GEP at hourly (R(2 ) = 0.77) to interannual (R(2 ) = 0.80) timescales.

163 nternational Prognostic Scoring System (IPSS-R) and presence of comorbidity graded according to the H

164 urg, Austria, were tested in ImmunoCAP ISAC((R)) for IgE reactivity to 112 single allergens.

165 We developed the IsotopicLabelling R package, a tool able to extract and analyze isotopic p

166 ced bone loss in adult female rats.-Chen, J.-R., Lazarenko, O.

167 activate the antiviral kinase protein kinase R (PKR), which potently inhibits virus replication.

168 of the innate immune effector protein kinase R, which phosphorylates the eukaryotic initiation factor

169 th, making furthering our understanding of L-R development an important concern.

170 n dand5 expression pattern and left-right (L-R) axis establishment.

171 rface was well represented by the power-law (R(2) > 0.77).

172 ucibility (%RSD < 10%; n = 6) and linearity (R(2) > 0.99).

173 ely 2.5%), accuracy (>/=90%), and linearity (R(2) >/= 0.99) were attained for all the studied compoun

174 tivity and specificity, excellent linearity (R(2)>0.988) low decision limits and detection capabiliti

175 Good linearity (R(2)=0.9990) was achieved for all samples using matrix-m

176 RR, 1.30; 95% CI, 1.20-1.41); or ZDV-3TC-LPV-R (75 of 167 [44.9%]; ARR, 1.21; 95% CI, 1.01-1.45).

177 TDF-FTC and lopinavir-ritonavir (TDF-FTC-LPV-R) (112 of 231 [48.5%]; ARR, 1.31; 95% CI, 1.13-1.52); z

178 ion in reservoirs exceeds carbon fixation (P<R); the global P/R ratio, however, varies significantly,

179 contains the absolutely conserved (679)LWYIK/R(683) sequence, proposed to embody a "cholesterol recog

180 was obtained from 1.0x10(-8) to 4.1x10(-7)M (R(2)=0.9987) with a detection limit of 2.5x10(-9)M.

181 ignificantly associated with PM2.5 in males (R(2) = 11.1%, P < 0.0001) and females (R(2) = 16.8%, P <

182 The correlation of the model (R(2) approximately 0.995) indicates that the peptide sep

183 Since then, many more R genes have been identified and characterized in numero

184 relapsed and/or refractory multiple myeloma (R/R MM) after a long period in which dexamethasone and m

185 New R ratio Hy's law better identifies risk for death compar

186 short (50-bp) single-end reads and Nextera (R) library preparation yield reliable results.

187 from the surface using n-alkylamines (NH2R', R' = n-butyl, n-hexyl, n-octyl) (</=0.01 carboxylates nm

188 ubstance P (SP) receptor neurokinin 1-R (NK1-R).

189 neurodegeneration in MoCD and introduce NMDA-R antagonists as potential therapeutics for this fatal d

190 gnaling effector in the common synaptic NMDA-R-CaMKII-SynGap-Ras-BRaf-MEK-ERK transduction cascade.

191 NOv) were measured by two methods (NObreath((R)) and NIOX Vero((R))).

192 isomers of 21.8, compared to 2.3 for Novozym(R) 435.

193 hecin which transiently stabilized nucleolar R-loops recruited RNase H1 to the nucleoli.

194 The basic reproduction number R 0 is calculated, and its numerical and sensitivity ana

195 s cleaved rather than the weaker aliphatic O-R bond.

196 tive complexes are reported, 1-I (R(1) =OEt, R(2) =H) and 2-I (R(1) =H, R(2) =NMe2 ).

197 G islands, together with the accumulation of R-loops and cytosolic ssDNA.

198 R-loop accumulation, and the accumulation of R-loops was exacerbated when both proteins were depleted

199 To enable precision analysis of R-loops in vivo, we develop an RNase-H-based approach; t

200 (OCT), and immunohistochemistry analysis of R/G opsin and rhodopsin.

201 n-vitro tests showed a linear correlation of R(2)=0.998 between sensor values and reference glucose v

202 osed mechanism, DNA-binding-domains (DBD) of R insert in major grooves of O pre-TS, forming most Coul

203 ined that the major virulence determinant of R. equi is the surface bound virulence associated protei

204 countercurrent heat exchanger in the head of R. prolixus, which decreases the temperature of the inge

205 Significantly, increased cellular load of R-loops and DSBs, which are normalized on RNaseH1-mediat

206 tions of GLIC in the absence and presence of R- or S-ketamine.

207 all biochemically established properties of R-loops.

208 (1)(A(-*)-R(*)), and subsequent reduction of R(*) only occurs in D(+*)-(1)(A(-*)-R(*)).

209 erein, we report the development of a set of R-based scripts that allow for pre- and postprocessing o

210 ds and stimulates the activity of RNaseH1 on R loops.

211 asgow Outcome Scale as a continuous outcome (R = 0.82; p = 0.001; z score, 3.39).

212 exceeds carbon fixation (P<R); the global P/R ratio, however, varies significantly, from 0.20 to 0.5

213 P2Y14 R is downregulated in hCPCs derived from HF patients wit

214 Additionally, P2Y14 R overexpression reversed senescence-associated morpholo

215 Augmenting P2Y14 R expression levels in aged/diseased hCPCs antagonizes s

216 ivity using a single dose-related parameter (R (2) = 0.66).

217 at baseline before therapy in all patients (R(2) = 0.28, P <0.01) and with CAL change after therapy

218 the degree of J-ST point elevation (Pearson R, 0.81; P<0.001).

219 fferent Partial Least Square-Regression (PLS-R) multivariate quantification methods.

220 gestible starch (SDS) correlated positively (R=0.816, p<0.05) with TPC and water absorption correlate

221 and water absorption correlated positively (R=0.995, p<0.05) with damage starch content.

222 e-H-based approach; this reveals predominant R-loop formation near gene promoters with strong G/C ske

223 Its prototype, (R)-6-neopentyl-2-(pyridin-2-ylmethoxy)-6,7-dihydropyrimi

224 , is the same as in the previously published R package for Boolean Networks BoolNet, which enhances c

225 n imaging results for both nucleus pulposus (R = 0.92) and annulus fibrosus (R = 0.83) regions.

226 QIIME, R package "Phyloseq" analysis was used to assess alpha a

227 etry (LC-MS) method to separate and quantify R- and S-9-PAHSA, and this approach identified R-9-PAHSA

228 n of the permeation rate, J, droplet radius, R, membrane permeance, k, water viscosity, mu, and the w

229 requires the reference standard method (RAMP(R) immunoassay)) or alternatively on the basis of the co

230 ar orbital (HOMO) with a rectification ratio R = 99, but junctions with radical units have a new acce

231 lly limited to a maximum rectification ratio R of approximately 10(3).

232 es with it the IL-2 beta and gamma receptor (R) subunits.

233 a genome sequence, little is known regarding R. typhi biology in flea vectors that, importantly, do n

234 The relevant R package miLineage is publicly available.

235 f 158 genes in a Rhodococcus representative, R. ruber.

236 The first plant disease resistance (R) genes were identified and cloned more than two decade

237 Resistance to Ralstonia solanacearum 1 (RRS1-R)WRKY.

238 tifocal tumour (F), and spontaneous rupture (R).

239 esulted in an interference with the kinase's R-Spine.

240 o override well-learned stimulus-response (S-R) associations.

241 The crystal structure of GLIC shows R-ketamine bound to an extracellular intersubunit cavity

242 ion of P-P bonds to produce silylphosphines (R(1)R(2)P-SiR(3)R(4)R(5)).

243 atsiougiannis, S., Chia, D., Kim, Y., Singh, R.

244 epithelial targeting peptide (P) and siRNA (R).

245 Here, we present an open source R package 'twoddpcr', which uses Poisson statistics to e

246 We used closed-loop SPW-R detection at goal locations to trigger optogenetic sil

247 In contrast, the place fields of SPW-R-silenced place cells remapped, and their spatial infor

248 nt with experimentally measured stabilities (R(2) = 0.93).

249 AM) flanking the target site, and subsequent R-loop formation and strand scission are driven by compl

250 , represents a superior replacement of Taxol(R) that mitigates the side effects associated with Cremo

251 We show here that R-2HG also exerts a broad anti-leukemic activity in vitr

252 These findings indicate that R-ketorolac treatment slows tumor progression in an aggr

253 rturbation experiments further indicate that R-loop induction correlates to transcriptional pausing.

254 Here we show that R-loops accumulate preferentially in breast luminal epit

255 We show that R-motif regulates translation in response to pattern-tri

256 The R package chngpt provides both estimation and hypothesis

257 For Patlak analysis, the R(2) between NLR-based and parametric-based (Patlak) tum

258 intermediate will assemble with HOPS and the R, Qa, and Qc SNAREs, and that this assembly undergoes r

259 ich have a hydroxyl group substituted at the R-3 position on the C ring, have outstanding antioxidant

260 ne, which had an OH group substituted at the R-6 and R-7 position on the ring A, showed similar antio

261 and 1-month were significantly lower for the R-E group than for the NR-E group (treatment main effect

262 hence demonstrating a distinct role for the R-Ras-Akt axis.

263 Here, we report a pivotal role for the R-spondin/leucine-rich repeat-containing G protein-coupl

264 not differ significantly for patients in the R-CHOP or intensive therapy cohorts when analyzed by rec

265 atients in the GP2013-CVP; three [1%] in the R-CVP group).

266 w WGS variant data format implemented in the R/Bioconductor package 'SeqArray' for storing variant ca

267 bly needs HOPS, lipid membranes to which the R- or Qa-SNARE and Ypt7:GTP are integrally bound, and ea

268 When polysulfide reacts with the R domain of FisR through the three conserved cysteine re

269 The (R)-BINOL Fc phosphate gave Fc-rearranged phosphonate in

270 Thus, R. typhi(GFPuv) bacteria are a novel, potent tool to stu

271 We demonstrate that both TNF-R and nucleotide-binding oligomerization domain stimulat

272 eakage at expanded CAG repeats occurs due to R-loop formation and reveal two mechanisms for CAG repea

273 importantly, do not suffer lethality due to R. typhi infection.

274 mutants to translation inhibition points to R-loops as precursors for R-lesions.

275 ersely, among patients who were resistant to R-CHOP, basal DLBCL mutations did not disappear from cfD

276 How the detection and response to R/FR are spatially linked and how this spatial coordinat

277 vely with the content of beta-glucans (up to R=0.77) and arabinoxylans (up to R=0.80) in bran and ref

278 cans (up to R=0.77) and arabinoxylans (up to R=0.80) in bran and refined flour fractions.

279 TAGGED 1 (TOE1)-miR172-resistant (35S::TOE1(R) ) and mutant (flowering locus T-10 (ft-10)) lines wer

280 in FL concentration, accumulation of toxic (R)-FL and formation of toxic (S)-NFL leads to much highe

281 TRAIL-R suppression in tumor cells impaired CCL2 production an

282 ever, whether and to what extent TRAIL/TRAIL-R signaling in cancer cells can affect the immune microe

283 strates for the formation of transcriptional R-loops.

284 utilized during activated sludge treatment ((R)-FL is 30x more toxic than (S)-FL; (S)-NFL is 10x more

285 Here, we provide the TSIS R package, which is the first tool for detecting signifi

286 to those for animals infected with wild-type R. typhi and develop comparable pathology and bacterial

287 and Rrm3 binding to tDNAs is increased upon R-loop stabilization.

288 hances IP1 through vasopressin receptor (V1A-R) but not alpha1 adrenergic receptor (alpha1-AR), sugge

289 by two methods (NObreath((R)) and NIOX Vero((R))).

290 ir, the best linear correlation achieved was R(2)=0.90 and by microwave was R(2)=0.88.

291 achieved was R(2)=0.90 and by microwave was R(2)=0.88.

292 The model fits the observed GPP well (R(2) = 0.79), which was confirmed by other model perform

293 es produce 4-piperidones in good yields when R = alkyl or aryl, but oxidation of 2H-pyrans also gives

294 ese impressive findings by examining whether R-E training could attenuate smoking-related craving and

295 When used in conjunction with R/Bioconductor packages, the SeqArray package provides u

296 CB17 SCID mice infected with R. typhi(GFPuv) succumb to the infection with kinetics s

297 duced callose after single inoculations with R. irregularis or P. putida, only the cultivar with high

298 1 enriches in nucleoli and co-localizes with R-loops in cultured human cells.

299 The final models with R(2) values ranging from 0.64 for p-xylene to 0.70 for b

300 adioligand used for the binding assay, with (R,R)-68 potentiating the radioligand and (S,S)-68 displa