ライフサイエンスコーパス: CCR

1 CCR allows efficient on-line control of NZG including VB

2 CCR can recover rearranged cancer contigs from karyotype

3 CCR expression in primary ASM cell cultures and airway b

4 CCR has been intensely studied in the model organisms Es

5 CCR has three components: continuous chest compressions

6 CCR improves survival of patients with cardiac arrest.

7 CCR is likely of great importance to Streptococcus pneum

8 CCR leachates had a mostly negative delta(11)B, ranging

9 CCR type 2 (CCR2) is responsible for pulmonary monocyte

10 CCR with FU/MMC has a statistically significant, clinica

11 CCRs are enriched in toxic elements, and their leachates

12 CCRs highlight protein domain families under high constr

13 gether this suggests a novel target of MCP-1/CCR-2 axis that could benefit ovarian cancer patients.

14 ty (TVA) coal ash spill affected waters; (2) CCR effluents from power plants in Tennessee and North C

15 iagnosed from January 2000 to December 2013; CCR records were linked to statewide birth certificate f

16 zontal lineCH(3,4,6-(F)3-C6H-2-yl)}Fe(PMe3)3(CCR) (R = Me, 4b-Me; R = Ph, 4b-Ph) were generated from

17 tially complement the irregular xylem gene 4 CCR mutation of Arabidopsis.

18 reated with imatinib mesylate who achieved a CCR.

19 ent from background, limiting their use as a CCR tracer.

20 hree-dimensional structure information for a CCR from a monocot species.

21 this is pertinent more broadly to advancing CCR.

22 , structurally distinct from the green algae CCRs used extensively for neural activation and from cry

23 yotype graph, and describe a novel algorithm CCR capable of solving CCCP in polynomial time.

24 ical residues and substrate preference among CCRs and provide, to our knowledge, the first three-dime

25 s a master regulator that controls anaerobic CCR in these bacteria.

26 damental differences between natural ACR and CCR conductance mechanisms and their underlying photoche

27 al antibody, serotype b-induced cytokine and CCR expression was inhibited; when TLR4 signaling was bl

28 tests showed the power density of IT-GAC and CCR anodes achieved at 2.92 and 2.55 W m(-2), the highes

29 Multiple IT-GAC and CCR anodes with multiple collectors effectively utilized

30 kinase/phosphatase) mutations on growth and CCR were evaluated.

31 mpair the interaction between the kinase and CCR domain.

32 ure calculations restrained with the RDC and CCR data, we observe collective motions on time scales s

33 abled detailed characterization of CAR-T and CCR-T cell activation to better understand their functio

34 Similarly, higher levels of cytokines and CCRs were detected in serotype b- or serotype K1-primed

35 tio (0.31 +/- 0.09), followed by Appalachian CCRs (283 +/- 34 Bq/kg; 0.67 +/- 0.09), and Powder River

36 We apply CCR on a prostate cancer dataset and demonstrate that it

37 airways in asthma, we hypothesized that ASM CCR activation could promote the increase in ASM mass se

38 226)Ra, and (210)Pb) in coals and associated CCRs from the Illinois, Appalachian, and Powder River Ba

39 characterized by C:G to A:T transversions at CCR sequence contexts that may have arisen due to error-

40 significant multivariate differences between CCR-receiving and reference lakes for surface water, por

41 he mga promoter and establish a link between CCR and Mga regulation in the GAS.

42 ving a canonical SDR catalytic triad in both CCR and CAD2 and an important role for an auxiliary cyst

43 including CXCR3, CXCR6, CCR1, and CCR5, but CCR expression on antigen-specific effector and memory T

44 h Carolina; (3) lakes and rivers affected by CCR effluents in North Carolina; and (4) porewater extra

45 ane-based induction chemotherapy followed by CCR for organ preservation in resectable stage III/IVA a

46 with cisplatin and fluorouracil, followed by CCR with three cycles of cisplatin.

47 xtracted from sediments in lakes affected by CCRs.

48 tes of metastases to evaluate whether T cell CCR/CXCR expression correlates with intratumoral accumul

49 ducting mutants of cation channelrhodopsins (CCRs) showed radical differences in their anion selectiv

50 ied conductance by cation channelrhodopsins (CCRs), not attributable to simply a modification of the

51 n; (b) cryptophyte cation channelrhodopsins (CCRs), structurally distinct from the green algae CCRs u

52 Contrary to cation channelrhodopsins (CCRs), the ion conducting state of ACRs develops in an L

53 eloped an exploratory method to characterize CCRs in the methylation data and identified the 200 gene

54 the Anal Canal], concurrent chemoradiation (CCR) with fluorouracil (FU) plus mitomycin (MMC) decreas

55 Taxane-based concurrent chemoradiotherapy (CCR) for head and neck cancers has proven to have a favo

56 erapy (IC) and concurrent chemoradiotherapy (CCR).

57 at least partly, by central chemoreceptors (CCRs) and the carotid bodies (CBs).

58 pressing central respiratory chemoreceptors (CCRs), is the site of such plasticity.

59 Finally, we identify highly constrained CCRs within genes lacking known disease associations.

60 The most constrained CCRs are enriched for pathogenic variants in ClinVar and

61 RT-PCR) to predict the duration of continued CCR, we monitored 85 patients treated with imatinib mesy

62 king surgery (completeness of cytoreduction [CCR], 2 or 3; P < .001), and not using HIPEC (P = .030)

63 he specific treatment approaches that define CCR, this alternative approach may represent the future

64 ion effects on female fertility traits (DPR, CCR and HCR).

65 d to receive fewer doses of cisplatin during CCR.

66 ded to reduce cisplatin to two cycles during CCR.

67 ing followed, but 40% for the 3 years during CCR.

68 The hprKV265F mutant enhanced CCR of the fruA and levD operons, a phenotype reversible

69 uces a metaplasia of the gastric epithelium, CCR decline, and subsequent commensal dysbiosis and epit

70 overall response): three (6.1%) experienced CCRs, and 17 (34.7%) experienced PRs.

71 CCR3 was the most frequently expressed CCR protein and was present on 79 +/- 14% of cells.

72 domestic cat BAC clone containing the feline CCR genes CCR1, CCR2, CCR3, and CCR5 to further analyze

73 bstantially depleted, providing evidence for CCR's involvement in coniferyl alcohol biosynthesis.

74 pe and G-type lignin, providing evidence for CCR's involvement in the biosynthesis of both lignin typ

75 grasses, the marker is only an indicator for CCR deficiency in general, but is a reliable marker in w

76 rrangements and are probably responsible for CCR.

77 To directly access the correlations from CCR, we develop a structure-free data analysis.

78 nts the quality of effluents discharged from CCR settling ponds or cooling water at ten sites and the

79 and trace elements in over 300 samples from CCR effluents, surface water from lakes and rivers at di

80 condary end points included global cure (GC; CCR without CDI recurrence) 30 days after EOT (end of st

81 econdary endpoints included global cure (GC; CCR without CDI recurrence) 30 days after EOT (end of st

82 Importantly, this "green" CCR protocol circumvents prefunctionalization, isolation

83 t genotype-dependent effects of field-grown, CCR-down-regulated poplar trees (Populus tremula x Popul

84 impacted with high B levels and 49 had high CCR-contaminant levels.

85 Illinois CCRs had the highest total Ra ((228)Ra + (226)Ra = 297 +

86 ents with SR-average disease did not improve CCR or OS, even in patients with higher MRD, in whom it

87 , and fish tissues as well as differences in CCR accumulation among North Carolina resident fish spec

88 reference lake levels and (2) differences in CCR accumulation patterns among abiotic and biotic compa

89 c acid hexoside and ferulic acid hexoside in CCR-RNAi lines, indicating a redirection of metabolite f

90 of specific enzymes and proteins involved in CCR.

91 tabolite profile and the cell wall matrix in CCR-RNAi lines.

92 cidic compounds into the cell wall matrix in CCR-RNAi lines.

93 acidolysis, pyrolysis-GC/MS and/or 2D-NMR in CCR-RNAi lines, providing new insights into the conseque

94 ch as ferulic acid) that are up-regulated in CCR-deficient poplar trees.

95 the hypothesis that CcpA has a major role in CCR and regulation of gene expression but revealed that

96 Overall, total NORM activities in CCRs are 7-10- and 3-5-fold higher than NORM activities

97 ificantly associated with drastic changes in CCRs throughout the genome.

98 used to predict total NORM concentrations in CCRs.

99 In contrast (87)Sr/(86)Sr ratios in CCRs were not always exclusively different from backgrou

100 Total Ra and (228)Ra/(226)Ra variations in CCRs correspond to the U and Th concentrations and ash c

101 report describes the first CcpA-independent CCR mechanism identified in the pneumococcus and the fir

102 tabolic enzymes, suggesting CcpA-independent CCR mechanisms predominate.

103 Bobrow et al. instituted CCR for out-of-hospital cardiac arrest in metropolitan a

104 Interestingly, CCR suppression substantially promoted pyrolytic breakdo

105 collected in areas near and away from known CCR disposal sites, and analyzed for Mo and inorganic ge

106 ple component analysis of census block-level CCR data that was linked to census data to address seven

107 information about regulatory processes like CCR in bacteria at a single cell level within a time spa

108 for many years despite recent laws to limit CCR discharge into surface waters in NC.

109 roximately P)-mediated regulation is a major CCR mechanism and an essential activity in the pneumococ

110 n S (SLS) production was under CcpA-mediated CCR, as was SLS hemolytic activity.

111 to increased resistance to glucose-mediated CCR when lactose was used to induce the lac operon, but

112 rom loss of HPr-Ser approximately P-mediated CCR in any species.

113 relapsed after a median time of 7.6 months; CCR and survival at 5 years only reached 12% and 33%, re

114 The compact configuration of multiple CCR anodes contacting each other did not deteriorate the

115 verts pyruvate to acetyl-phosphate under non-CCR-inducing growth conditions, was unable to form biofi

116 chronic HCV for flow cytometric analysis of CCR expression on CD8+ T cells.

117 Many components of CCR have since been incorporated in the 2005 ILCOR guide

118 t al. instituted the first two components of CCR in rural Wisconsin in 2004.

119 The first 2 components of CCR were first instituted in 2003 in Tucson, Arizona; in

120 Concentrations of CCR contaminants, including SO4, Ca, Mn, Fe, Se, As, Mo,

121 viding new insights into the consequences of CCR suppression in pine.

122 ploitation of rationally engineered forms of CCR and CAD2 for the targeted modification of monolignol

123 of various liganded and unliganded forms of CCR and CAD2 highlight substantial conformational flexib

124 ist that contribute to the implementation of CCR and NCR.

125 vironmental and human health implications of CCR disposal and accidental release to the environment i

126 tem transport rates and limited induction of CCR-repressed genes.

127 ngerprints, combined with elevated levels of CCR tracers, provide strong evidence for the leaking of

128 ese TREM-2(+) cells expressed high levels of CCR-7 and CD86 suggesting a potential role of TREM-2 in

129 passages (NPs) in response to high levels of CCR-ligands produced in these tissues.

130 arallel in the peripheral blood and lungs of CCR(+/+) mice, whereas CD11c(+) MHC class II(+) pre-DC w

131 lite control protein A (CcpA), a mediator of CCR in gram-positive bacteria.

132 nce regulator SmrC as potential mediators of CCR in connection with ManLMN.

133 In contrast, the rhizosphere microbiome of CCR-deficient and WT poplar trees featured highly overla

134 unted cytotoxic responses in the presence of CCR-specific stimuli or cognate leukemic cells.

135 The rate of CCR at 2 days after EOT was 77.6% (76 of 98 patients) wi

136 The rate of CCR at 2 days after EOT was 77.6% (76/98) with fidaxomic

137 However, strong down-regulation of CCR also affected biomass yield.

138 However, fine regulation of CCR is accomplished by the small molecule effectors, glu

139 gated whether an increase in the activity of CCRs accounts for this return.

140 tailed functional and structural analyses of CCRs from Medicago truncatula and Petunia hybrida and of

141 ing the retrotrapezoid nucleus, a cluster of CCRs, reduced breathing proportionally to arterial pH.

142 Large legacy depositions of CCRs within reservoir sediments are likely to sustain Se

143 of secretion of cytokines and expression of CCRs detected in DCs stimulated with different serotypes

144 nt with the expected isotope fingerprints of CCRs, but rather mimic the compositions of local litholo

145 The impact of CCRs is long-term, which influences contaminant accumula

146 g and evaluating the environmental impact of CCRs.

147 material from the complete set of 20-mo-old CCR-down-regulated trees, including bark and less effici

148 ntradict those reported in a recent study on CCR-deficient Arabidopsis.

149 m isotopic ratios of leaching experiments on CCRs from a variety of coal sources (Appalachian, Illino

150 RNAi suppression of PtrCCR2, the only CCR member highly expressed in SDX, caused a reciprocal

151 strates high selectivity for CCR1 over other CCR-family members, high microsomal stability, and good

152 Threonine-154 of SbCCR1 and other CCRs likely confers strong substrate specificity for fer

153 The highest-percentile CCRs complement existing variant prioritization methods

154 hese results support a model of pneumococcal CCR in which HPr-Ser approximately P directly affects th

155 activation of the prototypical Gram-positive CCR master regulator, ccpA, attenuates virulence in mice

156 er after CBD, consistent with its postulated CCR function.

157 hat, in rats, CB denervation may not produce CCR plasticity.

158 emical information, four additional putative CCR genes were discovered from sorghum genomic data.

159 alladium-catalyzed cross-coupling reactions (CCRs) of aryl and heteroaryl chlorides with readily acce

160 Complex chromosomal rearrangements (CCRs) have been known for some time but their mechanisms

161 l adipocytes binding to its cognate receptor CCR-2 on ovarian cancer cells facilitates migration and

162 ory T cells and Th2 cells via their receptor CCR type 4 (CCR4).

163 T lymphocytes bearing CC chemokine receptor (CCR) 1, CCR3, and CCR5 receptors for RANTES chemokine wa

164 ited to the liver by C-C chemokine receptor (CCR) 2, CCR5, and nucleotide-binding oligomerization dom

165 forms heteromers with CC chemokine receptor (CCR) 2, CCR5, the Na(+)/H(+) exchanger regulatory factor

166 les [eg, eotaxins and CC chemokine receptor (CCR) 3] in IL-13-mediated airway disease.

167 CC chemokine receptor (CCR) 4 was dispensable for donor Treg function in the tr

168 f chemokine (CC/CXC) and chemokine receptor (CCR) mRNAs, thereby helping to resolve physiological inf

169 whether cytokine and CC-chemokine receptor (CCR) production by DCs stimulated with different serotyp

170 ty complex class II, C-C chemokine receptor (CCR) type 1, CCR2, CX3C chemokine receptor 1 (CX3CR1), o

171 genetic deficiency of CC-chemokine receptor (CCR) type 5, the common receptor of chemokine (C-C motif

172 tween FcepsilonRI and CC chemokine receptor (CCR)-mediated signaling pathways in mast cells.

173 ligand (CCL)2, CCL4, C-C chemokine receptor (CCR)1, and CCR5, which are involved in monocyte recruitm

174 own-regulation of the CC chemokine receptor (CCR)5 in NY1DD mice but not in control mice.

175 ne ligand (CCL) 20, a CC chemokine receptor (CCR)6 ligand, in human keratinocyte monolayer and raft c

176 of the CCL20 receptor CC chemokine receptor (CCR)6, suggesting that Fpr2/3 regulates CCL20-CCR6-media

177 e mechanisms by which CC chemokine receptor (CCR)7 ligands are selectively presented on lymphatic end

178 ted CD69(+)CD45RA(-) C-C chemokine receptor (CCR)7(-) effector memory and perforin(+) granzyme B(+) c

179 t homing alpha4beta7 and chemokine receptor (CCR)9 by anti-CD3 preconditioning results from a reducti

180 tigen and a chimeric costimulatory receptor (CCR) that recognizes a second antigen.

181 n of CD45RO, chemokine (C-C motif) receptor (CCR) 5, CCR7, CD27, and CD28 to enumerate naive and memo

182 ignal in the chemokine (C-C motif) receptor (CCR) gene cluster on chromosome 3.

183 acellular loop (ECL)-2, chemokine receptors (CCR) contain a disulfide bridge between the N terminus a

184 e expression patterns of 9 homing receptors (CCR/CXCR) in naive and memory CD4+ and CD8+ T lymphocyte

185 ines, acting through CC chemokine receptors (CCRs) 1 to 5, is instrumental in shaping inflammatory re

186 Chemokine receptors (CCRs) are expressed on airway smooth muscle (ASM) cells.

187 hepatic T cells express chemokine receptors (CCRs), including CXCR3, CXCR6, CCR1, and CCR5, but CCR e

188 Fibronectin, C-C chemokine receptors (CCRs)2 and 7, and oxidative stress were all increased in

189 expressed chimeric costimulatory receptors (CCRs) lacking CD3zeta but containing DAP10 stimulatory d

190 combination of carbon capture and recycling (CCR) is an emerging area of research.

191 Cinnamoyl-coenzyme A reductase (CCR) catalyzes the reduction of hydroxycinnamoyl-coenzym

192 The enzymes cinnamoyl-CoA reductase (CCR) and cinnamyl alcohol dehydrogenase (CAD) catalyze t

193 drogenase (CAD) and cinnamoyl-CoA reductase (CCR) families in wood formation in Populus trichocarpa,

194 lignin-related gene cinnamoyl-CoA reductase (CCR) in the Pinus radiata tracheary element (TE) system

195 Cinnamoyl-CoA reductase (CCR), an enzyme central to the lignin biosynthetic pathw

196 down-regulated for cinnamoyl-CoA reductase (CCR), the enzyme catalyzing the first step in the monoli

197 gnins isolated from cinnamoyl CoA reductase (CCR)-deficient poplar.

198 Cinnamoyl CoA reductases (CCR) convert hydroxycinnamoyl CoA esters to their corres

199 ow that the stomach-like copper cell region (CCR) in the middle midgut controls distribution and comp

200 the midgut known as the copper cell region (CCR).

201 pe proximal to the central conserved region (CCR) of RSV G protein (mAb 131-2G) showed therapeutic ef

202 erences, occurs in cleavage cluster regions (CCRs), and is enriched in introns and lincRNA loci.

203 detailed map of constrained coding regions (CCRs) by leveraging variation observed among 123,136 hum

204 population-based California Cancer Registry (CCR) database as a model.

205 d 2011 using the California Cancer Registry (CCR) dataset merged with California Office of Statewide

206 f DLBCL from the California Cancer Registry (CCR) to survivors of breast, prostate, head and neck, an

207 The North Carolina Central Cancer Registry (CCR) was used to identify female AYA cancer survivors di

208 th data from the California Cancer Registry (CCR).

209 is (DA) and Correlated Component Regression (CCR) correctly estimated the percent of blocked lysine i

210 tive bacteria, carbon catabolite regulation (CCR) is mediated by the carbon catabolite control protei

211 nomena conditional concordant relationships (CCRs).

212 hat relates NMR cross-correlated relaxation (CCR) rates between dipolar interactions to residual dipo

213 uates virulence in mice but does not relieve CCR of most metabolic enzymes, suggesting CcpA-independe

214 e, the 6-year continuous complete remission (CCR) and OS rates for SC versus IC were 87.8% +/- 1.3% v

215 robability of continuous complete remission (CCR; 74% vs 35%; P < .0001) and of overall survival (80%

216 Carbon catabolite repression (CCR) allows bacteria to alter metabolism in response to

217 t accounts for carbon catabolite repression (CCR) control of the anaerobic catabolism of aromatic com

218 al mediator of carbon catabolite repression (CCR) in gram-positive bacteria, and growing evidence fro

219 that carry out carbon catabolite repression (CCR) in staphylococci and other Gram-positive bacteria.

220 Carbohydrate catabolite repression (CCR) in Streptococcus mutans can be independent of catab

221 Carbon catabolite repression (CCR) is a regulatory phenomenon implemented by bacteria

222 Carbon catabolite repression (CCR) is a regulatory phenomenon occurring in both lower

223 r some form of carbon catabolite repression (CCR), a regulatory network in which genes involved in th

224 lycolysis, and carbon catabolite repression (CCR)-mediated carbohydrate-dependent metabolic switches.

225 direct role in carbon catabolite repression (CCR).

226 's strategy of carbon catabolite repression (CCR).

227 tabolite and nitrogen catabolite repression (CCR, NCR), and has been shown to be important for virule

228 Carbon catabolite repressor (CCR)4 and CCR4-associated factor (CAF)1 in the CCR4-NOT

229 llowing decades of coal combustion residual (CCR) inputs.

230 fish species from coal combustion residual (CCR)-impacted lakes and paired reference lakes.

231 6 million tons of coal combustion residuals (CCRs) annually.

232 terials (NORM) in coal combustion residuals (CCRs) from different coal source basins have not been fu

233 Coal combustion residuals (CCRs), the largest industrial waste in the United States

234 Coal combustion residues (CCRs) are enriched in Mo, and thus present a potential a

235 30 million tons of coal combustion residues (CCRs) each year in the United States; yet their environm

236 cy endpoint was confirmed clinical response (CCR), 2 days after end of treatment (EOT).

237 y end point was confirmed clinical response (CCR), 2 days after the end of treatment (EOT).

238 ate achieve a complete cytogenetic response (CCR), some patients will relapse.

239 were responders (complete clinical response [CCR] or partial response [PR] as overall response): thre

240 oarcus sp. CIB controls succinate-responsive CCR of the central pathways for the anaerobic catabolism

241 ptsG gene in the manL mutant did not restore CCR of the lev or fru operons.

242 Both chronic calorie restriction (CCR) and intermittent calorie restriction (ICR) have sho

243 Cardiocerebral resuscitation (CCR) is a new approach for resuscitation of patients wit

244 Cardiocerebral resuscitation (CCR) represents a bundle of specific therapies designed

245 It is called cardiocerebral resuscitation (CCR), rather than cardiopulmonary resuscitation, as the

246 Using chemostat with cell retention (CCR) of Pseudomonas putida, we resolve this controversy

247 holography and a cornercube retroreflector (CCR).

248 ow that the carboxyl-terminal cysteine-rich (CCR) domain of this protein functions as a copper-bindin

249 ion and an upstream conserved cysteine-rich (CCR) domain.

250 - 34 Bq/kg; 0.67 +/- 0.09), and Powder River CCRs (213 +/- 21 Bq/kg; 0.79 +/- 0.10).

251 ted charcoal (IT-GAC) and carbon cloth roll (CCR)) and multiple anodes/electron collectors.

252 ocarpa transgenics caused a reduction in SDX CCR activity.

253 Severe CCR suppression almost halved lignin content in TEs base

254 also generated a library of the significant CCRs that may be of interest to future studies of the re

255 Thus, specific CCR/CXCR expression patterns on circulating T lymphocyte

256 valent self-association (aggregation) state, CCR-5 specificity, in vivo elimination half-life, and an

257 complications (P < .001), debulking surgery (CCR 2 or 3; P < .001), prior chemotherapy treatment (P =

258 source of Mo to the groundwater, rather than CCR-induced contamination.

259 We conclude that CCR down-regulation may become a successful strategy to

260 Furthermore, we demonstrated that CCR-gammadeltaT cells may offer the potential to avoid o

261 e compartments additionally highlighted that CCR pollution is a mixtures contamination issue.

262 The data show that CCR effluents contain high levels of contaminants that i

263 urces, and increasing evidence suggests that CCR is involved in regulating virulence gene expression

264 This observation suggests that CCRs may identify regions under strong purifying selecti

265 The CCR method advocates continuous chest compressions witho

266 The CCR method has been shown to dramatically improve surviv

267 The CCR-mediated proline auxotrophy was lifted when nonprefe

268 We also identify mutations in the CCR domain that lead to elevated levels of PI(3,5)P2 Tog

269 gly, inhibition of JAK/Stat signaling in the CCR specifically prevents age-related metaplasia, commen

270 rimary biosynthetic enzymes) proteins in the CCR versus batch culture.

271 e explored how ManLMN is integrated into the CCR regulatory framework in S. pneumoniae.

272 eal a regulatory mechanism that involves the CCR domain of Fab1 and contributes to dynamic control of

273 RSV G protein mAbs that react at or near the CCR and can block RSV G protein-mediated activities are

274 The role of the CCR and NCR-related factors in virulence varies greatly

275 The chemokine receptor genes of the CCR cluster on human chromosome 3p21 play important role

276 However, silencing of the CCR gene results in considerable flux changes of the gen

277 attributable to simply a modification of the CCR selectivity filter.

278 the endosphere were highly responsive to the CCR-deficient poplar genotype with remarkably different

279 s either at high seeding density or with the CCR-7 receptor inhibited migration against, rather than

280 b (130-6D) reactive to an epitope within the CCR of G protein, while treatment with a mAb specific fo

281 At 6 years, the CCR and OS rates among 635 nonrandomly treated patients

282 We linked their CCR records to a statewide database documenting hospital

283 These CCR-gammadeltaT cells did not exhibit tonic signaling bu

284 Expression of these CCRs was then examined on HCV-specific CD8+ T-cell subpo

285 Compared to CCR, ICR decreased tumor incidence in genetically engine

286 chemically induced rat models as compared to CCR.

287 owever, the direct evidence comparing ICR to CCR with respect to cancer prevention is controversial a

288 ant role for an auxiliary cysteine unique to CCR.

289 aline residue to confer anion selectivity to CCRs, is nevertheless conserved in all of the ACRs ident

290 arisons to ENCODE data reveal distinct TOP2A CCR clusters that overlap with marks of transcription, o

291 TOP2A CCRs are biased toward the distal regions of gene bodies

292 cogenic translocations overall contain TOP2A CCRs.

293 e utilized these isotopic ratios for tracing CCR contaminants in different environments: (1) the 2008

294 s constitute the majority of transcriptional CCR of galactose metabolism operons.

295 We identified two CCR genes in the model legume Medicago truncatula.

296 Patients treated with three versus two CCR cycles of cisplatin had improved 5-year postinductio

297 nd Wisconsin in 2003, patients treated using CCR appear to have improved outcomes compared with those

298 m shallow aquifers in a region of widespread CCR disposal in southeastern Wisconsin.

299 d xylem coloration typically associated with CCR down-regulation.

300 lower MRD and no improvement with IC (6-year CCR: SC, 77.5% +/- 4.8%; IC, 77.1% +/- 4.8%; P = .71).