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 expression in primary ASM cell cultures and airway b

3 CCR has been intensely studied in the model organisms Es

4 CCR has three components: continuous chest compressions

5 CCR improves survival of patients with cardiac arrest.

6 CCR is likely of great importance to Streptococcus pneum

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

8 CCR mRNA expression by liver DC subsets was evaluated by

9 CCR of maltose-inducible alpha-glucosidase, raffinose-in

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

11 CCRs are enriched in toxic elements, and their leachates

12 well as monocyte chemoattractant protein-1, CCR-2, platelet-derived growth factor C, and excessive a

13 10; CCL-2, -5, -6, -7, -8, -9, -11, and -19; CCR-1 and CCR-5), adhesion molecules (ICAM-1, CD18, Ly69

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 CC chemokine receptor 7 (CCR-7) is expressed on mature dendritic cells and T-cell

19 dentify residues on CC chemokine receptor 7 (CCR-7) that are involved in agonist-mediated receptor ac

20 reated with imatinib mesylate who achieved a CCR.

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

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

23 After CCR, BCR-ABL mRNA levels progressively declined for at l

24 With a median follow-up of 13 months after CCR (29 months after imatinib mesylate; median 6 RQ-PCR

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

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

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

28 -5, -6, -7, -8, -9, -11, and -19; CCR-1 and CCR-5), adhesion molecules (ICAM-1, CD18, Ly69, PSGL-1,

29 and 3.0-fold increases in interleukin-18 and CCR 5, respectively.

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

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

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

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

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

35 mpair the interaction between the kinase and CCR domain.

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

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

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

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

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

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

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

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

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 xtracted from sediments in lakes affected by CCRs.

47 f expansion of the effector memory (CD45RA(-)CCR-7(-)) population (P < .05), suggesting that protecti

48 7beta-estradiol also increased CD4(+) T cell CCR expression.

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

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

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

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

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

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

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

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

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

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

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

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

63 To effect CCR, CcpA binds a phosphoprotein, either HPr-Ser46-P or

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

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

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

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

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

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

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

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

72 rrangements and are probably responsible for CCR.

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

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

75 chemical signature in lignins resulting from CCR mutation.

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

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

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

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

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

81 We show that CcpA functions in CCR of lactose-inducible beta-galactosidase activity in

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

83 of specific enzymes and proteins involved in CCR.

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

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

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

87 detected in CD34+ cells from CML patients in CCR on imatinib, may contribute to persistence of small

88 in CD34+ cells isolated from CML patients in CCR on imatinib.

89 However, patients in CCR usually demonstrate evidence of residual BCR-ABL-pos

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

91 pA is the major transcriptional regulator in CCR in several gram-positive bacteria.

92 hypothesized to be functionally relevant in CCR.

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

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

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

96 used to predict total NORM concentrations in CCRs.

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

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

99 The increased CCR expression correlates with enhanced in vitro chemota

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

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

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

103 Interestingly, CCR suppression substantially promoted pyrolytic breakdo

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

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

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

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

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

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

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

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

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

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

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

115 We also describe two partial agonists of CCR-7 ([Nle(72)]CCL-19(6-77) and Ac-[Nle(72)]CCL-19(7-77

116 Moreover, in the case of CCR downregulation in tobacco, there were no NMR spectro

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 tic cells (DCs) resulted in the induction of CCR-7 chemokine receptor expression and cytokine release

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

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

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

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

131 d disease progression (predominantly loss of CCR).

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

133 rogression and control, and that measures of CCR status of circulating lymphocytes may have prognosti

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

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

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

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 cular mechanism of Crh-Ser46-P regulation of CCR, we determined the structure of a CcpA-(Crh-Ser46-P)

140 that CcpA, though not a global regulator of CCR in S. pneumoniae, is required for colonization of th

141 er a 2-log molecular response at the time of CCR or a 3-log response anytime thereafter is a signific

142 e to achieve a 2-log response at the time of CCR was an independent predictive marker of subsequent p

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

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

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

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

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

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

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

150 g and evaluating the environmental impact of CCRs.

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

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

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

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

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

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

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

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

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

160 First, we examined whether prominent CCRs on different monocyte subsets, CCR2 or CX3CR1, medi

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

162 cular response at the time of first reaching CCR.

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

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

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

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 The authors compared CC chemokine receptor (CCR) expression by mouse liver myeloid, "lymphoid-relate

169 Cytokine and CC chemokine receptor (CCR) gene expression was analyzed by RNase protection as

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

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

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

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

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

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

176 hocyte antigen (CLA) and chemokine receptor (CCR)4.

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

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

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

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

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

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

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

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

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

186 Chemokine receptors (CCR), normally expressed on lymphocytes, control immune

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

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

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

190 ated in part by such CC chemokine receptors (CCRs) as CCR2 and CCR5, respectively, plays a central ro

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

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

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

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 tructure in dwarfed cinnamoyl CoA reductase (CCR)-downregulated tobacco were also previously reported

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

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

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

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

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

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

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

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

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

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

209 of carbon catabolite repression/regulation (CCR).

210 nomena conditional concordant relationships (CCRs).

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

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

213 oter (-10 hexamer) and the amyE cre relieved CCR of amyE expression.

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

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

216 is involved in carbon catabolite repression (CCR) and regulates the expression of known virulence gen

217 CcpA) mediates carbon catabolite repression (CCR) by controlling expression of catabolite responsive

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

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

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

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

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

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

224 many bacteria, carbon catabolite repression (CCR) is central to such regulation, influencing hierarch

225 Carbon catabolite repression (CCR) is one of the most fundamental environmental-sensin

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

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

228 direct role in carbon catabolite repression (CCR).

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

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

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

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

233 6 million tons of coal combustion residuals (CCRs) annually.

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

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

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

237 30 million tons of coal combustion residues (CCRs) each year in the United States; yet their environm

238 ylate induces complete cytogenetic response (CCR) in a high proportion of chronic myelogenous leukemi

239 with rates of complete cytogenetic response (CCR) of more than 40% in patients after failure of inter

240 ho achieved a complete cytogenetic response (CCR) or major cytogenetic response (MCR) on IM (HR=5.31,

241 t the time of complete cytogenetic response (CCR), implicating mutations as a cause of disease persis

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

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

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

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

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

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

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

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

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

251 holography and a cornercube retroreflector (CCR).

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

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

254 - 34 Bq/kg; 0.67 +/- 0.09), and Powder River CCRs (213 +/- 21 Bq/kg; 0.79 +/- 0.10).

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

256 Severe CCR suppression almost halved lignin content in TEs base

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

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

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

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

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

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

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

264 Here, we show that CCR-LIKE (CCL) and SENESCENCE ASSOCIATED GENE 1 transcri

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

266 The CCR method advocates continuous chest compressions witho

267 The CCR method has been shown to dramatically improve surviv

268 The CCR-mediated proline auxotrophy was lifted when nonprefe

269 rom both Arabidopsis wild-type (Ler) and the CCR-irx4 mutant at both developmental stages revealed th

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

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

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

273 Hemin-induced HO-1 induction in the CCR-5, CXCR-4, and CD4 coexpressing GHOST(3) cells was c

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

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

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

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

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

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

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

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

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

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

284 rtant for high-affinity binding of CCL-19 to CCR-7.

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

297 e that abnormal lignin formation occurs when CCR activity is modulated.

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 Patients with CCR who achieve a profound reduction of BCR-ABL mRNA hav