ライフサイエンスコーパス: CDS

1 CDS activity maintains phosphoinositide 4,5 bisphosphate

2 CDS and PDS neurons-selected based on their responses to

3 CDS is widely used by the academic research community an

4 CDS neurons were strongly tuned for the direction of mot

5 CDSs having the bulkier cholesteryl group showed a bette

6 ulated; (ii) 360 (99%) of the arrayed PBCV-1 CDSs were expressed at some time in the virus life cycle

7 DS) and a 161,613-base pair plasmid with 173 CDSs.

8 Here we study a set of 176 CDS time series of financial institutions from 2002 to 2

9 e virus DNA synthesis begins; (iv) these 227 CDSs were grouped into two classes: 127 transcripts disa

10 There are 26 CDSs that have no viral homolog, and many did not necess

11 Additionally, 27 CDSs were identified which were present in all 47 low-pa

12 physical activity counseling (CDS arm, 45%; CDS + coaching arm, 25%; P < .001 compared with usual ca

13 ent of 39.2% and encompassed a total of 5362 CDS.

14 not support the hypothesis that the 7q22/5A3 CDS interval contains a myeloid TSG.

15 nt, we confirmed somatic deletion of the 5A3 CDS in the hematopoietic stem cell compartment.

16 ive ShE.coli meta-array gene sequences (6239 CDS) were used for in silico hybridization analysis.

17 mine whether haploinsufficiency for the 7q22 CDS contributes to myeloid leukemogenesis, we performed

18 ethyltetrahydro-beta-carboline in the active CDS extract.

19 lear localization causes elimination of Adi3 CDS activity and induction of cell death.

20 After CDS implementation, quarterly use decreased 20.1%, from

21 y angiography were compared before and after CDS implementation in August 2007.

22 nations per 1000 admissions before and after CDS, respectively; P = .008) observed 1 month after CDS

23 monary angiographic imaging before and after CDS.

24 spectively; P = .008) observed 1 month after CDS implementation was sustained over the ensuing 32-mon

25 hic examinations positive for acute PE after CDS (P = .65).

26 e 2 desensitizing dentifrices in alleviating CDS over time.

27 principle, the network of correlations among CDS spread time series could at least display some form

28 tion-based Chronic Disease Score (CDS)-1 and CDS-2 (c = 0.738, c = 0.718).

29 ed odds ratio, 2.28 [95% CI, 1.15-4.53]) and CDS + coaching arm (adjusted odds ratio, 2.60 [95% CI, 1

30 density and average nucleotide diversity and CDS (coding sequences) the lowest, in both humans and ma

31 For both DV and CDS, there was evidence of linkage to the same region on

32 negative relationship between expression and CDS length.

33 C Known Genes offers the highest genomic and CDS coverage among major human and mouse gene sets, more

34 nd 19.89% based on the ATP III, IDF, JIS and CDS criterion, respectively.

35 text of 5'- and 3'-untranslated regions, and CDS sections of aligned mRNA sequences.

36 RNA degradome data, we discovered uORFs and CDS regions potentially associated with stacked ribosome

37 mportance of separately examining 3' UTR and CDS sequences in gene expression analyses.

38 unbalanced expression of cognate 3' UTR and CDS sequences; many genes show high 3' UTR relative to C

39 the ratio of translation over 5' leaders and CDSes is conserved between human and mouse, and correlat

40 als that sequence features at both uORFs and CDSes modulate the translation of CDSes.

41 of gene models (i.e. transcription units and CDSs).

42 and dynamics comparable to that of annotated CDSs.

43 arify the boundaries of previously annotated CDSs in Trypanosoma brucei.

44 the KVP40 genome is coding, with an average CDS size of 587 bp.

45 Implementation of evidence-based CDS for inpatients was associated with a 12.3% immediate

46 Implementation of evidence-based CDS in the ED was associated with a significant decrease

47 onary angiography use increased 82.1% before CDS implementation, from 14.5 to 26.4 examinations per 1

48 nothing is known about the single T. brucei CDS gene (Tb927.7.220/EC 2.7.7.41) or its activity.

49 nd is the two-proline spacer containing CDS (CDS-PP), followed by the BTRA.

50 his meta-array lacked probes for many CFT073 CDS.

51 e shown to coelute with the active classical CDS extracts.

52 lan represent active components of classical CDS.

53 An intervention that included computerized CDS for pediatric clinicians and support for self-guided

54 imulated data set created from the Consensus CDS project and two experimental RNA-seq data sets gener

55 ompound is the two-proline spacer containing CDS (CDS-PP), followed by the BTRA.

56 r nutrition or physical activity counseling (CDS arm, 45%; CDS + coaching arm, 25%; P < .001 compared

57 Crude CDS from bovine lung was purified by reverse-phase high-

58 h shifted codon triplet usage to a different CDS with a hydrophilic C terminus, changing the canonica

59 toxin and immunity proteins, did not display CDS, whereas a strain of Burkholderia dolosa producing a

60 dex of antisocial substance dependence (DV + CDS).

61 Our composite index (DV + CDS) yielded the strongest evidence for linkage (logarit

62 genome: the exome-plus design and the exome-CDS design.

63 This reduced the size of the exome-CDS to approximately 71 Mb.

64 The exome-CDS was designed as a subset of the exome-plus by omitti

65 s, we estimated the performance of the exome-CDS.

66 ith full-length protein coding sequences (FL-CDS).

67 ders overrode alerts than when they followed CDS guidelines.

68 , and a novel region on chromosome 17q12 for CDS.

69 had the highest accuracy in rice (0.5648 for CDS, 0.4468 for exon, and 0.6695 nucleotide structure) a

70 otide structure) and A. thaliana (0.5808 for CDS, 0.5955 for exon, and 0.8839 nucleotide structure).

71 ion of Adi3 directs nuclear localization for CDS and that disruption of Adi3 nuclear localization may

72 on of PEMT and thereby put women at risk for CDS.

73 s to establish clear physiological roles for CDS.

74 Four CDSs were synthesized by segment-coupling method that pr

75 dicted protein-encoding open reading frames (CDS) and a 161,613-base pair plasmid with 173 CDSs.

76 tative protein-encoding open reading frames (CDSs), 30 tRNAs, 33 T4-like late promoters, and 57 poten

77 set of premenopausal women is protected from CDS.

78 accurately distinguish canonical ncRNAs from CDSs and UTRs (accuracies: >92% in human, mouse, worm an

79 suppresses the mitophagy induced by fundc1 (CDS+3'UTR) but not fundc1 (CDS) overexpression.

80 nduced by fundc1 (CDS+3'UTR) but not fundc1 (CDS) overexpression.

81 number of processed pseudogenes and the gene CDS GC content.

82 number of processed pseudogenes and the gene CDS length (R = -0.40; p < 0.001), i.e., the relatively

83 ith a total of 3,015 protein-encoding genes (CDS), and a GC content of 47.7%.

84 es to the PBCV-1 365 protein-encoding genes (CDSs) was constructed.

85 se was less common (47% for patients who had CDS and 31% for those who did not).

86 igh 3' UTR relative to CDS, others show high CDS to 3' UTR.

87 Considering that human CDS are devoid of >4 consecutive AAA codons, sensing of

88 34 behaved as an apparent inverse agonist in CDS assays involving TM cells but as a neutral prostamid

89 On average, responses began 6 ms earlier in CDS neurons than in PDS neurons.

90 n providers adhered to evidence presented in CDS were nearly double those seen when providers overrod

91 We compared the time course of responses in CDS and PDS neurons in opiate-anesthetized macaques, usi

92 portals adapted specifically for targets in CDS.

93 reveals that rare variants tend to reside in CDSs, whereas common variants tend to reside in the 3' U

94 lassified as lncRNAs due to their incomplete CDS, leading to higher false positive rate for lncRNA id

95 s the first good candidate domains for intra-CDS pairing of a miRNA in mammals.

96 p between Adi3 cellular localization and its CDS activity.

97 ear localization of Adi3 is required for its CDS activity and loss of nuclear localization causes eli

98 Four widely used criteria (ATPIII IDF JIS CDS) were used to measure the prevalence of MetS.

99 At least 99 KVP40 CDSs have homologs in the T4 genome (Blast alignments of

100 ymerase II (Pol II) progression through lacZ CDS in vivo.

101 ered late); and (vi) expression of most late CDSs is inhibited by adding the DNA replication inhibito

102 From these latter CDSs, an NAD salvage pathway was inferred that appears t

103 nd of the gene, and isolated the full-length CDS of the mNLRC5 of about 6 kb through conventional RT-

104 or patients with a Wells score of 4 or less, CDS alerts suggested d-dimer testing because acute PE is

105 ed miRNA:gene interactions from DIANA-microT-CDS for 4 species (human, mouse, nematode and fruit fly)

106 In silico analyses with DIANA-microT-CDS highlighted 5 putative targets in common between two

107 ithms (TargetScan, miRanda, and DIANA-microT-CDS), miR-18a-5p was predicted to be the top candidate m

108 o whether patients belonged to the CDS or no CDS group.

109 primary-cancer-directed surgery (CDS) or no CDS within 4 months of diagnosis.

110 ecificity for coding sequence (CDS) over non-CDS, and increased tolerance to base-substituting and fr

111 years versus 5.6 years for patients with non-CDS QOL.

112 an fibroblasts identifies thousands of novel CDSs, including micropeptides and variants of known prot

113 These results suggest that availability of CDS-controlled resynthesis of phosphoinositides is essen

114 ) most highly linked with the development of CDS (p < 0.00006) was located within 1 kb of the critica

115 llus thuringiensis (Bt) tested the impact of CDS recoding using different codon bias tables.

116 ths scarcely change over the entire range of CDS values.

117 state until 50-75 ms after the responses of CDS neurons had stabilized.

118 nducible PEMT expression, conferring risk of CDS in women.

119 eting differences between miRNAs in terms of CDS versus 3'-untranslated region targeting, and stable

120 olyadenylation signals leading to the use of CDS protein-coding region poly(A) sites are distinct fro

121 uORFs and CDSes modulate the translation of CDSes.

122 pared in patients in whom providers overrode CDS alerts (by performing CT pulmonary angiography in pa

123 ly double those seen when providers overrode CDS alerts.

124 or non-conserved microRNAs, whereas PACCMIT-CDS addresses the lack of similar portals adapted specif

125 d with a cohort of discordant sibling pairs (CDS) to derive a comparative similarity score.

126 The molecular architecture of the peptide CDS disguises its peptide nature from neuropeptide-degra

127 r mediating analgesia induced by the peptide CDS that delivered, retained, and then released the pept

128 ls of transposition than the native piggyBac CDS, whereas in the absence of induction its activity is

129 ine B-Raf pseudogene Braf-rs1 or its pseudo "CDS" or "3' UTR" develop an aggressive malignancy resemb

130 of the Panel Study of Income Dynamics (PSID-CDS).

131 en at 33.2% (95% CI: 22.4, 46.1) in the PSID-CDS and 26.2% (95% CI: 20.2, 33.2) in the NLSY79-Child.

132 d and 20.6% (95% CI: 16.0, 26.3) in the PSID-CDS.

133 ercent (6,469 of 9,011) of patients received CDS, and their 30-day postoperative mortality was 10%.

134 slated regions (UTRs) and the coding region (CDS).

135 lained by their conserved role in repressing CDS translation.

136 than medication-based Chronic Disease Score (CDS)-1 and CDS-2 (c = 0.738, c = 0.718).

137 dies, we defined a commonly deleted segment (CDS) of 1.5 Mb between D5S479 and D5S500 in patients wit

138 s, we delineated a commonly deleted segment (CDS) of 5 Mb within band 20q12 flanked by D20S206 (proxi

139 approximately 2-Mb commonly deleted segment (CDS) of 7q22 bounded by D7S1503 and D7S1841.

140 A 2.5-Mb commonly deleted segment (CDS) of chromosome band 7q22 is implicated as harboring

141 or gene within the commonly deleted segment (CDS), we have cloned and characterized the genes encodin

142 tive (PDS) or component direction selective (CDS).

143 MT component direction-selective (CDS) neurons respond to the individual gratings of a pla

144 t arising from cervical dentine sensitivity (CDS).

145 s carrying a wild-type TP53 coding sequence (CDS) and 1 or more 3'UTR SNVs had a better 5-year surviv

146 ger RNAs (mRNAs) consist of coding sequence (CDS) and 5' and 3' UTRs, typically expected to show simi

147 et gene which truncates the coding sequence (CDS) and targets the corresponding transcript for degrad

148 arative methods can improve coding sequence (CDS) annotation, the SSA method is extended to a Phylo-H

149 hat miR-107 paralogs target coding sequence (CDS) of mRNA; (iii) biochemical and computational studie

150 located in the 3'UTR or the coding sequence (CDS) of targets.

151 e increased specificity for coding sequence (CDS) over non-CDS, and increased tolerance to base-subst

152 translated region (3' UTR), coding sequence (CDS) region and 5' untranslated region (5' UTR) of targe

153 translated region (UTR) and coding sequence (CDS) sites exhibiting stronger interaction.

154 rsion of the PB transposase coding sequence (CDS) which provides transposition levels greater than th

155 located within the protein coding sequence (CDS).

156 on structure in the deduced coding sequence (CDS).

157 capacity of a genome [i.e., coding sequence (CDS)] as a reliable measure of proteome diversity, we fi

158 prising 116 098 ordered coding DNA sequence (CDS) gene models.

159 unctional allele with a coding DNA sequence (CDS) of 1521 bp and a promoter adjacent to the CDS.

160 n system to deliver the coding DNA sequence (CDS) of either full-length human dystrophin (DYS: 11.1 k

161 The upstream coding sequences (CDS) present a significant challenge for the translation

162 Protein-coding sequences (CDS) that are contiguous on annotated reference template

163 ection of 82,356 annotated coding sequences (CDS) to identify 2,325 patterns of presence or absence a

164 tic polyadenylation within coding sequences (CDS) triggers ribosome-associated quality control (RQC),

165 tion from long or G+C-rich coding sequences (CDS) without affecting the associated GAL1 promoter acti

166 nd its individual genes or coding sequences (CDS).

167 at uORFs are depleted near coding sequences (CDSes) and have initiation contexts that diminish their

168 ed to identify new protein-coding sequences (CDSs) and clarify the boundaries of previously annotated

169 the divergence time in the coding sequences (CDSs) and intergenic sequences (IGSs) is the same betwee

170 by comparing the predicted coding sequences (CDSs) in all 15 loci for synteny and homology.

171 d mRNA ends that mapped to coding sequences (CDSs) of Arabidopsis thaliana, rice (Oryza sativa), and

172 ces revealed 125 predicted coding sequences (CDSs) present in all highly pathogenic strains but absen

173 nd using native microalgal coding sequences (CDSs) with higher GC content improved transgene expressi

174 constrained for SNPs than coding sequences (CDSs), but more constrained than a neutral reference.

175 assumptions about protein-coding sequences (CDSs), e.g., they are conserved, do not overlap, and exc

176 39.3% G+C content, and 925 coding sequences (CDSs).

177 407 kbp, consisting of 485 coding sequences (CDSs).

178 of more than 450 predicted coding sequences (CDSs).

179 ition to annotated protein coding sequences (CDSs).

180 The shared CDSs represent 36% of all T4 CDSs but only 26% of those

181 total of 27%, 3.2%, and 5.2% of E. sibiricum CDS spotted on the DNA microarray detected differentiall

182 Termed contact-dependent signaling (CDS), this response promotes biofilm formation and other

183 enomenon called contact-dependent signaling (CDS).

184 l map and the identification of the smallest CDS will facilitate the molecular cloning of a myeloid l

185 PNI0373 showed only 15 lineage specific CDS when compared to the pan-genome of pneumococcus.

186 All these GIs had many strain-specific CDS, anomalous GC contents and/or significant dinucleoti

187 ells using cellular dielectric spectroscopy (CDS).

188 TBNA) or conventional diagnosis and staging (CDS), for further investigation and staging.

189 The Cornea Donor Study (CDS) showed that donor age is not a factor in survival o

190 nding sites, clonidine-displacing substance (CDS), has been a major goal for many years.

191 of evidence-based clinical decision support (CDS) for ordering computed tomographic (CT) pulmonary an

192 The cell death suppression (CDS) activity of Adi3 requires phosphorylation by 3-phos

193 er they had primary-cancer-directed surgery (CDS) or no CDS within 4 months of diagnosis.

194 Credit Default Swaps (CDS) spreads should reflect default risk of the underlyi

195 ed indexes of DV, conduct disorder symptoms (CDS), and a composite index of antisocial substance depe

196 atic steatosis (choline deficiency syndrome (CDS)).

197 Canine cognitive impairment syndrome (CDS) represents a group of symptoms related to the aging

198 aryotes, being produced by CDP-DAG synthase (CDS).

199 m of the enzyme CDP-diacylglycerol synthase (CDS), which catalyzes the formation of CDP-diacylglycero

200 m of the enzyme CDP-diacylglycerol synthase (CDS), which catalyzes the formation of CDP-diacylglycero

201 Chrysanthemyl diphosphate synthase (CDS), the first enzyme involved in the synthesis of tran

202 ntral role of CDP-diacylglycerol synthetase (CDS) in the regulation of VEGFA signaling and angiogenes

203 A brain-targeted chemical delivery system (CDS) based on retrometabolic drug design was applied to

204 The Celera Discovery System (CDS) is a web-accessible research workbench for mining g

205 of brain-targeted chemical delivery systems (CDS) for a kyotorphin analogue (Tyr-Lys) are described.

206 The shared CDSs represent 36% of all T4 CDSs but only 26% of those from KVP40.

207 We also found that CDS was characterized by the presence of reactive and se

208 Actually, it has been recognized that CDS spread time series did not anticipate but only follo

209 The CDS + coaching arm had a smaller magnitude of effect (-0

210 The CDS intervention, implemented after a baseline observati

211 but even among those older than age 75, the CDS rate was 69% (3,378 of 4,909).

212 or and similar recipient criteria as for the CDS PKP procedures, performed by 68 surgeons.

213 to the unrelated unaffected sibling from the CDS and then, sum over such individuals and pairs.

214 T-guided biopsy sample; the patient from the CDS group needed intercostal drainage and was admitted t

215 t of childhood obesity HEDIS measures in the CDS arm (adjusted odds ratio, 2.28 [95% CI, 1.15-4.53])

216 e arm, BMI increased less in children in the CDS arm during 1 year (-0.51 [95% CI, -0.91 to -0.11]).

217 sulted from an insertional disruption in the CDS by Sal-PIF, a 3100-bp PIF/Harbinger-like DNA transpo

218 ial images by the reading center used in the CDS Specular Microscopy Ancillary Study.

219 andomly permuting the affected status in the CDS.

220 ian cell loss after PK by 68 surgeons in the CDS.

221 leading to loss of 20q, we have narrowed the CDS to an approximately 250-kb interval encompassing two

222 o the affected than to the unaffected of the CDS (P value approximately 0.00001).

223 The activities of the CDS and BTRA, respectively, were antagonized by naloxone

224 nes were localized to the distal half of the CDS between D5S1983 and D5S500.

225 es represented 10.6%, 0.89%, and 2.3% of the CDS differentially expressed when grown at -2.5 degrees

226 (TSGs), we developed a transcript map of the CDS.

227 us positions of the 5'-terminal 30 nt of the CDS: in mammalian mRNAs, the 5'-UTR shows a greater cons

228 5'-UTR shows a greater conservation than the CDS, whereas the opposite trend holds for yeast mRNAs.

229 other Vps factors can be cross-linked to the CDS of genes induced by Gcn4 or Gal4 in a manner depende

230 of the mouse genome that is syntenic to the CDS of human 5q31.

231 NAs plays a role in guiding miR-103/7 to the CDS of targets; and (iv) there are major sequence-specif

232 tionship to whether patients belonged to the CDS or no CDS group.

233 statistical models applied previously to the CDS PK data were considered.

234 S) of 1521 bp and a promoter adjacent to the CDS.

235 r, intercistronic distance, overlap with the CDS, and initiation context most strongly influence tran

236 shift from a common to rare codon within the CDS facilitated miRNA binding downstream of the SNP, dra

237 The antinociceptive effect of the CDSs was naloxone-reversible and methylnaloxonium-irreve

238 considered early/late); (v) 133 (36%) of the CDSs were expressed after virus DNA synthesis begins (co

239 le in the laboratory; (iii) 227 (62%) of the CDSs were expressed before virus DNA synthesis begins; (

240 While 65% of the CDSs were unique to KVP40 and had no known function, the

241 ore extreme conservation patterns than their CDSs.

242 A great proportion (49.1%) of these CDSs are organized into paralogous gene families, which

243 ents to treatment: 66 to EBUS-TBNA and 67 to CDS (one later withdrew consent).

244 der for pulmonary angiography was exposed to CDS on the basis of the Wells criteria.

245 prokaryotes clearly evolve in proportion to CDS values, whereas those of eukaryotes are more randoml

246 In 5 practices randomized to CDS + coaching, decision support was augmented by indivi

247 In 5 practices randomized to CDS, pediatric clinicians received decision support on o

248 ces; many genes show high 3' UTR relative to CDS, others show high CDS to 3' UTR.

249 r period were positive for PE; subsequent to CDS implementation, yield by quarter increased 69.0%, fr

250 rained for indels than for SNPs, compared to CDSs.

251 f 19 genes) shows a broad range of 3' UTR-to-CDS expression ratios across neurons and tissues.

252 Further, for two genes examined, a 3' UTR-to-CDS ratio above a particular threshold in any given neur

253 ed poorer OS for patients with a mutant TP53 CDS.

254 reduce NuA4 occupancy in certain transcribed CDS.

255 e that the sequence composition of transgene CDSs can directly impact silencing, providing design str

256 ival rate than patients carrying a wild-type CDS and the reference 3'UTR, yet there is no statistical

257 cloetide (nt) sequence overlapping the UL136 CDS supported expression of a downstream cistron in a bi

258 included several previously uncharacterized CDSs that may encode novel virulence determinants includ

259 oeconomic status were less likely to undergo CDS; but even among those older than age 75, the CDS rat

260 f the mRNA [5'-untranslated region (5'-UTR), CDS and 3'-UTR] preferentially fold onto themselves, whi

261 and for all three regions of a mRNA (3' UTR, CDS and 5' UTR), STarMir output includes the computed bi

262 y characteristics and features of the 5'UTR, CDS and 3'UTR.

263 Loss of CDS2, 1 of 2 vertebrate CDS enzymes, results in vascular-specific defects in zeb

264 (s), a Gene Transfer Format (.GTF) file with CDS information and a SNP report(s) in an increasing sel

265 The median survival for patients with CDS QOL was 1.6 years versus 5.6 years for patients with

266 EBUS-TBNA (14 days; 95% CI 14-15) than with CDS (29 days; 23-35) resulting in a hazard ratio of 1.98

267 nal by complementation of a non-viable yeast CDS null strain and that it is essential in the bloodstr