ライフサイエンスコーパス: reading

1 involvement were compared with visual expert reading.

2 to histopathology results during prospective reading.

3 istic functions, becoming less selective for reading.

4 steps of the assay, including incubation and reading.

5 or easily correctable using the rest of the readings.

6 gher based on the mean SBP level of 2 seated readings.

7 ined as >95% limits of agreement between two readings.

8 CI: 0.80, 0.98) between the first and second readings.

9 rticular brain region become specialized for reading?

10 We applied this approach to the domain of reading, a crucial ability in which there are known to b

11 Thirty-eight adults with a wide range of reading abilities were shown random-dot displays spatial

12 hat, while the reading intervention enhanced reading abilities, learning to read did not affect motio

13 ation, race, menopausal status, and baseline reading ability, anxiety, and depressive symptoms.

14 nd strongly disrupts its histone methylation reading ability, causing it to disassociate from chromat

15 wn to develop only through experience (i.e., reading acquisition), and widespread literacy is too rec

16 READ measures, there was more improvement in reading acuity (difference, -0.11 logMAR, 95% CI, -0.15

17 imum reading speed, critical print size, and reading acuity (higher number indicates lower visual acu

18 At the second readings, agreement among senior and junior radiologists

19 ing an omnipotent RF in bacteria, capable of reading all three stop codons.

20 mpairment with delayed response times during reading aloud tasks, but not lexical decision tasks.

21 re not inferior to the results of the visual reading analysis was tested.

22 Consequently, CIE over-reading and confirmation by an experienced ECG reader ar

23 Experimental achievements include reading and manipulating single nuclear spins, exploitin

24 ciation of CHD with not meeting standards on reading and math end-of-grade examinations in third grad

25 opposite of those of rs174448, but only for reading and not significant after adjustment for parenta

26 d to assess the agreement between photograph reading and OCT in estimating CDR.

27 main via G protein signaling is required for reading and responding to guidance and survival cues con

28 nd there was >90% agreement between the TECS reading and the face-to-face findings of the physician.

29 All changes except Stroop word reading and total functional capacity remained significa

30 The library has facilities for reading and writing both NMR-STAR version 2.1 and 3.1 fo

31 Existing architectures enable reading and writing but do not offer random-access and e

32 Here we demonstrate the reading and writing of the magnetism of individual Ho at

33 magnetic stability combined with electrical reading and writing shows that single-atom magnetic memo

34 To demonstrate independent reading and writing, we built an atomic-scale structure

35 adiation risk was estimated based on the TLD readings and expressed as the dose absorbed by particula

36 A significant decrease in both keratometry readings and spherical equivalent (from -4.0 to -1.56 di

37 e (10:00 am-8:00 pm), 24-hour (all available readings), and nighttime (midnight-6:00 am) periods, sep

38 h thin corneas, to not place reliance on GAT readings, and abandon any correction formula.

39 te the effect of measurement technique on BP readings, and explore how ambulatory BP data from the SP

40 The 3.0mm diameter K-readings appear to be the most reliable choice for calcu

41 and that different neural implementations of reading are possible.

42 ime tl of a single measurement, the expected reading at time tl, and the factor 2/ln(2).

43 PMT readings at 8 different depths (from 3069 to 3349 m) of

44 In 2 readings at least 1 mo apart, readers performed either a

45 icantly larger VCDR and HCDR than photograph reading before and after stratifying eyes based on disc

46 alyzed men with rising PSA after RP with PSA readings between 0.05 and 1.0 ng/mL, considered eligible

47 h stability and reproducibility of potential readings between sensors as well as improved analytical

48 in the comparison of AL, ACD and keratometry readings between the Lenstar and IOLMaster.

49 th discordant interpretations at the primary reading, blinded to previous reports.

50 Conclusion Blood pressure readings, blood draws, injections, and number or duratio

51 etic resonance imaging experiments: (1) word reading (Braille for blind and print for sighted partici

52 FFA was reduced by 44.3, PV by 50.2, and FOS reading by 40.1% in com I whereas reductions of 41.6, 44

53 OCT and photograph reading by clinicians agree poorly in CDR assessment.

54 ations of this motif directly modulate proof-reading by eliminating or enhancing selectivity for vira

55 Here, we directly monitor RNA proof-reading by RIG-I and we show that it is controlled by a

56 rithm and stereoscopic optic disc photograph readings by glaucoma specialists.

57 A masked reading center (University of Wisconsin-Madison) determi

58 Panel of retina specialists, image reading center experts, retinal histologists, and optics

59 nual grades and ARIAS results were sent to a reading center for arbitration.

60 years determined by a central image analysis reading center from clinical specular or confocal centra

61 urements were performed by masked, certified Reading Center graders using the Visante's Internal Meas

62 ainst a manual consensus reading of 2 masked reading center graders.

63 Discrepancies were adjudicated by a reading center supervisor.

64 reased autofluorescence were quantified by a reading center.

65 Images were evaluated by staff at a central reading center.

66 MR elastograms were analyzed manually at two reading centers, and using a new automated technique.

67 grading of images at Moorfields Eye Hospital Reading Centre.

68 We measured VA with Radner reading charts and QoL with the Health Utilities Index i

69 he current state of knowledge of the brain's reading circuits, and then we describe opportunities to

70 lted in a significant reduction of equivocal readings compared with pBS, which implies an improved di

71 luate sustained silent reading speeds, while reading comprehension was assessed based on silent readi

72 oud and sustained silent reading speeds, and reading comprehension.

73 A retrospective reading data set of 7060 cases was created and randomly

74 solubility test based on spectrophotometric reading described in this study can differentiate S. pne

75 a collection of correlated risk factors for reading difficulties.

76 mined the degree to which different kinds of reading disabilities (defined as profiles or patterns of

77 pmental difficulties of children with unique reading disability profiles and reasons for their readin

78 y findings across children with quite varied reading disability profiles that we hypothesize compound

79 Dyslexia is a prevalent reading disability whose underlying mechanisms are still

80 ng disability profiles and reasons for their reading disability.

81 However, reading DNA sequence from sub-nanogram quantities is imp

82 e consequence of a lack, or poor quality, of reading experience.

83 t motion processing deficits are due to poor reading experience.

84 iable predictions limit their acquisition of reading expertise.

85 mane view on poverty that should be required reading for policy makers, particularly those interested

86 ficant disagreement between first and second readings for LSM and CAP when obtained back to back was

87 angiopoietin 4 (ANGPT4), chromosome 11 open reading frame (C11orf30/EMSY), and exocyst complex compo

88 lture, contained a 2,158-bp deletion in open reading frame (ORF) 12.

89 Remarkably, the approximately 1,100 bp open reading frame (ORF) encoding the envelope proteins is fu

90 p crinkle virus (TCV) coat protein (CP) open reading frame (ORF) has been found to promote internal e

91 The integrity of the putative BWRF1 open reading frame (ORF) is retained in over 80% of strains,

92 The open reading frame (ORF) lengths of TmELO1 and TmELO2 were 10

93 e introduction of a frameshift into the open reading frame (ORF) of the target gene which truncates t

94 that the last 36 nucleotides of the NSs open reading frame (ORF) were needed to ensure the efficient

95 mitochondrial clades based on the mtDNA open reading frame (ORF).

96 e has pointed to the existence of small open reading frame (smORF)-encoded microproteins in mammals,

97 An upstream open reading frame (uORF) confers the translational control o

98 nscriptionally regulated by an upstream open reading frame (uORF) located in its 5' untranslated regi

99 showed that amphoterin-induced gene and open reading frame 2 (Amigo2) was overexpressed in LV12 cells

100 ve primer set targeting the overlapping open reading frame 2/3 (ORF2/3) nucleotide sequence of HEV.

101 ous, tetradecanoyl phorbol acetate-, or open reading frame 50 (ORF50)/replication transactivator (RTA

102 We subsequently identified open reading frame 52 (ORF52), a multifunctional and abundant

103 ed promoter of the immediate early gene open reading frame 63 (ORF63).

104 Open reading frame 7 (ORF7) of VZV has been recognized as a n

105 acterized gene (C17orf99; chromosome 17 open reading frame 99), that is expressed in bone marrow and

106 Reading frame altering genomic variants can impact gene

107 s; for example, a single indel may shift the reading frame and incorrectly truncate a protein sequenc

108 mains of life, RelE has potential to improve reading frame and shed light on A-site occupancy in ribo

109 nly; attributes of the resulting transcript, reading frame and translated protein product are not rep

110 e features: TRmIND by the length of the open reading frame and TRmD both by a approximately 60 nucleo

111 itin gene is a unique, highly conserved open reading frame composed solely of tandem repeats, yet it

112 esolution and have yielded no information on reading frame due to problems inherent to MNase digestio

113 ors carrying the full-length dystrophin open-reading frame for transduction of human muscle derived c

114 ed increasing lengths of the dystrophin open reading frame in a foamy virus vector and quantified pac

115 ecise 3'-ends that for the first time reveal reading frame in bacteria.

116 g repressed the translation of the main open reading frame in cis, independent of the sequence of the

117 The nonclassical open reading frame in the FCGR2C gene (FCGR2C.nc-ORF) was str

118 The virion infectivity factor (Vif) open reading frame is conserved among most lentiviruses.

119 his quality control step produces defects in reading frame maintenance.

120 med by GFP accumulation from the second open reading frame of a polycistronic messenger RNA, which wo

121 sequences - most of them located in the open reading frame of CD95L.

122 We discuss that mutations in the open reading frame of CEBPA lead to an altered C/EBPalpha fun

123 embrane protease, serine 2) gene to the open reading frame of ERG, encoding an ETS family transcripti

124 uscular dystrophy caused by mutations in the reading frame of the dystrophin gene disrupting its prot

125 The I2L open reading frame of vaccinia virus (VACV) encodes a conserv

126 Additionally, open reading frame Ov8, unique to OvHV-2, was found to encode

127 express the NSs protein or have the NSs open reading frame replaced with a reporter gene.

128 hancing factor (PTEF) relieves upstream open reading frame repression and thereby facilitates VAR2CSA

129 f PTEF, and the alleviation of upstream open reading frame repression requires the proteolytic proces

130 ARv56es maintains the reading frame resulting in the inclusion of the C-termin

131 This isoform embraces an alternative reading frame that imparts a 50% change in CTD protein s

132 script variant lacking a small upstream open reading frame that would otherwise inhibit translation o

133 PR/Cas9 system despite their lacking an open reading frame to evaluate functional loss.

134 This RSV F open reading frame was evaluated in rB/HPIV3 in three forms:

135 Identical genomic and open reading frame was found to be present in close relatives

136 Here, we describe an alternative open reading frame within human insulin mRNA encoding a highl

137 is of the i-leader revealed a potential open reading frame within the leader sequence and the termina

138 ynamic during cellular transitions, preserve reading frame, and reveal intricacy of cell states invis

139 no termini of these proteins to the NP1 open reading frame, and splice site mutations that prevented

140 emming from variants that produce an altered reading frame, such as stop-lost variants and small inse

141 nserted sense or antisense to the luciferase reading frame, the XDP variants repressed or enhanced tr

142 ithin the coding region of the opposite open reading frame.

143 introduction of a TC tag into the muNS open reading frame.

144 ranslationally repressed by an upstream open reading frame.

145 ft -1 nt and continue translating in the new reading frame.

146 rational when combined with an upstream open reading frame.

147 r mutant analysis, we revised the rec27 open reading frame: the new start codon is in the previously

148 nstrated the translation of alternative open-reading frames (altORFs) in addition to annotated protei

149 ism and to the presence of the atypical open reading frames (ORFans) F-orf and M-orf, respectively in

150 Ribo-TISH can also predict novel open reading frames (ORFs) from regular ribosome profiling (r

151 Bam35, nearly half of the 32 annotated open reading frames (ORFs) have no homologs in databases (ORF

152 zed into operons consisting of discrete open reading frames (ORFs) in a single polycistronic mRNA.

153 The open reading frames (ORFs) involved have functions related to

154 68 substitutions that were localized in open reading frames (ORFs) likely associated with host cell e

155 ity leading to the formation of altered open reading frames (ORFs) that appear to be under relaxed se

156 equence containing 128 unique predicted open reading frames (ORFs), many of which were most closely r

157 oduce 21 transcripts with nine distinct open reading frames (ORFs).

158 Each genome encodes 21 open reading frames (ORFs).

159 oteins or translation of upstream small open reading frames (uORF).

160 of Kozak sequence composition, upstream open reading frames (uORFs), and secondary structure.

161 Upstream open reading frames (uORFs), located in transcript leaders (5

162 t also two pathogen-responsive upstream open reading frames (uORFsTBF1) of the TBF1 gene.

163 of HERV-K elements, still retain intact open reading frames and the capacity to produce certain viral

164 es carry a 7.5kb plasmid encoding eight open reading frames conventionally called plasmid glycoprotei

165 nscript is produced with small upstream open reading frames in its 5' untranslated region.

166 ts and sequenced the full gyrA and gyrB open reading frames in their respective sputum TB isolates.

167 pression of identified and unidentified open reading frames needed to deal with and overcome the many

168 g the repressive effect of the upstream open reading frames on gene expression and the mutational eff

169 RTC4 transcript contains small upstream open reading frames that prevent translation of the downstrea

170 d due to the presence of multiple small open reading frames upstream of the coding region.

171 shown that a fraction of putative small open reading frames within lncRNAs are translated.

172 mutations predicted to restore BRCA1/2 open reading frames, including two patients with multiple ind

173 tion of uridines to generate functional open reading frames, many of which encode components of the m

174 dN/dS ratio) located a region of overlapping reading frames, which is subject to positive selection i

175 ogenic functions of the plasmid-encoded open reading frames, which may motivate further investigation

176 as multi k-mer frequencies and relaxed open reading frames.

177 from 22.6-33.0 Kbp, consisting of 27-39 open reading frames.

178 l-CoA carboxylase subunit D (accD)-like open reading frames.

179 s and thereby generate mutations in all open reading frames.

180 n digits, objects, newswire articles, sensor readings from the Space Shuttle, and protein expression

181 Reading genotypes in the SeqArray package are two to thr

182 6 patients could use the device but had IOP readings greater than 5 mm Hg different from those obtai

183 a visual interpretation alone or a combined reading (i.e., visual plus quantitative data were availa

184 f our prosopagnosia cases exhibited a severe reading impairment with delayed response times during re

185 n complement the traditional method of close reading in detecting trends of continuity and change in

186 rten readiness and tested in mathematics and reading in grades 3 through 8.

187 anges in crowding may in part explain slower reading in older adults.

188 The Spot successfully obtained readings in 89.7% of patients.

189 subjective image parameters and on oncologic readings in whole-body (18)F-FDG PET/MRI.

190 Our data show that, while the reading intervention enhanced reading abilities, learnin

191 Here we used an intensive reading intervention program to test the causal relation

192 ops within the ventral visual stream because reading involves extracting linguistic information from

193 One may read this statement in 20-30 s, but reading it in less than five leaves us clueless.

194 acuity (BCVA) and normal maximum keratometry reading (Kmax) were measured at study entry and at the 1

195 gh analysis of maximum simulated keratometry readings (Kmax, diopters).

196 functional connectivity between hubs of the reading/language networks.

197 In two studies, reading literary art enabled the transformation of selfh

198 ns of these assays and the use of absorbance readings make them suitable for application by any labor

199 ce, measurements for AL, ACD and keratometry readings may be used interchangeability with both device

200 s from different immunoassays and visual PET readings may influence the use of CSF biomarkers and/or

201 Such a simple behaviour-reading mechanism has the potential to be widespread amo

202 t has been suggested that RIG-I has a 'proof-reading' mechanism for rejecting host RNA targets, and t

203 agreement between manual and novel automated reading methods.

204 ve investigated musical abilities related to reading music scores [13, 14] and singing familiar songs

205 Given the aim of reading neural activity in the peripheral nervous system

206 s at least "moderate difficulty" with either reading newsprint or near work.

207 stic curves, 0.87 versus 0.69; P<0.001) with readings obtained in the endocardial myocardium performi

208 ent was evaluated against a manual consensus reading of 2 masked reading center graders.

209 ate that Mt/AFM-SECM enables high throughput reading of dense nanoarrays, with a sensitivity and a re

210 ve image quality was evaluated with a masked reading of each simulated PET compared with the dose of

211 There was also a difference in reading of histopathology samples of BE tissues between

212 The diagnostic reading of PET/MR patients with brain tumors did not cha

213 der was originally developed to simplify the reading of Protein Data Bank (PDB) files containing glyc

214 a direct readout mechanism that involves the reading of the base sequence in the DNA major groove at

215 on histone tails and thereby facilitate the reading of the histone code.

216 ry low power consumption is required for the reading of the optical responses and data transmission t

217 e R213I mutant of RF2 showed 5-fold improved reading of the RF1-specific UAG codon relative to UAA, t

218 ction of the time interval from the previous reading of the same non-word.

219 n's nosology are illustrated through a close reading of their essays on hebephrenia, catatonia, and c

220 as 2 consecutive intraocular pressure (IOP) readings of <6 mmHg with vision loss or >17 mmHg without

221 ithm allowed for analysis, hence physiologic readings of the parameters in all 4 limbs of all lambs w

222 t, we obtained a high stability of potential readings of the resulting ion-selective electrodes toget

223 For samples with a 5-20ppm reading on a first test, replicate analyses provided res

224 mutations is now essential for radiologists reading oncology cases.

225 ical interference from the nanomaterial when reading optical density, and the residue left from the e

226 the odds of not meeting standards in either reading or math (95% confidence interval, 1.12-1.37), wi

227 Reading out the combined activity of all neurons, a mach

228 atio of 10(6) ), and long-term stability for reading out with human breath.

229 gnificantly affected the maximal keratometry reading (p = .036), the vertical keratometry reading (p

230 reading (p = .036), the vertical keratometry reading (p = .04), and the index of height asymmetry (p

231 of other infiltrate and normal for both the reading panel and the arbitration panel (32% and 30% of

232 Two members of a 14-person reading panel, who had undertaken training and standardi

233 A second reading performed 1 month later used predefined classifi

234 ," or "always" in distance straight ahead or reading positions on the Diplopia Questionnaire.

235 ntia and the connectionist triangle model of reading, previous empirical work has shown that healthy

236 bilities (defined as profiles or patterns of reading problems) contribute to brain morphology results

237 odality test r=-0.374, p<0.0001; Stroop word reading r=-0.248, p=0.0033), total functional capacity (

238 regularities in benefitting dyslexics' oral reading rate.

239 Test of Attention performance (P < 0.02) and reading scores (P < 0.001) in boys but with better readi

240 (P < 0.03) and for the associations between reading scores and rs174448 and rs2397142 (P < 0.01).

241 g scores (P < 0.001) in boys but with better reading scores in girls (P </= 0.002).

242 Why does a reading-selective region develop at this anatomical loca

243 ork for language while 102 participants were reading sentences.

244 ution (acuity) limit that was independent of reading skill.

245 n sensitivity showed the same improvement in reading skills as children with typical motion sensitivi

246 relationship between motion sensitivity and reading skills has been debated for more than thirty yea

247 ular side effect of this focus on individual reading skills, the Protestant territories were the firs

248 ual sensitivity to motion is correlated with reading skills.

249 within each domain were blurry vision (32%), reading small print (34%), medical costs (26%), and dryn

250 older adults exhibited significantly slower reading speed (a decrease by 30%) and larger crowding: a

251 not associated with a decrement in sustained reading speed (beta = -10.1, 95% CI: -22.4, 2.1, P = .10

252 5% CI, -0.15 to -0.07; P < .001) and maximum reading speed (mean increase of 21.0 words/min; 95% CI,

253 so observed significant correlations between reading speed and each of the crowding measures.

254 microperimetry, low-luminance visual acuity, reading speed assessments, and patient-reported outcomes

255 Reading speed was measured with short blocks of text.

256 Read maximum reading speed, sustained-silent reading speed, and comprehension score.

257 es (baseline to end of treatment) in maximum reading speed, critical print size, and reading acuity (

258 OUTCOME MEASURES: MNRead maximum reading speed, sustained-silent reading speed, and compr

259 d was used to assess short-duration out-loud reading speed.

260 also plays a role in age-related changes in reading speed.

261 n to play a role in developmental changes in reading speed.

262 1), but there was no difference in sustained reading speeds between groups (beta = 0.99, 95% CI: -41.

263 (AMD) on short out-loud and sustained silent reading speeds, and reading comprehension.

264 g test was used to evaluate sustained silent reading speeds, while reading comprehension was assessed

265 novel magnetic information devices with high reading speeds.

266 ions had significantly better performance in reading, spelling, and math computation, with increased

267 t three-way interaction between "pre-morbid" reading status, stimulation, and word type, such that TM

268 ved, multicenter, multireader, retrospective reading study, between July 2011 and March 2013.

269 c sensitivity and specificity for visual PET readings supported by voxel-based statistical analyses f

270 In the PERCIST reading, target lesions were above the liver threshold w

271 g comprehension was assessed based on silent reading test text.

272 Sustained silent reading test was used to evaluate sustained silent readi

273 erformance in the d2 Test of Attention and a reading test were analyzed in multiple regression models

274 ive assessments done were the National Adult Reading Test, Wechsler Abbreviated Scale of Intelligence

275 Dyslexia is a developmental disorder in reading that exhibits varied patterns of expression acro

276 variants into cells as pooled libraries and reading the barcodes out using massively multiplexed flu

277 ide a useful background and set of tools for reading the bloom literature and to give some suggestion

278 mpact is mediated by TORC1 signaling through reading the FAD-dependent ATP level.

279 wo of which engage the tail of histone H3 by reading the H3-Lys-4 trimethylation and H3-Arg-8 asymmet

280 eta-analysis of cognitive empathy using the 'Reading the Mind in the Eyes' Test (Eyes Test) in 88,056

281 ication (affective speech recognition (ASR), reading the mind in the eyes, olfactory identification,

282 including the Penn emotion recognition task, reading the mind in the eyes, the awareness of social in

283 A mobile phone "app" was also capable of reading the test result and transmitting this to a remot

284 GRO-Seq analysis showed the polymerase reading through the termination signal in the downstream

285 BT plus synthetic 2D imaging increased image reading time and the time needed for invasive assessment

286 r of blood draws, injections, blood pressure readings, trauma to the at-risk arm, and number of fligh

287 visual ability and in 4 functional domains (reading, visual information, visual motor, and mobility)

288 3 to 20/200 improved more in visual ability (reading, visual motor, and overall).

289 h participants self-reported difficulty with reading, visuospatial tasks (ie, close-up work or findin

290 ming distance is then obtained by applying a reading voltage to the memristors and summing all the re

291 Oncologic reading was performed first according to PERCIST in each

292 Significant disagreement between two readings was defined as >95% limits of agreement between

293 he average improvement in corneal topography readings was slightly lower than the Dresden protocol in

294 hypothesis that the results of the combined reading were not inferior to the results of the visual r

295 resence of corneal abnormalities, CH and CRF readings were available for 382 Indian persons.

296 struction in PET/CT for confident radiologic reading when compared with other reconstruction paramete

297 epresent a new principle of mechanical proof-reading, whereby only reactions supporting anchorage of

298 sion for 37 atypical S. aureus isolates (156 readings) with MHA supplemented with 5% sheep's blood (B

299 s was defined by a good technique and an IOP reading within 5 mm Hg of that obtained by a clinician u

300 ipants vary in their reliance on meaning for reading words with atypical correspondences between spel