ライフサイエンスコーパス: naming

1 chy underlying word comprehension and object naming.

2 g the results to universal patterns in color naming.

3 on somatosensory or auditory feedback during naming.

4 ty-independent convergence region for proper naming.

5 cluded motor, sensory, counting, and picture naming.

6 ific levels of word comprehension and object naming.

7 d through evidence from tasks such as object naming.

8 fy cortical sites critical for visual object naming.

9 function, episodic memory and confrontation naming.

10 herefore reflected the semantic component of naming.

11 f general aphasia severity, agrammatism, and naming.

12 versal and language-specific forces in color naming.

13 By consistently annotating and naming 10,899 microRNA genes in these organisms, we show

14 constraining temporal context is faster than naming a picture after a weakly constraining temporal co

15 For example, naming a picture following a strongly constraining tempo

16 that brain changes associated with improved naming ability in chronic aphasia rely on preservation a

17 Results suggest that preserved naming ability in HS patients following anterior tempora

18 The bimodal distribution in pitch-naming ability signifies AP as a distinct perceptual tra

19 ) of whom proved to have extraordinary pitch-naming ability.

20 that neural responsivity measures relate to naming accuracy and fluid intelligence.

21 tion, we document a gradual decline in pitch-naming accuracy with age, characterized by a perceptual

22 ent semantic information is linked to higher naming accuracy, a measure of task-specific performance.

23 of universal or recurrent patterns in color naming across cultures is paralleled by the observation

24 roposal by Jameson and D'Andrade: that color naming across languages reflects optimal or near-optimal

25 Dichromats' color naming also could account for their color preferences, w

26 ggest a potential role of the hippocampus in naming, although this is inconsistent with neurocognitiv

27 In support, we found that color naming among Tsimane' had relatively low communicative e

28 Color-naming among Tsimane' was boosted when naming artificial

29 ming, suggesting that the variation in color naming-among the individuals and across the color wheel-

30 ults demonstrate a strong link between color naming and color memorization both across different indi

31 they contribute to networks underlying both naming and comprehension of objects.

32 Color naming and comprehension was assessed.

33 ce recognition (familiarity, identification, naming and cross-modal matching) and equivalent measures

34 On the expressive semantic tests of naming and fluency, average performance was worse in the

35 ciations of TDP-43 with greater memory loss, naming and functional decline, and smaller hippocampal v

36 quantitative assessments of episodic memory, naming and grammatical comprehension.

37 est, the King-Devick test, uses rapid number naming and has been tested in multiple athlete cohorts.

38 visional 16S rRNA based taxonomic scheme for naming and identifying unnamed canine bacterial taxa.

39 the operations they perform, their arbitrary naming and lack of documentation, however, mean that the

40 her behavioral predictors of dyslexia, rapid naming and letter knowledge, did not correlate with volu

41 ior frontal gyrus correlated with both odour naming and matching.

42 ed much more pronounced impairments of odour naming and matching.

43 es were significantly correlated with Boston naming and mini-mental state examination results.

44 re sensitive to this principled link between naming and object representation by age 12 mo.

45 c stroke using a battery of oral and written naming and other lexical tests, and with magnetic resona

46 This relationship between color naming and preference also was present for trichromat ma

47 We review the history of naming and provide keys and character lists for all spec

48 The potential interaction between color naming and psychophysical color recognition has been his

49 culty but the contrasting difference between naming and reading illustrates how the demands on somato

50 Specifically, they exhibit deficits in naming and repetition in the context of spared semantic,

51 Levels of activation to the auditory naming and reversed speech conditions did not differ in

52 als, whereas Pappworth believed that only by naming and shaming could any expose act as a deterrent.

53 intensities were only correlated with Boston naming and Trails B results in the cognitively impaired.

54 -Verbal Learning Test delayed recall, Boston naming and Trails B scores as measures of specific domai

55 ral spinal fluid amyloid-beta1-42 and Boston naming and Trails B.

56 hes based on individual differences in color naming and variation of color name density along the col

57 In 33 human subjects with PPA, object naming and word comprehension were explored with N400 po

58 nventional tests of semantic memory, such as naming and word-to-picture matching.

59 ge in two other similar tasks, spoken action naming and written object naming, each of which was inde

60 ated decrease (fluid intelligence and object naming) and a syntactic comprehension task that shows ag

61 , phonological memory, and rapid automatized naming), and (3) electrophysiological markers of SiN per

62 al Paired Associates, Logical Memory, Animal Naming, and Controlled Oral Word Association Test).

63 ecall, Logical Memory delayed recall, Boston Naming, and Digit-Symbol Substitution.

64 We describe here the challenges of mapping, naming, and quantifying tRNA-derived RNAs and present a

65 ex positively related to spontaneous speech, naming, and repetition scores.

66 cognitive performance (problems with memory, naming, and word finding).

67 elated with both (i) change in spoken object naming; and (ii) structural adaptation in the two peak c

68 (HR, 3.79; 95% CI, 1.57-9.15; P = .003) and naming animals (HR, 2.41; 95% CI, 1.04-5.59; P = .04) we

69 nosing diseases, prescribing treatments, and naming animals and objects using written information as

70 ge network, leading to impairments of object naming (anomia) and word comprehension.

71 The different patterns of naming areas identified in patients with and without HS

72 Color-naming among Tsimane' was boosted when naming artificially colored objects compared with natura

73 perature with weak hydrogen-bonded structure naming Au nanoparticles (NPs)-treated (AuNT) water via t

74 a novel cytokine, FAM150B, which we propose naming augmentor-alpha (AUG-alpha), as a ligand for ALK.

75 We propose naming bacteria that express the previously described 20

76 f curated domain architectures in support of naming bacterial proteins in RefSeq.

77 T scores on GP-NDH, WAIS-IIIDS, Stroop Color-Naming; better motor and SIP summary T scores.

78 al-time surveillance with consistent cluster naming between studies and allows for outbreak detection

79 rs 5 years before expected onset in tests of naming (Boston Naming Test -0.7; SE 0.3) and executive f

80 lex Figure Test), and visual confrontational naming (Boston Naming Test Short Form) once per day over

81 nce that a network of brain regions supports naming, but separate components of this network are diff

82 The six known types of CA, which we propose naming CA1 through CA6, use a range of molecular mechani

83 Meaningful speech, as exemplified in object naming, calls on knowledge of the mappings between word

84 : Silent Sentence Completion (SSC), category naming (CAT) and verbal fluency (FAS), in localizing the

85 gher in most visual cortical areas for color naming compared to diverted attention.

86 how treatment-related improvement in correct naming compared with cases where the same areas were int

87 trademarks, feature films produced, and baby-naming conformity.

88 ceae; we suggest resolving the long-standing naming conundrum by renaming it Peptoclostridium diffici

89 HACA-PD1 was adopted as the naming convention for aglycosylated tracer variants.

90 We suggest a naming convention to resolve this issue.

91 set of experimental features with consistent naming conventions and units.

92 The lack of standardized naming conventions for diastereotopic atoms of small mol

93 There were no overall trends in naming conventions, though ligand-specific trends were p

94 ndard and organism-specific protein and gene-naming conventions, visualization of protein architectur

95 Two prominent patterns of color naming could be accounted for by the decoding results: t

96 e formalize this idea, test it against color-naming data from a broad range of languages and show tha

97 ect concepts by analysing 43 sets of picture-naming data from patients with semantic dementia.

98 ant hippocampus will likely result in visual naming decline postoperatively.

99 ortical stimulation mapping protects against naming decline when resection includes the hippocampal r

100 esection exhibited significant postoperative naming decline, despite preresection mapping and preserv

101 hippocampal resection showed no significant naming decline, suggesting a clinical benefit from corti

102 rk, non-HS patients exhibited post-operative naming decline, whereas HS patients did not.

103 ilepsy (TLE) carries risk for post-operative naming decline.

104 -temporal atrophy (when matched on degree of naming deficit to a set of cases with more extensive lef

105 also displayed higher levels of apathy and a naming deficit.

106 ond group of PPA patients showed more severe naming deficits-the object name was neither verbalized n

107 rocesses underlying oral and written picture naming depend on intact function of different, but overl

108 Even accurate overt naming did not necessarily imply normal semantic process

109 ntensification of the semantic factor as the naming disorder becomes more severe.

110 Phonological errors in naming (e.g. GHOST named as 'goath') are commonly seen i

111 sks, spoken action naming and written object naming, each of which was independently associated with

112 ultures smell talk is more frequent and odor naming easier.

113 hat the cross-linguistic similarity in color-naming efficiency reflects colors of universal usefulnes

114 An informal system for naming eggplant wild relatives largely based on crossing

115 that are comparable to the traditional color-naming emotional Stroop.

116 ymptom mapping analysis of 1718 phonological naming errors collected from 106 individuals with divers

117 We gathered picture-naming errors from 86 individuals with poststroke langua

118 Surprisingly many of the naming errors reflected pure retrieval failures, without

119 Naming errors were attributed to pure retrieval failure

120 locus of lesions that give rise to semantic naming errors.

121 gnitive mechanisms that contribute to object naming failures in PPA.

122 frontal anodal tDCS during an overt picture-naming fMRI study.

123 The traditional Naming Game corresponds to setting w at infinity.

124 The Naming Game has proven to be an important model of opini

125 We investigate the two-word Naming Game on two-dimensional random geometric graphs.

126 In addition to naming genomic loci we manually curate genes into family

127 Whilst synchronised gene naming has been actively pursued between human and mouse

128 s to transmodal representations required for naming have not been put forward.

129 The color naming idiolects of 2,367 WCS informants fall into three

130 F NfL levels were moderately associated with naming impairment as measured by the Boston Naming Test

131 e language network, frequently causes object naming impairments.

132 rolled oral word association task (vegetable naming), implementing a reverse-time longitudinal modeli

133 We assessed postoperative changes in visual naming in 33 patients, 14 who underwent left temporal re

134 e activated during reading aloud and picture naming in a patient with left putamen damage.

135 ch showed significantly more activation than naming in both SII/OP1 and STS bilaterally.

136 speculated that the relative preservation of naming in post-operative HS patients might reflect corti

137 rophysiologic responses to picture and voice naming in the human left ATL.

138 l (i.e., transmodal) dispositions for proper naming in the left ATL.

139 id not consider drug exposure, partly due to naming inconsistencies in the data.

140 Forty years after its naming, interleukin-1 (IL-1) is experiencing a renaissan

141 s pattern might implicate direct hippocampal naming involvement.

142 a has allowed us to uncover unsuspected note-naming irregularities suggestive of a "perceptual magnet

143 Standardized gene naming is crucial for effective communication about gene

144 Naming is mediated by perisylvian cortex in the left (la

145 These findings suggest that, although object naming is more error prone than reading, subjects can af

146 ccipital cortex is also critical for picture naming, it is likely that bilateral occipital damage is

147 mantic interference effect was observed with naming latencies longer in HOM versus HET blocks.

148 Whereas naming latencies were unaffected by phoneme repetition,

149 in the high-frequency band predicted picture-naming latencies.

150 pment, by somewhat subjective describing and naming main changes of oocytes, have been criticized for

151 e recognized but not retrieved during verbal naming, N400s in picture-word trials were also abnormal,

152 importance of Broca's area within the normal naming network and as such indicate that Broca's area ma

153 ed to illuminate brain reorganization of the naming network in comparison with healthy controls.

154 d to higher processing efficiency within the naming network.

155 vations basically overlapping with premorbid naming networks observed in healthy subjects.

156 Based on the established naming nomenclature for KMTs, we propose to rename FAM17

157 Based on the established naming nomenclature for similar enzymes, we suggest that

158 We also present a uniform murine OCT layer naming nomenclature system that is consistent with human

159 Nomenclature Committee (HGNC) guidelines for naming not only protein-coding but also RNA genes and ps

160 Confrontation naming, noun fluency, recognition, and perceptual organi

161 ity of word finding at baseline based on CAT Naming Objects test scores).

162 erms for odors, odor talk is infrequent, and naming odors is difficult.

163 to the kidney exchange paired recipient, the naming of alternative recipients, and the potential to u

164 the past two decades, particularly after the naming of Australopithecus bahrelghazali and Kenyanthrop

165 The naming of colors has long been a topic of interest in th

166 suggest that universal processes control the naming of colors.

167 e and unintended consequence of the gendered naming of hurricanes, with important implications for po

168 slexics was associated with the faster rapid naming of letters and numbers (RANln), a measure that is

169 are about to lead to dramatic changes in the naming of medically important molds and yeasts.

170 here lesions can be associated with impaired naming of people regardless of modality (e.g., picture o

171 tion affected behavior, primarily during the naming of pseudowords, and modulated brain activity in t

172 Based on the previous naming of similar enzymes, we have redubbed FAM86A and Y

173 Based on the previous naming of similar enzymes, we suggest the renaming of hu

174 e chemistry, electrical engineering, and the naming of species.

175 identity of each subunit, plus hierarchical naming of taxa and coloring are included.

176 Some 100 y after the description and naming of the first vitamin, this conference on the stat

177 he initial discovery, conceptualization, and naming of the salience network, highlighting aspects tha

178 The naming of these HLA genes and alleles and their quality

179 The naming of these HLA genes and alleles and their quality

180 The naming of these HLA genes and alleles, and their quality

181 s as 'type material', thereby preventing the naming of uncultivated organisms.

182 stimulus colors and performed either a color-naming or diverted attention task.

183 ed this process to other vertebrate species, naming over 14000 protein-coding genes in cow and dog an

184 es neither produced a significant deficit in naming pictures of famous faces on the computer, nor did

185 -native speakers of English who were overtly naming pictures of objects and reading their written nam

186 ied areas of the brain that are critical for naming pictures of objects, using a new methodology for

187 presentations underlying the complex task of naming pictures.

188 In naming population groups, we think a chief aim is to use

189 We suggest that naming preferences are a product of this frequency-size

190 Furthermore, identifying and naming printed words in these languages raises common th

191 evidence that the level of impairment in the naming process reflects the distribution of tissue dysfu

192 rious areas can predict the component of the naming process that is disrupted.

193 on the basis of the primary component of the naming process that was impaired (defined as visual, sem

194 with particular levels of impairment in the naming process were largely consistent with evidence for

195 the focus on comprehensively identifying and naming protein phosphatases in available apicomplexan ge

196 ties often enforce disparate conventions for naming proteins, the PNU supports grouping rules into us

197 has expanded largely owing to an increase in naming pseudogenes and non-coding RNA genes, and we now

198 Rapid automatized naming (RAN) tasks provide insight into this system, act

199 ree familiar speech production tasks: object naming, reading and repeatedly saying "1-2-3." Bilateral

200 s suggests that the changes in spoken object naming reflected variation at the level of word-retrieva

201 challenge for human color categorization and naming research.

202 Furthermore, faster naming responses correlated with decreased blood oxygen

203 web-based database for storing and applying naming rules to identify and correct syntactically incor

204 users to generate and manage collections of naming rules, optionally building upon the growing body

205 state "E0H(+)", following the Lowe-Thorneley naming scheme.

206 se with damage to both had worse reading and naming scores.

207 In picture naming, semantic errors (horse for goat) generally resul

208 mands, and lower (figure copying) or higher (naming, semantic fluency) semantic demands.

209 ction mapping and preservation of all visual naming sites (p < or = 0.02).

210 nts exhibited a greater proportion of visual naming sites above the superior temporal sulcus, whereas

211 the previously reported pattern of auditory naming sites anterior to visual naming sites, auditory n

212 language mapping with preservation of visual naming sites from resection, removal of an intact domina

213 es anterior to visual naming sites, auditory naming sites had a significantly more posterior distribu

214 On the other hand, critical naming sites have been found in anterior, lateral tempor

215 to determine whether preservation of visual naming sites identified via cortical stimulation mapping

216 Visual object naming sites identified via electrical stimulation were

217 mpared the topography of auditory and visual naming sites in 12 patients with HS and 12 patients with

218 tients exhibited a more even distribution of naming sites in anterior and posterior temporal regions

219 HS patients had proportionally fewer overall naming sites in anterior temporal cortex, the region typ

220 the superior temporal sulcus, whereas visual naming sites in HS patients were scattered across superi

221 ermore, their more posterior distribution of naming sites is consistent with the more anterior propag

222 of auditory naming sites anterior to visual naming sites, auditory naming sites had a significantly

223 ssessed-testing each patient's spoken object naming skills and acquiring structural brain scans twice

224 emory (P = .006), working memory (P < .001), naming speed (P < .001), and cognitive fluency (P = .007

225 P < 0.001), working memory (P < 0.001), oral naming speed (P < 0.001), and cognitive flexibility (P <

226 activity was positively correlated with oral naming speed in both lateral frontal lobes (rho = 0.48 a

227 fferentially associated with phonological or naming speed subtypes and showed comparable mean reading

228 ', although impaired sustained attention and naming speed were associated with DL(co)(corr).

229 and Symbol Search (WAIS-IIISS), Stroop Color-Naming, Stroop Word-Reading, Trail-Making Test-A (TMT-A)

230 ptual color matching is not related to color naming, suggesting that the variation in color naming-am

231 t all patients showed impairments in picture naming, syntactic comprehension and executive function.

232 tifs," where each motif is a different color-naming system based on a subset of a universal glossary

233 owever, little is understood about the color naming systems at the least technologically advanced end

234 or categorization and the evolution of color naming systems in human societies are discussed.

235 performed within multiple gene- and protein-naming systems.

236 orse than SYN-AD on a temporal lobe-mediated naming task (t(27) = 2.1, p = 0.04).

237 etwork at rest and during an auditory covert naming task in five bilaterally anophthalmic subjects, w

238 lography (MEG) was recorded during a picture naming task to provide a direct measure of neural activi

239 eta (15-30 Hz) activities during an auditory-naming task were animated on the average surface image i

240 during the task relative to a neutral color-naming task while activation in functionally defined wor

241 f these complementary processes in a picture naming task with blocks of semantically heterogeneous (H

242 o demands (No Task), language-related (Color-naming Task), or action-related (Imitation Task) demands

243 ed to between-category colors) for the color-naming task, but not for the diverted attention task.

244 ngruence effect can be detected in the color-naming task, but only in the late, practiced trials.

245 subtypes were severely impaired on an odour naming task, in comparison with an age-matched control g

246 data using two extreme versions of the color-naming task, in three groups: the Tsimane', a remote Ama

247 stimuli of famous U.S. politicians during a naming task.

248 Finally, in both recognition (study 3) and naming tasks (study 4), Chinese icon priming increased a

249 percent error in auditory comprehension and naming tasks as a function of infarct volume using a non

250 ng, 20 adults performed lexical decision and naming tasks on words and pseudowords during functional

251 rs in both auditory comprehension and object naming tasks.

252 We examined if the animal naming test (ANT1 ) (maximum number of animals listed in

253 ther extra-scanner performance on the Boston Naming Test (BNT) and Semantic Fluency Test (SFT), neuro

254 abody Picture Vocabulary Test (PPVT), Boston Naming Test (BNT), Controlled Oral Word Association Test

255 naming impairment as measured by the Boston Naming Test (r(s) =-0.32, p=0.002) and with smaller grey

256 rieve personally relevant words in a picture naming test (with 10% mean difference in change consider

257 re expected onset in tests of naming (Boston Naming Test -0.7; SE 0.3) and executive function (Trail

258 ty derived from their responses to a picture-naming test and a computational model of word production

259 n, r = -0.63), recall (r = -0.44) and graded naming test scores (r = -0.50) over 1-year post-temporal

260 elated with postoperative verbal fluency and naming test scores.

261 ), and visual confrontational naming (Boston Naming Test Short Form) once per day over at least two c

262 tric Hepatic Encephalopathy Score and animal naming test to detect MHE.

263 Digit Symbol Substitution Test, and Category Naming Test) in the modified intention-to-treat populati

264 er Abbreviated Scale of Intelligence, Graded Naming Test, Birt Memory and Information Processing Batt

265 Rey Auditory-Verbal Learning Test or Boston Naming Test.

266 peech therapy for 3 weeks, with standardized naming tests and brain magnetic resonance imaging before

267 made associative semantic errors in picture naming that SD patients did not make.

268 nits (NuoL, NuoM, and NuoN, Escherichia coli naming) that are considered to be involved in the proton

269 a cell lysates as the gene product of DHX36, naming the enzyme G4 Resolvase 1 (G4R1).

270 urrently no coherent nor accepted scheme for naming the expanding phylogenetic diversity of SARS-CoV-

271 RR, 0.68; 95%CI, 0.47, 0.99) and among those naming the health center as their principal source of fe

272 y members of the Porifera phylum, we suggest naming the newly described taxon Candidatus Porisulfidus

273 ng the disease; recovering, identifying, and naming the virus; and describing the epidemic.

274 ys) gene family of putative fw2.2 orthologs, naming them Cell Number Regulator (CNR) genes.

275 We propose naming these disorders Behcet's spectrum disorders to hi

276 We therefore suggest naming this entity autosomal recessive cerebellar ataxia

277 We suggest naming this entity high myopia-excavated optic disc anom

278 On the basis of these findings, we are naming this new enzyme 5'-deoxyadenosine deaminase (DadD

279 We propose naming this new South American member of the Lyme borrel

280 tructure for memory, without contribution to naming, this pattern might implicate direct hippocampal

281 g linguistic tests (verb generation, picture naming) to test for hemispheric dominance in patients wi

282 suppressed (relative to rest) during object naming, to a lesser extent when repeatedly saying "1-2-3

283 NGO1024 homologues, which we suggest naming UfaA, form a distinct lineage within the 2-nitrop

284 he underlying source of cross-language color-naming universals or derived from category boundaries th

285 ames manually, we have developed the Protein Naming Utility (PNU).

286 ontrasts: (1) Task vs. No Task and (2) Color-naming vs. Imitation Task.

287 e decoding results: the greater precision in naming warm colors compared to cool colors evident by an

288 vent related responses revealed that picture naming was associated with a bilateral frontotemporal ne

289 Improved naming was associated with increased brain activation in

290 e is occurring here, change in spoken object naming was correlated with change in two other similar t

291 pseudoisochromatic plates, but simple color naming was normal in 8/9 tested patients.

292 decline in verbal memory and confrontational naming was observed in individual patients.

293 etermined SII/OP1 deactivation during object naming, we searched the whole brain for areas where acti

294 is mostly due to high ambiguity in resource naming, which is compounded by the on-going introduction

295 Change in written object naming, which requires word-retrieval but not articulati

296 t accounts for universal tendencies in color naming while also accommodating some observed cross-lang

297 investigated the physiological basis of odor naming with a paradigm where olfactory and visual object

298 nts showed the greatest deficits on tests of naming, word finding, and visual/verbal episodic memory.

299 with phonemic verbal fluency (walking while naming words beginning with a single letter), and comple

300 with phonemic verbal fluency (walking while naming words, alternating between two letters of the alp