ライフサイエンスコーパス: naming

1 ific levels of word comprehension and object naming.

2 d through evidence from tasks such as object naming.

3 fy cortical sites critical for visual object naming.

4 function, episodic memory and confrontation naming.

5 herefore reflected the semantic component of naming.

6 roke in 87 individuals with impaired picture naming.

7 n was associated with improvement in picture naming.

8 and superordinate semantic errors in picture naming.

9 the source of universal tendencies in color naming.

10 versal and language-specific forces in color naming.

11 chy underlying word comprehension and object naming.

12 on somatosensory or auditory feedback during naming.

13 ty-independent convergence region for proper naming.

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

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

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

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

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

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

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

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

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

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

24 Naming also correlated with lexical retrieval in all pat

25 Impaired naming also correlated with semantic memory and visual p

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

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

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

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

30 Of the seven patients who had auditory naming (AN) sites removed, six declined post-operatively

31 of ECoG HGA with respect to ECS was 78% for naming and 81% for mouth-related motor function, and equ

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

33 Color naming and comprehension was assessed.

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

35 relative to both ECS-induced impairments of naming and ECS disruption of mouth-related motor functio

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

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

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

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

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

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

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

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

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

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

46 When ECS maps of naming and mouth-related motor function were combined, t

47 tation naming predicts ECS interference with naming and mouth-related motor function with good specif

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

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

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

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

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

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

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

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

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

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

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

59 Two additional priming tests, picture-naming and word-stem completion, invoke both conceptual

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

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

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

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

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

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

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

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

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

69 (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

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

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

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

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

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

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

76 We propose naming bacteria that express the previously described 20

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

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

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

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

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

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

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

84 hods, including a longitudinal assessment of naming, comprehension, picture and word association, as

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

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

87 We suggest a naming convention to resolve this issue.

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

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

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

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

92 genome sequences have not evolved with gene naming conventions.

93 fic groups of patients and, correspondingly, naming correlated with cortical atrophy in partially dis

94 e. if it affected the mouth, lips or tongue, naming could not be tested with ECS at the same cortical

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

96 We examine color-naming data from languages of 110 nonindustrialized soci

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

98 analyzed the World Color Survey (WCS) color-naming data set by using k-means cluster and concordance

99 (www.icsi.berkeley.edu/wcs/), a large color-naming database obtained from informants of mostly unwri

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

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

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

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

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

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

106 n between AN site removal and post-operative naming decline.

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

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

109 resence of verbal fluency deficits, although naming deficits have been described in other studies.

110 We found significant naming deficits in all patient groups.

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

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

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

114 This makes naming difficult and impacts any downstream analysis suc

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

116 Because naming during ECoG involved these muscles of articulatio

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

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

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

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

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

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

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

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

125 Naming errors were attributed to pure retrieval failure

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

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

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

129 The confrontation naming fMRI task also revealed impaired activation in le

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

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

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

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

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

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

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

137 We tested this hypothesis by correlating naming impairments with voxel-based morphometric (VBM) a

138 e language network, frequently causes object naming impairments.

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

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

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

142 erfere with a lexical retrieval component of naming in AD, FTD and CBD.

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

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

145 its on both letter fluency and confrontation naming in the ALS group.

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

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

148 search has demonstrated intact confrontation naming in the presence of verbal fluency deficits, altho

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

150 s pattern might implicate direct hippocampal naming involvement.

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

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

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

154 Visual object naming is the gold standard for identifying 'essential'

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

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

157 Naming latencies were longer in PPA and PRAD patients th

158 Whereas naming latencies were unaffected by phoneme repetition,

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

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

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

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

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

164 d to higher processing efficiency within the naming network.

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

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

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

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

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

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

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

172 suggest that universal processes control the naming of colors.

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

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

175 We tested oral and written naming of nouns and verbs, matched in difficulty, in pat

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

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

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

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

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

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

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

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

184 Oral Word Association Test FAS and in color naming on the Stroop Color and Word Test.

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

186 priming on the word-identification, picture-naming, or word-stem completion tests.

187 correlation of the complete chromatic color-naming patterns obtained from individual WCS informants.

188 2 to 10, we found that (i) the average color-naming patterns of the clusters all glossed easily to si

189 The aphasic patients' picture naming performance improved considerably with phonemic c

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

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

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

193 presentations underlying the complex task of naming pictures.

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

195 event-related ECoG HGA during confrontation naming predicts ECS interference with naming and mouth-r

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

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

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

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

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

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

202 tive interruption of other components of the naming process, including semantic and visual perceptual

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

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

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

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

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

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

209 challenge for human color categorization and naming research.

210 Furthermore, faster naming responses correlated with decreased blood oxygen

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

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

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

214 signs cell identities based on the canonical naming scheme.

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

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

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

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

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

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

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

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

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

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

225 Visual object naming sites identified via electrical stimulation were

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

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

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

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

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

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

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

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

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

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

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

237 inical ECS mapping used a subset of the same naming stimuli at each cortical site.

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

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

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

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

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

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

244 re 'ecologically valid' auditory description naming task in our pre-resection cortical mapping protoc

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

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

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

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

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

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

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

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

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

254 rs in both auditory comprehension and object naming tasks.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

273 We therefore suggest naming this entity autosomal recessive cerebellar ataxia

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

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

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

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

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

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

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

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

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

283 al' language cortex; however, sparing visual naming (VN) sites has not reliably prevented post-operat

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

285 Improved naming was associated with increased brain activation in

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

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

288 nfirmation of previous work, rapid automatic naming was not predicted by the anatomical risk index, b

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

290 In addition to visual object naming, we included a more 'ecologically valid' auditory

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

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

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

294 e employed, letter fluency and confrontation naming, which were developed for use with an older and p

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

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

297 Analysis of concordance in color naming within WCS languages revealed small regions in co

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