コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 negative affective and amygdala response to facial affect stimuli returned to baseline levels while
2 in, negative affect and amygdala response to facial affect stimuli were reduced, whereas positive aff
3 behaving mice, we found that while an abrupt facial air puff triggered transient increases in noradre
4 ls and interleukin-35 (IL-35) in suppressing facial allodynia and facial grimacing in animals with ex
7 reveal the development of a neornithine-like facial anatomy despite the retention of a maxilla-premax
10 stor possessed maxillae and premaxillae with facial and palatal laminae, and that these bones underwe
11 play a classical FSHD phenotype with typical facial and scapular muscle weakness, whereas 20.1% prese
13 lates of emotion perception as influenced by facial and vocal information by measuring changes in oxy
14 Despite evidence of interactions between facial and vocal processing, these findings suggest some
18 cause of the potential need to sacrifice the facial and/or spinal accessory nerves and because of a l
19 man Immunodeficiency Centromeric Instability Facial Anomalies (ICF) 4 syndrome is a severe disease wi
20 munodeficiency, centromeric instability, and facial anomalies (ICF) syndrome is a genetically heterog
21 e hypothesis posits that long-term partners' facial appearance converges with time due to their share
22 ge, they do not converge over time, bringing facial appearance in line with other personal characteri
23 t would be important to be able to place the facial appearance of a patient with congenital or acquir
24 n the EEG data, we reveal representations of facial attractiveness after 150-200 ms of cortical proce
25 already early perceptual representations of facial attractiveness convey idiosyncratic attractivenes
29 lly specific, and genuine representations of facial attractiveness, which may underlie fast attractiv
32 In study 1, 966 judges rated the composites (facial averages) of women with higher OS as more attract
34 hlight the importance of natural patterns of facial behaviour in emotional expressions, and demonstra
35 with depigmentation of 0.5% or more of their facial body surface area (BSA) and 3% or more of their n
37 iodontal phenotype, maintaining or enhancing facial bone thickness, accelerating tooth movement, expa
38 size of the gap between the implant and the facial bone wall may play a role on peri-implant tissues
41 rface area (BSA) and 3% or more of their non-facial BSA were randomly assigned (1:1:1:1:1) by use of
42 h no, one, or ten missing teeth would have a facial centroid size of 511.83, 510.81, or 501.70 mm, re
43 Linear discriminant analysis distinguished facial change determined by the emotional valence of the
44 n by promoting the extraction of distinctive facial characteristics and suppressing redundant or irre
45 nt and easily recognizable patterns of human facial characteristics co-vary with genomic ancestry, an
46 liance on single-trait-based versus holistic facial characteristics for species discrimination, with
47 O recommends the SAFE (Surgery, Antibiotics, Facial cleanliness, and Environmental improvement) strat
51 Significant difference of linear changes of facial contour was noted over time and not between the g
52 dings highlight the relative significance of facial cues compared to bodily cues on interpersonal out
54 rown group) birds also exhibit constraint on facial development(8,9), they have comparatively diverse
56 her the psychological trauma associated with facial disfigurement alters their perception of FT and i
63 tooth abnormality, intellectual disability, facial dysmorphism, attention-deficit hyperactivity diso
64 Here, we report a syndrome characterized by facial dysmorphism, colobomatous microphthalmia, ptosis
65 ximal shortening of the limbs, contractures, facial dysmorphism, congenital cataracts, ichthyosis, sp
66 /hyperactivity disorder (ADHD), autism, mild facial dysmorphism, craniosynostosis, and multiple osteo
67 ity, self-harm, hetero-aggressive behaviour, facial dysmorphism, left facial paralysis, post-axial po
70 h sleep disturbance, cerebellar atrophy, and facial dysmorphisms, and suggesting a recognizable syndr
71 delay and/or intellectual disability, subtle facial dysmorphisms, behavioral and psychiatric problems
72 linically variable symptoms, such as typical facial dysmorphisms, short stature, developmental delay,
74 ial mimicry is emotion-specific, we measured facial electromyography (EMG) from five muscle sites (co
75 investigation of this pathway using combined facial electromyography and functional magnetic resonanc
76 ecorded alongside skin conductance level and facial electromyography from the corrugator supercilii a
79 -SEA), which comprises the faux pas test and Facial Emotion Recognition Test (FERT); Mini-Mental Stat
80 Participants from two countries completed a facial emotion recognition test, and a subsample additio
82 has been shown to be a key regulator of both facial-emotion processing and brain dynamics, and 5-HT a
85 on the responsivity of brain dynamics during facial-emotion processing in individuals with and withou
87 limbic regions during processing of negative facial emotions in adults with ASD-but not in neurotypic
91 nd a double dissociation of areas processing facial expression and those processing head orientation.
95 we examined the extent to which 16 types of facial expression occurred systematically in thousands o
96 e correlates with asymmetry, indicating that facial expression of the mouse is itself correlated with
97 ain activation in regions involved in infant facial expression processing and empathic and mentalizin
98 nd the left fusiform gyrus, recruited during facial expression processing, were positively correlated
99 A popular hypothesis holds that efficient facial expression recognition cannot be achieved by visu
100 dividuals can achieve normotypical efficient facial expression recognition despite a congenital absen
103 image onset, and identity across a change in facial expression was uniquely associated with neural pa
104 hes in the STS fundus were most sensitive to facial expression, as was the amygdala, whereas those on
105 cifically painful, angry, happy, and neutral facial expressions and questionnaires including a measur
106 hich measured amygdala responsivity to angry facial expressions and ventral striatum responsivity to
110 Understanding the degree to which human facial expressions co-vary with specific social contexts
112 evidence linking social context to specific facial expressions is sparse and is largely based on sur
114 esults reveal fine-grained patterns in human facial expressions that are preserved across the modern
116 , regions varied in how frequently different facial expressions were produced as a function of which
119 ade trials with pain faces relative to other facial expressions, indicating a difficulty disinhibitin
120 completed the anti-saccade task with dynamic facial expressions, specifically painful, angry, happy,
121 Emotion processing-including signals from facial expressions-is often altered in individuals with
127 odological approach combining trial-by-trial facial eye-blink startle electromyography and brainstem-
128 e brain focuses on a task-relevant subset of facial features and assessing log likelihood of a face u
129 aniofacial and tooth development, dysplastic facial features and delayed development of the ossicles
132 uate a stranger's trustworthiness from their facial features in a fraction of a second, despite commo
133 It remains uncertain whether prototypical facial features in emotional expressions are being cover
134 We investigated the association between the facial features of 97 postmenopausal women and their lev
135 cial defects possibly akin to the dysmorphic facial features seen in individuals harboring putatively
136 cterized by developmental disability, coarse facial features, and fifth digit/nail hypoplasia that ar
137 y have intellectual disabilities, dysmorphic facial features, and ocular alterations such as ptosis,
138 dividuals with strikingly similar dysmorphic facial features, especially midface hypoplasia, and inte
144 he size of a domestication phenotype-a white facial fur patch-is linked to their degree of affiliativ
147 (IL-35) in suppressing facial allodynia and facial grimacing in animals with experimental autoimmune
148 ology is characterized by excessive vertical facial growth with severe disarrangement of jaws and tee
151 e memory guidance is specific for associated facial identities, it does not only occur for the specif
152 sharpened tuning of visuocortical neurons to facial identity cues, indicating the behavioral relevanc
154 realistic, normalized versions of any given facial image, and objectively measures the perceptual di
155 sly measured arousal signal from the thermal facial imagery was moderate and did not correlate with s
156 between the features of artificial composite facial images and attributions of personality traits by
157 study, we isolated the level of error in 3D facial images attributable to four sources, using the 3d
158 rum by reexamining this hypothesis using the facial images of 517 couples taken at the beginning of t
160 dimensional personality profiles from static facial images using ANNs trained on large labelled datas
168 tment claims to rejuvenate skin by improving facial lines, wrinkles and skin pigmentation associated
169 eservation at the esthetic concern area (mid-facial margin and 2 to 6 mm above) at the final 12-month
170 verall, we find no support for the idea that facial masculinity is a condition-dependent male ornamen
171 te activation patterns across muscles during facial mimicry and to provide evidence for distinct patt
172 ng covertly mimicked and also whether covert facial mimicry involves distinct facial muscle activatio
174 dividual emotion categories, suggesting that facial mimicry is emotion-specific, rather than just val
176 MRI findings and NDD diagnoses together with facial morphological variants and genetic copy number va
178 When combining the presence of MRI findings, facial morphological variants, and CNVs, statistically s
179 etween MRI findings and any NDD diagnosis or facial morphological variants; however, MRI findings wer
180 health traits were related to the macaques' facial morphology and their observed behaviour supportin
184 ion despite a congenital absence of relevant facial motor representations and, therefore, unaided by
185 been claimed that certain configurations of facial movements are universally recognized as emotional
186 dyads that were able to see their partner's facial movements mapped onto their avatars liked each ot
187 hesis that people infer emotional meaning in facial movements using emotion knowledge embrained by cu
193 ther covert facial mimicry involves distinct facial muscle activation patterns across muscles per emo
194 to provide evidence for distinct patterns of facial muscle activation when viewing individual emotion
197 ed by local infiltration around the lids and facial nerve (n = 6), topical anesthesia (n = 5), and ge
205 d in 7 of 27 articles and included transient facial nerve weakness, persistent blue dye staining of t
210 n neuronal death and glial activation in the facial nucleus in the brain stem, and on axon degenerati
211 ical structures (0.47 ug . g(-1) +/- 0.10 in facial nucleus, 0.39 ug . g(-1) +/- 0.10 in choroid plex
212 showed reduced microglial activation in the facial nucleus, whereas the levels of neuronal death wer
214 nd an overlapping spectrum of symptoms, with facial pain and loss of smell being the most differentia
215 p period, patients recorded daily ratings of facial pain intensity and duration; the product was comp
222 gressive behaviour, facial dysmorphism, left facial paralysis, post-axial polydactyly, and for the fi
223 bility of these fish to discriminate complex facial patterns tracked categorical rather than metric d
225 alized morphometric changes may underlie the facial phenotype seen in human patients with severe OI.
226 ions at the Xq13.2-q13.3 locus with a common facial phenotype, intellectual disability (ID), distinct
228 tiple signals with associations to different facial phenotypes, and there is evidence for potential c
229 MRD2, and levator function were measured and facial photography was taken before, 1 month, and at lea
230 tment-driven classification for tooth-bound, facial PMMDs in non-molar sites, consisting of three dif
232 Since the improvement of LF patients on facial profile and occlusion is often difficult and lack
233 OX9 expression during a restricted window of facial progenitor development at distances up to 1.45 Mb
236 n lower physical effort and greater negative facial reactions during reward anticipation, especially
237 gh naltrexone led to a reduction in positive facial reactions to liked rewards during reward consumpt
238 Subjective ratings, physical effort, and facial reactions to matched primary social (affective to
239 it stands in sharp contrast to variation in facial recognition ability, which is driven mostly by ge
240 -2 VF MD remained a significant predictor of facial recognition after adjusting for potential confoun
241 heir facial similarity (human judgment and a facial recognition algorithm), we show that while spouse
242 there was a significant correlation between facial recognition and 10-2 VF MD (P < .0001 better, wor
244 aucomatous macular damage exhibit diminished facial recognition, which is partly mediated through dim
249 linical report of the first documented human facial retransplantation is proof-of-concept that the lo
250 ve faces, represent an attentional effect to facial salience rather than to their rewarding propertie
254 pproaches risk missing potentially important facial signals and within-person variability in expressi
255 two independent methods of estimating their facial similarity (human judgment and a facial recogniti
256 continue to regulate the number of teeth and facial size of modern humans in a coordinated manner.
259 d tissue, smaller airways, and smaller lower facial skeletons from measurements of the mandible and l
260 to evaluate the uptake of APIs within human facial skin and confirm accurate drug delivery, a select
261 hat the skin organoids are equivalent to the facial skin of human fetuses in the second trimester of
263 testing of an integrated system for decoding facial strains and for predicting facial kinematics.
264 at the brain's neural suppression of average facial structure facilitates recognition by promoting th
265 rate that the dynamic suppression of average facial structure plays a prominent role in the responses
266 s that the brain computes and stores average facial structure, which it then uses to efficiently dete
269 nt of Sox9 dosage perturbation to developing facial structures through context-specific enhancer acti
271 y outcomes, subjects reported less bruising, facial swelling, and use of ice pack for the ERL group.
277 experiments with live guenons, showing that facial traits critical for accurate classification influ
278 ation is proof-of-concept that the loss of a facial transplant after CAMR can be mitigated successful
279 ograft necrosis and the eventual loss of the facial transplant, the desensitisation protocol used for
280 plantation in a man, 8 years after his first facial transplantation because of extensive disfiguremen
281 oughout the planning and operative stages of facial transplantation by performing a critical analysis
283 istidine (His134) of the 2-His-1-carboxylate facial triad, instead of assuming the offline-binding mo
285 epidemiological dynamics of Tasmanian devil facial tumor disease (DFTD), a fatal, transmissible canc
292 a 25% or higher improvement from baseline in facial Vitiligo Area Scoring Index (F-VASI) at week 24 w
294 patients, which persisted in 3 at 4 months; facial weakness in 3 patients, which persisted in 1 at 4
295 reas 20.1% present incomplete phenotype with facial weakness or scapular girdle weakness, 6.7% displa
296 rats and mice, where the arrangement of the facial whiskers is preserved in the arrangement of cell
297 ats, employ cyclic scanning motions of their facial whiskers to explore their proximal surrounding, a
298 ienced influences the rate of growth of this facial white patch, and this suggests a mechanistic link
299 ntrast, we find that Boc deletion results in facial widening that correlates with increased HH target
300 ived BoNT injections to treat hyperhidrosis, facial wrinkles, migraine prophylaxis, spasticity, and s