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1 hat measured the skin (r = -0.48, P < .001), lips (r = -0.21, P = .001), and lip rhytids (r = -0.32,
2 in's lymphoma (HR, 3.0; 95% CI, 1.7 to 5.3), lip cancer (HR, 3.4; 95% CI, 2.0 to 6.0), and nonepithel
3 t other metals in a convenience sample of 32 lip products used by young Asian women in Oakland, Calif
7 , P < .001), lips (r = -0.21, P = .001), and lip rhytids (r = -0.32, P < .001) correlated with the re
8 recorded M1 neurons in the anterior bank and lip of the central sulcus as monkeys performed more natu
10 icant positive correlation between blood and lip tissue DNA methylation, indicating blood as a suitab
11 Cancers of the breast, uterine cervix, and lip or oral cavity are three of the most common malignan
12 tial coherence between left motor cortex and lip movements and this partial coherence directly predic
13 zed patients with dry eyes and dry mouth and lip biopsies from the Sjogren's International Collaborat
15 stive mouth movements (tongue protrusion and lip smacking) for the purposes of social communication:
21 ion that was most pronounced on the face and lips and was associated with nail pigmentation, blue pig
25 tats showed greater plasticity for apertural lip thickness and apertural area in the presence of crab
26 threat), fearful (fear grin), and appeasing (lip smack)--were presented to the subjects in a blocked
27 orehead, glabella, lateral periorbital area, lips, and marionette lines), with scores ranging from 0
29 de-by-side computer-generated monkey avatars lip-smacking at natural versus sped-up or slowed-down rh
30 sociated increases in affiliative behaviors--lip smacking, visual attention to a caregiver, and time
31 consistently oriented toward the blastopore lip in dorsal and lateral cells, but oriented parallel t
32 e apical surfaces of cells at the blastopore lip, and it functions during blastopore formation and cl
34 -water distribution coefficient (K(lipw) = C(lip)/C(w)) as 450 L/kg lipid, which is independent of do
35 ounty-level mortality rates from 29 cancers: lip and oral cavity; nasopharynx; other pharynx; esophag
37 nsistent with the hypothesis that chimpanzee lip-smacks function to coordinate and prolong social gro
47 observed wider de novo deletions among cleft lip and palate (CLP) cases than seen among cleft palate
51 ry such as ophthalmology (88, 28%) and cleft lip and palate surgery (70, 22%) were also frequently pe
52 of limb deficiency, cleft palate, and cleft lip cases were, respectively, 1.8 (95% CI: 1.1, 3.1), 1.
55 ctrodactyly, ectodermal dysplasia, and cleft lip/palate (EEC) syndrome is caused by single point muta
56 ctrodactyly, ectodermal dysplasia, and cleft lip/palate (EEC) syndrome patients with p63 mutations as
57 associated with cognitive defects and cleft lip/palate, its role in mammalian development and physio
58 y of Fallot, coarctation of the aorta, cleft lip, cleft palate, anorectal atresia/stenosis, and limb
60 sed risk of anencephaly, spina bifida, cleft lip with or without cleft palate (CLP), or cleft palate
61 -agonists were found for spina bifida, cleft lip, anal atresia, severe congenital heart defects in ge
62 aniofacial defects including bilateral cleft lip and palate and tongue agenesis, following the loss o
63 The proband presented with bilateral cleft lip and palate, malformed auricles, and bilateral ectrod
65 n saliva, and patients with the common cleft lip and palate have a higher prevalence of dental caries
66 ns or liver consumption would decrease cleft lip with or without cleft palate (CL +/- P) risk and tha
68 candidate genes for genetic disorders (cleft lip and palate, certain forms of cancer) or solute uptak
69 ing characteristic facial dysmorphism, cleft lip and/or palate, craniosynostosis, learning disability
71 he cellular mechanism demonstrated for cleft lip pathogenesis, we found that either SHH ligand additi
74 ed testes, hypospadias, hydrocephalus, cleft lip/palate, and clubfoot) was determined by physical exa
79 use of abnormal development (including cleft lip and/or palate, craniosynostosis and facial dysostose
82 three affected siblings with isolated cleft lip and palate, we discovered that they share a novel mi
84 ung adults who were born with isolated cleft lip only did not differ significantly from unaffected in
86 lateral choanal atresia, hearing loss, cleft lip and/or palate, and other craniofacial dysmorphisms.
87 lly treatable conditions (breast mass, cleft lip/palate, club foot, hernia or hydrocele [adult and pa
88 nout, expansion of the facial midline, cleft lip, extensive exencephaly, and microphthalmia or anopht
90 known candidate genes for nonsyndromic cleft lip and/or palate through genome-wide linkage analysis.
91 e genetic contribution to nonsyndromic cleft lip and/or palate through the analysis of family pedigre
92 icated in the etiology of nonsyndromic cleft lip with or without cleft palate (NSCL/P) in populations
101 es to the etiology and pathogenesis of cleft lip through antagonistic interactions with other gene re
102 (TGFA) polymorphisms with the risk of cleft lip with or without cleft palate (CL/P) or cleft palate
103 understanding the genetic etiology of cleft lip with or without cleft palate, relatively little is k
106 senting 14 specialties (ophthalmology, cleft lip/palate, multidisciplinary teams, orthopaedics, cardi
107 t surgical specialties (ophthalmology, cleft lip/palate, multidisciplinary teams, orthopaedics, cardi
109 cts, middle-ear defects, cleft palate, cleft lip, limb defects, limb-reduction defects, polydactyly,
111 ts (OFCs), which include non-syndromic cleft lip with or without cleft palate (CL/P), are among the m
119 Wnt9b mutations are associated with cleft lip and cleft palate in mice; however, the cause of thes
120 al outcome assessment in patients with cleft lip and for the rehabilitation of patients with facial n
121 ling pathway have been associated with cleft lip and palate in humans and mice, the mechanisms involv
124 rge multi-ethnic human population with cleft lip identified clusters of single-nucleotide polymorphis
125 e authors identified associations with cleft lip with cleft palate (aOR = 1.23) and anorectal atresia
127 is commonly found in individuals with cleft lip/palate (CL/P), we used four large cohorts to evaluat
129 o investigate if genes associated with cleft lip/palate were also associated with oral cancer, we gen
131 ith isolated cleft palate (ie, without cleft lip) had increased mortality (hazard ratio, 3.4; 95% CI,
134 me model is proposed as reference to compare lip movement during speech in similar population groups.
135 , seen in a mirror, spoke with corresponding lip movements, and for half of the participants this was
137 mined whether the three electrically coupled lip motoneurons C15/16/17 are controlled by the buccal C
144 ics of the macaque monkey vocal tract during lip-smacking (a rhythmic facial expression) versus chewi
145 mild systemic reaction to peanut experienced lip swelling, stomach cramping, and objective tiredness.
149 hic frequencies of lesions were as followed: lips and oral cavity (n = 46 [93%]) and pharynx and vest
150 xtract three-dimensional coordinate data for lip shape during four spoken words decomposed into seven
151 jectable with low viscosity may be ideal for lip enhancement wherein softness is required, whereas a
152 study was to develop an outcome measure for lip shape during speech using statistical shape analysis
153 both kiss initiators and kiss recipients for lip kissing, and took into consideration differences due
160 Irf6 cKO), bypassing the role of the gene in lip and palate morphogenesis and thus ensuring survival
161 We identified small yet consistent shifts in lip representation contralateral to the missing hand tow
162 ured the McGurk effect (in which incongruent lip-voice pairs evoke illusory phonemes), and also ident
163 tutive shell shape development and inducible lip thickening have evolved jointly to form an effective
164 e interactions (mutual gaze and intermittent lip-smacking) with human caregivers display increased so
165 and a clinical trial of a minimally invasive lip treatment in the United Kingdom and France (clinical
166 Stimulation of the nose, upper lip, lower lip, and chin caused a somatotopic lateral-to-medial, ip
169 with Van der Woude express pits on the lower lip that continuously or intermittently drain saliva, an
172 ween the nipple-areola complex and the lower lips, moves as a rigid body with the cycling motion of t
173 movement, then one hypothesis is that monkey lip-smacking versus chewing should also exhibit these di
174 ch communicative gesture in macaque monkeys, lip-smacking, has motor parallels with speech in its rhy
176 und that TMS-induced disruption of the motor lip representation modulated specifically the early audi
179 rded from 10 patients with clinically normal lips (mean [SD] age, 34.5 [6.1] years), 16 patients with
181 confocal microscopy (RCM) features of normal lips of different phototypes and to identify features th
185 macules (MAC) are the most frequent cause of lip pigmentation and sometimes difficult to differentiat
188 spectrometry and used previous estimates of lip product usage rates to determine daily oral intakes.
191 ls of taste buds including the epithelium of lips and olfactory epithelium, and ii) mechanosensory ce
192 ssociated angioedema (defined as swelling of lips, tongue, pharynx, or face during ACE inhibitor use
195 on the ear (RR, 4.67; 95% CI, 1.28-17.12) or lip (RR, 4.55; 95% CI, 1.41-14.69), invasion beyond subc
198 than repression and formation of the palate, lip, and characteristic folds of the closed Antirrhinum
200 g high-frequency vocalizations at the phonic lips, a constriction in the nasal passages just beneath
201 Groomers were also more likely to produce lip-smacks during face-to-face grooming where the visual
206 canonical variate discriminated the resting lip shape from articulation of the utterances and accoun
210 , indicating that VZ/SVZ-derived and rhombic lip-derived progenitor cells show differential requireme
212 the dorsal-most region of the caudal rhombic lip, gives rise to the cochlear and precerebellar nuclei
217 odelling of mutations in mouse lower rhombic lip progenitors that generate WNT-subgroup tumours ident
219 Wls-positive cells in the Math1-null rhombic lip indicates that Wls expression is independent of Math
220 interactions during the presence of Rhombic lip versus the presence of distinct internal granule lay
222 contains two germinative zones, the rhombic lip (RL) and the ventricular zone (VZ), which generate d
224 on of cerebellar cell types from the rhombic lip and its upregulation inhibits their production.
225 ved from neuronal progenitors of the rhombic lip and that cerebellar ectopia were derived from granul
227 e of spatial compartmentation in the rhombic lip and the interplay between Wls, Math1, and Pax6 in th
230 These findings suggest that the rhombic lip is dynamically patterned by the expression of Wls, M
231 between Wls, Math1, and Pax6 in the rhombic lip provides novel views of early cerebellar development
232 orsal interneurons that comprise the rhombic lip relay sensory information and coordinate motor outpu
233 he cells in the interior face of the rhombic lip throughout normal mouse cerebellar development.
234 ives rise to isthmic nuclei, and the rhombic lip, which generates deep cerebellar nuclei and granule
238 ain specification and generate upper rhombic lip derivatives on exposure to bone morphogenetic protei
239 ones, the ventricular zone and upper rhombic lip, which give rise to distinct cell types in the matur
240 ioning of fissures, whereas in upper rhombic lip-derived cells the genes are more important in regula
241 precerebellar nuclei originate from rhombic lips, the first analysis of neuronal migrations from the
242 ve knock-out of P/Q-type channels in rhombic-lip-derived neurons including the PF and MF pathways (qu
244 een oscillatory brain activity and speaker's lip movements and demonstrated significant entrainment i
246 nt a case of a 15-year-old boy with a severe lip abscess requiring incision and drainage and hospital
247 scales that measure appearance of the skin, lips, and facial rhytids (ie, overall, forehead, glabell
252 ed syllables were least likely to engage the lip sensorimotor area and they were least impaired by TM
254 ptical fibre probe is used to illuminate the lip and acquire fluorescence emission spectra in approxi
255 y cilia of the CNC-derived mesenchyme in the lip and palate region in mice and is a strong candidate
257 ing PDGF-C have been linked to clefts of the lip and/or palate in humans, and ablation of PDGF-C in 1
259 om the vermillion and/or mucosal part of the lip were recorded from 10 patients with clinically norma
261 onsive to the red spots in the callus of the lip, and PeMYB12 participated in the full pigmentation i
266 for whom lymphocytic foci per 4 mm(2) on the lip biopsies was either 0 (F = 0), <1 (F <1) or > 3 (F >
268 t of multiple articulators (for example, the lips, jaw, tongue and larynx) over rapid time scales.
270 and usually present with enlargement of the lips, tongue, nose, hands, and feet and are diagnosed by
271 sented with chronic verrucous papules on the lips, tongue, and buccal mucosa refractory to multiple e
277 cally the early auditory-cortex responses to lip-articulated speech sounds when they were attended.
279 s that include a prominent maxilla and upper lip that readily reveal the upper gingiva, widely spaced
280 s cNCC mesenchyme proliferation during upper lip morphogenesis, and that disruption of this sequence
284 tinoic acid is a critical regulator of upper lip and primary palate development in Xenopus laevis.
285 f IQR, P-value 0.0371), and wrinkle on upper lip (7.7% more wrinkle on upper lip per increase of IQR,
287 understand how retinoic acid regulates upper lip and palate morphogenesis we searched for genes downr
288 eyes, a narrow nasal bridge, a tented upper lip, a high palate, an open mouth, tightly adherent skin
289 r understand the complex nature of the upper lip and primary palate development which will lead to im
297 poral narrowing, broad nasal tip, thin upper lip, posteriorly rotated or low-set ears, and microretro
298 re-biased patch (MCP) located on the ventral lip of the posterior superior temporal sulcus (STS) in a
299 erium simum), a large African herbivore with lips specialized for grazing in open savannahs, relates
300 the ventilated patient who can mouth words, lip-reading interpretation offers an opportunity for com
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