ライフサイエンスコーパス: pharyngeal

1 240 participants had serious adverse events (pharyngeal abscess and keratitis), which were not consid

2 resence of its food (bacteria) by regulating pharyngeal activity (pumping).

3 2 randomized studies; and laryngeal mask and pharyngeal administration, in 1 observational study each

4 of the tongue that dilates and stiffens the pharyngeal airway.

5 1; P <0.05), but did not significantly alter pharyngeal anatomy/collapsibility, upper-airway gain, or

6 One hundred pharyngeal and 100 rectal gonorrhea infections in 190 me

7 on; gemifloxacin/azithromycin cured 15 of 15 pharyngeal and 5 of 5 rectal infections.

8 sel progenitors to the interface between the pharyngeal and cardiac mesoderm, identify the transcript

9 y laser ablation of connectivity between the pharyngeal and central nervous system indicating signals

10 plication of the pan-IAV RT FRET-PCR to oral-pharyngeal and cloacal swab specimens collected from hea

11 Pharyngeal and food specimens were cultured for GAS by t

12 In severe cases, it extends to pharyngeal and laryngeal structures.

13 ted in 13.7% of urine specimens; addition of pharyngeal and rectal collections to the analysis result

14 Pharyngeal and rectal gonorrhea DNA persisted in 8% of m

15 eria gonorrhoeae DNA following treatment for pharyngeal and rectal gonorrhea.

16 Among 200 baseline pharyngeal and rectal isolates, there were 10 with ceftr

17 a gonorrhoeae and Chlamydia trachomatis from pharyngeal and rectal specimens among patients with a hi

18 Nasal/pharyngeal and rectal swabs were collected from HRSC mem

19 second heart field (SHF) progenitors in the pharyngeal and splanchnic mesoderm (SpM), but how these

20 al magnetic stimulation (TMS) to co-localise pharyngeal and thenar representation in the cortex and c

21 US case-control studies (1981-2006) of oral, pharyngeal, and laryngeal cancers (6,772 cases and 8,375

22 objective of the study was to compare nasal, pharyngeal, and sputum eosinophil peroxidase (EPX) level

23 ay proved to be a superior option as topical pharyngeal anesthetic before an UGE.

24 e effect of a bupivacaine lozenge as topical pharyngeal anesthetic compared with standard treatment w

25 mutations of TBX1 cause malformations in the pharyngeal apparatus and cardiac outflow tract.

26 lossus muscles that are derived from the 4th pharyngeal arch (PA); however, the tensor veli palatini,

27 elop in the maxillary and mandibular buds of pharyngeal arch 1 (PA1).

28 The mandibular portion of pharyngeal arch 1 is patterned dorsally by Jagged-Notch

29 arily sequestered in the mesodermal cores of pharyngeal arch 2 (PA2), where they downregulate nkx2.5

30 The pharyngeal arch arteries (PAAs) are a series of paired e

31 to join the OFT, instead contributing to the pharyngeal arch arteries (PAAs), and second, a loss of f

32 Development of the cerebral vessels, pharyngeal arch arteries (PAAs). and cardiac outflow tra

33 Growth and remodeling of the pharyngeal arch arteries are vital for the development o

34 ion in outflow tract size and loss of caudal pharyngeal arch arteries.

35 onsible for craniofacial skeleton formation, pharyngeal arch artery remodeling and cardiac outflow tr

36 holaminergic cells associated with zebrafish pharyngeal arch blood vessels, and propose a new model f

37 ts exhibit a non-cell-autonomous increase in pharyngeal arch cell death accompanied by alterations in

38 defect of cNCCs, resulting in abnormal chick pharyngeal arch development.

39 r, our data indicate that the extreme distal pharyngeal arch expression domain of Hand1 defines a nov

40 h is a major source of myocardium and of the pharyngeal arch mesoderm that gives rise to skeletal mus

41 e performed gene profiling of microdissected pharyngeal arch one (PA1) from Tbx1(+/+) and Tbx1(-/-) e

42 d in the ectopic expression of Sema3c in the pharyngeal arch region.

43 In the first pharyngeal arch we observed a shift in the expression of

44 g within the mandibular portion of the first pharyngeal arch, from which the lower jaw arises.

45 in dlx1/2 and emx2 expression in the second pharyngeal arch, presaging the differentiation of the re

46 nting with bi- or unilateral OME, the fourth pharyngeal arch-derived levator veli palatini muscles we

47 lar identity during development of the first pharyngeal arch.

48 tation on cells derived from mouse embryonic pharyngeal arch.

49 logue Numblike (Nbl) depletes CPCs in second pharyngeal arches (PA2s) and is associated with an atrop

50 (crNCCs) migrate from the neural tube to the pharyngeal arches (PAs) of the developing embryo and, su

51 r beta1 integrin were able to migrate to the pharyngeal arches and associate with endothelial lined a

52 embryo and distribute to the thoracic wall, pharyngeal arches and heart.

53 es of reiterated structures that segment the pharyngeal arches and help pattern the vertebrate face.

54 we show that morphogenetic movements of the pharyngeal arches and patterning of the neural crest req

55 ived cells to control the remodelling of the pharyngeal arches and the septation of the heart and out

56 in neural crest-derived cells (NCCs) of the pharyngeal arches display a malformed stapes.

57 f Jagged1-Notch2 signaling in patterning the pharyngeal arches from fish to mouse to man, despite the

58 middle ear bones derived from the equivalent pharyngeal arches of mammals.

59 skeletal elements derived from the first two pharyngeal arches of zebrafish.

60 d halting in their migration midway from the pharyngeal arches to the conotruncal cushions.

61 CaV1.2 is expressed in the first and second pharyngeal arches within the subset of cells that give r

62 wed strong expression in the developing eye, pharyngeal arches, and limb bud.

63 including immobility, small eyes, diminished pharyngeal arches, curved body axis, edema, underdevelop

64 e from embryonic neural folds and migrate to pharyngeal arches, which give rise to most mid-facial st

65 cells also failed to condense correctly into pharyngeal arches.

66 ation and proliferation within the posterior pharyngeal arches.

67 housands of genes in distinct regions of the pharyngeal arches.

68 of condensing neural crest cells within the pharyngeal arches.

69 expressed early in the developing kidney and pharyngeal arches.

70 rning of neural crest cells (NCC) within the pharyngeal arches.

71 y associated with blood vessels in anamniote pharyngeal arches.

72 mature derivatives from the first and second pharyngeal arches.

73 hypoplastic or aplastic at the conclusion of pharyngeal artery formation and compared these against t

74 ugh a catheter placed in the right ascending pharyngeal artery.

75 ek-old wild-type Balb/c mice were exposed by pharyngeal aspiration nine times over 3 weeks to DEP at

76 Third, light causes a novel pharyngeal behavior, reversal of flow or "spitting," whi

77 was associated with a 49% lower risk of oral/pharyngeal cancer death relative to no/occasional coffee

78 me-wide association study of oral cavity and pharyngeal cancer in 6,034 cases and 6,585 controls from

79 nated coffee, and tea intake with fatal oral/pharyngeal cancer in the Cancer Prevention Study II, a p

80 ee intake was inversely associated with oral/pharyngeal cancer mortality.

81 r free at enrollment, 868 deaths due to oral/pharyngeal cancer occurred during 26 years of follow-up.

82 9%; melanoma, 0.5% and 0.6%; and oral cavity/pharyngeal cancer, 0.8% and 0.8%.

83 take is associated with reduced risk of oral/pharyngeal cancer.

84 Oral and pharyngeal cancers combined were associated with loci at

85 anogenital cancers, as well as both oral and pharyngeal cancers.

86 Conventional methods for detecting pharyngeal carriage of Neisseria meningitidis are comple

87 Thus, GAS M1 protein-Fg binding reduces GAS pharyngeal cell adherence and colonization in a fashion

88 ng and relieved its inhibitory effect on GAS pharyngeal cell adherence.

89 ed more early biofilms on lung cells than on pharyngeal cells.

90 S) in causing programmed cell death of human pharyngeal cells.

91 This suggests that pharyngeal cholinergic motor neurons are normally rhythm

92 .3 +/- 4.3 l min(-1); P < 0.05) and improved pharyngeal collapsibility (mean +/- s.d. 3.4 +/- 1.4 l m

93 Pharyngeal collapsibility was quantified as the ventilat

94 at occurs during sleep and thereby decreases pharyngeal collapsibility.

95 of 85.7% of males with T. vaginalis-positive pharyngeal collections indicated strictly heterosexual p

96 Inverse associations were observed on oral, pharyngeal, colon, liver, prostate, endometrial cancer a

97 lipid bilayers and inhibit the physiological pharyngeal contractions in Caenorhabditis elegans, a new

98 e transcranial magnetic stimulation over the pharyngeal cortex in 12 healthy individuals.

99 Ten minutes of PAS to the unlesioned pharyngeal cortex reversed (bilaterally) the cortical su

100 rectal GC, 8.4% for urogenital CT, 2.9% for pharyngeal CT, and 14.1% for rectal CT.

101 ectal GC, 81.4% for urogenital CT, 31.7% for pharyngeal CT, and 45.9% for rectal CT.

102 eeth during evolution but retain a posterior pharyngeal dentition that requires retinoic acid (RA) ce

103 All T. vaginalis pharyngeal detections were confirmed by TMA-based altern

104 -1 contribute to the regulation of pha-1 and pharyngeal development through the Zn-finger protein SUP

105 hat are distinct from its role in regulating pharyngeal development with SUP-35.

106 of the E2 enzyme UBC-18, which functions in pharyngeal development.

107 triggers upper airway collapse is decreased pharyngeal dilator muscle activity during sleep.

108 he number of swallows evoked by upper airway/pharyngeal distensions was not significantly reduced by

109 y by modifications downstream of a conversed pharyngeal DV patterning program.

110 e LC concentration and results in persistent pharyngeal dysfunction and in a significant reduction of

111 o promote plasticity by combining peripheral pharyngeal (electrical) with cortical stimulation.

112 n mice to dissect the roles of Nkx2.5 in the pharyngeal endoderm and mesoderm.

113 biting endothelin 1 (Edn1) expression in the pharyngeal endoderm of the dorsal arch, thus preventing

114 ng the ciliary band, in the apical plate and pharyngeal endoderm, and 4-6 serotonergic neurons that a

115 velopment, including the second heart field, pharyngeal endoderm, outflow tract and atrioventricular

116 heart field pharyngeal mesoderm, as well as pharyngeal endodermal cells underlying the second heart

117 valuated in assays using monolayers of human pharyngeal epithelial and umbilical vein endothelial cel

118 significantly, corynebacterial adherence to pharyngeal epithelial cells was strictly correlated with

119 are known to mediate bacterial adherence to pharyngeal epithelial cells.

120 l step in GAS infection-interaction with the pharyngeal epithelium.

121 on in a given patient between both nasal and pharyngeal EPX levels and the eosinophil percentage of i

122 s correlation coefficients for nasal EPX and pharyngeal EPX levels compared to induced sputum eosinop

123 ory connections between the conserved cardio-pharyngeal factor Tbx1/10 and muscle determinant COE, as

124 n by changes developmentally downstream from pharyngeal FGF signaling.

125 beta (IFNbeta) and IL-33 levels in the nasal pharyngeal fluids (NPF).

126 All invasive and pharyngeal GAS isolates had an identical mutation in a g

127 as at least 5.7% in rectal GC, rectal CT, or pharyngeal GC at their last test.

128 Pharyngeal GC infection was highly associated with recta

129 tested positive for urogenital GC, 7.9% for pharyngeal GC, 10.2% for rectal GC, 8.4% for urogenital

130 .9% were tested for urogenital GC, 65.9% for pharyngeal GC, 50.4% for rectal GC, 81.4% for urogenital

131 ened for urogenital GC/CT, rectal GC/CT, and pharyngeal GC.

132 netic features, along with robust support of pharyngeal gill slits as a shared deuterostome character

133 ng plesiomorphies of Ambulacraria, including pharyngeal gill slits, a single axocoel, and paired hydr

134 which is associated with the development of pharyngeal 'gill' slits, the foremost morphological inno

135 Pharyngeal gills are a fundamental feature of the verteb

136 mes and gnathostomes, and a single origin of pharyngeal gills prior to the divergence of these two an

137 openings that subsequently were co-opted as pharyngeal gills.

138 biotrophic parasite secretes effectors from pharyngeal glands, some of which were acquired by horizo

139 In addition, 8 participants had positive pharyngeal gonococcal cultures, and 4 had positive recta

140 the proportion of repeat positive tests for pharyngeal gonorrhea 7-180 days following treatment amon

141 spective analysis of patients diagnosed with pharyngeal gonorrhea during 1993-2011, at a sexually tra

142 isease Control and Prevention guidelines for pharyngeal gonorrhea treatment recommend dual therapy wi

143 A total of 1440 cases of pharyngeal gonorrhea were diagnosed during the study per

144 For pharyngeal gonorrhea, positivity of N. gonorrhoeae DNA o

145 ftriaxone-based regimens in the treatment of pharyngeal gonorrhea.

146 e have not been effective methods to reverse pharyngeal hypotonia pharmacologically in sleeping human

147 Gentamicin/azithromycin cured 10 of 10 pharyngeal infections and 1 of 1 rectal infection; gemif

148 zed by craniofacial anomalies including velo-pharyngeal insufficiency, facial muscle hypotonia and fe

149 ristaltic contractions of the muscles in the pharyngeal isthmus and function systemically to regulate

150 and quantified shape variation of the lower pharyngeal jaw (LPJ) using geometric morphometrics.

151 Pharyngeal jaw diversification is associated with the ex

152 two eco-morphological traits: body shape and pharyngeal jaw morphology.

153 Here, I test the hypothesis that pharyngeal jaw shape and tooth morphology are adaptive i

154 We present evidence that the modified pharyngeal jaws of cichlid fishes and several marine fis

155 he M1 protein reduced GAS adherence to human pharyngeal keratinocytes by 2-fold, and this difference

156 Conjunctival and oral/pharyngeal lesions with subepithelial splitting were fou

157 es of early CWD pathogenesis have implicated pharyngeal lymphoid tissue as the earliest sites of prio

158 Increased size of the pharyngeal lymphoid tissue, rather than enlargement of t

159 ths of at least two cells-the sisters of the pharyngeal M4 motor neuron and the AQR sensory neuron-by

160 In CeMM medium, signalling from the pharyngeal MC neurons and body wall muscles slows larval

161 Respiratory diphtheria with the absence of a pharyngeal membrane was the most common presentation (50

162 Only 10 Hz cerebellar rTMS increased cortico-pharyngeal MEP amplitudes (mean bilateral increase 52%,

163 smooth muscle cells, while proliferation of pharyngeal mesoderm and differentiation of mesodermal de

164 ory network with cardiac progenitor cells in pharyngeal mesoderm of the second heart field (SHF) and

165 In vertebrates, pluripotent pharyngeal mesoderm progenitors produce the cardiac prec

166 rect contact with myoblasts derived from the pharyngeal mesoderm, and Dlx5 disruption leads to altere

167 early first heart field, second heart field pharyngeal mesoderm, as well as pharyngeal endodermal ce

168 cells that have expressed markers of cranial pharyngeal mesoderm, whereas other muscles in the neck a

169 Inhibition of pharyngeal motoneurons accompanies REM sleep and is a ca

170 Thus, tDCS to the contralateral pharyngeal motor cortex reverses the neurophysiological

171 nd produce short-term enhancement of cortico-pharyngeal motor evoked potentials, suggesting the feasi

172 against it as a major mechanism of REM sleep pharyngeal motor inhibition.

173 te growth in Celegans TRH-like peptides from pharyngeal motor neurons are required for normal body si

174 the major cause of REM sleep inhibition at a pharyngeal motor pool critical for effective breathing.

175 th hemispheres by intraluminal recordings of pharyngeal motor-evoked responses (PMEPs) to single-puls

176 The majority of lesions were found in the pharyngeal mucosal space (n=16) with squamous cell carci

177 ancy arising from the superior aspect of the pharyngeal mucosal space, associated with latent Epstein

178 ody size, and knockdown of their receptor in pharyngeal muscle cells reduces growth.

179 successfully profiled proteins expressed in pharyngeal muscle cells, and in the process, identified

180 asic ontogenetic motif underlies cardiac and pharyngeal muscle development and evolution in chordates

181 quiescence during DTQ results from a loss of pharyngeal muscle excitability, whereas feeding quiescen

182 lier/OLF/EBF) orchestrates the transition to pharyngeal muscle fate both by promoting an MRF-associat

183 agonism underlies a fundamental heart versus pharyngeal muscle fate choice that occurs in a conserved

184 shes pumping, and optogenetic stimulation of pharyngeal muscle in these animals causes abnormal contr

185 esult in segregation of larval, cardiac, and pharyngeal muscle progenitors.

186 olecular mechanisms that govern heart versus pharyngeal muscle specification within this lineage rema

187 rm an ancient conserved regulatory state for pharyngeal muscle specification, whereas their regulator

188 nitors are primed to activate both heart and pharyngeal muscle transcriptional programs, which progre

189 s, intestinal epithelial cells, neurons, and pharyngeal muscle) or state-selective (heat-shock) promo

190 ated cholinergic transmission from MC to the pharyngeal muscles by activating the Gsalpha signaling p

191 Mitoflash activity in Caenorhabditis elegans pharyngeal muscles peaked on adult day 3 during active r

192 essential for development of the ABa-derived pharyngeal muscles, specification of neural cell fate in

193 le precursors that form most of the juvenile pharyngeal muscles.

194 genitors of the second heart field (SHF) and pharyngeal muscles.

195 y activates neurotransmission from M4 to the pharyngeal muscles.

196 been shown to directly evoke responses from pharyngeal musculature and produce short-term enhancemen

197 eatment failure, involving urethral (n = 4), pharyngeal (n = 2), and rectal (n = 3) sites.

198 pine, while hyoid elevation was predicted by pharyngeal neck length and initial hyoid distance from t

199 llowing were examined for relationships with pharyngeal neck length, and initial hyo-laryngeal positi

200 released acetylcholine, and suggest that the pharyngeal nervous system entrains contraction rate and

201 limited coexpression, and only a fraction of pharyngeal neurons are labeled.

202 mbryogenesis, and amphid sensory neurons and pharyngeal neurons in adults.

203 The I2 pharyngeal neurons increase calcium in response to light

204 eristics of neuromuscular disorders, such as pharyngeal neuropathy or weakness, macroglossia, bulbar

205 fts into the neck and increases Rph, because pharyngeal obstruction causes OSA.

206 uid shift could facilitate OSA if it induces pharyngeal obstruction, but could also facilitate CSA if

207 he animals (169/1,839) or 6.3% of their oral-pharyngeal or cloacal swabs (233/3,678) were positive fo

208 Men who had sex with men diagnosed with pharyngeal or rectal gonorrhea underwent swabbing from t

209 We estimated the frequency and positivity of pharyngeal or urine specimens tested for GC and CT on th

210 the diagnostic workup of patients with oral, pharyngeal, or laryngeal cancer.

211 an inverted body-wall musculature or a novel pharyngeal organ.

212 e thymus and parathyroids develop from third pharyngeal pouch (3rd pp) endoderm.

213 a shared endodermal primordium in the third pharyngeal pouch (3rd pp).

214 shown that the Hoxa3 null mutant lacks third pharyngeal pouch derivatives, the thymus and parathyroid

215 e cell type-specific roles of Hoxa3 in third pharyngeal pouch development, we analyzed tissue-specifi

216 ltimobranchial body epithelium emerging from pharyngeal pouch endoderm in early organogenesis, differ

217 erlying ectoderm, core paraxial mesoderm and pharyngeal pouch endoderm of the mandibular arch as well

218 ling: an early phase during which FGFs drive pharyngeal pouch formation, and a later phase when they

219 type is likely to be secondary to defects in pharyngeal pouch formation.

220 development in jawed vertebrates, including pharyngeal pouch morphogenesis, patterning of the oral s

221 re, Hoxa3 was required for survival of third pharyngeal pouch-derived organs, but expression in eithe

222 The pharyngeal pouches are a segmental series of epithelial

223 vertebrate head, endodermal branches, called pharyngeal pouches, form through the transient stratific

224 which direct Eya1 expression to the somites, pharyngeal pouches, the preplacodal ectoderm (the common

225 The pharyngeal pouches, which form by budding of the foregut

226 omplex, and expression has been described in pharyngeal precursors and body wall muscles during embry

227 that occurs in a conserved lineage of cardio-pharyngeal progenitors.

228 where disruption of the stronger (dominant) pharyngeal projection alters swallowing neurophysiology

229 1 Hz rTMS pre-conditioning to the strongest pharyngeal projection.

230 egans requires two distinct feeding motions, pharyngeal pumping and isthmus peristalsis.

231 We examined pharyngeal pumping and observed that clozapine-induced i

232 lin/IGF-1 signaling (IIS) in the recovery of pharyngeal pumping during starvation.

233 IIS are required to maintain high levels of pharyngeal pumping during starvation.

234 In C. elegans, pharyngeal pumping is regulated by the presence of bacte

235 Our data demonstrate that the pharyngeal pumping of C elegans is significantly and sel

236 ficient for TRH signaling have no defects in pharyngeal pumping or isthmus peristalsis rates, but the

237 0) phenotypes, including developmental rate, pharyngeal pumping rate, brood size, body movement, acti

238 bserved that clozapine-induced inhibition of pharyngeal pumping requires sms-1, a finding that may ex

239 nes on five behaviors modulated during sleep-pharyngeal pumping, defecation, locomotion, head movemen

240 hspan and muscle health, including increased pharyngeal pumping, swimming movement, and reduced perce

241 the nervous system and muscle in generating pharyngeal pumping.

242 nce interval [CI]: 0.91-0.97 P < 0.0001) and pharyngeal reconstruction (OR: 0.05; CI: 0.02-0.13, P <

243 Simultaneous esophageal and pharyngeal reconstruction by colopharyngoplasty allows r

244 = 0.67) CONCLUSIONS:: The need to associate pharyngeal reconstruction during esophageal reconstructi

245 Triple-site testing (using pharyngeal, rectal, and urethral/first-void urine sample

246 abs were taken to form a pooled sample (PS) (pharyngeal, rectal, and urine specimens).

247 omites, but mainly form from mesoderm in the pharyngeal region.

248 l crest cell (NCC)-derived structures in the pharyngeal region.

249 al progenitors and for Fgf8 signaling in the pharyngeal region.

250 le SAT serotypes for extended periods in the pharyngeal region.

251 Pharyngeal responses to HGNS were characterized by the c

252 Pharyngeal samples (n = 300) were collected from pediatr

253 trachomatis and N. gonorrhoeae in rectal and pharyngeal samples from 224 men and 175 women reporting

254 tening Lemierre's syndrome, and screening of pharyngeal samples may be warranted for its early detect

255 atis was detected from 59 rectal swabs and 8 pharyngeal samples, with 97.7% and 99.5% agreement betwe

256 norrhoeae was detected from 30 rectal and 40 pharyngeal samples, with 99.5% and 97.5% agreement betwe

257 n Aptima, but with more false positives from pharyngeal samples.

258 while both systems were 100% sensitive from pharyngeal samples.

259 is linked to the aspiration of contaminated pharyngeal secretions around the endotracheal tube.

260 in barx1 mutant animals are present in every pharyngeal segment, and are associated with disrupted at

261 The fly pharyngeal sense organs lie at the transition between ex

262 Together, our data demonstrate that pharyngeal sense organs play an important role in direct

263 f the palatal skeleton and hypoplasia of the pharyngeal skeleton.

264 ae and Chlamydia trachomatis from rectal and pharyngeal sources.

265 sources among Neotropical cichlids such that pharyngeal specialization has increased access to otherw

266 ytic groups C/G using rapid antigen-negative pharyngeal specimens (n = 161).

267 ters were managed by collection of urine and pharyngeal specimens and 19.1% by the addition of a thir

268 ar diagnostic evidence of influenza virus in pharyngeal specimens collected during clinical illness.

269 On that date, 86.5% had either urine or pharyngeal specimens collected, and 56.1% had both speci

270 Rapid accurate detection of GAS in pharyngeal specimens from individuals suffering from pha

271 A total of 38.1% of T. vaginalis-positive pharyngeal specimens were derived from symptomatic patie

272 respectively) than of other STI agents, 858 pharyngeal specimens yielded a 2.9% T. vaginalis detecti

273 EPX levels measured in the nasal and pharyngeal swab samples derived from the same patients w

274 ds in the Kosi River area provided stool and pharyngeal swab samples that were tested for polioviruse

275 From pharyngeal swab samples, Xpert was 98% sensitive (95% CI

276 Pharyngeal swab specimens were collected, and Neisseria

277 During this period, 58 103 FRI pharyngeal swab specimens were studied, yielding 37 048

278 se-dependent amplification assay using 1,192 pharyngeal swab specimens.

279 offered the opportunity to collect their own pharyngeal swab.

280 cted) and health care worker (HCW)-collected pharyngeal swabs for detection of GAS by PCR.

281 ocess employing patient- or parent-collected pharyngeal swabs for group A Streptococcus (GAS) testing

282 Self-collected pharyngeal swabs provide a reliable alternative to HCW c

283 ificity of 99.6% for the detection of GAS in pharyngeal swabs using the illumigene assay.

284 A total of 796 pharyngeal swabs were collected at three separate clinic

285 Three pharyngeal swabs were collected from 999 pupils aged 10

286 Deep pharyngeal swabs were collected on days 3, 14, 28, and 3

287 Pharyngeal swabs were performed on attendees, household

288 Here we investigate the function of pharyngeal sweet gustatory receptor neurons, demonstrati

289 ion in the legs and labial palps have intact pharyngeal sweet taste, which is both necessary and suff

290 FCs, 63.1% were symptom free; excluding oral-pharyngeal symptoms, 95.2% were symptom free.

291 a distinct disorder, usually mild, with oral/pharyngeal symptoms, in the context of hay fever or poll

292 Using the C. elegans pharyngeal system as a paradigm, we report a previously

293 mble the sclerotized circumoral elements and pharyngeal teeth expressed in tardigrades, stem-group eu

294 The radial elements and pharyngeal teeth resemble the sclerotized circumoral ele

295 ntition of fish species that retain anterior pharyngeal teeth such as medaka but that medaka do not e

296 dramatic anterior expansion of the number of pharyngeal teeth that later form and shifts anteriorly t

297 have both convergently evolved more ventral pharyngeal teeth through heritable genetic changes.

298 al lymph node, nasopharyngeal lymph node and pharyngeal tonsil collected at the peak of clinical dise

299 olved an approximate twofold gain in ventral pharyngeal tooth number compared with their ancestral ma

300 Pharyngeal tooth number, diversity and the frequency of