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 One hundred pharyngeal and 100 rectal gonorrhea infections in 190 me

4 ssays for MG detection in urine samples, oro-pharyngeal and anal swabs.

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

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

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

8 tracing to test the embryonic origin of the pharyngeal and paired fin skeleton in the skate (Leucora

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

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

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

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

13 e reference method for the detection of both pharyngeal and rectal N. gonorrhoeae and C. trachomatis.

14 e reference method for the detection of both pharyngeal and rectal N. gonorrhoeae and C.trachomatis.

15 Pharyngeal and rectal Neisseria gonorrhoeae and Chlamydi

16 Pharyngeal and rectal Neisseriagonorrhoeae and Chlamydia

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

18 ance of assays to detect those infections in pharyngeal and rectal specimens to support regulatory su

19 Patient-collected pharyngeal and rectal swabs and urine were 92%, 96%, 96%

20 We collected pharyngeal and rectal swabs from participants.

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

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

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

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

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

26 NG/CT anal, pharyngeal, and urine (APU) samples from MSM attending t

27 suggest different combinations of anorectal, pharyngeal, and urogenital testing based on age, sex, an

28 ); APU samples every 6 months (S3); anal and pharyngeal (AP) samples every 6 months (S4); and AP samp

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

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

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

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

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

34 rch arteries with failure of the 3rd and 4th pharyngeal arch arteries to form correctly.

35 eractions during normal morphogenesis of the pharyngeal arch artery system.

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

37 echanisms underlying evolutionary changes in pharyngeal arch development, here we investigate embryos

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

39 s arise by E7.5 in the SHF and contribute to pharyngeal arch endothelium between E7.5 and E9.5.

40 these divergent patterns correlate with the pharyngeal arch expression of Pou3f3 orthologs.

41 l of cardiac progenitors present in anterior pharyngeal arch mesoderm at mid-gestation.

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

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

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

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

46 lar identity during development of the first pharyngeal arch.

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

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

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

50 e deleted genes, is expressed throughout the pharyngeal arches and is considered a key gene, when mut

51 ng with the developmental progression of the pharyngeal arches and show that experimentally altering

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

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

54 Consequently, SHF-derived ECs in the pharyngeal arches form a plexus of small blood vessels,

55 In most vertebrates, pharyngeal arches form in a stereotypic anterior-to-post

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

57 rlying targeting of vagus motor axons to the pharyngeal arches in zebrafish.

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 : (1) accumulation of SHF-derived ECs in the pharyngeal arches, (2) remodeling of the EC plexus in th

61 anterior embryonic structures, including the pharyngeal arches, heart, and anterior somites.

62 g dynamic contribution of SHF-derived ECs to pharyngeal arches, the remodeling of endothelial plexus

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

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

65 Met is required for vagus innervation of the pharyngeal arches.

66 y associated with blood vessels in anamniote pharyngeal arches.

67 mature derivatives from the first and second pharyngeal arches.

68 cells also failed to condense correctly into pharyngeal arches.

69 l progenitors, which contribute to posterior pharyngeal arches.

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

71 orhabditis elegans postembryonic gonadal and pharyngeal BMs.

72 Viral RNA was detectable in pharyngeal, bronchial, and colonic mucosa but not bile.

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

74 genomic expression analysis of the E2/E4/E5 pharyngeal cancer subtype is defined by activation of th

75 9%; melanoma, 0.5% and 0.6%; and oral cavity/pharyngeal cancer, 0.8% and 0.8%.

76 es in the gums and throat, and possibly oral pharyngeal cancer.

77 Oral and pharyngeal cancers combined were associated with loci at

78 Half of HPV positive cervical and pharyngeal cancers comprised a subtype with increase in

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

80 ticipants (n = 15/group) were intubated with pharyngeal catheters.

81 The gnathostome pharyngeal cavity functions in food transport and respir

82 connect to a population of cells inside the pharyngeal cavity that express periderm markers, yet do

83 This suggests that pharyngeal cholinergic motor neurons are normally rhythm

84 The site and severity of pharyngeal collapse combine to determine oral appliance

85 eses that oral appliance therapy (i) reduces pharyngeal collapsibility preferentially in patients wit

86 orly-located tongue and less-severe baseline pharyngeal collapsibility.

87 at occurs during sleep and thereby decreases pharyngeal collapsibility.

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

89 Further, it significantly suppresses GAS pharyngeal colonization in mice mucosal infection model.

90 erpreted as jaws situated within an expanded pharyngeal complex.

91 define a shallow network architecture of the pharyngeal connectome.

92 MS interval induced the greatest increase on pharyngeal cortical excitability (F(1,13) = 21.244; P <

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

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

95 l-aged children in Pittsburgh, Pennsylvania, pharyngeal cultures were obtained from children at 2-wee

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

97 Similar to skeletal postural muscles, pharyngeal dilator muscles responsible for maintaining a

98 Proper function of pharyngeal dilator muscles, including the genioglossus m

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

100 is orchestrated by signals dependent on the pharyngeal ECM microenvironment, extrinsic to the endoth

101 done using data from four studies involving pharyngeal electrical stimulation in acute stroke patien

102 ctively) and in response to an intervention, pharyngeal electrical stimulation, in a published meta-a

103 Pax9 is expressed in the pharyngeal endoderm and is downregulated in Tbx1 mutant

104 We conclude that in zebrafish the pharyngeal endoderm becomes overlain by cells with a per

105 lled signalling mechanism emanating from the pharyngeal endoderm is required for crucial tissue inter

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

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

108 of this Tbx1-Pax9 genetic interaction is the pharyngeal endoderm, therefore revealing that a Tbx1-Pax

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

110 dhere to and subsequently invade Detroit 562 pharyngeal epithelial cells.

111 bsequently cover the entire endoderm-derived pharyngeal epithelium [Rosa et al., 2019, Sci.

112 pithelial invasion and how this modifies the pharyngeal epithelium.

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

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

115 inical practice, particularly for rectal and pharyngeal exposure sites that can harbor asymptomatic i

116 on of upper airway (UA) obstruction based on pharyngeal factors is important for obstructive sleep ap

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

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

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

120 Pharyngeal GC infection was highly associated with recta

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

122 .9% were tested for urogenital GC, 65.9% for pharyngeal GC, 50.4% for rectal GC, 81.4% for urogenital

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

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

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

126 Pharyngeal gills are a fundamental feature of the verteb

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

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

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

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

131 th nucleic acid amplification test-diagnosed pharyngeal gonorrhea in a single-arm, unblinded clinical

132 have sex with men (MSM) with NAAT-diagnosed pharyngeal gonorrhea in a single-arm, unblinded clinical

133 cacy of gentamicin alone in the treatment of pharyngeal gonorrhea is uncertain.

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

135 point estimate for gentamicin's efficacy for pharyngeal gonorrhea.

136 More empirical data on pharyngeal gonorrhoea infections, and the role of transm

137 Subsets of cardiac and pharyngeal/head muscles share a common origin in the car

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

139 synthesis inhibitor)-dependent reduction in pharyngeal infection and increase in lifespan.

140 For participants with a pharyngeal infection, a greater proportion receiving cef

141 ock, which reduces early mortality caused by pharyngeal infection.

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

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

144 Pharyngeal jaw diversification is associated with the ex

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

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

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

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

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

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

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

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

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

154 Based on the changes in pharyngeal MEPs, the optimal preconditioned 1 Hz and 5 H

155 ates, multipotent progenitors located in the pharyngeal mesoderm form cardiomyocytes and branchiomeri

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

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

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

159 c outflow tract, right ventricle and atrium, pharyngeal mesoderm, peripheral neurons, and hindlimbs.

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

161 MS interval was most optimal for suppressing pharyngeal motor cortex (F(1,13) = 13.547; P = 0.003).

162 e for enhanced directional metaplasticity in pharyngeal motor cortex and new insights into its clinic

163 inducing functional metaplasticity in human pharyngeal motor cortex have been identified.

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

165 directional metaplastic properties in human pharyngeal motor cortex using preconditioned rTMS.

166 icipants received 10 min of 1 Hz rTMS to the pharyngeal motor cortex which elicited the largest PMEPs

167 s have investigated such mechanisms in human pharyngeal motor cortex.

168 Baseline pharyngeal motor evoked potentials (PMEPs) and swallowin

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

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

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

172 comparison to conventional measures such as pharyngeal Mp deoxyribonucleic acid (DNA) and serum anti

173 1 vs. 0.32), liver (2.77 vs. 1.69), and oral/pharyngeal mucosa (4.88 vs. 2.57) was significantly lowe

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

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

176 fication (TMA) assay performed on rectal and pharyngeal mucosal swabs.

177 piratory arousal threshold without impairing pharyngeal muscle activity to reduce OSA severity, with

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 influx and hypercontraction of the head and pharyngeal muscle cells, ultimately resulting in rapid n

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 ling maintains multipotency and promotes the pharyngeal muscle fate, whereas signal termination permi

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

185 forming first and second heart lineages and pharyngeal muscle precursors and characterize the molecu

186 soderm to distinct fate-restricted heart and pharyngeal muscle precursors.

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

188 s of airway pressure, zolpidem did not alter pharyngeal muscle responsiveness during natural sleep.

189 indings that showed paradoxical increases in pharyngeal muscle responsiveness during transient manipu

190 s in arousal threshold without any change in pharyngeal muscle responsiveness, zolpidem does not alte

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

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

193 mV, induced by BWM action potentials, and in pharyngeal muscle, measured in simultaneous optical and

194 e giant UNC-89 isoforms, dis-organization of pharyngeal muscle, small body size, and reduced muscle f

195 accessibility, which govern later heart vs. pharyngeal muscle-specific expression profiles, demonstr

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

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

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

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

200 eculate that the overall architecture of the pharyngeal nervous system may be reminiscent of the arch

201 n, we re-evaluate here the connectome of the pharyngeal nervous system, providing a novel and more de

202 likely sensory neurons and most, if not all, pharyngeal neurons also classify as motor neurons.

203 euron classes, we provide evidence that most pharyngeal neurons are also likely sensory neurons and m

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

205 Compared with the somatic nervous system, pharyngeal neurons both physically associate with a larg

206 The I2 pharyngeal neurons increase calcium in response to light

207 Contrasting the previous classification of pharyngeal neurons into distinct inter- and motor neuron

208 with the extensive cross-connectivity among pharyngeal neurons, which is more widespread than previo

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

210 suggests that the structure and severity of pharyngeal obstruction determine the phenotype of sleep

211 ng and different markers, we investigated if pharyngeal openings enable epithelial invasion and how t

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

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

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

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

216 ey had a diagnosis of uncomplicated genital, pharyngeal, or rectal gonorrhoea.

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

218 ure of chondrichthyan-like and plesiomorphic pharyngeal patterning in Ptomacanthus challenges the ide

219 ff at a UK teaching hospital using naso-/oro-pharyngeal PCR testing and immunoassays for IgG antibodi

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

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

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

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

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

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

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

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

228 also showed that healthspan measures such as pharyngeal pumping and tap-induced stimulated reversals

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

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

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

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

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

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

235 the nervous system and muscle in generating pharyngeal pumping.

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

237 Simultaneous esophageal and pharyngeal reconstruction by colopharyngoplasty allows r

238 = 0.67) CONCLUSIONS:: The need to associate pharyngeal reconstruction during esophageal reconstructi

239 When compared to esophagocoloplasty alone, pharyngeal reconstruction had a significant negative imp

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

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

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

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

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

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

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

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

248 We compared clinician-taken rectal and pharyngeal samples with self-taken samples for diagnosti

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

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

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

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

253 If urogenital, plus rectal and pharyngeal, samples are analysed the diagnostic cost is

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

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

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

257 es and mostly from respiratory tract and oro-pharyngeal sites, where Redondoviridae was the second mo

258 ring sleep, and surgical modification of the pharyngeal soft tissues or facial skeleton to enlarge th

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

260 dentified the small GTPase RAP-3 (Rap1) as a pharyngeal-specific PAT-2/PAT-3 activator that modulates

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

262 ally transmitted disease clinic provided 506 pharyngeal specimens and 410 rectal specimens with valid

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

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

265 High viral RNA loads in nasal and pharyngeal specimens were associated with fatal outcome.

266 We collected pharyngeal specimens, cultured Neisseria species, and me

267 and HRs of the combined outcome laryngeal or pharyngeal squamous cell carcinoma (n = 39) were decreas

268 crease over time after surgery was found for pharyngeal squamous cell carcinoma.

269 er antireflux surgery prevents laryngeal and pharyngeal squamous cell carcinoma.

270 seems to increase the risk of laryngeal and pharyngeal squamous cell carcinoma.

271 squamous cell carcinoma and possibly also of pharyngeal squamous cell carcinoma.

272 as well as obstruction as a result of other pharyngeal structures (e.g. epiglottis).

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

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

275 Pharyngeal swab specimens were collected, and Neisseria

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

277 ine sample or urethral swab, rectal swab, or pharyngeal swab, respectively, during PrEP care.

278 offered the opportunity to collect their own pharyngeal swab.

279 respiratory syndrome coronavirus 2 at nasal-pharyngeal swabbing, negative chest CT findings, and inc

280 was selected for vaccination with 4CMenB and pharyngeal swabbing.

281 Furthermore, a high proportion of the pharyngeal swabs (78.3%) yielded a Factor H-Binding Prot

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

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

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

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 e chain reaction (RT-PCR) assay of nasal and pharyngeal swabs.

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

291 e that the earliest interactions to generate pharyngeal teeth encompass those between different epith

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

293 ve evidence that the epithelial component of pharyngeal teeth in zebrafish (the enamel organ) is deri

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

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

296 For MSMTW, two site anorectal and pharyngeal testing versus single site anorectal testing

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

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

299 Pharyngeal tooth number, diversity and the frequency of

300 Pharyngeal virus shedding was very high during the first

301 ted as follows: oral rinse, tongue base, and pharyngeal wall brushes, then tonsil tissue (tonsillecto