ライフサイエンスコーパス: tracheal

1 ckening, inflammatory small airways disease, tracheal abnormalities, interstitial lung abnormalities,

2 bronchiectasis, airway wall thickening, and tracheal abnormalities.

3 de generation and lung pathology after intra-tracheal administration of bleomycin to WT and STC1 Tg m

4 rom aspiration associated with laryngeal and tracheal afferent nerve activation.

5 VEGF-C overexpression in tracheal allografts induced epithelial activation, neutr

6 After 28 days, luminal obliteration of tracheal allografts was reduced from 89%+/-21% in untrea

7 e, obliterative airway disease (OAD)] in rat tracheal allografts.

8 me quantitative polymerase chain reaction in tracheal and amniotic fluid of CDH patients undergoing F

9 al diaphragmatic hernia (CDH) and changes in tracheal and amniotic fluid of fetuses undergoing fetosc

10 not have established place in diagnostics of tracheal and bronchi disorders and its potential has not

11 We took paired tracheal and cloacal swabs and fresh feces samples.

12 contrast to some animal models of AHR, human tracheal and main bronchial smooth muscle contractility

13 Serum, tracheal, and cloacal swabs were randomly collected from

14 Main bronchi and tracheal ASM were significantly hyposensitive in subject

15 In human preterm infants, tracheal aspirate Clec9a expression positively correlate

16 To this end, we analyzed tracheal aspirate samples from infant patients suffering

17 rated (n = 438) or induced sputum (n = 128), tracheal aspirates (n = 71), bronchoalveolar lavage flui

18 The genome yield from tracheal aspirates and bronchoalveolar lavage samples we

19 Tracheal aspirates from premature human infants were col

20 ice, Escherichia coli lipopolysaccharide, or tracheal aspirates from preterm infants exposed to chori

21 The IL1beta:IL1ra ratio in tracheal aspirates from preterm infants with respiratory

22 Bronchoalveolar lavage samples and tracheal aspirates had significantly higher genome fract

23 Tracheal aspirates had viral loads similar to those in b

24 Tracheal aspirates yielded significantly higher MERS-CoV

25 were nasopharyngeal swab specimens, 30 were tracheal aspirates, and 3 were bronchoalveolar lavage sp

26 one showing laryngeal atresia and the other, tracheal atresia.

27 out of the niche, tracking along a subset of tracheal branches destined for destruction.

28 nsion mutants, unicellular and intracellular tracheal branches develop bubble-like cysts with enlarge

29 Like other tracheal branching events, invasion requires the Branchl

30 of models, including border cell migration, tracheal branching, blood vessel sprouting, and the migr

31 locked HKU1 virus infection of primary human tracheal-bronchial epithelial (HTBE) cells.

32 ween 1980 and 2014, including 5656423 due to tracheal, bronchus, and lung cancer; 2484476 due to colo

33 gallbladder and biliary; pancreatic; larynx; tracheal, bronchus, and lung; malignant skin melanoma; n

34 ges, meniscus, intervertebral disc, rib, and tracheal cartilages on samples from 5-6 different indivi

35 All vATPase-deficient tracheal cells had reduced apical domains and terminal c

36 In tracheal cells of the freeze-tolerant goldenrod gall fly

37 apical ECM (aECM) and the apical F-actin in tracheal cells.

38 iary rootlets of multiciliated ependymal and tracheal cells.

39 he calcineurin/NFAT signaling pathway during tracheal chondrogenesis.

40 gated Ca(2+) channel Cav3.2 is essential for tracheal chondrogenesis.

41 superior to conventional cuffs in preventing tracheal colonization and VAP.

42 Cumulative tracheal colonization greater than 10(3) cfu/ml at Day 2

43 prophylaxis, subglottic secretion drainage, tracheal cuff monitoring).

44 Tracheal cytotoxin (TCT), a monomer of DAP-type peptidog

45 to Gram-negative bacteria through sensing of tracheal cytotoxin (TCT), whereas PGRP-LCy may have a mi

46 etect at least a 30% reduction in minor axis tracheal diameter from inspiration to end-expiration.

47 This ferret tracheal differentiated primary epithelial cell culture

48 In this study, we developed a ferret tracheal differentiated primary epithelial cell culture

49 vivo models, which used cell lines and mouse tracheal EC.

50 gnificant increase in neutrophil tracking in tracheal epithelia of the treatment calves compared to c

51 th satellite proteins in human multiciliated tracheal epithelia, and its loss inhibits motile cilioge

52 inked receptor to be able to attach to human tracheal epithelial and alveolar cells.

53 Using tracheal epithelial cell cultures, we show that enhanced

54 Human tracheal epithelial cells (HTEpC) were cultured with IL-

55 utophagy in vivo and in differentiated mouse tracheal epithelial cells (MTECs).

56 ladesh, and HeV were determined in bronchial/tracheal epithelial cells (NHBE) and small airway epithe

57 pregulation of cytokines and chemokines from tracheal epithelial cells (TECs) in vitro and tracheal t

58 interaction of M. gallisepticum with chicken tracheal epithelial cells (TECs) mediated the upregulati

59 nt in many lung cell lines and primary human tracheal epithelial cells but is absent from intestinal

60 We recently demonstrated that tracheal epithelial cells continuously secrete soluble m

61 Influenza-infected tracheal epithelial cells from caspase-1-deficient mice

62 Mouse tracheal epithelial cells grown at an air-liquid interfa

63 Recent work in mouse tracheal epithelial cells links microtubules with both e

64 we now observed that conditioning of DCs by tracheal epithelial cells regulated 98 genes under homeo

65 Indeed, exposure of mouse tracheal epithelial cells to IL-1beta or IL-1alpha resul

66 d differentiated human primary bronchial and tracheal epithelial cells to investigate cellular tropis

67 Cultures of mouse tracheal epithelial cells undergoing differentiation in

68 Addition of exogenous TNF-alpha to mouse tracheal epithelial cells was sufficient to attenuate SP

69 as examined using PLA2 inhibitors and murine tracheal epithelial cells with Pla2g10 deletion.

70 of the IFN response in primary renal cells, tracheal epithelial cells, and a chicken cell line.

71 tion of not only primary AT2 cells, but also tracheal epithelial cells, and C2C12 myoblasts.

72 Primary tracheal epithelial cells, mice lacking the gene for Grx

73 of allergic asthma, as well as primary mouse tracheal epithelial cells, to evaluate the relevance of

74 this paper, using primary cultures of mouse tracheal epithelial cells, we show that Cby facilitates

75 l and mucin-deficient mice, as well as mouse tracheal epithelial cells, were investigated in vitro an

76 thymic stromal lymphopoietin and GM-CSF from tracheal epithelial cells.

77 ewal and differentiated into pneumocytes and tracheal epithelial cells.

78 dentified as up-regulated in ciliating mouse tracheal epithelial cells.

79 the transcriptional profile of multiciliated tracheal epithelial cells.

80 We report the child's clinical progress, tracheal epithelialization and costs over the 4 years.

81 r time, we lesioned small areas of the mouse tracheal epithelium (1 to 12 cells) using a femtosecond

82 cally, we followed the regeneration of mouse tracheal epithelium after ablation of luminal cells by i

83 intestinal epithelium of the fly and in the tracheal epithelium of mice exhibit transient activation

84 n IAVs (hIAVs) showed that they infected the tracheal epithelium with various efficiencies depending

85 e, and infection and growth in horse and dog tracheal explant cultures.

86 Tracheal explants from wild-type swine demonstrated a di

87 Inoculation of the viruses into tracheal explants revealed similar levels of infection a

88 (LAIV), which was attenuated in mice and dog tracheal, explants compared to CIV H3N8 wild type.

89 that zelda directly controls CNS midline and tracheal expression of the link (CG13333) gene, as well

90 y of recovery of neuromuscular function upon tracheal extubation cannot be guaranteed.

91 isplay increased miR-200 expression in their tracheal fluid at the time of balloon removal.

92 emonstrated similar sensitivities for bovine tracheal force development and phosphorylation of RLC, M

93 Fifth, tracheal homogenates contained NAADP-binding sites of hi

94 Third, tracheal homogenates could synthesize NAADP by base exch

95 The embryonic tracheal inducer branchless FGF (fibroblast growth facto

96 Thus, reactivation of an embryonic tracheal inducer in decaying branches directs outgrowth

97 ary bacterial infection after a single intra-tracheal instillation at a very low dosage of 0.1 mg/kg.

98 Pseudomonas aeruginosa tracheal instillation led to an acute pneumonia with a r

99 Ethanol mice given a tracheal instillation of LPS demonstrated early lung flu

100 ittle is known about the association between tracheal intubation and survival in this setting.

101 ngoscopy attempts in children with difficult tracheal intubation are associated with a high failure r

102 th immediate recognition was the most common tracheal intubation associated events (n = 167, 9%).

103 in 20% of intubations (n = 372), with severe tracheal intubation associated events in 6% (n = 115).

104 Self-reported adverse tracheal intubation associated events occurred frequentl

105 Severe tracheal intubation associated events were associated wi

106 Adverse tracheal intubation associated events were reported in 2

107 nd operational definitions including adverse tracheal intubation associated events.

108 provider were associated with occurrence of tracheal intubation associated events.

109 tion status was associated with fewer severe tracheal intubation associated events.

110 n, and establish the effect of more than two tracheal intubation attempts on complications.

111 plications was associated with more than two tracheal intubation attempts, a weight of less than 10 k

112 Tracheal intubation can be avoided by the start of the N

113 We analyzed 5,096 tracheal intubation courses from July 2010 to March 2014

114 registry consists of prospectively collected tracheal intubation data from 13 children's hospitals in

115 To determine whether tracheal intubation during adult in-hospital cardiac arr

116 Exposures: Tracheal intubation during cardiac arrest .

117 ic patients with in-hospital cardiac arrest, tracheal intubation during cardiac arrest compared with

118 Tracheal intubation during cardiac arrest.

119 and January, 2015, 1018 difficult paediatric tracheal intubation encounters were done.

120 One thousand seven hundred fifteen tracheal intubation encounters were reported (averaging

121 Tracheal intubation failed in 19 (2%) of cases.

122 ication, these findings do not support early tracheal intubation for adult in-hospital cardiac arrest

123 ed Injury Severity Score >/= 3) who received tracheal intubation for at least 48 hours in the ICU bet

124 do not support the current emphasis on early tracheal intubation for pediatric in-hospital cardiac ar

125 were prospectively collected for all initial tracheal intubation in 15 PICUs from July 2010 to Decemb

126 All adult patients requiring tracheal intubation in the ICU were eligible.

127 namic instability and oxygenation failure as tracheal intubation indications were associated with car

128 Tracheal intubation is common during adult in-hospital c

129 Importance: Tracheal intubation is common during pediatric in-hospit

130 e and training level), and practice factors (tracheal intubation method and use of neuromuscular bloc

131 ilation (oxygenation) is always possible and tracheal intubation normally simple.

132 Tracheal intubation of ICU patients is frequently associ

133 k or a high-flow nasal cannula oxygen during tracheal intubation of ICU patients.

134 ressions more than 1 minute occurring during tracheal intubation or within 20 minutes after tracheal

135 ed patient, clinician, and practice data and tracheal intubation outcomes.

136 r Children was feasible to characterize PICU tracheal intubation procedural process of care and safet

137 ldren registry is a feasible tool to capture tracheal intubation process of care and outcomes.

138 Tracheal intubation quality improvement data were prospe

139 Tracheal intubation quality improvement data were prospe

140 ated respiratory infections during prolonged tracheal intubation requires further investigation.

141 Elective tracheal intubation status was associated with fewer sev

142 The most frequently attempted first tracheal intubation techniques were direct laryngoscopy

143 tion, establish the success rates of various tracheal intubation techniques, catalogue the complicati

144 Ninety-eight percent of primary tracheal intubation were successful; 86% were successful

145 Ninety percent of tracheal intubation were with cuffed tracheal tubes.

146 th in-hospital cardiac arrest, initiation of tracheal intubation within any given minute during the f

147 nt factors (demographics and indications for tracheal intubation), provider factors (discipline and t

148 the complications of children with difficult tracheal intubation, and establish the effect of more th

149 ) to characterise risk factors for difficult tracheal intubation, establish the success rates of vari

150 Tracheal intubation-associated cardiac arrest was define

151 Tracheal intubation-associated cardiac arrest was report

152 Tracheal intubation-associated cardiac arrests occurred

153 Tracheal intubation-associated cardiac arrests were much

154 Occurrence of any tracheal intubation-associated events and severe trachea

155 Adverse tracheal intubation-associated events are common in PICU

156 rage had a significantly higher frequency of tracheal intubation-associated events during nights and

157 Little is known about how the incidence of tracheal intubation-associated events is affected by the

158 Higher occurrence of tracheal intubation-associated events was observed durin

159 Frequency of a priori-defined tracheal intubation-associated events was the primary ou

160 heal intubation-associated events and severe tracheal intubation-associated events were more common d

161 nd weekends but was not fully protective for tracheal intubation-associated events.

162 ds are associated with a higher frequency of tracheal intubation-associated events.

163 actice factors are important contributors to tracheal intubation-associated events.

164 evel clustering and patient factors: for any tracheal intubation-associated events: adjusted odds rat

165 Critically ill children requiring tracheal intubation.

166 onate, 3 mg/kg, or placebo 15 minutes before tracheal intubation.

167 out complications in children with difficult tracheal intubation.

168 acheal intubation or within 20 minutes after tracheal intubation.

169 were prospectively collected for all initial tracheal intubations in 25 PICUs from July 2010 to March

170 We hypothesize that tracheal intubations occurring during nights and weekend

171 A total of 5,232 pediatric tracheal intubations were evaluated.

172 d cardiac arrests were much more common with tracheal intubations when the child had acute hemodynami

173 procedures were prospectively studied: 1,007 tracheal intubations, 1,272 arterial and 2,586 central v

174 cardiac arrests occurred during 1.7% of PICU tracheal intubations.

175 We propose that tracheal invasion is controlled by an AP-1-dependent swi

176 while marginal virus titers were detected in tracheal lavage fluid cells of N4-blind MV-infected host

177 s, but only the wild-type virus was found in tracheal lavage fluids and urine.

178 tissue or muscle, large defects >50% of the tracheal length still present a clinical challenge.

179 lowing 1918 infection correlated with severe tracheal lesions.

180 ability, and alveolar hemorrhage after intra-tracheal lipopolysaccharide (LPS).

181 lls, was the major source of TF during intra-tracheal LPS-induced ALI.

182 m organization and reduced fluid flow in the tracheal lumen.

183 nd avidity indices of IgG in sera and IgA in tracheal, lung, and intestinal secretions, significantly

184 as measured through fluoroscopic tracking of tracheal markers.

185 lar structures, were determined with US, and tracheal measurements were performed by using US.

186 learning [9] and is thought to phonate with tracheal membranes [10, 11] instead of the two independe

187 Instead of the main sound source, the tracheal membranes constitute a morphological specializa

188 Birds with experimentally disabled tracheal membranes were still able to phonate.

189 two oscine-like labial pairs and the unique tracheal membranes, which collectively represent the lar

190 r larvae (L3), cells constituting the second tracheal metamere (Tr2) reenter the cell cycle.

191 d using an internal pressure sensor within a tracheal model upon cuff inflation up to 30 cm H2O.

192 Cuffs were tested within a tracheal model, oriented 30 degrees above horizontal to

193 udied inward short-circuit currents (Isc) in tracheal mucosa from human, sheep, pig, ferret, and rabb

194 By providing stabilized access to the tracheal mucosa without intubation, our setup uniquely a

195 infiltration of inflammatory cells into the tracheal mucosa.

196 from M. gallisepticum populations present on tracheal mucosae during a 7-day experimental infection i

197 a glpK mutant, R(low), or growth medium, and tracheal mucosal thickness and lesion scores were assess

198 velocity and pressure drops around a distal tracheal narrowing.

199 Fetoscopic endoluminal tracheal occlusion (FETO) stimulates lung growth and imp

200 of fetuses undergoing fetoscopic endoluminal tracheal occlusion (FETO) to reverse severe lung hypopla

201 and Scopus databases for clinical studies on tracheal occlusion and CDH.

202 male sex, term birth, high illness severity, tracheal or noninvasive ventilation, parental absence an

203 oked by electrical stimulation of either the tracheal or the laryngeal mucosa occurred at stimulation

204 , mild and attenuated IBV strains in ex vivo tracheal organ culture (TOC).

205 Priming of chicken primary fibroblasts and tracheal organ cultures with chIFN-kappa imparted cellul

206 By examining Drosophila tracheal outgrowth during metamorphosis, we show that pr

207 Both the increase in tracheal perfusion pressure and action potential dischar

208 The diaphragm was assessed by twitch tracheal pressure in response to bilateral anterior magn

209 hragm dysfunction was evaluated using twitch tracheal pressure in response to bilateral anterior magn

210 pressure within the safe range, transmitted tracheal pressure is extremely heterogeneous and differs

211 ertness, glottal muscle electrical activity, tracheal pressure, SpO2, and respiratory movements.

212 clinical setting, a patient who underwent a tracheal reconstruction with a vascularized myofascial f

213 Although there are various methods for tracheal reconstruction, such as a simple approximation

214 , we used a vascularized myofascial flap for tracheal reconstruction.

215 ation, suggesting its suitability for use in tracheal reconstruction.

216 The primary outcome was tracheal reintubation for any cause within 7 days of ran

217 standard oxygen therapy reduced the risk of tracheal reintubation within 7 days.

218 is needed to develop bioengineered pediatric tracheal replacements with lower morbidity, better biome

219 treme oxygen demand of insect flight muscle, tracheal (respiratory) tubes ramify not only on its surf

220 esponse to sHA was evaluated in the isolated tracheal ring assay in tracheal rings from TSG-6(-/-) or

221 Moreover, TSG-6(-/-) tracheal ring non-responsiveness to sHA was reversed by

222 antagonist Ned-19 inhibited contractions in tracheal rings and calcium increases in isolated smooth

223 In tracheal rings and lung parenchyma strips, OVA caused a

224 Regulation of contraction of murine tracheal rings expressing GRK2 C terminus was also asses

225 Tracheal rings from Iqgap1-/- mice generated greater ago

226 line-induced force generation was reduced in tracheal rings from ROCK1(+/-) and ROCK2(+/-) vs. WT mic

227 uated in the isolated tracheal ring assay in tracheal rings from TSG-6(-/-) or TSG-6(+/+), with or wi

228 lenge, and the diminished contraction of the tracheal rings in these mice was reversed by IL-17A.

229 Analyses of tracheal rings obtained at necropsy (day 12) documented

230 of Plk1 also diminished contraction of mouse tracheal rings.

231 ressure of sediment methane to inflate their tracheal sacs.

232 Cultured cells repopulated tracheal scaffolds in a heterotopic transplantation xeno

233 The primary objective was to compare the tracheal sealing performance of polyvinyl chloride taper

234 endotracheal tube cuff material and shape on tracheal sealing performance remains debated.

235 cal rather than a cylindrical shape increase tracheal sealing.

236 4% of the instilled microspheres per gram of tracheal secretions, whereas 0.22% +/- 0.25% and 0.97% +

237 y airway human smooth muscle cells and mouse tracheal sections revealed colocalization of p190A-RhoGA

238 ation of NM myosin heavy chain on Ser1943 in tracheal SM tissues, which can regulate NM myosin IIA fi

239 sin during contractile stimulation of canine tracheal SM tissues.

240 aling mechanisms were identified in cultured tracheal SMC and verified by in vivo reconstitution expe

241 of human embryonic kidney cells (HEK293) and tracheal smooth muscle cells (SMCs) were tested with ibu

242 Tracheal smooth muscle contains significant amounts of m

243 her NAADP functions as a second messenger in tracheal smooth muscle contraction, we used the criteria

244 Acetylcholine stimulation of tracheal smooth muscle tissues induces the recruitment o

245 Contractile stimulation of tracheal smooth muscle tissues stimulates phosphorylatio

246 ses concurrently with tension development in tracheal smooth muscle tissues.

247 nothing is known about its possible role in tracheal smooth muscle, a muscle type that is clinically

248 hat NAADP functions as a second messenger in tracheal smooth muscle, and therefore, steps in the NAAD

249 y electric field stimulation (EFS) in bovine tracheal smooth muscle.

250 85, was enriched in mouse, as well as bovine tracheal smooth muscle.

251 on (PCR) from nasopharyngeal swabs and lower tracheal specimens via intubation tube.

252 ng multilayered skin, bone, vascular grafts, tracheal splints, heart tissue and cartilaginous structu

253 ave been confounded by the low prevalence of tracheal stenosis and a limited number of studies.

254 is indicates a trend toward a higher rate of tracheal stenosis and an increased risk of major bleedin

255 g this channel (Cav3.2(-/-)) show congenital tracheal stenosis because of incomplete formation of car

256 significant difference in the prevalence of tracheal stenosis or major bleeding between percutaneous

257 wing percutaneous tracheostomy, particularly tracheal stenosis, are unclear.

258 en to estimate the pooled risk difference of tracheal stenosis, bleeding, and wound infection compari

259 eta-analysis suggests a higher prevalence of tracheal stenosis, wound infection, and major bleeding f

260 neuropeptides, sculpt the growth of specific tracheal subsets.

261 use of incomplete formation of cartilaginous tracheal support.

262 ts FGF from T-tubules to surface, increasing tracheal surface ramification and preventing invasion.

263 orientation directs particles to the ventral tracheal surface.

264 es and females (iv), and whether cloacal and tracheal swabs might be used to detect herpesvirus.

265 The Drosophila tracheal system is a branched tubular network that forms

266 At the molt, the tracheal system is shed and replaced with a new, larger

267 In Drosophila development, tip cells of the tracheal system lead the migration of each branch and co

268 The LIV can then enter the tracheal system of the adult beetle for dispersal to a n

269 Here, we used the Drosophila tracheal system to study the complex relationship betwee

270 ain tissues (mesoderm, digestive system, and tracheal system) required more than one pgant, suggestin

271 ysiological and morphological changes in the tracheal system, metabolic reorganization, and suppressi

272 In the Drosophila tracheal system, mutations in oak gall (okg) and conjoin

273 In the Drosophila tracheal system, two tube types connect within single ce

274 rient-dependent plasticity of the Drosophila tracheal system: a network of oxygen-delivering tubules

275 terrestrial lineages that exchange gases via tracheal systems, most taxa have a dorsal heart that dri

276 In Drosophila, stellate-shaped tracheal terminal cells make seamless tubes, with single

277 We use Drosophila tracheal terminal cells, a component of the insect respi

278 ses of complications, such as aberrations of tracheal, thyroidal, and vascular structures, were deter

279 racheal epithelial cells (TECs) in vitro and tracheal tissue ex vivo in response to virulent strain R

280 ia, elevation in plasma histamine level, and tracheal tissue mast cell degranulation in mice in a dos

281 CnPnV was detected in the tracheal tissues of 29/205 kenneled dogs.

282 ct on muscarinic force responses in isolated tracheal tissues.

283 lung transplantation, we used an established tracheal transplant model inducing BO-like lesions to in

284 ed fifty-two adult patients intubated with a tracheal tube allowing subglottic secretion suctioning w

285 ow and pressure measured at the inlet of the tracheal tube and expressed as resistance (Rrs) and reac

286 After replacing the tracheal tube by a double-lumen one, we initiated latera

287 thway in promoting cell intercalation during tracheal tube morphogenesis in Drosophila embryogenesis,

288 e pressure ventilation by an endotracheal or tracheal tube, a PaO2:FiO2 less than 200 mm Hg with at l

289 of mechanical ventilation, the prevalence of tracheal tubes, and behavioral "learned nonuse" may all

290 cent of tracheal intubation were with cuffed tracheal tubes.

291 Seventy-two ex vivo pig tracheal two-lung blocks.

292 swallowing reflexes evoked by laryngeal and tracheal vagal afferent nerve stimulation in anaesthetiz

293 o assess the association between duration of tracheal ventilation (TV) and exposure to opioids, sedat

294 The tapered cuffs showed the lowest tracheal wall contact area (n: 96, p < 0.001).

295 The tracheal wall pressure distribution pattern was heteroge

296 f-trachea contact area and the percentage of tracheal wall pressure measurements greater than 50 cm H

297 as heterogeneous, and the percentage of high tracheal wall pressure significantly differs among the c

298 The extent of transmitted tracheal wall pressure throughout the cuff-trachea conta

299 ize very-long-chain fatty acids required for tracheal waterproofing and that adult oenocytes produce

300 ir-liquid interface cultures, and an in vivo tracheal xenograft model.