ライフサイエンスコーパス: mite

1 ature inverted-repeat transposable elements (MITEs).

2 regulation of immune response to house dust mite.

3 hogen enhances reproduction of the parasitic mite.

4 only studied airway allergen, the house dust mite.

5 ates a swift and accurate kick to remove the mite.

6 line and after sensitization with house dust mite.

7 increasing sum of specific IgE to cat/grass/mite.

8 such as Alternaria alternata and house dust mite.

9 1 allergens, group 2 allergens, or both) in mite.

10 tory challenge with an extract of house dust mite.

11 inst staple food antigens but not house dust mites.

12 local allergic rhinitis (LAR) to house dust mites.

13 on the beetle in the presence and absence of mites.

14 n a well-studied experimental system of soil mites.

15 are transmitted by the larvae of trombiculid mites.

16 f genes involved in xenobiotic metabolism in mites.

17 t for the host shift in native macrodinychid mites.

18 ape, which involves two generalist predatory mites.

19 ially high among rotifers, oligochaetes, and mites.

20 stent fitness benefits of breeding alongside mites.

21 organs for chemical defense in most oribatid mites.

22 , while symbiotic bacteria prevailed in prey mites.

23 and functionality compared to the classified MITEs.

24 We show that mites: 1) cause beetles to reduce the antibacterial acti

25 Four longitudinal trajectories emerged for mite: (1) no/low sensitization; (2) group 1 allergens; (

26 IT in children/adults allergic to house dust mite (10 trials), grass pollen or other inhalants.

27 he prevalence of sensitization to house dust mite (-4.3%; 95% CI, -6.0% to -2.6%) and cat (-2.1%; 95%

28 mothy grass/birch, (3) molds, (4) house dust mites, (5) peanut/wheat flour/mugwort, (6) peanut/soybea

29 We found that when a mite (a parasitic pest for Drosophila) touches the wing

30 monstrating that DWV, vectored by the Varroa mite, adversely affects humoral and cellular immune resp

31 ce with Aspergillus fumigatus and house dust mite allergen and compared the effects on airway eosinop

32 NC/Nga mice were sensitized with house dust mite allergen and treated topically with HOCl hydrogel b

33 of IgE responses differed between grass and mite allergen components, with temporal differences (ear

34 Dust mite allergen exposure modifies the estimated effect of

35 ith asthma are modified by the level of dust mite allergen exposure.

36 In addition, we discuss of house dust mite allergen extracts as a prototypical complex extract

37 A genome-wide interaction analysis of dust mite allergen level and lung function was performed in a

38 ificant interaction effect on FEV1 with dust mite allergen level in PRGOAL (interaction P = 3.1 x 10(

39 ed with FEV1 in children exposed to low dust mite allergen levels, but negatively associated with FEV

40 ve been no genome-wide G x E studies of dust mite allergen on asthma-related phenotypes.

41 Diverse factors contribute to house dust mite allergenicity through the activation of innate immu

42 r Phl p 1 from grass pollen (26.5%), group 2 mite allergens (18.2%), Bet v 1 from birch pollen (16.3%

43 nce enzyme immunoassays recognizing domestic mite allergens (DM), Fel d 1, Can f 1, and Mus m 1.

44 House dust contains mite allergens as well as bacterial products such as lip

45 assayed with a set of 178 peptides spanning mite allergens group Der p 1, 2, 23 and Der f group 1 an

46 IgE specific for staple foods and house dust mite allergens in DOCK8-deficient patients and healthy c

47 MS-based analyses confirmed the presence of mite allergens recorded by IUIS in D. pteronyssinus and

48 rmer synergizes with LPS and grass pollen or mite allergens to enhance the Toll-like receptor 4-media

49 antage of the prevailing enzymatic nature of mite allergens, we have developed a broad-spectrum bioch

50 or a small percentage of the IgE response to mite allergens, which is dominated by Der p 1 and Der p

51 es for mAb and IgE Ab recognition in group 1 mite allergens.

52 ownregulation in a mouse model of house dust mite allergic airway inflammation.

53 tribute to the clinical status of house dust mite-allergic patients.

54 d and reduces the CPT reaction in house dust mite-allergic patients.

55 Specifically, for patients with house dust mite allergies, which are often underestimated and diffi

56 e TNPT were randomized to receive placebo or mite allergoid SCIT 6667, 20 000, 50 000 or 100 000 AUeq

57 In this mite allergoid SCIT dose finding study in HDM-induced AR

58 The safety and tolerability of a mite allergoid subcutaneous allergen immunotherapy (SCIT

59 containing carbamylated monomeric house dust mite allergoids was to determine the most effective and

60 r-old Prevention and Incidence of Asthma and Mite Allergy (PIAMA) cohort.

61 of current allergic rhinitis (AR) related to mite allergy and asthma were based on yearly interviews

62 Dutch Prevention and Incidence of Asthma and Mite Allergy birth cohorts.

63 centrated in the transposition activities of MITEs among different ecotype accessions within a specie

64 This unique association between mite and bee persists due to the evolution of low Varroa

65 ic prevalence of sensitization to house dust mite and cat did not differ between year-of-birth cohort

66 s of sensitization, especially to house dust mite and cat, after the age of 20 years.

67 Here we find that extracts from dust mite and cockroach induce sustained Ca(2+) elevations in

68 hinitis, focusing on responses to house dust mite and grass.

69 many different biological systems, including mite and insect cuticles, pollen grains, fungal spores,

70 tease and major allergen from the house dust mite and is associated with allergic rhinitis and allerg

71 Mite and mold sensitization was low.

72 evere as the degree of sensitization to dust mite and mouse increase.

73 nificantly reduced risk of SPT reactivity to mite and other perennial allergens, and maternal ascaria

74 erved when considering specific IgE to grass/mite and symptoms on exposure to pollen/dust.

75 ved between specific IgE levels to cat/grass/mite and the risk of symptoms on each allergen-related e

76 measurement of allergen-specific IgE to dust mites and cockroach in plasma.

77 s including insect allergens from house dust mites and cockroaches contribute to allergic inflammator

78 The interactions between MITEs and homologous genes across 19 accessions provided

79 he lack of toxic agents that are specific to mites and not to the host honey bee.

80 a reduction in SPT reactivity to house dust mites and perennial allergens.

81 e of 7 with asthma, atopy (grass, house dust mite, and cat skin prick test) and atopic vs. non-atopic

82 enge with Alternaria alternata or house dust mite, and secretion of IL-33 and activation of subsequen

83 ergies (e.g. grass and ragweed pollens, dust mites, and cat) and those that induce life-threatening a

84 hSP-D) has been shown to suppress house dust mite- and Aspergillus fumigatus-induced allergic inflamm

85 Through comparison with the potential MITEs annotated in Repbase, the widely used eukaryotic r

86 After exposure to house dust mite antigen, Zbtb46-negative CD64(+) inflammatory cells

87 was also intranasally exposed to house dust mite antigen.

88 sensitized differed by study group for four mite antigens: Dermatophagoides farinae (Der-f1, Der-f2)

89 Mites are frequent ant symbionts, yet the exact nature o

90 In contrast, internally deleted sequences (MITEs) are preferred substrates of mariner transposition

91 ature inverted repeat transposable elements (MITEs) are prevalent in eukaryotic genomes, including pl

92 ature inverted repeat transposable elements (MITEs) are prevalent in eukaryotic genomes.

93 munities in populations of predator and prey mites, as well as the occurence of potential acaropathog

94 we test the novel hypothesis that P. carabi mites assist burying beetles in clearing the carcass of

95 e and fitness consequences for the beetle of mite-associated changes to the bacterial community on th

96 ability favored the coexistence of predatory mites at a low density of the intraguild prey.

97 ces the proportion of children sensitized to mites at age 18 months.

98 Exposure to mites at age 6 and 18 months was assessed by measuring D

99 l patients have IgEs to allergens present in mite bodies and feces.

100 rovince, where no previous incidence of this mite borne disease had been reported.

101 ualism between burying beetles and P. carabi mites, but more work is needed to understand the functio

102 empel-Ziv complexity algorithm to filter out MITE candidates with low complexity, and utilizes the po

103 ific IgE to common aeroallergens (house dust mite, cat, and grass) and total IgE levels were measured

104 underwent skin prick testing for house dust mite, cat, grasses and moulds.

105 re also decreased in the lungs of house dust mite-challenged ERp57-deleted mice.

106 2-fold in pulmonary epithelium of house dust mite-challenged mice.

107 Several mites' characteristics, such as their protective morphol

108 These mites complete their development on a single host, sucki

109 House dust mite concentrations varied across cohorts.

110 With the exception of integrated mite control implemented during the 1980s, pest control

111 , 80.7% of them were previously unclassified MITEs, demonstrating a different genomic distribution an

112 Es on a genome-wide scale than other popular MITE detection tools.

113 e conventional string matching algorithms in MITE detection, adopts the Lempel-Ziv complexity algorit

114 crucial in supporting the idiosyncrasies of mite detoxification and will further support the expandi

115 Chelicerate mites diverged from other arthropod lineages more than 4

116 ergenic components of timothy grass and dust mite during childhood.

117 nd TH2 polarization, as seen in a house dust mite exposure model.

118 promoted allergic TH responses to house dust mite exposure.

119 t in both the ovalbumin (OVA) and house dust mite extract (HDM) murine models of respiratory inflamma

120 xposed to allergens (ovalbumin or house dust mite extract) to decipher in vivo the implication of Rac

121 ce following acute challenge with house dust mite extract.

122 robust approach to assess the complexity of mite extracts and highlights the critical importance of

123 program CD-HIT to cluster similar MITEs into MITE families.

124 the significance of the phoretic stage, when mites feed on adult bees for a few days, is not clear.

125 onfirming a unique habit in the evolution of mite feeding strategies and suggesting that the entire g

126 ing leafrollers, mealybugs, leafhoppers, and mites for improved phytosanitary performance, and contri

127 n, it is not clear whether the preference of mites for nurses observed in the laboratory also happens

128 geography of hosts predicted the lineages of mites found on them; 27% of the total molecular variance

129 e climate discourages cockroach, fungal, and mite growth and (2) dander allergens are known to be pre

130 House dust mites have been implicated in the etiology and exacerbat

131 gene expression suggests that migrations of MITEs have no detectable effect on the expression level

132 The house dust mite (HDM) allergen Der p 13 could be a lipid-binding pr

133 ield study, sublingual tablets of house dust mite (HDM) allergen extracts (STG320) were efficacious i

134 ous CD4(+) T cells specific for a house dust mite (HDM) allergen form and function.

135 y and efficacy of challenges with house dust mite (HDM) allergen in the Fraunhofer allergen challenge

136 eding sensitization to the common house dust mite (HDM) allergen remains to be elucidated.

137 House dust mite (HDM) allergens are a common cause of allergy and a

138 Upon inhalation, house dust mite (HDM) allergens are deposited at the nasal and oral

139 Mice were sensitized with house dust mite (HDM) allergens from days 3, 15, or 60 after birth.

140 aled that IgE from crustaceans or House dust mite (HDM) allergic patients showed cross-reactivity to

141 py (AIT) lack recommendations for house dust mite (HDM) allergy.

142 ld-type mice were challenged with house dust mite (HDM) and infected with RV1B to determine lung infl

143 were challenged over 3 weeks with house dust mite (HDM) antigen.

144 that Streptococcus pneumoniae and house dust mite (HDM) bear similar phosphorylcholine (PC) epitopes.

145 g antigen (SEA) immunization, and house dust mite (HDM) challenge without affecting cytotoxic T lymph

146 of airborne allergens such as the house dust mite (HDM) effectively activates both innate and adaptiv

147 through the intranasal route with house dust mite (HDM) extract derived from Dermatophagoides pterony

148 lphaT-catenin knockout mice and a house dust mite (HDM) extract model of atopic asthma, with assessme

149 were intranasally challenged with house dust mite (HDM) extract or PBS five days per week for four we

150 s of intranasal administration of house dust mite (HDM) extract.

151 h prolonged i.n exposure to crude house dust mite (HDM) extract.

152 d DNA damage responses induced by house dust mite (HDM) in vivo and in vitro.

153 nfirmed in reporter assays and in house-dust-mite (HDM) induced AAI and primary human bronchial epith

154 Sensitization to house dust mite (HDM) is a risk factor for the development of aller

155 luated in the ovalbumin (OVA) and house dust mite (HDM) murine models.

156 Mice were sensitized to house dust mite (HDM) or cockroach at day 0, treated with IL-6R inh

157 challenged with saline, DEPs, or house dust mite (HDM) or DEP+HDM.

158 As house dust mite (HDM) sensitization is dependent on TLR4 and HDM De

159 lammation was induced following a house dust mite (HDM) sensitization protocol.

160 he last 8 weeks of treatment in 2 house dust mite (HDM) SLIT-tablet trials (n = 1768).

161 olled, randomized clinical trial, house dust mite (HDM) sublingual AIT was found to be efficacious in

162 The house dust mite (HDM) sublingual allergen immunotherapy (SLIT) tabl

163 The house dust mite (HDM) sublingual immunotherapy (SLIT) tablet (MK-82

164 hallenged with ovalbumin (OVA) or house dust mite (HDM), and accessed for TH2 inflammation.

165 to common human allergens such as house dust mite (HDM), in the absence of additional adjuvants, infl

166 o environmental antigens, such as house dust mite (HDM), often leads to T helper 2 (Th2) cell-driven

167 Exposure to allergens, such as house dust mite (HDM), through the skin often precedes allergic inf

168 24) was predicted to be active in house dust mite (HDM)- and helminth-elicited Il4(gfp+)alphabeta(+)C

169 e were assessed in sera from 1302 house dust mite (HDM)-allergic patients living in various areas.

170 ng induced by DCs is critical for house dust mite (HDM)-driven allergic airway inflammation (AAI) in

171 herapeutic efficacy of SAHM1 in a house dust mite (HDM)-driven asthma model.

172 1c promotor) to acute and chronic house dust mite (HDM)-driven asthma models.

173 address the role of B cells in a house dust mite (HDM)-driven TH2-high asthma mouse model.

174 mice were evaluated in a model of house dust mite (HDM)-induced AAI.

175 nd cytokine production to prevent house dust mite (HDM)-induced airway inflammation and remodeling.

176 immune responses in patients with house dust mite (HDM)-induced airways disease.

177 s and in response to DEP-enhanced house dust mite (HDM)-induced allergic airway inflammation.

178 several dosages in patients with house dust mite (HDM)-induced allergic rhinoconjunctivitis (ARC) us

179 nasal epithelium of patients with house dust mite (HDM)-induced AR and in an HDM-induced murine model

180 nfiltration, protecting mice from house dust mite (HDM)-induced asthma or Leishmania major infection.

181 OVA- and house dust mite (HDM)-induced murine asthma models were used in thi

182 timulatory effects of IL-1beta on house dust mite (HDM)-induced release of thymic stromal lymphopoiet

183 s been developed for treatment of house dust mite (HDM)-induced respiratory allergic disease.

184 investigate the role of TPL-2 in house dust mite (HDM)-mediated allergic airway inflammation.

185 histosoma mansoni or the allergen house dust mite (HDM).

186 , transcriptome and microbiome of house dust mites (HDM) has shown that Staphylococcus aureus (S. aur

187 House dust mites (HDM) may serve as carriers of bacteria responsibl

188 lls, BEAS-2B, directly exposed to house dust mites (HDM) resulted in enhanced DNA damage, as measured

189 The most frequent allergens are house dust mites (HDM), which act in vivo on the bronchial epitheli

190 House dust mite/HDM atopy patch test/APT elicits positive reactions

191 s dominated by a single allergen (house dust mite; HDM).

192 Twenty-three adults allergic to house dust mites (HDMs) (M+) and 15 nonsensitive, nonallergic (M-)

193 ntries demonstrate sensitivity to house dust mites (HDMs).

194 dance with an asthma exacerbation to receive mite-impermeable (active group) or control (placebo grou

195 To evaluate the use of house dust mite-impermeable bedding and its impact on severe asthma

196 Mite-impermeable encasings are effective in reducing the

197 ergen was present in 17.2% and to house dust mite in 8.7%.

198 allergen levels of dog, cat, and house dust mite in bed dust samples at 1 year.

199 (Blo t) mite species is considered a storage mite in temperate climate zones and an important source

200 0) showed evidence for interaction with dust mite in the Childhood Asthma Management Program (P = .02

201 es of allergic asthma provoked by house dust mite in vivo.

202 ive analysis by characterizing and comparing MITEs in 19 Arabidopsis thaliana accessions.

203 Control of these mites in beehives is a challenge in part due to the lack

204 ensive and accurate genome-wide detection of MITEs in various eukaryotic genomes can improve our unde

205 We also find that mites increase bacterial diversity and richness on the c

206 Experimental acute canine house dust mite-induced AD lesions exhibit an activation of innate

207 During house dust mite-induced airway allergy, rEos features remained unch

208 A-HSP65 and CpG/CFP downregulated house dust mite-induced allergic airway inflammation via distinct p

209 to the airways of mice undergoing house dust mite-induced allergic response.

210 -finding study, 131 patients with house dust mite-induced allergic rhinoconjunctivitis were randomize

211 of NP-CpG could prevent and treat house dust mite-induced allergy by modulating immunity directly in

212 ne responses were dispensable for house dust mite-induced endoplasmic reticulum stress and airways fi

213 ed, subjected to an ovalbumin- or house dust mite-induced experimental asthma protocol.

214 Peanut- and dust mite-induced expression of TH2 cytokines was reduced in

215 Blockade of Runx2 inhibited the house dust mite-induced goblet cell differentiation with a 75% redu

216 mice into WT recipients increases house dust mite-induced Th2/Th17 inflammation in the airway.

217 t-generation sequencing, we investigated how mites influence the bacterial communities on the carcass

218 e molecular structure of (particularly) dust mite, insect and mould allergens in dogs and horses, res

219 clustering program CD-HIT to cluster similar MITEs into MITE families.

220 Our results suggest that the Varroa mite is a highly adapted parasite for honey bees.

221 Dust mite is a known risk factor for asthma morbidity.

222 agnosis and immunotherapy of allergy against mites is based on complex extracts from large-scale cult

223 pa) to reproduce, the fitness benefit to the mites is not immediate but delayed.

224 ddresses the interactions between the varroa mite, its environment, and the honey bee host, mediated

225 nd, together with other (non-haematophagous) mites, lack a gene encoding haem oxygenase.

226 ur data indicate that exposure to house dust mite markedly reduces Sema3E expression in mouse airways

227 ng rat, mouse, cockroach, cat, dog, and dust mites, measured in dust samples collected from inner-cit

228 xperimental asthma (ovalbumin and house dust mite); miRNAs deregulated in both models were further te

229 Mite, mouse, cat, and dog allergens were mostly higher i

230 Mechanical stimuli that mimic the mites' movement evoke a similar kicking behavior.

231 fitness, although due to the fact that each mite must find a second host (a pupa) to reproduce, the

232 ely, comprehensively, and efficiently detect MITEs on a genome-wide scale than other popular MITE det

233 Finally, analysis of the impact of MITEs on gene expression suggests that migrations of MIT

234 induced in mice using intranasal house dust mite or aerosol ova-albumin challenge, and chloroquine o

235 The oribatid mite Oribatula tibialis uses the cyanogenic aromatic est

236 kicking response against invading parasitic mites over their wing margin with ultrafast speed and hi

237 et can compensate the deleterious effects of mite parasitization.

238 pests, beet army worm or two-spotted spider mites; pesticidal efficacy exceeded that of commercial f

239 will further support the expanding field of mite-plant interactions.

240 Burying beetles also carry phoretic mites (Poecilochirus carabi complex), which breed alongs

241 s, extracts, and allergen mixtures including mites, pollen, drugs, and food.

242 esent in all samples from predatory and prey mite populations (core OTUs): the intracellular symbiont

243 We show that Varroa mites prefer nurses over both newly emerged bees and for

244 cal method for the standardization of native mite products.

245 he direct transmission route that the Varroa mite provides.

246 ic airway inflammation induced by house dust mites, pulmonary function and cytokine profiles in Htr4-

247 A total of 343485 MITE putative sequences, including canonical, diverse an

248 tly different between the microbiota of prey mites reared with and without N. cucumeris.

249 e (ie, ABC) had significantly higher risk of mite-related AR and asthma than unsensitized participant

250 us molecules, which in turn predicts current mite-related AR and current/future asthma.

251 rom Aspergillus fumigatus and the house dust mite, resulting in an asthma-like pathology characterize

252 ldren and correlated with IgE levels to dust mite, ryegrass, and fungi but not cat, ragweed, or food

253 Kairomones are used at all stages of the mite's life cycle, and the exploitation of bees' brood p

254 miochemicals regulating crucial steps of the mite's life cycle.

255 ens; (3) group 2 allergens; and (3) complete mite sensitization.

256 dermatitis skin lesions with high house dust mite sensitization.

257 286 (mean age, 7.7 yr; male sex, 65.8%) were mite sensitized, and 284 were randomized (146 to the act

258 Among mite-sensitized children across all populations and at d

259 We randomized mite-sensitized children with asthma (ages 3-17 yr) afte

260 ings are effective in reducing the number of mite-sensitized children with asthma attending the hospi

261 Within the entire population of MITEs sequences, 80.7% of them were previously unclassif

262 Generally, myrmecophilous mites show adaptations for dispersal through phoresis, b

263 nged with a bacterial disease or a parasitic mite, similar to bees selected using a phenotype-based a

264 availability of genomic resources for other mite species has allowed researchers to study the lineag

265 The Blomia tropicalis (Blo t) mite species is considered a storage mite in temperate c

266 ens (ie, grass, olive/ash pollen, house dust mites), specific IgE did not show marked differences bet

267 Mite-specific AIT should rely upon a mixture of D. ptero

268 opulations and at different ages, house dust mite-specific IgG/IgE ratios (but not IgG4/IgE ratios) w

269 t to diagnose, the efficacy of SQ house dust mite sublingual immunotherapy tablets has been demonstra

270 nt with SQ (standardised quality) house dust mite sublingual tablet for 1 year resulted in a decrease

271 day (from 11% [placebo] to 5% [SQ house dust mite sublingual tablet]) and an increased probability of

272 ay (from 16% [placebo] to 34% [SQ house dust mite sublingual tablet]).

273 eared predators are fed with factitious prey mites such as Tyrophagus putrescentiae.

274 ooccurrence of hosts and parasites in spider mites (Tetranychidae), a globally distributed group of p

275 an acaricide resistant strain of the spider mite Tetranychus urticae upon exposure to synergists suc

276 The study of the two-spotted spider mite, Tetranychus urticae, for which a high-quality Sang

277 on as the I1017F mutation reported in spider mites that confers etoxazole resistance.

278 200-fold increase of relative pad area from mites to geckos.

279 ation of Dermatophagoides farinae house dust mites to sensitized atopic dogs.

280 inst the progression of IgE sensitization to mites toward AR and asthma.

281 essions provided a fine source for analyzing MITE transposition activities and their impacts on genom

282 Neoseiulus cucumeris is a predatory mite used for biological control of arthropod pests.

283 multifactorial syndrome, with the parasitic mite Varroa destructor and the associated deformed wing

284 for honey bees challenged with the parasitic mite Varroa destructor associated to the Deformed Wing V

285 The ecto-parasitic mite Varroa destructor has transformed the previously in

286 (DWV) and infestation with the ectoparasitic mite Varroa destructor have been linked to colony collap

287 eformed wing virus (DWV) and its vector, the mite Varroa destructor, are a major threat to the world'

288 y Iflaviridae, together with its vector, the mite Varroa destructor, is likely the major threat to th

289 The varroa mite, Varroa destructor, is a devastating ectoparasite o

290 The Varroa mite, Varroa destructor, is an acarine ecto-parasite on

291 ccount for the remarkable importance of this mite-virus interaction in the induction of honey bee col

292 ic sensitization to cat, dog, and house dust mites was diagnosed longitudinally using skin prick test

293 to certain allergens (cockroach, mouse, dust mite) was significantly associated with enhanced cytokin

294 rching for a specific toxic target of varroa mites, we investigated two closely related neuropeptider

295 , parental hay fever, and higher exposure to mites were associated with a broader polymolecular IgE s

296 From 2009 to 2013, 60 small animals and 2250 mites were collected in the vicinity of the school.

297 Moreover, a significant proportion of MITEs were found located in the last exon of genes besid

298 tal bacteria were more abundant in predatory mites, while symbiotic bacteria prevailed in prey mites.

299 tMITE has been shown to find known and novel MITEs with a complete structure and full-length copies i

300 y caused by sensitization against house dust mites with a nearly complete penetrance of the allergen,