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1 ir monocultures or mixtures without pine and birch.
2 t data: (1) dog/cat/horse, (2) timothy grass/birch, (3) molds, (4) house dust mites, (5) peanut/wheat
3 ive quantification of Bet v 1 in 30 marketed birch allergen products in one laboratory, simulating th
4 urement of Bet v 1 in a panel of 'real-life' birch allergen products indicated better repeatability o
8 eding decreased the risk of sensitization to birch allergen; introduction of oats <5.1 months and bar
10 h sensitization to wheat, timothy grass, and birch allergens; the introduction of 1-2 food items at 4
12 black spruce, burned black spruce and paper birch, allowing us to determine vegetation and edaphic d
13 neighbourhood scale, where the proportion of birch among neighbouring trees varied, but not at the pl
16 ergenic proteins shared by many pollens (eg, birch and alder) and foods (eg, apple, peach, and soy).
17 haw in unburned dominant forest types (paper birch and black spruce) associated with location on elev
18 d the (3)He chemical shifts observed for the Birch and dihydroanthracene reduction products, the two
19 pollen were analyzed regarding IgE to major birch and grass pollen allergens Bet v 1 and Phl p 1/p 5
22 notherapy with mixed depigmented-polymerized birch and grass pollen extract in 285 patients with alle
25 , indicating T-cell cross-reactivity between birch and hazelnut allergens in all patients of the stud
28 n updated include respiratory allergens from birch and ragweed pollen, midge larvae, and horse dander
31 elterwood system with mixed stands of silver birch and spruce in combination with regular harvest of
33 community biomass response, and responses of birch and willow, to warming by 19%, 46%, and 11%, respe
34 with American beech, sugar maple, and yellow birch, and negatively with red spruce and balsam fir - g
35 ing three types of wood logs, namely, beech, birch, and spruce, were chemically characterized using t
37 the major pollen allergen Bet v1 from silver birch as examples and showed that these purified recombi
38 resent analyses we included 28 children with birch atopy and randomly selected 28 nonatopic children
39 nd (2) IgE responses to birch (children with birch atopy) or no IgE response at all to 9 common aeroa
41 om timothy grass (Phl p 7), alder (Aln g 4), birch (Bet v 4), turnip rape (Bra r 1), lamb's quarter (
43 mbling aspen (Populus tremuloides) and paper birch (Betula papyrifera) to the north vs. eastern cotto
45 berian larch (Larix sibirica Ledeb.), silver birch (Betula pendula Roth.) and black alder (Alnus glut
48 tity with an ACC oxidase from European white birch (Betula pendula), and phylogenetic analyses clearl
49 al plant community were taken, namely silver birch (Betula pendula), Norway spruce (Picea abies), bir
50 )-D-Xylp, which was previously identified in birch (Betula verrucosa) and spruce (Picea abies) GX.
52 elevant nonphylogenetically related species: birch (Betula verrucosa), pine (Pinus sylvestris), and r
54 ears, and 13 years) and (2) IgE responses to birch (children with birch atopy) or no IgE response at
55 al susceptibility when growing with pine and birch compared with their monocultures or mixtures witho
57 e synthesis applies the previously developed Birch-Cope sequence to create the key arylic quaternary
59 tivity to recombinant Bet v 1.0101 (Bet v 1; birch), Cor a 1.0401 (Cor a 1; hazelnut), and Dau c 1.01
62 ionally occurring pollen allergens (ragweed, birch, cypress), IgE sensitization was significantly ass
63 e forest tree (Betula alleghaniensis, yellow birch) displayed responses to increased CO2 that were bo
65 s for moderate-to-severe peanut allergy in a birch-endemic region and to create an oral-peanut challe
67 There is cross-reactivity between beech and birch family which related with oral allergic syndrome.P
68 and suggests that chewing damage on mountain birch foliage could significantly increase reactive VOC
69 es along replicated natural transitions from birch forest (Betula pubescens), through deciduous shrub
72 year period, we observed a nonlinear loss of birch forests and a relatively continuous gain of spruce
73 stimates a transition of ~15 km(2) or ~7% of birch forests to wetlands, where the greatest change fol
75 erbivore-induced VOC emissions from mountain birch in laboratory experiments and assessed the impact
79 of electron-deficient pyrroles using either Birch (Li/NH(3)) or ammonia-free (Li/di-tert-butyl biphe
84 re <6 GPa, the PAW-GGA can be described by a Birch-Murnaghan equation of state with = 687.4 A(3), = 5
86 receiving steroids after SCIT against grass, birch or both were 0.65, 0.83 and 0.72, respectively (P
87 d He@C(60)H(36) have been synthesized by the Birch or dihydroanthracene reduction of C(60) and isolat
91 -10) protein family and allergic rhinitis to birch pollen (ARbp) from early childhood up to age 16 ye
95 3) and patients with mild allergic asthma to birch pollen (n = 12) before and after birch allergen pr
98 lied to evaluate the therapeutic efficacy of birch pollen AIT on birch pollen-related food allergy.
99 ovocation (COLAP) test using the recombinant birch pollen allergen Bet v 1 (rBet v 1) for in vivo dia
100 gellin A from Listeria monocytogenes and the birch pollen allergen Bet v 1 (recombinant flagellin A [
101 ions and T-cell responses to the recombinant birch pollen allergen Bet v 1 and recombinant hypoallerg
102 inly results from sensitization to the major birch pollen allergen Bet v 1 and subsequent cross-react
104 ntibodies and T cells specific for the major birch pollen allergen Bet v 1 cross-react with structura
105 t fusion proteins of flagellin and the major birch pollen allergen Bet v 1 for suitability as allergy
107 genetically engineered variant of the major birch pollen allergen Bet v 1 that lacks the typical Bet
108 gs which had been immunized with recombinant birch pollen allergen Bet v 1 using patch delivery syste
109 er 25 years ago, the gene encoding the major birch pollen allergen Bet v 1 was the first such gene to
110 ved from the IgE-reactive areas of the major birch pollen allergen Bet v 1 were fused to the hepatiti
111 an ELISA for the quantification of the major birch pollen allergen Bet v 1, established as a referenc
112 minent member of the PR-10 family, the major birch pollen allergen Bet v 1, is the main cause of spri
113 effect of intranasal administration of major birch pollen allergen Bet v 1, omalizumab or placebo on
118 ution of specific surface areas of the major birch pollen allergen Bet v 1.0101 to binding IgE of ind
119 r Tlr4(-/-) BALB/c mice were sensitized to a birch pollen allergen extract (BPEx), then received eith
121 llergic patients using recombinant (r) major birch pollen allergen rBet v 1 and major timothy grass p
122 Art v 4 are compared with those of Bet v 2 (birch pollen allergen) as well as with other allergenic
124 ble for quantification of Bet v 1, the major birch pollen allergen, in preceding phases of BSP090.
125 ed by co-sensitization to Bet v 1, the major birch pollen allergen, its cross-reactive food allergens
126 tides (COPs) derived from Bet v 1, the major birch pollen allergen, showed good clinical tolerability
127 aneous immunotherapy with Bet v 1, the major birch pollen allergen, to intervene in birch pollen alle
130 lind placebo-controlled pilot trial in which birch pollen allergic subjects were challenged intranasa
132 ut AD (group 2), 5 allergic patients without birch pollen allergy (group 3), and 5 nonallergic subjec
135 le to activate T-cell lines from donors with birch pollen allergy and from mice immunized with the pa
136 ergenicity of hazelnut in individuals with a birch pollen allergy and reactivity to raw hazelnut.
138 4 sera from Bet v 1-sensitized subjects with birch pollen allergy was determined by using direct ELIS
139 pecific immune responses of 16 patients with birch pollen allergy were characterized up to 54 months
140 ctions in not only most of the patients with birch pollen allergy with AD (11/15) but also in most of
141 ical study was conducted in 15 patients with birch pollen allergy with AD (group 1), 5 patients with
142 ent late reactions not only in patients with birch pollen allergy with AD but also in those without A
144 ontaining Bet v 1 fragments in patients with birch pollen allergy with and without atopic dermatitis
145 n allergy with AD (group 1), 5 patients with birch pollen allergy without AD (group 2), 5 allergic pa
156 symptoms, conjunctival provocation test with birch pollen and Bet v 1, and in vitro tests (tIgE, sIgE
157 zations to nuts in individuals sensitized to birch pollen and examine cross-reactivities between birc
158 n an environmental exposure chamber (EEC) to birch pollen at an average concentration of 3500 +/- 500
160 patients allergic to grass pollen and 94 to birch pollen completed two questionnaires (RCAT and RQLQ
161 ll subjects with skin prick tests (SPTs) for birch pollen conducted during 1997-2013 in the Skin and
165 exposed to native or heat-inactivated white birch pollen extract (BPEx) intratracheally and injected
167 ly increased reactivity to grass compared to birch pollen extract in Bet v 2 only sensitized patients
168 with >90% of Bet v 1 content present in the birch pollen extract, while displaying a weak cross-reac
170 recombinant rBet v 1.0101 as well as native birch pollen extracts were measured independently at lea
174 r allergen-specific immunotherapy (AIT) with birch pollen improves birch pollen-related food allergy.
178 ections of ALK Alutard (containing 1000 SQ-U birch pollen or grass pollen) or placebo (ALK diluent).
179 se reactions to food, GI tract symptoms, and birch pollen pollinosis and five healthy controls underw
181 total of 40 patients with a clear history of birch pollen rhinoconjunctivitis and associated OAS to a
183 d in autumn 2007 and spring 2008, before the birch pollen season, in 32 Dutch adults with symptoms of
189 for inhalant allergies; however, successful birch pollen SIT does not correlate well with the amelio
190 ted from patients before and during AIT with birch pollen were added to the allergen prior to intrana
191 ients with positive skin prick test (SPT) to birch pollen were analyzed regarding IgE to major birch
192 showed that allergen-Ab complexes formed in birch pollen, as well as food allergy, contained IgE, Ig
194 for a PreS carrier-based peptide vaccine for birch pollen, which, in addition to the established redu
198 IgE immunoblotting studies with sera from birch pollen-allergic individuals demonstrate that cleav
201 , Mal d 1, and Cor a 1 were determined in 42 birch pollen-allergic patients before and during BP-SIT.
202 grass pollen-allergic patients and 45.7% of birch pollen-allergic patients receiving guideline-conco
203 blingual challenge tests in a high number of birch pollen-allergic patients that inter alia can be ap
204 ntraperitoneally allergen-reactive PBMC from birch pollen-allergic patients together with birch polle
207 L) and clones (TCC) established from PBMC of birch pollen-allergic patients with carrot allergy were
208 tained from three healthy individuals and 23 birch pollen-allergic patients with/without oral allergy
217 ristics, efficacy, and safety in ragweed- or birch pollen-induced seasonal allergic rhinitis (SAR).
218 role of other immunoglobulin isotypes in the birch pollen-plant food syndrome has not been investigat
219 we analyzed the Fc glycosylation pattern of birch pollen-reactive serum IgGs after successful allerg
228 lls were quantified in peripheral blood, and birch pollen-specific IgE and IgG antibody levels were d
239 umber of patients, ILIT with grass-pollen or birch-pollen extracts appears to reduce nasal allergic s
243 ysis at Tyr(6)-Val(7) and Trp(35)-Ala(36) in birch profilin and at Trp(32)-Ala(33) in human profilin,
245 e (MFC), nanofibrillated cellulose (NFC) and birch pulp derivate, nanofibrillated anionic dicarboxyli
247 and alginate were produced using unmodified birch pulp, microfibrillated cellulose (MFC), nanofibril
249 and challenging with optimal doses of grass, birch, recombinant house dust mite (rDer p2) allergen or
252 resistant to acidic, basic, Lewis acid, and Birch reduction conditions and was assessed as a polymer
253 smoothly and stereoselectively reduced under Birch reduction conditions to give trans-4,5-disubstitut
254 was found that ambident substrate 12, under Birch reduction conditions, underwent smooth partial red
260 1,4-cyclohexadienes 2, obtained through the Birch reduction of arenes 1, have found widespread use a
265 olution, the mass spectral signature for the Birch reduction products of M+@C60-COT*3- and C60-COT*3-
267 the oxazolidine, followed by N-acylation and Birch reduction, completed the syntheses of 2 and 3.
268 ls-Alder, dipolar and ketene cycloadditions, Birch reduction, many types of nucleophilic additions, a
269 ylation, a variant of the nearly century-old Birch reduction, occurs on single-walled carbon nanotube
270 olving three reactions: the enantioselective Birch reduction-allylation, enol ether hydrolysis, and t
274 nge thus results from a cyclic one-electron (Birch) reduction/protonation/reoxidation (by phenoxyl ra
275 also report that SmI2(H2O)n cleanly mediates Birch reductions of substrates bearing at least two arom
276 el (the Na(2)K-SG(I) reagent) cleanly effect Birch reductions of substrates with at least two or more
281 thus cannot be fitted to a linear relation, Birch's law, which has been used to extrapolate measured
282 mbination with regular harvest of leaves and birch sap and an understory of ground elder, it is poten
287 across dominant groupings of species (dwarf birch shrubs, willow shrubs, other deciduous shrubs, gra
288 d might be helpful to evaluate the effect of birch-specific immunotherapy on pollen-associated food a
289 rent lignocellulosic biomass, namely, beech, birch, spruce, ash, oak, and pine as well as commercial
290 e and organic matter deposition in aspen and birch stands at the Aspen FACE facility in northern Wisc
293 iterpene isolated from the bark of the white birch tree, has been reported to be a selective inducer
294 An alternative approach is the coppicing of birch trees in combination with an understory of ground
299 plots containing preferred species (pine and birch) while intermediate preference species (larch and
300 ionships of Empetrum (crowberry) and Betula (birch) with millennial-scale changes in climate, fire ac
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