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1 t data: (1) dog/cat/horse, (2) timothy grass/birch, (3) molds, (4) house dust mites, (5) peanut/wheat
7 ive quantification of Bet v 1 in 30 marketed birch allergen products in one laboratory, simulating th
8 urement of Bet v 1 in a panel of 'real-life' birch allergen products indicated better repeatability o
13 black spruce, burned black spruce and paper birch, allowing us to determine vegetation and edaphic d
14 neighbourhood scale, where the proportion of birch among neighbouring trees varied, but not at the pl
17 ergenic proteins shared by many pollens (eg, birch and alder) and foods (eg, apple, peach, and soy).
18 haw in unburned dominant forest types (paper birch and black spruce) associated with location on elev
19 EAACI definitions on pollen season for both birch and grass and for a variety of geographical locati
20 pollen were analyzed regarding IgE to major birch and grass pollen allergens Bet v 1 and Phl p 1/p 5
23 used to investigate the correlation between birch and grass pollen concentrations during the birch a
24 notherapy with mixed depigmented-polymerized birch and grass pollen extract in 285 patients with alle
25 h and grass pollen concentrations during the birch and grass pollen season defined via the EAACI crit
28 ollen proteases of Kentucky bluegrass, white birch and hazel selectively destroy integrity and anchor
29 , indicating T-cell cross-reactivity between birch and hazelnut allergens in all patients of the stud
32 n updated include respiratory allergens from birch and ragweed pollen, midge larvae, and horse dander
35 elterwood system with mixed stands of silver birch and spruce in combination with regular harvest of
38 with American beech, sugar maple, and yellow birch, and negatively with red spruce and balsam fir - g
39 ing three types of wood logs, namely, beech, birch, and spruce, were chemically characterized using t
41 the major pollen allergen Bet v1 from silver birch as examples and showed that these purified recombi
42 d respective treatment with AIT primarily to birch as the representative allergen of the Fagales tree
43 gic sensitization; however, sensitization to birch as well as grass pollen Phl p 1 and cat Fel d 1 al
44 resent analyses we included 28 children with birch atopy and randomly selected 28 nonatopic children
45 nd (2) IgE responses to birch (children with birch atopy) or no IgE response at all to 9 common aeroa
46 y a relatively frequent byproduct of burning birch bark (a natural tinder) under common, i.e., aerobi
47 ively undemanding connection between burning birch bark and the production of birch tar would have be
49 uire a cognitively demanding setup, in which birch bark is heated in anaerobic conditions, a setup wh
54 om timothy grass (Phl p 7), alder (Aln g 4), birch (Bet v 4), turnip rape (Bra r 1), lamb's quarter (
55 growth of the dominant vegetation, Himalayan birch Betula utilis and Himalayan fir Abies spectabilis,
56 experiment at three sites with paired paper birch (Betula neoalaskana) and black spruce (Picea maria
57 mbling aspen (Populus tremuloides) and paper birch (Betula papyrifera) to the north vs. eastern cotto
62 formers, leaf miners and rollers) on silver birch (Betula pendula) trees growing in one-, two-, thre
63 al plant community were taken, namely silver birch (Betula pendula), Norway spruce (Picea abies), bir
64 plots distributed across 1 km(2) of treeline birch (Betula pubescens) forest and willow (Salix lappon
65 re, by manipulating the stem weight of downy birch (Betula pubescens) trees, we show that cambial dev
66 elevant nonphylogenetically related species: birch (Betula verrucosa), pine (Pinus sylvestris), and r
67 tightly constrains the colonization of dwarf birch (Betula, a thermophilous shrub) to 5.9 +/- 0.1 ka,
69 ears, and 13 years) and (2) IgE responses to birch (children with birch atopy) or no IgE response at
73 ionally occurring pollen allergens (ragweed, birch, cypress), IgE sensitization was significantly ass
74 y significantly lower TSS during the 24-week birch EEC session for 7 DU and 12 DU compared to placebo
75 s for moderate-to-severe peanut allergy in a birch-endemic region and to create an oral-peanut challe
77 There is cross-reactivity between beech and birch family which related with oral allergic syndrome.P
78 lying regulation by combining an accelerated birch flowering program with a recessive mutation at the
79 and suggests that chewing damage on mountain birch foliage could significantly increase reactive VOC
80 es along replicated natural transitions from birch forest (Betula pubescens), through deciduous shrub
83 year period, we observed a nonlinear loss of birch forests and a relatively continuous gain of spruce
84 stimates a transition of ~15 km(2) or ~7% of birch forests to wetlands, where the greatest change fol
88 significant correlation (slightly higher for birch) has been found between the Total Nasal Symptom an
89 ity and sequential pollen seasons within the birch homologous group create a prolonged symptomatic al
90 cross-reactivity towards allergens from the birch homologous group has been observed in basic resear
92 re the representative allergen source of the birch homologous group including several Fagales trees b
96 erbivore-induced VOC emissions from mountain birch in laboratory experiments and assessed the impact
101 ere also highest for the postexposure silver birch leaves; scanning electron microscopy showed that U
105 re <6 GPa, the PAW-GGA can be described by a Birch-Murnaghan equation of state with = 687.4 A(3), = 5
108 uggested increased risks of sensitization to birch (odds ratio [OR] = 1.12 [95% CI = 1.01-1.25] per 1
115 -10) protein family and allergic rhinitis to birch pollen (ARbp) from early childhood up to age 16 ye
119 oms were positively correlated with airborne birch pollen abundance, and nasal birch pollen challenge
121 linical trial data show that the efficacy of birch pollen AIT is not only related to birch pollen all
122 lied to evaluate the therapeutic efficacy of birch pollen AIT on birch pollen-related food allergy.
123 gellin A from Listeria monocytogenes and the birch pollen allergen Bet v 1 (recombinant flagellin A [
124 ions and T-cell responses to the recombinant birch pollen allergen Bet v 1 and recombinant hypoallerg
125 inly results from sensitization to the major birch pollen allergen Bet v 1 and subsequent cross-react
127 t fusion proteins of flagellin and the major birch pollen allergen Bet v 1 for suitability as allergy
130 gs which had been immunized with recombinant birch pollen allergen Bet v 1 using patch delivery syste
131 er 25 years ago, the gene encoding the major birch pollen allergen Bet v 1 was the first such gene to
132 an ELISA for the quantification of the major birch pollen allergen Bet v 1, established as a referenc
133 minent member of the PR-10 family, the major birch pollen allergen Bet v 1, is the main cause of spri
134 effect of intranasal administration of major birch pollen allergen Bet v 1, omalizumab or placebo on
139 ution of specific surface areas of the major birch pollen allergen Bet v 1.0101 to binding IgE of ind
140 ed Timothy grass pollen allergen Phl p 7 and birch pollen allergen Bet v 4 to study these effects.
141 llergic patients using recombinant (r) major birch pollen allergen rBet v 1 and major timothy grass p
142 Art v 4 are compared with those of Bet v 2 (birch pollen allergen) as well as with other allergenic
143 ble for quantification of Bet v 1, the major birch pollen allergen, in preceding phases of BSP090.
144 ed by co-sensitization to Bet v 1, the major birch pollen allergen, its cross-reactive food allergens
145 tides (COPs) derived from Bet v 1, the major birch pollen allergen, showed good clinical tolerability
146 aneous immunotherapy with Bet v 1, the major birch pollen allergen, to intervene in birch pollen alle
150 lind placebo-controlled pilot trial in which birch pollen allergic subjects were challenged intranasa
152 ut AD (group 2), 5 allergic patients without birch pollen allergy (group 3), and 5 nonallergic subjec
153 le to activate T-cell lines from donors with birch pollen allergy and from mice immunized with the pa
154 solated from peripheral blood of donors with birch pollen allergy and stimulated with GM-CSF, IFN-gam
155 y of birch pollen AIT is not only related to birch pollen allergy but extends to pollen from other tr
157 , meaning that the majority of patients with birch pollen allergy suffer from secondary pollen food s
158 4 sera from Bet v 1-sensitized subjects with birch pollen allergy was determined by using direct ELIS
159 ctions in not only most of the patients with birch pollen allergy with AD (11/15) but also in most of
160 ical study was conducted in 15 patients with birch pollen allergy with AD (group 1), 5 patients with
161 ent late reactions not only in patients with birch pollen allergy with AD but also in those without A
163 ontaining Bet v 1 fragments in patients with birch pollen allergy with and without atopic dermatitis
164 n allergy with AD (group 1), 5 patients with birch pollen allergy without AD (group 2), 5 allergic pa
177 zations to nuts in individuals sensitized to birch pollen and examine cross-reactivities between birc
178 to current guidelines on allergen products, birch pollen are the representative allergen source of t
180 h airborne birch pollen abundance, and nasal birch pollen challenge led to downregulation of type I a
181 patients allergic to grass pollen and 94 to birch pollen completed two questionnaires (RCAT and RQLQ
183 ll subjects with skin prick tests (SPTs) for birch pollen conducted during 1997-2013 in the Skin and
186 cy and safety of sublingual high-dose liquid birch pollen extract (40,000 allergy units native [AUN]/
187 exposed to native or heat-inactivated white birch pollen extract (BPEx) intratracheally and injected
189 ly increased reactivity to grass compared to birch pollen extract in Bet v 2 only sensitized patients
191 roles of Bet v 1 and other components of the birch pollen extract, remain incompletely understood.
192 with >90% of Bet v 1 content present in the birch pollen extract, while displaying a weak cross-reac
194 recombinant rBet v 1.0101 as well as native birch pollen extracts were measured independently at lea
197 explanation for the limited effectiveness of birch pollen immunotherapy in birch pollen-related food
198 r allergen-specific immunotherapy (AIT) with birch pollen improves birch pollen-related food allergy.
202 ly ARC total combined score (TCS) during the birch pollen season (BPS) analyzed for subjects with dia
203 eatment was started 3 to 6 months before the birch pollen season and continued during the season in 4
204 pollen challenges were conducted outside the birch pollen season and included four birch and two oak
208 for inhalant allergies; however, successful birch pollen SIT does not correlate well with the amelio
209 ted from patients before and during AIT with birch pollen were added to the allergen prior to intrana
210 ients with positive skin prick test (SPT) to birch pollen were analyzed regarding IgE to major birch
211 ) T cells from donors sensitized to grass or birch pollen were stimulated with autologous allergen-pu
212 of AIT in dual-allergic patients (grass and birch pollen) using active untargeted treatments as cont
216 grass pollen-allergic patients and 45.7% of birch pollen-allergic patients receiving guideline-conco
217 blingual challenge tests in a high number of birch pollen-allergic patients that inter alia can be ap
218 ntraperitoneally allergen-reactive PBMC from birch pollen-allergic patients together with birch polle
220 L) and clones (TCC) established from PBMC of birch pollen-allergic patients with carrot allergy were
221 tained from three healthy individuals and 23 birch pollen-allergic patients with/without oral allergy
229 ents the development of cardinal features of birch pollen-induced allergic asthma in a strain-specifi
231 properly mirror symptom loads for grass and birch pollen-induced allergic rhinitis in other European
232 n 406 adult patients with moderate-to-severe birch pollen-induced allergic rhinoconjunctivitis with o
235 role of other immunoglobulin isotypes in the birch pollen-plant food syndrome has not been investigat
243 fectiveness of birch pollen immunotherapy in birch pollen-related food allergy and indicate a dominan
247 ted between populations, as egg-specific and birch pollen-specific IgE was more common in Finland.
256 umber of patients, ILIT with grass-pollen or birch-pollen extracts appears to reduce nasal allergic s
259 e (MFC), nanofibrillated cellulose (NFC) and birch pulp derivate, nanofibrillated anionic dicarboxyli
261 and alginate were produced using unmodified birch pulp, microfibrillated cellulose (MFC), nanofibril
263 and challenging with optimal doses of grass, birch, recombinant house dust mite (rDer p2) allergen or
265 ounds at anoxic sites, catalyze a biological Birch reduction beyond the negative limit of this redox
270 ed dearomatization and a subsequent directed Birch reduction, enabled by an intramolecular H-source.
271 n a four-step process by means of an initial Birch reduction, followed by an isomerization of the C=C
273 also report that SmI2(H2O)n cleanly mediates Birch reductions of substrates bearing at least two arom
274 ides as new organic photoredox catalysts for Birch reductions performed at ambient temperature and dr
279 mbination with regular harvest of leaves and birch sap and an understory of ground elder, it is poten
283 across dominant groupings of species (dwarf birch shrubs, willow shrubs, other deciduous shrubs, gra
284 rent lignocellulosic biomass, namely, beech, birch, spruce, ash, oak, and pine as well as commercial
285 e and organic matter deposition in aspen and birch stands at the Aspen FACE facility in northern Wisc
288 able surfaces provides useable quantities of birch tar in a single work session (3 h; including birch
289 cal hard surface, such as an adjacent stone, birch tar is naturally deposited and can be easily scrap
292 we demonstrate that recognizable amounts of birch tar were likely a relatively frequent byproduct of
293 een burning birch bark and the production of birch tar would have been readily discoverable multiple
295 We report the discovery of a 50,000-y-old birch tar-hafted flint tool found off the present-day co
296 In contrast, associational resistance of birch to leaf miners was not trait-mediated but driven d
298 An alternative approach is the coppicing of birch trees in combination with an understory of ground
299 aracterized by zymography and those of white birch were fully identified for the first time as serine