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1 cations and the limits of detection for each bisphenol.
2 eceptor, which are two known main targets of bisphenols.
3 ylhexyl phthalate (DEHP) and polychlorinated bisphenol 153 (PCB153), were detected in adult dog teste
6 Our results propose a new mode of action for bisphenol A (10) that advocates a reduced exposure to th
8 By combination with an antibody directed to bisphenol A (alphaBPA), this conducting polymer-based bi
10 hinylestradiol (EE2)] and two xenoestrogens [bisphenol A (BPA) and 4-n-nonyl-phenol (NP)] in surface
14 ence regarding associations for exposures to bisphenol A (BPA) and phthalates with type 2 diabetes (T
15 is growing concern that prenatal exposure to bisphenol A (BPA) and phthalates, which are widely used
21 erns, variability, and predictors of urinary bisphenol A (BPA) concentrations in 337 children from th
22 n expert panel reviewed associations between bisphenol A (BPA) exposure and reproductive health outco
27 ticipants previously randomly selected for a bisphenol A (BPA) exposure study who had unusually high
29 As concern regarding the toxic effects of bisphenol A (BPA) grows, BPA in many consumer products i
33 Prenatal exposure to nonylphenol (NP) and/or bisphenol A (BPA) has been reported to be associated wit
34 Widespread environmental contamination by bisphenol A (BPA) has created the need to fully define i
36 We report on an innovative heterogeneous bisphenol A (BPA) immunoassay based on an electrolyte-ga
38 ead use of the endocrine disrupting chemical bisphenol A (BPA) in consumer products has resulted in n
40 s increasingly been used as a substitute for bisphenol A (BPA) in some "BPA-free" consumer goods and
41 ectrochemical biosensor for the detection of Bisphenol A (BPA) in water has been developed by immobil
42 y bottles, little attention has been paid to bisphenol A (BPA) intake from packaged water consumption
55 ure to the environmental endocrine disruptor bisphenol A (BPA) is ubiquitous and associated with the
60 products from store shelves after reports of bisphenol A (BPA) leaching from baby bottles, reusable d
61 oprobe is designed for the quantification of bisphenol A (BPA) levels in the blood after human exposu
62 rly-life exposure to the endocrine disruptor bisphenol A (BPA) may contribute to the development of o
63 tory actions and public concerns, the use of bisphenol A (BPA) may decrease, while the use of BPA alt
69 ion on the homogeneous Fenton degradation of bisphenol A (BPA) used as a model pollutant, was investi
73 scharge of the endocrine disrupting compound bisphenol A (BPA) with wastewater treatment plant (WWTP)
74 sed on the MS results these were assigned to bisphenol A (BPA), 2,4-di-tert-butylphenol, and a possib
77 t chronic exposure of synthetic xenoestrogen bisphenol A (BPA), a component of consumer plastic produ
83 al models suggests that prenatal exposure to bisphenol A (BPA), a ubiquitous endocrine-disrupting che
86 S (BPS) are increasingly used to substitute bisphenol A (BPA), a widespread environmental endocrine
91 to investigate the carcinogenic property of Bisphenol A (BPA), an environmental estrogen, by long-te
94 crine-disrupting chemicals (EDCs), including bisphenol A (BPA), are environmental ubiquitous pollutan
96 phenoxyethanol (2-PE), 4-nonylphenol (4-NP), bisphenol A (BPA), benzylbuthyl phthalate (BBP) and dime
97 al samples were analyzed for the presence of bisphenol A (BPA), bis (2-ethylhexyl) phthalate (DEHP),
98 like activity is attributed to EDCs, such as bisphenol A (BPA), bisphenol AF (BPAF), and zearalenone
99 ion of bisphenol F diglycidyl ether (BFDGE), bisphenol A (BPA), bisphenol B (BPB), bisphenol F (BPF)
101 ironment of some of these chemicals, such as bisphenol A (BPA), external contamination during handlin
104 of environmental contaminants, particularly bisphenol A (BPA), is understudied with regard to PTB.
105 vestigated the direct effects of exposure to bisphenol A (BPA), mono-n-butyl phthalate (Pht), and pol
106 With the pressure to ban or limit the use of bisphenol A (BPA), production of alternatives such as bi
107 hlorophenol (25-DCP), benzophenone-3 (BP-3), bisphenol A (BPA), triclosan (TCS), butyl paraben (B-PB)
108 Analytes included parabens, phthalates, bisphenol A (BPA), triclosan, ethanolamines, alkylphenol
120 ime polymerase chain reaction indicated that bisphenol A and bisphenol AF consistently activated endo
121 e strain CBDB1 completely converted TBBPA to bisphenol A and BPB to phenol red with a stepwise remova
123 ansgenic reporter demonstrated that the EEDs bisphenol A and genistein preferentially activate estrog
128 g and toxic pollutants, many of which (e.g., bisphenol A and substituted phenols) are known to be ins
132 ained from horse radish peroxidase (HRP) and bisphenol A assays were 12.5 ng/ml (2.84x10(-10) M ) and
133 ata values, with diethyl hexyl phthalate and bisphenol A being the most ubiquitous compounds detected
134 esorcinol bis(diphenylphosphate) (RBDPP) and bisphenol A bis(diphenylphosphate) (BPA-BDPP) are two ha
135 fication and temporal variability in urinary bisphenol A concentrations among couples in Utah-the HOP
136 e were no measured chlorinated byproducts of bisphenol A despite occasionally high concentrations of
140 A), bisphenol B (BPB), bisphenol F (BPF) and bisphenol A diglycidyl ether (BADGE) down to 0.50ng/mL;
145 cerol dimethacrylate (PMGDM) and ethoxylated bisphenol A dimethacrylate (EBPADMA) at mass ratio of 1:
146 xanediol dimethacrylate (HDDMA), ethoxylated bisphenol A dimethacrylate (EBPADMA), and urethane dimet
147 lectivity towards closely related compounds (bisphenol A dimethacrylate, and dibutyl phthalate).
148 d respiratory health, with ethyl-paraben and bisphenol A exhibiting some consistency across respirato
150 which factor, the dimethacrylate component, bisphenol A glycerolate dimethacrylate (BisGMA) or photo
151 2-hydroxyethyl methacrylate (HEMA) and 5% of bisphenol A glycidyl dimethacrylate (BisGMA) (PEHB).
153 als composed of a trimethacrylate monomer or bisphenol A glycidyl methacrylate, which is a monomer st
157 see that in these kind of food the amount of bisphenol A increases with an increase in the amount of
159 visualization of dose-dependent induction of Bisphenol A inducible genes showed a weak gene activatio
162 method was applied for the determination of bisphenol A migrated from some polycarbonate plastic pro
165 , the UV filter benzophenone-2 (BP2) and the bisphenol A substitute bisphenol S (BPS) was deciphered
167 intramolecular glycosylations using a rigid bisphenol A template supplemented with linkers of variou
168 ith FEV1% (beta=-0.59; 95% CI: -1.24, 0.05); bisphenol A tended to be associated with increased rates
169 free chlorine alone, while for triclosan and bisphenol A the free iodine mediated transformations wer
170 at levels ranging from 0.6 to 4.6ngg(-1) and bisphenol A was detected in all the samples at concentra
171 lutants) and nonpersistent (some phthalates, bisphenol A) environmental pollutants, and exposure to a
173 f other xenoestrogens (e.g., alkylphenols or bisphenol A) that are sometimes found in surface water.
175 mmonly targeted EDC and their isobars (e.g., bisphenol A, (Z)- and (E)-diethylstilbestrol, hexestrol,
176 water consumption was associated with higher bisphenol A, 2,4-dichlorophenol, and 2,5-dichlorophenol
178 e concentrations of 8 phthalate metabolites, bisphenol A, 25 polychlorinated biphenyls (PCBs), 6 orga
179 an environmentally relevant concentration of bisphenol A, a nearly ubiquitous environmental contamina
180 environmental contaminants (benzo[a]pyrene, bisphenol A, and acrolein) in human serum via a competit
182 hyl paraben, propyl paraben, benzophenone-3, bisphenol A, and triclosan in urine collected during 199
183 unds that contain a phenolic ring (parabens, bisphenol A, and triclosan) were completely transformed
185 hemical detection of the endocrine disruptor bisphenol A, as well as the capture of living nonadheren
186 ere used to examine the sorption affinity of bisphenol A, atrazine, and diuron to five soils of varyi
187 Exposure to environmental phenols (e.g., bisphenol A, benzophenone-3, and triclosan) and parabens
188 erum testosterone concentrations and urinary bisphenol A, benzophenone-3, triclosan, and paraben leve
191 s had overall false positive rates of </=5%, bisphenol A, caffeine, NP, OP, and triclosan had false p
193 d disinfection byproducts of salicylic acid, bisphenol A, gemfibrozil, naproxen, diclofenac, technica
194 ct on pbPPARG, while hexabromocyclododecane, bisphenol A, oxychlordane, and endosulfan were weak anta
195 ed for phthalates and to a lesser extent for bisphenol A, synthetic musks, some pesticides, and PAHs.
196 actone, genistein, daidzein, benzophenone-3, bisphenol A, the sum of parabens (methyl, ethyl, and pro
197 n significantly reduce the teratogenicity of bisphenol A, triclosan and 17alpha-ethinyl estradiol wit
200 oducts, namely methylparaben, propylparaben, bisphenol A, triclosan, galaxolide, and 4- methylbenzili
201 y diarylpropionitrile, genistein, equol, and bisphenol A, whereas its coactivation at the AP-1 site i
202 gel-filled, and water-filled (most labeled "bisphenol A-free"), were collected from the U.S. market
208 utrition Examination Survey in which urinary bisphenol A; triclosan; benzophenone-3; propyl, methyl,
216 lastic derived endocrine disruptor compounds bisphenol-A (BPA), bis(2-ethylhexyl)phthalate (DEHP) and
217 ny endocrine disrupting chemicals, including bisphenol-A (BPA), induce non-monotonic dose response (N
219 that gestational, but not adult, exposure to bisphenol-A increased the development of experimental au
226 A (BPA), production of alternatives such as bisphenol AF (BPAF) and bisphenol S (BPS) are increasing
227 such as BPA analogues bisphenol S (BPS) and bisphenol AF (BPAF) in production of consumer products;
228 tributed to EDCs, such as bisphenol A (BPA), bisphenol AF (BPAF), and zearalenone (Zea), but mechanis
229 s, bisphenol S (BPS), bisphenol F (BPF), and bisphenol AF (BPAF), in 616 archived samples collected f
230 hain reaction indicated that bisphenol A and bisphenol AF consistently activated endogenous ER target
233 the urinary concentrations of BPA and three bisphenol analogs, bisphenol S (BPS), bisphenol F (BPF),
234 mined vertical profiles of concentrations of bisphenol analogues in sediment cores from the U.S. and
236 study, concentrations and profiles of eight bisphenol analogues were determined using high-performan
239 silico evaluation of the interaction between bisphenols and ERs or other members of the nuclear hormo
240 ographic analysis of the interaction between bisphenols and ERs reveals two discrete binding modes, r
241 the chemical replacements, however, are also bisphenols and may have similar physiological effects in
242 ethylhexyl) tetrabromophthalate, halogenated bisphenols and phenols, and hydroxylated PBDEs were foun
243 Common environmental contaminants such as bisphenols and phthalates and persistent contaminants su
244 amount of the sum of nine bisphenols (Sigma9 bisphenols) and 5 benzophenones (Sigma5 benzophenones) l
248 diglycidyl ether (BFDGE), bisphenol A (BPA), bisphenol B (BPB), bisphenol F (BPF) and bisphenol A dig
249 Parabens (p-hydroxybenzoic acid esters), bisphenols, benzophenone-type UV filters, triclosan, and
250 bisalkylsulfonyl fluorides (AA monomers) and bisphenol bis(t-butyldimethylsilyl) ethers (BB monomers)
252 the toxicity and teratogenic effects of the bisphenols BPA, BPS, BPF, and BPAF in zebrafish embryo-l
260 se extraction method for the enrichment of 5 bisphenol derivatives using hexagonal boron nitride (BN)
262 FDGE), bisphenol A (BPA), bisphenol B (BPB), bisphenol F (BPF) and bisphenol A diglycidyl ether (BADG
265 to structurally similar compounds including bisphenol F (BPF) or bisphenol S (BPS) even at much high
267 three bisphenol analogs, bisphenol S (BPS), bisphenol F (BPF), and bisphenol AF (BPAF), in 616 archi
269 ery sensitive, allowing for determination of bisphenol F diglycidyl ether (BFDGE), bisphenol A (BPA),
270 Bisphenol A diglycidyl ether (BADGE)- and bisphenol F diglycidyl ether (BFDGE)-based epoxy resins
271 omatography-tandem mass spectrometry, BADGE, bisphenol F glycidyl ether (BFDGE), 3-ring NOGE, and eig
273 ethod for simultaneous determination of five bisphenols in canned energy drinks by UPLC with fluoresc
274 to determine contamination levels from these bisphenols in forty energy drinks of different brands, c
276 henols ( summation operatorBPs; sum of eight bisphenols) in dust were in the range of 0.026-111 mug/g
277 We assessed the potential EA of both a new bisphenol monomer used to synthesize polymeric coatings
280 le absorption of BPA or the BPA alternatives bisphenol S (BPS) and 4-hydroxyphenyl 4-isoprooxyphenyls
281 of alternate chemicals such as BPA analogues bisphenol S (BPS) and bisphenol AF (BPAF) in production
283 alternatives such as bisphenol AF (BPAF) and bisphenol S (BPS) are increasing, but little is known on
285 lar compounds including bisphenol F (BPF) or bisphenol S (BPS) even at much higher concentration.
288 enone-2 (BP2) and the bisphenol A substitute bisphenol S (BPS) was deciphered in eight human and zebr
289 than the accepted human daily exposure) and bisphenol S (BPS), a common analog used in BPA-free prod
290 trations of BPA and three bisphenol analogs, bisphenol S (BPS), bisphenol F (BPF), and bisphenol AF (
296 ompounds in surface water, like caffeine and bisphenol-S, five dihydroxydiphenylmethane isomers were
301 s of BPF were generally lower than for other bisphenols, the 95th percentile concentration of BPF was
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