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1 micals such as phthalates and phenols (e.g., bisphenol A).
2 ahistidine peptide for the quantification of bisphenol A.
3 ates, diethylhexyl adipate, alkylphenols and bisphenol A.
4 her than the corresponding concentrations of bisphenol A.
5 co-crystallized with an alkyl derivative of bisphenol A.
8 Our results propose a new mode of action for bisphenol A (10) that advocates a reduced exposure to th
10 trations of BADGE and its three derivatives, bisphenol A (2,3-dihydroxypropyl) glycidyl ether [BADGE.
11 water consumption was associated with higher bisphenol A, 2,4-dichlorophenol, and 2,5-dichlorophenol
13 e concentrations of 8 phthalate metabolites, bisphenol A, 25 polychlorinated biphenyls (PCBs), 6 orga
14 hydroxypropyl) glycidyl ether [BADGE.H(2)O], bisphenol A (3-chloro-2-hydroxypropyl) (2,3-dihydroxypro
15 the approach allows the direct detection of bisphenol A, a low molecular weight (228 Da) target usua
16 an environmentally relevant concentration of bisphenol A, a nearly ubiquitous environmental contamina
19 midispersive solid phase extraction of eight bisphenols (A, AF, AP, C, BP, G, M, and Z) from river wa
20 By combination with an antibody directed to bisphenol A (alphaBPA), this conducting polymer-based bi
27 ime polymerase chain reaction indicated that bisphenol A and bisphenol AF consistently activated endo
28 e strain CBDB1 completely converted TBBPA to bisphenol A and BPB to phenol red with a stepwise remova
30 ansgenic reporter demonstrated that the EEDs bisphenol A and genistein preferentially activate estrog
33 cals as EDCs, and we use diethylstilbestrol, bisphenol A and perchlorate as examples to illustrate th
36 minent plastic-associated chemicals, such as bisphenol A and phthalates, have been thoroughly studied
37 g and toxic pollutants, many of which (e.g., bisphenol A and substituted phenols) are known to be ins
39 dichlorophenols, triclosan, benzophenone-3, bisphenol A) and 11 phthalate metabolites were measured
40 b copper, 5 ppb cadmium, 10 ppb lead, 10 ppb bisphenol A, and 1 ppb paraoxon, tested as safety limits
41 environmental contaminants (benzo[a]pyrene, bisphenol A, and acrolein) in human serum via a competit
42 to exhibit the highest sorption capacity for bisphenol A, and it was almost irreversible, probably du
44 hyl paraben, propyl paraben, benzophenone-3, bisphenol A, and triclosan in urine collected during 199
45 unds that contain a phenolic ring (parabens, bisphenol A, and triclosan) were completely transformed
49 hemical detection of the endocrine disruptor bisphenol A, as well as the capture of living nonadheren
50 ained from horse radish peroxidase (HRP) and bisphenol A assays were 12.5 ng/ml (2.84x10(-10) M ) and
51 ere used to examine the sorption affinity of bisphenol A, atrazine, and diuron to five soils of varyi
52 ata values, with diethyl hexyl phthalate and bisphenol A being the most ubiquitous compounds detected
53 Exposure to environmental phenols (e.g., bisphenol A, benzophenone-3, and triclosan) and parabens
54 erum testosterone concentrations and urinary bisphenol A, benzophenone-3, triclosan, and paraben leve
55 ihydroxypropyl) ether [BADGE.HCl.H(2)O], and bisphenol A bis (2,3-dihydroxypropyl) ether [BADGE.2H(2)
56 esorcinol bis(diphenylphosphate) (RBDPP) and bisphenol A bis(diphenylphosphate) (BPA-BDPP) are two ha
60 hinylestradiol (EE2)] and two xenoestrogens [bisphenol A (BPA) and 4-n-nonyl-phenol (NP)] in surface
63 al was to provide a definitive evaluation of bisphenol A (BPA) and explain disparities between tradit
66 cerns exist regarding children's exposure to bisphenol A (BPA) and other phenols because of the highe
67 the impact of serially assessed exposure to bisphenol A (BPA) and phthalates on measures of kidney f
68 ence regarding associations for exposures to bisphenol A (BPA) and phthalates with type 2 diabetes (T
69 is growing concern that prenatal exposure to bisphenol A (BPA) and phthalates, which are widely used
76 erns, variability, and predictors of urinary bisphenol A (BPA) concentrations in 337 children from th
78 ivity, bisphenol S (BPS) as a substitute for bisphenol A (BPA) could actually increase the risk of en
79 ry method for the determination of different bisphenol A (BPA) derivatives such as bisphenol A diglyc
80 ent study revealed that prenatal exposure to bisphenol A (BPA) disrupted the transcriptome profiles o
82 n expert panel reviewed associations between bisphenol A (BPA) exposure and reproductive health outco
87 ticipants previously randomly selected for a bisphenol A (BPA) exposure study who had unusually high
89 As concern regarding the toxic effects of bisphenol A (BPA) grows, BPA in many consumer products i
94 Prenatal exposure to nonylphenol (NP) and/or bisphenol A (BPA) has been reported to be associated wit
95 Widespread environmental contamination by bisphenol A (BPA) has created the need to fully define i
96 widespread environmental disrupting chemical bisphenol A (BPA) has estrogenic activity, but its impli
99 We report on an innovative heterogeneous bisphenol A (BPA) immunoassay based on an electrolyte-ga
101 ead use of the endocrine disrupting chemical bisphenol A (BPA) in consumer products has resulted in n
104 s increasingly been used as a substitute for bisphenol A (BPA) in some "BPA-free" consumer goods and
105 ectrochemical biosensor for the detection of Bisphenol A (BPA) in water has been developed by immobil
106 y bottles, little attention has been paid to bisphenol A (BPA) intake from packaged water consumption
127 ure to the environmental endocrine disruptor bisphenol A (BPA) is ubiquitous and associated with the
134 products from store shelves after reports of bisphenol A (BPA) leaching from baby bottles, reusable d
135 oprobe is designed for the quantification of bisphenol A (BPA) levels in the blood after human exposu
136 rly-life exposure to the endocrine disruptor bisphenol A (BPA) may contribute to the development of o
137 tory actions and public concerns, the use of bisphenol A (BPA) may decrease, while the use of BPA alt
144 ion on the homogeneous Fenton degradation of bisphenol A (BPA) used as a model pollutant, was investi
149 to replace the endocrine disrupting chemical bisphenol A (BPA) while exerting estrogenic effects of c
150 scharge of the endocrine disrupting compound bisphenol A (BPA) with wastewater treatment plant (WWTP)
151 sed on the MS results these were assigned to bisphenol A (BPA), 2,4-di-tert-butylphenol, and a possib
154 t chronic exposure of synthetic xenoestrogen bisphenol A (BPA), a component of consumer plastic produ
161 al models suggests that prenatal exposure to bisphenol A (BPA), a ubiquitous endocrine-disrupting che
164 S (BPS) are increasingly used to substitute bisphenol A (BPA), a widespread environmental endocrine
166 perimental laboratory evidence suggests that bisphenol A (BPA), an endocrine disruptor, is a neurodev
170 to investigate the carcinogenic property of Bisphenol A (BPA), an environmental estrogen, by long-te
173 crine-disrupting chemicals (EDCs), including bisphenol A (BPA), are environmental ubiquitous pollutan
175 phenoxyethanol (2-PE), 4-nonylphenol (4-NP), bisphenol A (BPA), benzylbuthyl phthalate (BBP) and dime
176 al samples were analyzed for the presence of bisphenol A (BPA), bis (2-ethylhexyl) phthalate (DEHP),
177 like activity is attributed to EDCs, such as bisphenol A (BPA), bisphenol AF (BPAF), and zearalenone
178 ion of bisphenol F diglycidyl ether (BFDGE), bisphenol A (BPA), bisphenol B (BPB), bisphenol F (BPF)
179 e promising lignin-derivable alternatives to bisphenol A (BPA), but limited bioassay data are availab
181 ironment of some of these chemicals, such as bisphenol A (BPA), external contamination during handlin
184 of environmental contaminants, particularly bisphenol A (BPA), is understudied with regard to PTB.
185 docrine disrupting compounds (EDCs), such as bisphenol A (BPA), may cause adverse health effects in w
186 vestigated the direct effects of exposure to bisphenol A (BPA), mono-n-butyl phthalate (Pht), and pol
187 in (GEN), and in industrial chemicals, e.g., bisphenol A (BPA), present in plastics and other product
188 With the pressure to ban or limit the use of bisphenol A (BPA), production of alternatives such as bi
189 on ROS scavengers inhibited the oxidation of bisphenol A (BPA), suggesting the possible involvement o
190 hlorophenol (25-DCP), benzophenone-3 (BP-3), bisphenol A (BPA), triclosan (TCS), butyl paraben (B-PB)
191 Analytes included parabens, phthalates, bisphenol A (BPA), triclosan, ethanolamines, alkylphenol
200 like estrogen, the well-studied xenoestrogen bisphenol A (BPA, a plastics monomer), induces strong br
201 A-seq in endometrial cancer cells exposed to bisphenol A (BPA; found in plastics), genistein (GEN; fo
211 lastic derived endocrine disruptor compounds bisphenol-A (BPA), bis(2-ethylhexyl)phthalate (DEHP) and
212 ny endocrine disrupting chemicals, including bisphenol-A (BPA), induce non-monotonic dose response (N
213 t famous member of this family of compounds, bisphenol-A (BPA), when spiked (at 1 mug.g(-1) concentra
214 s had overall false positive rates of </=5%, bisphenol A, caffeine, NP, OP, and triclosan had false p
217 Linking Academic and Regulatory Insights on Bisphenol-A (CLARITY-BPA) is a rare collaboration of gui
218 the formation of chlorinated derivatives of Bisphenol A (ClxBPA), that have higher estrogenic activi
219 fication and temporal variability in urinary bisphenol A concentrations among couples in Utah-the HOP
220 in diastolic BP were observed with maternal bisphenol-A concentrations (0.7 mm Hg [95% CI: 0.1 to 1.
221 e patterns were observed on spin-coated poly(bisphenol A decane ether) (BA-C10) films prepared with c
222 e were no measured chlorinated byproducts of bisphenol A despite occasionally high concentrations of
226 p-Hydroxybenzoic acid esters (parabens) and bisphenol A diglycidyl ether (BADGE) are widely present
227 A), bisphenol B (BPB), bisphenol F (BPF) and bisphenol A diglycidyl ether (BADGE) down to 0.50ng/mL;
228 ferent bisphenol A (BPA) derivatives such as bisphenol A diglycidyl ether (BADGE), bisphenol F diglyc
232 against similarly filled methacrylate-based bisphenol A diglycidyl ether dimethacrylate / triethylen
234 th were randomized to amalgam or composites (bisphenol-A-diglycidyl-dimethacrylate composite for perm
235 cerol dimethacrylate (PMGDM) and ethoxylated bisphenol A dimethacrylate (EBPADMA) at mass ratio of 1:
236 xanediol dimethacrylate (HDDMA), ethoxylated bisphenol A dimethacrylate (EBPADMA), and urethane dimet
237 lectivity towards closely related compounds (bisphenol A dimethacrylate, and dibutyl phthalate).
238 lutants) and nonpersistent (some phthalates, bisphenol A) environmental pollutants, and exposure to a
239 d respiratory health, with ethyl-paraben and bisphenol A exhibiting some consistency across respirato
243 gel-filled, and water-filled (most labeled "bisphenol A-free"), were collected from the U.S. market
244 d disinfection byproducts of salicylic acid, bisphenol A, gemfibrozil, naproxen, diclofenac, technica
245 which factor, the dimethacrylate component, bisphenol A glycerolate dimethacrylate (BisGMA) or photo
246 2-hydroxyethyl methacrylate (HEMA) and 5% of bisphenol A glycidyl dimethacrylate (BisGMA) (PEHB).
248 als composed of a trimethacrylate monomer or bisphenol A glycidyl methacrylate, which is a monomer st
249 ies show that bisphenol A (BPA) leaches from bisphenol A-glycidyl methacrylate (bisGMA)-based dental
253 ens, including the environmental contaminant bisphenol A, have also been linked to reproductive probl
256 In this study, the sorption and release of bisphenol A in marine water were investigated through la
257 osensor capable of detecting the presence of bisphenol A in ultra-low concentrations, yielding a wave
259 that gestational, but not adult, exposure to bisphenol-A increased the development of experimental au
260 see that in these kind of food the amount of bisphenol A increases with an increase in the amount of
262 visualization of dose-dependent induction of Bisphenol A inducible genes showed a weak gene activatio
270 method was applied for the determination of bisphenol A migrated from some polycarbonate plastic pro
271 ribe a mixture of phthalates, pesticides and bisphenol A (mixture N1) detected in pregnant women of t
273 ct on pbPPARG, while hexabromocyclododecane, bisphenol A, oxychlordane, and endosulfan were weak anta
275 or by four major endocrine disruptor classes:bisphenol A, polychlorinated biphenyls, organophosphates
279 , the UV filter benzophenone-2 (BP2) and the bisphenol A substitute bisphenol S (BPS) was deciphered
281 ed for phthalates and to a lesser extent for bisphenol A, synthetic musks, some pesticides, and PAHs.
283 intramolecular glycosylations using a rigid bisphenol A template supplemented with linkers of variou
284 ith FEV1% (beta=-0.59; 95% CI: -1.24, 0.05); bisphenol A tended to be associated with increased rates
285 f other xenoestrogens (e.g., alkylphenols or bisphenol A) that are sometimes found in surface water.
286 free chlorine alone, while for triclosan and bisphenol A the free iodine mediated transformations wer
287 actone, genistein, daidzein, benzophenone-3, bisphenol A, the sum of parabens (methyl, ethyl, and pro
288 compounds detected, one plastics component (bisphenol A), three pharmaceuticals (carbamazepine, sulf
289 rders of magnitude from a low of 0.6 ppm for bisphenol A to a high of > 180,000 ppm for methyl parabe
290 n significantly reduce the teratogenicity of bisphenol A, triclosan and 17alpha-ethinyl estradiol wit
293 oducts, namely methylparaben, propylparaben, bisphenol A, triclosan, galaxolide, and 4- methylbenzili
294 utrition Examination Survey in which urinary bisphenol A; triclosan; benzophenone-3; propyl, methyl,
295 dence of associations between raised urinary bisphenol A (uBPA) and increased incidence of reported c
296 at levels ranging from 0.6 to 4.6ngg(-1) and bisphenol A was detected in all the samples at concentra
298 y diarylpropionitrile, genistein, equol, and bisphenol A, whereas its coactivation at the AP-1 site i
299 cles can serve as transportation vectors for bisphenol A, which may constitute an ecological risk.
300 mmonly targeted EDC and their isobars (e.g., bisphenol A, (Z)- and (E)-diethylstilbestrol, hexestrol,