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1 a widely spread nephrotoxic food contaminant mycotoxin.
2 urkholderia) that produces rhixozin, a plant mycotoxin.
3 one gave dramatically enhanced levels of the mycotoxin.
4 ples (98%) were contaminated by at least one mycotoxin.
5 d grains are often contaminated with harmful mycotoxins.
6 by determining zearalenone and aflatoxin B1 mycotoxins.
7 eserving food that may exert some effects on mycotoxins.
8 als, leading to contamination of grains with mycotoxins.
9 ts cause is hypothesised to involve Fusarium mycotoxins.
10 was applied in this work to the screening of mycotoxins.
11 nated by various fungi, capable of producing mycotoxins.
12 were lower than 10mugkg(-1) for the selected mycotoxins.
13 e lower than TDI for all legislated Fusarium mycotoxins.
14 80% of analyzed samples contained mycotoxins.
15 echnologies and also referred to as "masked" mycotoxins.
16 xic, mutagenic, teratogenic and carcinogenic mycotoxins.
17 ol and beauvericin were the most predominant mycotoxins.
18 l as a cross-reactivity study with 25 common mycotoxins.
19 le, although very low levels, of two or more mycotoxins.
20 C3 hydroxyl moiety of several trichothecene mycotoxins.
21 se enzymes with coenzyme A and trichothecene mycotoxins.
22 ushroom poisonings and the toxicokinetics of mycotoxins.
23 e the most potent genotoxic and carcinogenic mycotoxins.
24 , but significantly higher than the original mycotoxins.
25 sceptible to fungal contamination as well as mycotoxins.
26 identified including two to seven different mycotoxins.
27 ereal samples were contaminated with several mycotoxins.
28 ble to that of the enniatins and beauvericin mycotoxins.
29 , 3 hexabromocyclododecane (HBCD) isomers, 6 mycotoxins, 6 inorganic compounds) together with chemica
31 ipal enzymes responsible for detoxifying the mycotoxin aflatoxin B(1) (AFB(1)) and GST dysfunction is
32 amples (90%) were positive for the following mycotoxins: aflatoxin B1 (50 mug/kg), alternariol monome
33 n of their marker - ergosterol and important mycotoxins (aflatoxins B1, B2, G1 and G2, and ochratoxin
34 nal bioaccessibility for both mycotoxins and mycotoxin-AITC conjugates, with duodenal fractions repre
35 od for the determination of three Alternaria mycotoxins (alternariol, alternariol monomethyl ether, a
38 polymer microspheres selective to Alternaria mycotoxins, alternariol (AOH) and alternariol monomethyl
41 hibition of biosynthesis of the carcinogenic mycotoxin and secondary metabolite, aflatoxin B1 in the
43 s in electrochemical affinity biosensors for mycotoxins and covers complete literature from the first
45 d by LC-MS for simultaneous determination of mycotoxins and fungicide residues in wheat grains suscep
47 tive recognition from aptamers to the target mycotoxins and further "on-the-move" fluorescence quench
49 ms to assess the co-occurrence of twenty-one mycotoxins and metabolites present in breakfast cereals
50 gher than duodenal bioaccessibility for both mycotoxins and mycotoxin-AITC conjugates, with duodenal
52 Relatively high levels of the main regulated mycotoxins and presence of non-regulated mycotoxins in f
53 a followed first order kinetics for analysed mycotoxins and thermal constant rates (k) were calculate
54 S system to confirm the identity of detected mycotoxins and to identify other possible microbial meta
56 ght into the mode of action of trichothecene mycotoxins and uncover a critical role for mitochondrial
58 gs support the hypothesis that trichothecene mycotoxins, and in particular NIV, have the potential to
67 ds have been already reported for legislated mycotoxins as trichothecenes and zearalenone (ZON) separ
68 ectronic properties of LMOF-241 and selected mycotoxins, as well as the extent of mycotoxin-LMOF inte
69 ith unlabeled OTA we were able to detect the mycotoxin at concentrations lower than E.U. specificatio
71 lenol and beta-zearalenol), and six emergent mycotoxins, beauvericin and five enniatins (A, A1, B, B1
72 s that plays an important role in regulating mycotoxin biosynthesis and virulence of F. graminearum.
74 r ultrasensitive detection of AFB1 and other mycotoxins by replacing the core recognition sequence of
81 edge on health effects posed by ingestion of mycotoxins-contaminated food and feed by humans and live
82 serious health and economic consequences of mycotoxin contamination have created the need for rapid,
83 t and barley that leads to reduced yield and mycotoxin contamination of grain, making it unfit for hu
87 rns pertaining towards fungal occurrence and mycotoxins contamination in agri-food commodities has be
89 ore, millet flour is commonly susceptible to mycotoxin contaminations, so the Ochratoxin A residues w
92 component of the early wheat response to the mycotoxin deoxynivalenol (DON), which is a virulence fac
94 scent biolabels for immunoassay detection of mycotoxin deoxynivalenol in food and feed, CdSe/CdS/ZnS
95 were successfully used for determination of mycotoxin deoxynivalenol in wheat and maize samples by f
96 s to almost the same extent as the prominent mycotoxin deoxynivalenol, while NX-2 is far less toxic,
97 t study is to determine the incidence of the mycotoxins deoxynivalenol (DON) and fumonisin B1 (FB1) i
98 he study was mainly focused on the following mycotoxins: deoxynivalenol, deoxynivalenol-3-glucoside,
99 e frequently contaminated by the presence of mycotoxins derived from Fusarium fungus, and, in particu
100 ich produced none of the known trichothecene mycotoxins despite causing normal disease symptoms.
101 development of a user friendly biosensor for mycotoxin detection at both academic and industrial leve
103 aptasensor, enzymatic sensors and others for mycotoxin detection with a reference to label and label
104 nt of an innovative immunosensing method for mycotoxin detection, based on antibody-immobilized micro
105 aspects in the development of biosensors for mycotoxin detection, current challenges and future prosp
106 Remarkable accuracy (Er < 5%) during the mycotoxin determination in certified reference material
107 od is an accurate, safe and rapid method for mycotoxins determination in meat products to ensure thei
109 ween 25.5 and 96.8%, appeared for all of the mycotoxins, especially for deepoxy-deoxynivalenol, zeara
112 n exposure; to evaluate associations between mycotoxin exposure and child stunting; and to investigat
114 vestigate EED as a potential pathway linking mycotoxin exposure to child stunting, to inform potentia
115 tween agricultural and harvest practices and mycotoxin exposure; to evaluate associations between myc
117 the recipe formulation has an impact on the mycotoxins extractability by affecting the biscuit micro
121 Samples were surveyed for the presence of 22 mycotoxins (four aflatoxins, ochratoxin A, diacetoxiscyr
123 t the isolation of secalonic acid-D (SAD), a mycotoxin from a novel source that exhibits potent antia
124 optimized for the selective isolation of the mycotoxins from aqueous samples coupled to HPLC with flu
125 Here we report that PCD triggered by the mycotoxin fumonisin B1 (FB1) can be suppressed by PTI in
126 activity and sensitivity to the PCD-inducing mycotoxin fumonisin B1 (FB1) were increased by ssSPTa ov
128 xhibited reduced sensitivity to PCD-inducing mycotoxin fumonisin B1 as well as oxidative stress induc
129 stance to the programmed cell death-inducing mycotoxin fumonisin B1, with an accompanying reduced acc
130 reliable assessment of two highly concerning mycotoxins (fumonisin B1 (FB1) and ocratoxin A (OTA)) ha
132 heoretical and experimental CCS obtained for mycotoxin glucuronides suggested the potential of the CC
133 against cell and DNA damage induced by both mycotoxins, implying that OTA and FB1 cytogenotoxicity m
135 flatoxin B2 was the most frequently detected mycotoxin in water samples, with a maximum concentration
137 f beer and beer-based drinks, the occurrence mycotoxins in 154 beer samples was topic of investigatio
138 assay was successfully validated for these 3 mycotoxins in a corn-based feed sample after a simple sa
139 r nearly two years the occurrence of various mycotoxins in a field cropped with winter wheat of the v
140 ysite, and tests for efficient adsorption of mycotoxins in animals' stomachs are also carried out.
141 different Fusarium toxins including modified mycotoxins in beer (deoxynivalenol-3-glucoside, deoxyniv
142 is necessary to establish maximum levels of mycotoxins in beer in Brazil and other countries in orde
143 luated the ability of these fungi to produce mycotoxins in both native grass and wheat hosts using bi
144 s of arid regions), reduce human exposure to mycotoxins in buildings and our food-supply chain, preve
146 onal report to study the presence of several mycotoxins in different types of cereal (rice, wheat, ma
148 ferences between levels or incidence for the mycotoxins in different years of harvest, variety of bar
156 contamination levels (<1100mug/kg) of these mycotoxins in multicereal baby food and its intakes coul
157 ped for the simultaneous determination of 11 mycotoxins in plant-based beverage matrices, using a QuE
160 applied to detect the presence of the target mycotoxins in real samples (fruits and juices) purchased
162 ing time play important roles for minimizing mycotoxins in the final products, while the recipe formu
164 ining towards fungal occurrence and level of mycotoxins in various oil seeds and their edible oils.
165 an analytical method for the detection of 25 mycotoxins in wheat grain based on simultaneous extracti
167 ensitivity to monitor contamination of these mycotoxins in wheat in accordance with European Commissi
168 In order to explore the early detection of mycotoxins in wheat three standardized approaches (Fusar
179 the percentage of moldy and fermented beans, mycotoxins levels, phenolic acids content, pasting prope
180 elected mycotoxins, as well as the extent of mycotoxin-LMOF interactions, employing theoretical metho
185 A stable isotope dilution LC-MS/MS multi-mycotoxin method was developed for 12 different Fusarium
190 g toxicity, we demonstrate that the volatile mycotoxin, N-methyl-N-nitrosoisobutyramide, is the domin
192 he present study, the occurrence of eighteen mycotoxins, nine trichothecenes (deoxynivalenol, 3-acety
196 ainst cytotoxicity and DNA damage induced by mycotoxins ochratoxin A (OTA) and fumonisin B1 (FB1).
197 tested for the simultaneous detection of the mycotoxins ochratoxin A (OTA), aflatoxin B1 (AFB1) and d
198 nd rapid method for the determination of ten mycotoxins (ochratoxin A, fumonisin B1, fumonisin B2, de
200 sorbent for the extraction of a group of six mycotoxins of interest including zearalenone, alpha-zear
201 method achieves the quantification of those mycotoxins of major concern and mycotoxins that are not
202 omplex isolates, known to produce the target mycotoxins on pure cultures, were analyzed and alternari
208 ations commonly consume food contaminated by mycotoxins, particularly aflatoxins (predominantly found
210 hows a limited cross-reactivity to different mycotoxins, paving the way to a highly specific techniqu
211 markable symbiosis is reduced deoxynivalenol mycotoxin, potentially benefiting millions of subsistenc
212 l of 32 compounds, classified as pesticides, mycotoxins, process-induced toxicants or packaging conta
213 chratoxin A (OTA), is a natural carcinogenic mycotoxin produced by Aspergillus and Penicillium fungi
214 f Ochratoxin A (OTA), a natural carcinogenic mycotoxin produced by Aspergillus and Penicillium fungi,
216 widespread and abundant natural carcinogenic mycotoxin produced by several species of Aspergillus and
217 nes are a class of photoactivated polyketide mycotoxins produced by fungal plant pathogens that notab
218 s and alkaloids that are produced by plants; mycotoxins produced by fungi; antimicrobials and acarici
221 Fumonisins are a group of polyketide-derived mycotoxins produced by Fusarium verticillioides, a filam
225 any agronomically important plant pathogens, mycotoxin producers, and opportunistic human pathogens.
226 it secondary metabolite syntheses in several mycotoxin producing filamentous fungi, these effects are
227 ical methodology for the characterization of mycotoxin-producing fungal species from the genera Asper
228 c profiles were able to discriminate between mycotoxin-producing fungi from different sections and to
231 seed from native grasses for the presence of mycotoxin-producing Fusarium species and evaluated the a
233 ction is important for host colonization and mycotoxin production and may provide a promising target
240 between causes of mortality, consumption of mycotoxin-prone foods, and socioeconomic variables were
241 n to test the hypotheses that consumption of mycotoxin-prone staple foods is 1) related to the incide
243 assays for Fusarium spp. identification and mycotoxin quantification) and a novel untargeted metabol
248 vergent and operationally simple approach to mycotoxin-related 4-amino-substituted 1-hydroxydihydroxa
250 ethod for the determination of a total of 12 mycotoxins simultaneously, nine trichothecenes (NIV, DON
254 idiation) and production of the carcinogenic mycotoxin sterigmatocystin (ST) in the model filamentous
255 DeltappoC mutants were unable to produce the mycotoxin sterigmatocystin (ST) in vitro or in planta bu
257 mponents and developmental regulators in the mycotoxin sterigmatocystin biosynthesis in the model fun
258 ted the effect of light on production of the mycotoxin sterigmatocystin in a veA wild-type and the ve
261 ed beverages have been analysed, and certain mycotoxins, such as deoxynivalenol, aflatoxin B1, aflato
264 ion of those mycotoxins of major concern and mycotoxins that are not frequently studied in milk, such
265 Trichothecenes are phytotoxic sesquiterpenic mycotoxins that can act as virulence factors in plant di
267 An emerging concern is frequent exposure to mycotoxins that contaminate a wide range of staple foods
268 l chemicals (including pesticides, hormones, mycotoxins) that we measured specifically for this valid
270 red to produce sesquiterpene (trichothecene) mycotoxins, the endoplasmic reticulum (ER) of the phytop
273 recommended to study food processing fate of mycotoxins through naturally contaminated materials (inc
275 Typically, electrochemical biosensors for mycotoxins use specific antibodies or aptamers as affini
277 simultaneous immunodetection of these three mycotoxins was demonstrated via the laminar flow pattern
280 rinciple, deoxynivalenol (DON), an important mycotoxin, was captured using an SPR gold chip containin
294 to a rare class of fungal tetracycline-like mycotoxins, were subjected to comprehensive spectroscopi
296 d nanoparticles that can efficiently prevent mycotoxins with minimal risk to health and environment.
297 ollows: suitable linearity ranges for all 23 mycotoxins with p-value >0.05; limits of detection (1.2-
298 on of the antiangiogenic activity of a novel mycotoxin, with potential application as a cancer-select
299 as concerned with the fate of these Fusarium mycotoxins within malting, brewing, milling and baking,
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