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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
30                                              Mycotoxins affect a broad range of agricultural products
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
36                    Among them, the "emerging mycotoxin" alternariol and alternariol-methyl ether arou
37              The stability of two Alternaria mycotoxins, alternariol (AOH) and alternariol monomethyl
38 polymer microspheres selective to Alternaria mycotoxins, alternariol (AOH) and alternariol monomethyl
39                       The method applied for mycotoxin analyses included high performance liquid chro
40 fore fulfilling the current requirements for mycotoxins analysis.
41 hibition of biosynthesis of the carcinogenic mycotoxin and secondary metabolite, aflatoxin B1 in the
42 sion confers increased root tolerance to the mycotoxin and spike resistance to the fungus.
43 s in electrochemical affinity biosensors for mycotoxins and covers complete literature from the first
44 e Mediterranean area, estimate the intake of mycotoxins and evaluate the risk assessment.
45 d by LC-MS for simultaneous determination of mycotoxins and fungicide residues in wheat grains suscep
46 consumed cereals, and can be contaminated by mycotoxins and fungicides.
47 tive recognition from aptamers to the target mycotoxins and further "on-the-move" fluorescence quench
48 tandardized approaches were able to quantify mycotoxins and identify Fusarium spp.
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
51             This is the first study in which mycotoxins and other microbial metabolites occurring in
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
55 soil organic matter, was investigated for 29 mycotoxins and two phytoestrogens.
56 ght into the mode of action of trichothecene mycotoxins and uncover a critical role for mitochondrial
57 ON) produced by the pathogen is an important mycotoxins and virulence factor.
58 gs support the hypothesis that trichothecene mycotoxins, and in particular NIV, have the potential to
59        However, the co-occurrence of several mycotoxins, and therefore synergic or additive effects,
60                                  Tremorgenic mycotoxins are a group of indole alkaloids which include
61                                              Mycotoxins are highly toxic secondary metabolites produc
62                                Trichothecene mycotoxins are natural contaminants of small grain cerea
63                                              Mycotoxins are secondary metabolites of fungi that cause
64                                              Mycotoxins are secondary metabolites that are naturally
65                                        Three mycotoxins are suspected to contribute to poor child hea
66            The ecotoxicological relevance of mycotoxins as newly identified aquatic micropollutants h
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
70     The method enabled quantification of the mycotoxin at the levels set by European legislation and
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.
73 odetection of low concentrations of multiple mycotoxins by microcantilever resonator arrays.
74 r ultrasensitive detection of AFB1 and other mycotoxins by replacing the core recognition sequence of
75                                        These mycotoxins can enter human food chain via use of edible
76 icide 2,4-dichlorophenoxyacetic acid and the mycotoxin citrinin were used as model analytes.
77 n increasing health concern due to potential mycotoxins combined effects.
78         Baking temperature, time and initial mycotoxin concentration in the raw materials were assaye
79                   The influence of excessive mycotoxin concentrations on yeast growth, productivity a
80                   Human exposure to multiple mycotoxins constitutes an increasing health concern due
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
84                                    The multi-mycotoxin contamination of ninety-eight (98) couscous se
85            A reliable exposure assessment of mycotoxin contamination relies on their unambiguous iden
86 production, resulting in both yield loss and mycotoxin contamination.
87 rns pertaining towards fungal occurrence and mycotoxins contamination in agri-food commodities has be
88                                              Mycotoxins contamination in both food and feed is inevit
89 ore, millet flour is commonly susceptible to mycotoxin contaminations, so the Ochratoxin A residues w
90  have been scarcely explored regarding their mycotoxin content.
91                          The biosynthesis of mycotoxin deoxynivalenol (DON) in Fusarium graminearum i
92 component of the early wheat response to the mycotoxin deoxynivalenol (DON), which is a virulence fac
93 l suspension cultures in the presence of the mycotoxin deoxynivalenol (DON).
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
102                                              Mycotoxin detection in food and feedstock in particular
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
108  Fusarium verticillioides produces fumonisin mycotoxins during colonization of maize.
109 ween 25.5 and 96.8%, appeared for all of the mycotoxins, especially for deepoxy-deoxynivalenol, zeara
110 lues were between 82.6 and 94.4% for all the mycotoxins, except for fumonisins.
111 whole set of neutral toxins, largely because mycotoxins exhibit highly complex structures.
112 n exposure; to evaluate associations between mycotoxin exposure and child stunting; and to investigat
113               We summarize the evidence that mycotoxin exposure is associated with stunting, and prop
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
116   No toxicological concern was associated to mycotoxins exposure for average beer consumers.
117  the recipe formulation has an impact on the mycotoxins extractability by affecting the biscuit micro
118 omise for future adaptation to include other mycotoxins for multiplex detection.
119                                    The major mycotoxin found was enniatin B4; it was detected in 40%
120                    Fumonisins are a group of mycotoxins found in various foods whose consumption is k
121 Samples were surveyed for the presence of 22 mycotoxins (four aflatoxins, ochratoxin A, diacetoxiscyr
122                      Ochratoxin A (OTA) is a mycotoxin frequently encountered in coffee.
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
127 ckbone and are targets for inhibition by the mycotoxin fumonisin B1 (FB1).
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
131 identified: a fungal serine protease and the mycotoxin gliotoxin.
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
134 s suppress pest-associated fungal growth and mycotoxin in corn.
135 flatoxin B2 was the most frequently detected mycotoxin in water samples, with a maximum concentration
136             Deoxynivalenol was the prevalent mycotoxin in wheat grain and epoxiconazole was the fungi
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
145        The simultaneous quantification of 15 mycotoxins in cow milk by liquid chromatography-mass spe
146 onal report to study the presence of several mycotoxins in different types of cereal (rice, wheat, ma
147 d for the detection and quantification of 23 mycotoxins in different varieties of sorghum.
148 ferences between levels or incidence for the mycotoxins in different years of harvest, variety of bar
149 nted and validated for the trace analysis of mycotoxins in drinking bottled waters.
150 ally relevant to the research on presence of mycotoxins in edible plant based oils.
151 ted mycotoxins and presence of non-regulated mycotoxins in feed samples were found.
152                              The presence of mycotoxins in food samples has been widely studied as we
153 esized and applied to the extraction of both mycotoxins in food samples.
154 gy was developed to determine pesticides and mycotoxins in food supplements.
155 ochemical biosensors in the determination of mycotoxins in foods.
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
158 e routine monitoring of the major Alternaria mycotoxins in pomegranates.
159  thermal treatment, may have implications on mycotoxins in products available for consumers.
160 applied to detect the presence of the target mycotoxins in real samples (fruits and juices) purchased
161 ed to provide good analytical results for 14 mycotoxins in rice.
162 ing time play important roles for minimizing mycotoxins in the final products, while the recipe formu
163 ecific technique, able to identify different mycotoxins in the sample.
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
166 y role in the diversity of fungal genera and mycotoxins in wheat grains.
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
169 tion for accurate quantification of patulin (mycotoxin) in strawberries.
170  graminearum produced more deoxynivalenol, a mycotoxin, in the primed treatment.
171 que for sensitive and selective detection of mycotoxins including PHO-A.
172 ctivity was observed in mature leaves during mycotoxin-induced cell death.
173 sis methods were applied to convert modified mycotoxins into their free aflatoxins.
174                    This low molecular weight mycotoxin is analyzed using an indirect competitive immu
175                                   The masked mycotoxins issue is of increasing relevance in the field
176 ole of aristolochic acid over the ubiquitous mycotoxin known as ochratoxin A.
177        This research work aimed to study how mycotoxin levels may be influenced by modifying the tech
178 meter can be a useful tool for prediction of mycotoxin levels.
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
181 ion in contamination with toxic elements and mycotoxins may be accomplished.
182                                              Mycotoxins may be found in syrups resulting from the use
183                               Xenoestrogenic mycotoxins may contaminate food and feed posing a public
184                                   This multi-mycotoxin method was applied to analyse plant-based beve
185     A stable isotope dilution LC-MS/MS multi-mycotoxin method was developed for 12 different Fusarium
186  analyzed by using the newly developed multi-mycotoxin method.
187 te risk assessment of children's exposure to mycotoxins mixtures in food.
188                              The presence of mycotoxins mixtures in foodstuffs as cereals has been re
189                                  ENB was the mycotoxin most found and levels in pasta and baby food r
190 g toxicity, we demonstrate that the volatile mycotoxin, N-methyl-N-nitrosoisobutyramide, is the domin
191        In rice cultures, a new trichothecene mycotoxin (named NX-2) was characterized by liquid chrom
192 he present study, the occurrence of eighteen mycotoxins, nine trichothecenes (deoxynivalenol, 3-acety
193         This study investigated the Fusarium mycotoxin Nivalenol (NIV) on the metabolism of bovine ar
194              Official methods of analysis of mycotoxins normally requires sophisticated instrumentati
195                  In the samples analyzed for mycotoxins occurrence, DON and FBs were present in 18% a
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
199                               Destruxin A, a mycotoxin of entomopathogenic fungus, Metarhizium anisop
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
203                       Co-exposure of mice to mycotoxins or DEP during pregnancy inhibited the LPS-ind
204          Some of the mice were co-exposed to mycotoxins or diesel exhaust particles (DEP) during preg
205             Although natural toxins, such as mycotoxins or phytoestrogens are widely studied and were
206                       Natural toxins such as mycotoxins or phytotoxins (bioactive compounds from fung
207                                         Both mycotoxins, OTA (4 mumol/l) and FB1 (20 mug/ml), induced
208 ations commonly consume food contaminated by mycotoxins, particularly aflatoxins (predominantly found
209             This study demonstrates that the mycotoxin patulin suppresses Toll-like receptor- and RIG
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,
215                      Fusaric acid (FSA) is a mycotoxin produced by several fusaria, including the ric
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
219                               Fumonisins are mycotoxins produced by Fusarium species that commonly li
220          Enniatins A, A1, B and B1 (ENs) are mycotoxins produced by Fusarium spp. and are normal cont
221 Fumonisins are a group of polyketide-derived mycotoxins produced by Fusarium verticillioides, a filam
222            Fumonisins are polyketide-derived mycotoxins produced by several plant pathogenic fungi.
223 r with negligible cross-reactivity for other mycotoxins produced by the same fungi species.
224                Trichothecenes are isoprenoid mycotoxins produced in wheat infected with the filamento
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
229              Head blight, which is caused by mycotoxin-producing fungi of the genus Fusarium, is an e
230                                              Mycotoxin-producing Fusarium graminearum and related spe
231 seed from native grasses for the presence of mycotoxin-producing Fusarium species and evaluated the a
232                                              Mycotoxin-producing Fusarium species were shown to be pr
233 ction is important for host colonization and mycotoxin production and may provide a promising target
234                               In Aspergilli, mycotoxin production and sporulation are governed, in pa
235  rtfA gene in a DeltaveA background restored mycotoxin production in a medium-dependent manner.
236 nt and the curcumin standard interfered with mycotoxin production.
237  Aspergillus cultures alters sporulation and mycotoxin production.
238 lationship between fungicide application and mycotoxin production.
239 uranocoumarin compounds, including the major mycotoxin products of Aspergillus flavus.
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
242 r pharmaceutical (antibiotics) and/or toxic (mycotoxins) properties.
243  assays for Fusarium spp. identification and mycotoxin quantification) and a novel untargeted metabol
244 e two sources largely explained the loads of mycotoxins quantified in river waters.
245                                     From the mycotoxins quantified in wheat (3-acetyl-deoxynivalenol,
246 tion mechanism provides useful knowledge for mycotoxin reduction and elimination.
247                                              Mycotoxin reductions were dose-dependent, and ZEA levels
248 vergent and operationally simple approach to mycotoxin-related 4-amino-substituted 1-hydroxydihydroxa
249                               Aflatoxins are mycotoxins secreted by Aspergillus flavus, which can col
250 ethod for the determination of a total of 12 mycotoxins simultaneously, nine trichothecenes (NIV, DON
251 l synthesis of a mimotope peptide simulating mycotoxin-specific antibodies.
252 molecular recognition of OTA; simulating the mycotoxin-specific antibody.
253 ed the importance of temperature and time in mycotoxin stability in heat treatments.
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
256 several secondary metabolites, including the mycotoxin sterigmatocystin (ST).
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
259  in production of oxylipins, conidia and the mycotoxin sterigmatocystin.
260                                              Mycotoxins, such as aflatoxins and ochratoxin A, are pre
261 ed beverages have been analysed, and certain mycotoxins, such as deoxynivalenol, aflatoxin B1, aflato
262                                Trichothecene mycotoxins synthesized by Fusarium species are potent in
263                  Fumonisin B(1) (FB(1)) is a mycotoxin that inhibits ceramide synthases (CerS) and ca
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
266        Ochratoxin A (OTA) is one of the main mycotoxins that can be found in food.
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
269 btained were higher than 70% for the studied mycotoxins the four cereal.
270 red to produce sesquiterpene (trichothecene) mycotoxins, the endoplasmic reticulum (ER) of the phytop
271 cies belonging to the genus Fusarium and the mycotoxins they produce.
272       The exposure of European population to mycotoxins through beer consumption was assessed.
273 recommended to study food processing fate of mycotoxins through naturally contaminated materials (inc
274                                              Mycotoxin toxicity in foodstuff can occur at very low co
275    Typically, electrochemical biosensors for mycotoxins use specific antibodies or aptamers as affini
276                             Co-occurrence of mycotoxins was also present in major cereals.
277  simultaneous immunodetection of these three mycotoxins was demonstrated via the laminar flow pattern
278 t pathogen related to the early detection of mycotoxins was discovered.
279 n of the tested fruits with toxic metals and mycotoxins was low.
280 rinciple, deoxynivalenol (DON), an important mycotoxin, was captured using an SPR gold chip containin
281 ion tool for samples that contain the target mycotoxins, was used.
282  since the ergot alkaloids and the regulated mycotoxins were below their regulated limits.
283                    To this purpose, thirteen mycotoxins were considered and analyzed using drift time
284                                    The three mycotoxins were detected in less than 20min at concentra
285           The concentrations of the targeted mycotoxins were determined using liquid chromatography c
286                                              Mycotoxins were dosed at varying concentrations to 11.5
287                  The toxicities of the novel mycotoxins were evaluated utilizing two in vitro transla
288                                              Mycotoxins were not found in any of the analyzed samples
289                                              Mycotoxins were not present in grains from all storage c
290                            Emerging Fusarium mycotoxins were predominant in Italian samples compared
291                                              Mycotoxins were regularly quantified in whole wheat plan
292                           The contents of 14 mycotoxins were studied in samples of different cereals
293                       Thirty-three different mycotoxins were surveyed over nearly two years in a typi
294  to a rare class of fungal tetracycline-like mycotoxins, were subjected to comprehensive spectroscopi
295                    Citrinin is a nephrotoxic mycotoxin which can be synthesized by Monascus mold duri
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,
300 he determination of food contaminants, using mycotoxin zearalenone (ZEN) as a model.

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