Metabolism of the masked mycotoxin deoxynivalenol-3-glucoside in rats. - Wikidata - awgldk - TriplyDB

Metabolism of the masked mycotoxin deoxynivalenol-3-glucoside in rats.

Metabolism of the masked mycotoxin deoxynivalenol-3-glucoside in rats.

http://www.wikidata.org/entity/Q36250222

about

Mycotoxin Contamination in the EU Feed Supply Chain: A Focus on Cereal Byproducts The impact of Fusarium mycotoxins on human and animal host susceptibility to infectious diseases Prevalence and effects of mycotoxins on poultry health and performance, and recent development in mycotoxin counteracting strategies Faces of a changing climate: semi-quantitative multi-mycotoxin analysis of grain grown in exceptional climatic conditions in Norway.Anomericity of T-2 toxin-glucoside: masked mycotoxin in cereal crops Low toxicity of deoxynivalenol-3-glucoside in microbial cells.Evaluation of an oral subchronic exposure of deoxynivalenol on the composition of human gut microbiota in a model of human microbiota-associated rats Comparison of anorectic and emetic potencies of deoxynivalenol (vomitoxin) to the plant metabolite deoxynivalenol-3-glucoside and synthetic deoxynivalenol derivatives EN139528 and EN139544.Effects of oral exposure to naturally-occurring and synthetic deoxynivalenol congeners on proinflammatory cytokine and chemokine mRNA expression in the mouse.A Versatile Family 3 Glycoside Hydrolase from Bifidobacterium adolescentis Hydrolyzes β-Glucosides of the Fusarium Mycotoxins Deoxynivalenol, Nivalenol, and HT-2 Toxin in Cereal Matrices Biochemical Characterization of a Recombinant UDP-glucosyltransferase from Rice and Enzymatic Production of Deoxynivalenol-3-O-β-D-glucoside.Metabolism of deoxynivalenol and deepoxy-deoxynivalenol in broiler chickens, pullets, roosters and turkeys.Risk Assessment of Deoxynivalenol by Revisiting Its Bioavailability in Pig and Rat Models to Establish Which Is More Suitable.The human fecal microbiota metabolizes deoxynivalenol and deoxynivalenol-3-glucoside and may be responsible for urinary deepoxy-deoxynivalenol.Multi-mycotoxin screening reveals the occurrence of 139 different secondary metabolites in feed and feed ingredients Occurrence of deoxynivalenol and deoxynivalenol-3-glucoside in hard red spring wheat grown in the USA.From the gut to the brain: journey and pathophysiological effects of the food-associated trichothecene mycotoxin deoxynivalenol.Oxidative stress-mediated cytotoxicity and metabolism of T-2 toxin and deoxynivalenol in animals and humans: an update.Fate of deoxynivalenol and deoxynivalenol-3-glucoside during cereal-based thermal food processing: a review study.Do Plant-Bound Masked Mycotoxins Contribute to Toxicity?Proposal of a comprehensive definition of modified and other forms of mycotoxins including "masked" mycotoxins.6-Plex microsphere immunoassay with imaging planar array detection for mycotoxins in barley.Chemical Synthesis of Deoxynivalenol-3-β-d-[(13)C₆]-glucoside and Application in Stable Isotope Dilution Assays.In vivo contribution of deoxynivalenol-3-β-D-glucoside to deoxynivalenol exposure in broiler chickens and pigs: oral bioavailability, hydrolysis and toxicokinetics.Study of the natural occurrence of T-2 and HT-2 toxins and their glucosyl derivatives from field barley to malt by high-resolution Orbitrap mass spectrometry.Deoxynivalenol and Its Modified Forms: Are There Major Differences?In vitro glucuronidation kinetics of deoxynivalenol by human and animal microsomes and recombinant human UGT enzymes.Glucuronidation of deoxynivalenol (DON) by different animal species: identification of iso-DON glucuronides and iso-deepoxy-DON glucuronides as novel DON metabolites in pigs, rats, mice, and cows.Masked trichothecene and zearalenone mycotoxins withstand digestion and absorption in the upper GI tract but are efficiently hydrolyzed by human gut microbiota in vitro.Deoxynivalenol (DON) sulfonates as major DON metabolites in rats: from identification to biomarker method development, validation and application.Risks to human and animal health related to the presence of deoxynivalenol and its acetylated and modified forms in food and feed Scientific Opinion on the risks for human and animal health related to the presence of modified forms of certain mycotoxins in food and feed Humans significantly metabolize and excrete the mycotoxin deoxynivalenol and its modified form deoxynivalenol-3-glucoside within 24 hours.UDP-Glucosyltransferases from Rice, Brachypodium, and Barley: Substrate Specificities and Synthesis of Type A and B Trichothecene-3-O-β-d-glucosides.Traditionally Processed Beverages in Africa: A Review of the Mycotoxin Occurrence Patterns and Exposure Assessment Relationship between lutein and mycotoxin content in durum wheat

P2860

Q26764898-CC654CAB-3774-45B9-91F5-D65345188C75 Q27004696-FCB019A4-F88D-4609-A2D6-6A7DA21AAD00 Q28829928-CFC32A89-FBA8-4B4F-B429-08E96343F931 Q30670962-2A7615F4-C177-4F12-9EA1-B4142201CE3D Q35002227-B8EFAFD9-55C7-4E1D-BD93-00F67F6847AF Q35003703-DF6F3589-A1CD-4D6C-A383-7F80B005C03C Q35049126-08E6DDA3-5C39-4A97-87FA-22F5C57D9F42 Q35102616-561AE501-9D56-46F9-B1FB-B271176D634B Q35534227-8610A2AC-5B41-4772-A4E2-B7C20DD0EB63 Q35829393-EBDC558E-86B6-4A78-A05A-EB370CA43E7F Q35894734-643FB516-A8C7-4423-95A7-E95DB8C4153D Q36329617-4DAFCE8F-DF06-457F-A379-EB6FF77CCC6E Q36401463-6884739C-44DA-422E-86FB-F4A68E157AE2 Q36668142-F5FACE3C-D182-4B30-B41A-E9A86F33E8A4 Q36993872-1FD30C1D-1F4D-4240-8D4E-8AFFC57046BA Q37416021-B61DA1F5-976F-4BB0-9C0D-B1AF0A8FF14A Q38101247-E7140C30-8400-43C5-A2A6-75090EDAF98D Q38217411-94E052E7-8B09-471F-AEFF-C922C49AB94D Q39014562-2CB68B32-39FE-401F-A16A-0B030317C0E3 Q39164094-48E2F63C-7F1E-4AD0-A893-E0B6EEC7F076 Q39170408-70FB8377-5F73-465F-8E4B-71A7C9320587 Q39177207-BA2DAE99-5C22-4268-998F-125385192199 Q39645709-91360D29-1D21-4C79-981C-C74FE21EEE2B Q39834534-168225C3-FA8F-45BF-AAC7-BB6D815D0BD2 Q40963601-ADA3D264-0899-4D3B-ACC8-61BCB7A79106 Q42082243-7A0151CA-3F4F-4B35-8282-E678D26F398A Q42705230-D0672D13-6532-4307-A28D-2324CEC3FA42 Q46346369-CF0150D6-C71F-4CD6-8DE3-A7206F9BB271 Q46449924-EAB687C8-1B0C-4E96-80DC-E471265525A5 Q46822538-08F6D647-A161-4016-941C-743DEC500E12 Q47160469-07A4B195-2205-4FAF-89F1-05967595DF88 Q47163111-814C9361-D950-48C7-85B9-2E346CBBC209 Q52626721-B2E3410C-E3C7-40E9-A85D-F96942C06FF6 Q52728567-C955ECDA-E1A4-45ED-81C4-3BBA89E90A9F Q56838767-5DCFD367-4091-487B-B659-57C9611FEFEC Q56838875-7CFFC803-7DC2-46EC-9A13-B3BA90718CFD

P2860

Metabolism of the masked mycotoxin deoxynivalenol-3-glucoside in rats.

http://www.wikidata.org/entity/Q36250222

description

2012 nî lūn-bûn

@nan

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

2012年论文

@zh

2012年论文

@zh-cn

name

Metabolism of the masked mycotoxin deoxynivalenol-3-glucoside in rats.

@ast

Metabolism of the masked mycotoxin deoxynivalenol-3-glucoside in rats.

@en

type

label

Metabolism of the masked mycotoxin deoxynivalenol-3-glucoside in rats.

@ast

Metabolism of the masked mycotoxin deoxynivalenol-3-glucoside in rats.

@en

prefLabel

Metabolism of the masked mycotoxin deoxynivalenol-3-glucoside in rats.

@ast

Metabolism of the masked mycotoxin deoxynivalenol-3-glucoside in rats.

@en

P1433

Q36250222-26A9A510-81F6-4CFF-9763-F9A6B226D398

P1476

Q36250222-B3207BD3-D38E-4FB7-BFA8-B918963FCA05

P2093

Q36250222-1863B29D-E78A-4287-93AE-AEC63E250721

Q36250222-2AB107BE-EBD9-48D3-A546-4C87A5D3EAA9

Q36250222-8560745E-0566-4723-9ADA-3EEFABA1DA30

Q36250222-AC075A2F-A898-401D-87C8-D7B731ADDC30

Q36250222-BEFC7D68-443C-48F0-9DD4-76EC663CBE8E

P2860

Q36250222-07838D7A-B6C1-46AA-956B-014463750971

Q36250222-0C6DD2B6-83A1-4104-A81E-0561AFF466E7

Q36250222-0EA8CBC8-5FED-4FA7-8892-8715EEF01A74

Q36250222-0F80EDD1-6ED8-468B-93FD-6E74A20EB725

Q36250222-110A5F91-4759-4E41-BF24-AF4A0CE314E6

Q36250222-26EA74B5-2C5C-473B-9FBA-2F4C46D046AF

Q36250222-2E289D92-8A98-40AE-BAEF-25BBC4803F48

Q36250222-30801035-4F71-4505-A711-7D083E4CD566

Q36250222-33401CA2-A7CF-4AB0-AE78-DBEE77F4863C

Q36250222-3C7E9222-7F7C-41E2-BCB0-6CEA4F884AF7

P304

Q36250222-48C62D70-FBF4-4528-A8FF-94C4E486EB0E

P31

Q36250222-091C9F0D-E37B-438D-973D-DAEC4A9BC1B2

P356

Q36250222-EDB7B23C-F8D5-4D4B-8388-CE022B2063AA

P433

Q36250222-EFF3BA84-A666-49AD-94FD-ED7CE4EAFCB2

P478

Q36250222-7A3A61AE-E88B-46F7-B9E8-B927F14F89B9

P50

Q36250222-4A3F2BEA-EE1B-48AC-B7F8-E8F093B14E36

Q36250222-6105C2A7-0EB2-44AF-90DD-73863D8FE17C

Q36250222-DAD22549-6AC5-4619-A6BC-D01A6A438638

P577

Q36250222-B1C3D658-45D6-4B0A-B3D4-C7A2D5E99238

P5875

Q36250222-9BA672BD-AE54-4B9C-AB6B-1BAB7438B97C

P698

Q36250222-7C4FAFD1-7A24-4AF1-BDFB-99DBFFD06A53

P921

Q36250222-F0AFB2A1-A566-4ABE-B508-8CE9BEADEB7D

P932

Q36250222-569401EC-D100-434C-9F80-B23729C6FE41

P356

J.TOXLET.2012.07.024

P1433

Toxicology Letters

P1476

Metabolism of the masked mycotoxin deoxynivalenol-3-glucoside in rats

@en

P2093

Gerhard Adam

http://www.w3.org/2001/XMLSchema#string

Heidi Schwartz

http://www.w3.org/2001/XMLSchema#string

Rudolf Krska

http://www.w3.org/2001/XMLSchema#string

Siegfried Knasmüller

http://www.w3.org/2001/XMLSchema#string

Veronika Nagl

http://www.w3.org/2001/XMLSchema#string

P2860

Detoxification of the Fusarium mycotoxin deoxynivalenol by a UDP-glucosyltransferase from Arabidopsis thaliana.

Report from SCOOP task 3.2.10 "collection of occurrence data of Fusarium toxins in food and assessment of dietary intake by the population of EU member states". Subtask: trichothecenes.

Synthesis and characterization of deoxynivalenol glucuronide: its comparative immunotoxicity with deoxynivalenol.

Effects of trichothecene mycotoxins on eukaryotic cells: a review.

A biomarker survey of urinary deoxynivalenol in China: the Shanghai Women's Health Study.

Hydrolytic fate of deoxynivalenol-3-glucoside during digestion

Formation, determination and significance of masked and other conjugated mycotoxins.

Analytical and compositional aspects of isoflavones in food and their biological effects.

Deoxynivalenol: mechanisms of action, human exposure, and toxicological relevance.

Toxicology of deoxynivalenol (vomitoxin).

P304

367-373

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1016/J.TOXLET.2012.07.024

http://www.w3.org/2001/XMLSchema#string

P433

3

http://www.w3.org/2001/XMLSchema#string

P478

213

http://www.w3.org/2001/XMLSchema#string

P50

Mathias Ritzmann

Franz Berthiller

Wulf-Dieter Moll

P577

2012-08-04T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

230655989

http://www.w3.org/2001/XMLSchema#string

P698

22884771

http://www.w3.org/2001/XMLSchema#string

P921

P932

3448059

http://www.w3.org/2001/XMLSchema#string