Aromatic hydrocarbon responsiveness-receptor agonists generated from indole-3-carbinol in vitro and in vivo: comparisons with 2,3,7,8-tetrachlorodibenzo-p-dioxin
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Influence of light on aryl hydrocarbon receptor signaling and consequences in drug metabolism, physiology and diseaseThe aryl hydrocarbon receptor: a perspective on potential roles in the immune systemCruciferous vegetables and human cancer risk: epidemiologic evidence and mechanistic basisLipid G protein-coupled receptor ligand identification using beta-arrestin PathHunter assayProblems for risk assessment of endocrine-active estrogenic compoundsFlavonoids as aryl hydrocarbon receptor agonists/antagonists: effects of structure and cell contextMucosal Interactions between Genetics, Diet, and Microbiome in Inflammatory Bowel DiseaseNew Trends in Aryl Hydrocarbon Receptor BiologyAryl hydrocarbon receptor control of adaptive immunityAntifungal Th Immunity: Growing up in FamilyCellular and molecular pathways through which commensal bacteria modulate sensitization to dietary antigensThe rainbow trout liver cancer model: response to environmental chemicals and studies on promotion and chemopreventionAntioxidant Functions of the Aryl Hydrocarbon ReceptorRole of Aryl Hydrocarbon Receptor in Circadian Clock Disruption and Metabolic DysfunctionPlant-derived 3,3'-Diindolylmethane is a strong androgen antagonist in human prostate cancer cellsNatural aryl hydrocarbon receptor ligands control organogenesis of intestinal lymphoid folliclesA direct interaction between the aryl hydrocarbon receptor and retinoblastoma protein. Linking dioxin signaling to the cell cycleDietary flavonols quercetin and kaempferol are ligands of the aryl hydrocarbon receptor that affect CYP1A1 transcription differentiallyInduction of cytochrome P4501A1 by 2,3,7,8-tetrachlorodibenzo-p-dioxin or indolo(3,2-b)carbazole is associated with oxidative DNA damageMetabolism and biomarkers of heterocyclic aromatic amines in molecular epidemiology studies: lessons learned from aromatic aminesFire Usage and Ancient Hominin Detoxification Genes: Protective Ancestral Variants Dominate While Additional Derived Risk Variants Appear in Modern HumansThe Brassica-derived phytochemical indolo[3,2-b]carbazole protects against oxidative DNA damage by aryl hydrocarbon receptor activation.Molecular basis of dioxin actions: evidence supporting chemoprotection.Inhibition of vinyl carbamate-induced pulmonary adenocarcinoma by indole-3-carbinol and myo-inositol in A/J miceIndole-3-carbinol as a chemopreventive and anti-cancer agent.Activation of the aryl hydrocarbon receptor dampens the severity of inflammatory skin conditions.Use of natural AhR ligands as potential therapeutic modalities against inflammatory disorders.Mechanistic aspects--the dioxin (aryl hydrocarbon) receptor.D-amino acid oxidase generates agonists of the aryl hydrocarbon receptor from D-tryptophan.Inhibition of lung carcinogenesis and critical cancer-related signaling pathways by N-acetyl-S-(N-2-phenethylthiocarbamoyl)-l-cysteine, indole-3-carbinol and myo-inositol, alone and in combination.The micronutrient indole-3-carbinol: implications for disease and chemoprevention.Low levels of 3,3'-diindolylmethane activate estrogen receptor α and induce proliferation of breast cancer cells in the absence of estradiol.Intersection of AHR and Wnt signaling in development, health, and disease.Indolocarbazole natural products: occurrence, biosynthesis, and biological activity.Fish models for environmental carcinogenesis: the rainbow trout.Enhanced inhibition of lung adenocarcinoma by combinatorial treatment with indole-3-carbinol and silibinin in A/J mice.Ring-substituted analogs of 3,3'-diindolylmethane (DIM) induce apoptosis and necrosis in androgen-dependent and -independent prostate cancer cells.Broccoli sprouts: an exceptionally rich source of inducers of enzymes that protect against chemical carcinogensGinsenosides are novel naturally-occurring aryl hydrocarbon receptor ligandsCross-species transcriptomic analysis elucidates constitutive aryl hydrocarbon receptor activity
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Q23919671-E83F7080-E848-4EE6-84E5-B402966777C1Q24338766-416B8391-4734-48E2-8BD3-1C000CD918A1Q24641921-5116EE49-EC93-4B1D-99EF-51DDEE0FE055Q24654730-40456BC6-326B-4864-A854-87237199118AQ24812789-563A53D6-3335-4475-ACAE-0FC9AE41AA1AQ24816974-534C9AF2-D9CB-4CAA-A41A-B645399B1BAEQ26741117-806E94FF-948B-4BF3-A474-40C59EA840B9Q26744482-97CCADB5-715A-4E2C-8F6C-B6862906EE00Q26991793-2177262D-82EA-449B-834F-648E90142FBDQ27002920-3E763D18-6B6B-4F9C-9A8C-A368241C425EQ27021336-EB52FA2E-B036-4FD7-BCF0-DC793B1587CAQ27691366-4D7B866A-ACF8-4665-94CC-BAF3A62C2C47Q28073170-469B3AE3-4617-4DEA-928E-80FC1A061A7BQ28076926-489C5276-0429-40DD-BBFE-5928C58E151EQ28187403-DD62EA5B-9DFF-409F-A90C-CD103C861425Q28251675-EC3E01AA-D944-4E49-A444-41313B17A809Q28280266-054D79F2-ED19-4A24-9956-9DC917FEF26EQ28343363-25AFA5C4-1EB6-4A00-92EE-20860F95C485Q28378843-A00AFD35-F538-4770-A9DF-95D0EAD159D3Q28391158-323EB0ED-45EC-450E-9FE9-FC865DEE52F2Q28595433-EDDA1E8A-7B3F-4DD3-9951-51E779142532Q30315579-636EB207-CB57-4CDB-8D8F-54EA8A60CDAEQ32052600-EAEB2EDD-4D85-4B62-B506-2F6717DF73A2Q33615285-8E1CF351-F94D-441F-B7A3-964D77571E70Q33622450-DF61DEAC-83A9-4BEB-88B4-EB4505DE1B79Q33795308-8C1B6D05-8E10-4A4B-AF4B-3A303077D069Q33827813-FBFD54C9-A011-4E83-994B-873C30366553Q33911313-AD2648E4-1EB7-4B82-9B6A-2D2DEF2DC0F7Q34073887-AF3C8267-34FB-4F6A-8F14-B2B79C58DAD1Q34094986-090A4F87-F871-4E7F-A6C4-D856DDBC38DAQ34153223-A5FD319C-9C26-41C0-952F-49B50D62D6E9Q34468550-21AFF40D-742A-4D6C-B4C3-5334204A17ACQ34486670-2F80069F-32F6-424E-89FD-585384802EBFQ34583547-C2133FD7-63DC-4A09-8676-0CE20CF5CD8FQ34636569-86021601-9D37-4F9B-A0F9-111EEDFBFC88Q34734130-F6220524-1FFF-4808-928D-96383EE240B6Q34741141-53C674EE-8B72-40A6-9B47-85FFB9E04D8AQ34742872-F953D6A7-D410-4B79-BE13-FE0538CBD798Q34776476-673D9850-99C5-49EC-BC1B-E3685DDCE839Q34994927-AE81CBF7-5688-446C-B25F-ACB3C2618059
P2860
Aromatic hydrocarbon responsiveness-receptor agonists generated from indole-3-carbinol in vitro and in vivo: comparisons with 2,3,7,8-tetrachlorodibenzo-p-dioxin
description
1991 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
article publié dans les Procee ...... f the United States of America
@fr
artículu científicu espublizáu en 1991
@ast
im November 1991 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: November 1991)
@en
vedecký článok (publikovaný 1991/11/01)
@sk
vědecký článek publikovaný v roce 1991
@cs
wetenschappelijk artikel (gepubliceerd op 1991/11/01)
@nl
наукова стаття, опублікована в листопаді 1991
@uk
name
Aromatic hydrocarbon responsiv ...... ,8-tetrachlorodibenzo-p-dioxin
@ast
Aromatic hydrocarbon responsiv ...... ,8-tetrachlorodibenzo-p-dioxin
@en
Aromatic hydrocarbon responsiv ...... ,8-tetrachlorodibenzo-p-dioxin
@nl
type
label
Aromatic hydrocarbon responsiv ...... ,8-tetrachlorodibenzo-p-dioxin
@ast
Aromatic hydrocarbon responsiv ...... ,8-tetrachlorodibenzo-p-dioxin
@en
Aromatic hydrocarbon responsiv ...... ,8-tetrachlorodibenzo-p-dioxin
@nl
prefLabel
Aromatic hydrocarbon responsiv ...... ,8-tetrachlorodibenzo-p-dioxin
@ast
Aromatic hydrocarbon responsiv ...... ,8-tetrachlorodibenzo-p-dioxin
@en
Aromatic hydrocarbon responsiv ...... ,8-tetrachlorodibenzo-p-dioxin
@nl
P2093
P2860
P3181
P356
P1476
Aromatic hydrocarbon responsiv ...... ,8-tetrachlorodibenzo-p-dioxin
@en
P2093
C A Bradfield
J C Bartholomew
L F Bjeldanes
P2860
P304
P3181
P356
10.1073/PNAS.88.21.9543
P407
P577
1991-11-01T00:00:00Z