INT45079
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
The increased protection is not related to interaction of these drugs with the Ah receptor. | |||||||||||||||
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Since the primers for AhR amplify both rat and mouse AhR, these results indicate that N2a-R? | |||||||||||||||
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Although immunoreactivity for AhR was not detected in the N2a-Vc and Neuro2a cells, the protein band corresponding to the molecular weight of AhR was clearly detected in N2a-R?. | |||||||||||||||
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The AhR primers were designed for rat AhR, but also specifically recognize and amplify mouse AhR under identical PCR conditions (Fig 2A). | |||||||||||||||
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The AhRArnt heterodimers then bind to their recognition sequence, the dioxin-responsive element (DRE) (Mimura and Fujii-Kuriyama 2003). | |||||||||||||||
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Once these xenobiotics are recognized by AhR, the AhRligand complexes translocate into the nucleus and form heterodimers with its partner coactivator, AhR nuclear translocator (Arnt). | |||||||||||||||
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The AhR is activated by binding to ligands, including dioxins, translocates from the cytoplasm to the nucleus and then binds to the consensus sequence known as XRE (xenobiotic responsive element) [7]. | |||||||||||||||
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The AhR is activated by binding to ligands, including dioxins, translocates from the cytoplasm to the nucleus and then binds to the consensus sequence known as XRE (xenobiotic responsive element) [7]. | |||||||||||||||
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AhR regulates the transcription of diverse genes through binding to the xenobiotic-responsive element (XRE). | |||||||||||||||
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To target the AhR we used the following shRNA sequences: 1. 5? | |||||||||||||||
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Recent studies revealed a connection between the AhR pathway and prostate cancer both in vitro and in vivo, showing that the AhR interacts and inhibits the AR. | |||||||||||||||
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The AhR primers were designed for rat AhR, but also specifically recognize and amplify mouse AhR under identical PCR conditions (Fig 2A). | |||||||||||||||
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This raises the question: Why is EB not associated with AHR if eosinophils contribute to AHR? | |||||||||||||||
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The binding of 3-MC to the aryl hydrocarbon receptor (AHR) forms a AHR/3-MC complex, which upregulates CYP1A1, CYP1A2, and CYP1B1 expression by binding, together with the AHR nuclear translocator (ARNT), to the XREs of these genes [30]. | |||||||||||||||
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The binding of 3-MC to the aryl hydrocarbon receptor (AHR) forms a AHR/3-MC complex, which upregulates CYP1A1, CYP1A2, and CYP1B1 expression by binding, together with the AHR nuclear translocator (ARNT), to the XREs of these genes [30]. | |||||||||||||||
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The impairment of COX-2 expression and activity caused by the antisense oligonucleotide was associated with a worsening of AHR. | |||||||||||||||
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Furthermore, TTX and MK801 differentially affected the association of AhR and its transcriptional co-activator cAMP-responsive-element binding protein with the cytochrome P450 1A1 (cyp1A1) gene enhancer. | |||||||||||||||
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In that same study, an increased expression and production of IL-9 in the lung was associated with AHR in DBA/J2 mice. | |||||||||||||||
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No association was also observed between metabolic syndrome and AHR or asthma and AHR in all children or in boys and girls separately. | |||||||||||||||
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Conclusion: There was no association between metabolic syndrome at age 10 to 11 and prevalent asthma or AHR, but we are in the process of recruiting children for the third wave of the SAGE study and soon will have results on the association between metabolic syndrome and incident asthma at age 12 years.
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