Study of the aryl hydrocarbon receptor as a target for rational drug design
The aryl hydrocarbon receptor (AhR) heterodimerizes with the aryl hydrocarbon receptor nuclear translocator (Arnt) for transcriptional regulation. We generated three N-terminal deletion constructs of the human AhR of 12-24 KDa in size—namely D1 (aa 84-295), D2 (aa 84-192) and D3 (aa 191-295)—to supp...
Main Author: | Xie, Jinghang |
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Format: | Others |
Published: |
Scholarly Commons
2014
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Subjects: | |
Online Access: | https://scholarlycommons.pacific.edu/uop_etds/140 https://scholarlycommons.pacific.edu/cgi/viewcontent.cgi?article=1139&context=uop_etds |
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