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oai:www.ideals.illinois.edu:2142/84926 2023-07-11 col_2142_5131 col_2142_14797 com_2142_5130 com_2142_14796 com_2142_397

2001 Jeffery, Elizabeth H. Nho, Chu Won 2015-09-25T22:31:01Z 2015-09-25T22:31:01Z 10000-01-01 2001 In conclusion, there is a molecular interaction between crambene and I3C that explains the synergism in phase II enzyme induction after exposure to combinations of these two components. In addition to this, active glucosinolate breakdown products studied here also have anti-promotional effects through inhibition of AP-1 induced tumor promotion in vitro. Made available in DSpace on 2015-09-25T22:31:01Z (GMT). No. of bitstreams: 2 license.txt: 4848 bytes, checksum: 96035ab3f5e1c23cc7138a224ce498bd (MD5) 3023152.pdf: 5610690 bytes, checksum: 433b680060c915438dce8a73ca8715e9 (MD5) Previous issue date: 2001 Embargo set by: Seth Robbins for item 86207 Lift date: Forever Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs U of I Only 123 p. Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2001. http://hdl.handle.net/2142/84926 (MiAaPQ)AAI3023152 eng Biology, Molecular Regulation of Hepatic Detoxification Enzymes by Glucosinolate Breakdown Products in Cruciferous Vegetables text Nutritional Sciences Nutritional Sciences University of Illinois at Urbana-Champaign Dissertation Ph.D.