pubmed-article:7966413 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:7966413 | lifeskim:mentions | umls-concept:C0014930 | lld:lifeskim |
pubmed-article:7966413 | lifeskim:mentions | umls-concept:C0441655 | lld:lifeskim |
pubmed-article:7966413 | lifeskim:mentions | umls-concept:C1521761 | lld:lifeskim |
pubmed-article:7966413 | lifeskim:mentions | umls-concept:C0015272 | lld:lifeskim |
pubmed-article:7966413 | lifeskim:mentions | umls-concept:C0720298 | lld:lifeskim |
pubmed-article:7966413 | lifeskim:mentions | umls-concept:C0054658 | lld:lifeskim |
pubmed-article:7966413 | pubmed:issue | 23 | lld:pubmed |
pubmed-article:7966413 | pubmed:dateCreated | 1994-12-16 | lld:pubmed |
pubmed-article:7966413 | pubmed:abstractText | Indole-3-carbinol (I3C) and related compounds have been identified in vegetables of the Brassica genus. I3C and its acid-derived condensation product, indolo[3,2-b]carbazole (ICZ), bind to the aryl hydrocarbon (Ah) receptor and induce CYP1A1/1A2 gene expression in both in vivo and in vitro models. I3C also inhibits mammary tumor development in rodent models. | lld:pubmed |
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pubmed-article:7966413 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7966413 | pubmed:language | eng | lld:pubmed |
pubmed-article:7966413 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7966413 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:7966413 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:7966413 | pubmed:month | Dec | lld:pubmed |
pubmed-article:7966413 | pubmed:issn | 0027-8874 | lld:pubmed |
pubmed-article:7966413 | pubmed:author | pubmed-author:BjeldanesL... | lld:pubmed |
pubmed-article:7966413 | pubmed:author | pubmed-author:LiuHH | lld:pubmed |
pubmed-article:7966413 | pubmed:author | pubmed-author:SafeS HSH | lld:pubmed |
pubmed-article:7966413 | pubmed:author | pubmed-author:WormkeMM | lld:pubmed |
pubmed-article:7966413 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:7966413 | pubmed:day | 7 | lld:pubmed |
pubmed-article:7966413 | pubmed:volume | 86 | lld:pubmed |
pubmed-article:7966413 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:7966413 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:7966413 | pubmed:pagination | 1758-65 | lld:pubmed |
pubmed-article:7966413 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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pubmed-article:7966413 | pubmed:meshHeading | pubmed-meshheading:7966413-... | lld:pubmed |
pubmed-article:7966413 | pubmed:meshHeading | pubmed-meshheading:7966413-... | lld:pubmed |
pubmed-article:7966413 | pubmed:meshHeading | pubmed-meshheading:7966413-... | lld:pubmed |
pubmed-article:7966413 | pubmed:meshHeading | pubmed-meshheading:7966413-... | lld:pubmed |
pubmed-article:7966413 | pubmed:year | 1994 | lld:pubmed |
pubmed-article:7966413 | pubmed:articleTitle | Indolo[3,2-b]carbazole: a dietary-derived factor that exhibits both antiestrogenic and estrogenic activity. | lld:pubmed |
pubmed-article:7966413 | pubmed:affiliation | Department of Veterinary Physiology and Pharmacology, Texas A&M University, College Station 77843-4466. | lld:pubmed |
pubmed-article:7966413 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:7966413 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:7966413 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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