| pubmed-article:1438532 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1438532 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
| pubmed-article:1438532 | lifeskim:mentions | umls-concept:C0029282 | lld:lifeskim |
| pubmed-article:1438532 | lifeskim:mentions | umls-concept:C0765250 | lld:lifeskim |
| pubmed-article:1438532 | lifeskim:mentions | umls-concept:C1521840 | lld:lifeskim |
| pubmed-article:1438532 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:1438532 | pubmed:dateCreated | 1992-11-27 | lld:pubmed |
| pubmed-article:1438532 | pubmed:abstractText | Interest in ornithine decarboxylase (ODC) and the therapeutic effects of its inhibition with the consequent depletion of polyamine biosynthesis has been widespread since the late 1970s and 1980s. This review covers new information about the properties of ODC, recent findings with ODC inhibitors and a discussion of the mechanism of inactivation of ODC by eflornithine. Recent in vivo therapeutic approaches of ODC inhibition are also discussed including: cancer and cancer chemoprevention; autoimmune diseases; polyamines and the blood-brain barrier, ischemia and hyperplasia; the NMDA receptor and modulation by polyamines; hearing loss; African trypanosomiasis; Pneumocystis carinii pneumonia and Cryptosporidium in AIDS; and other infectious diseases/organisms. | lld:pubmed |
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| pubmed-article:1438532 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1438532 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1438532 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1438532 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:1438532 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1438532 | pubmed:issn | 0163-7258 | lld:pubmed |
| pubmed-article:1438532 | pubmed:author | pubmed-author:PeggA EAE | lld:pubmed |
| pubmed-article:1438532 | pubmed:author | pubmed-author:McCannP PPP | lld:pubmed |
| pubmed-article:1438532 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1438532 | pubmed:volume | 54 | lld:pubmed |
| pubmed-article:1438532 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1438532 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1438532 | pubmed:pagination | 195-215 | lld:pubmed |
| pubmed-article:1438532 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
| pubmed-article:1438532 | pubmed:meshHeading | pubmed-meshheading:1438532-... | lld:pubmed |
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| pubmed-article:1438532 | pubmed:meshHeading | pubmed-meshheading:1438532-... | lld:pubmed |
| pubmed-article:1438532 | pubmed:year | 1992 | lld:pubmed |
| pubmed-article:1438532 | pubmed:articleTitle | Ornithine decarboxylase as an enzyme target for therapy. | lld:pubmed |
| pubmed-article:1438532 | pubmed:affiliation | Marion Merrell Dow Inc., Indianapolis, IN 46268-0470. | lld:pubmed |
| pubmed-article:1438532 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1438532 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:1438532 | pubmed:publicationType | Review | lld:pubmed |
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