| pubmed-article:15203185 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15203185 | lifeskim:mentions | umls-concept:C0204727 | lld:lifeskim |
| pubmed-article:15203185 | lifeskim:mentions | umls-concept:C0205409 | lld:lifeskim |
| pubmed-article:15203185 | lifeskim:mentions | umls-concept:C0596988 | lld:lifeskim |
| pubmed-article:15203185 | lifeskim:mentions | umls-concept:C0036576 | lld:lifeskim |
| pubmed-article:15203185 | lifeskim:mentions | umls-concept:C0683598 | lld:lifeskim |
| pubmed-article:15203185 | lifeskim:mentions | umls-concept:C0162610 | lld:lifeskim |
| pubmed-article:15203185 | lifeskim:mentions | umls-concept:C0064170 | lld:lifeskim |
| pubmed-article:15203185 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:15203185 | pubmed:dateCreated | 2004-6-18 | lld:pubmed |
| pubmed-article:15203185 | pubmed:abstractText | The accumulation of molecular damage from attack by reactive oxygen species is one cause of aging. Therefore, some mutant organisms showing increased resistance to reactive oxygen species should live longer. We show that selection for Caenorhabditis elegans mutants that are resistant to juglone, a reactive oxygen species-generating compound, leads to the identification of long-lived mutants. Indeed, four of six resistant mutants isolated were also long-lived. This study illustrates once more the strong relationship between oxidative stress and the aging processes. | lld:pubmed |
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| pubmed-article:15203185 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:15203185 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:15203185 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15203185 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:15203185 | pubmed:issn | 0891-5849 | lld:pubmed |
| pubmed-article:15203185 | pubmed:author | pubmed-author:JohnsonThomas... | lld:pubmed |
| pubmed-article:15203185 | pubmed:author | pubmed-author:de... | lld:pubmed |
| pubmed-article:15203185 | pubmed:author | pubmed-author:Hegi de... | lld:pubmed |
| pubmed-article:15203185 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15203185 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:15203185 | pubmed:volume | 37 | lld:pubmed |
| pubmed-article:15203185 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15203185 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15203185 | pubmed:pagination | 139-45 | lld:pubmed |
| pubmed-article:15203185 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
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| pubmed-article:15203185 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:15203185 | pubmed:articleTitle | Isolation of long-lived mutants in Caenorhabditis elegans using selection for resistance to juglone. | lld:pubmed |
| pubmed-article:15203185 | pubmed:affiliation | Institute for Behavioral Genetics, University of Colorado at Boulder, 80309, USA. | lld:pubmed |
| pubmed-article:15203185 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15203185 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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