| pubmed-article:9175861 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9175861 | lifeskim:mentions | umls-concept:C0035203 | lld:lifeskim |
| pubmed-article:9175861 | lifeskim:mentions | umls-concept:C0521451 | lld:lifeskim |
| pubmed-article:9175861 | lifeskim:mentions | umls-concept:C0596562 | lld:lifeskim |
| pubmed-article:9175861 | lifeskim:mentions | umls-concept:C0439659 | lld:lifeskim |
| pubmed-article:9175861 | lifeskim:mentions | umls-concept:C1704970 | lld:lifeskim |
| pubmed-article:9175861 | lifeskim:mentions | umls-concept:C1704211 | lld:lifeskim |
| pubmed-article:9175861 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:9175861 | pubmed:dateCreated | 1997-7-1 | lld:pubmed |
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| pubmed-article:9175861 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9175861 | pubmed:abstractText | Genes that encode mitochondrial homologues to the bacterial enzymes of fatty acid synthesis were found in various eukaryotic species. Inactivation of these genes leads to a disturbed mitochondrial respiration and an increase in mitochondrial lysophospholipids. We postulate that there is a mitochondrial biosynthetic system providing fatty acids for phospholipid repair. The mitochondrial acyl carrier protein may also play another role, supporting the formation of the respiratory NADH:ubiquinone oxidoreductase. | lld:pubmed |
| pubmed-article:9175861 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9175861 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9175861 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:9175861 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9175861 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9175861 | pubmed:month | May | lld:pubmed |
| pubmed-article:9175861 | pubmed:issn | 0014-5793 | lld:pubmed |
| pubmed-article:9175861 | pubmed:author | pubmed-author:SchneiderRR | lld:pubmed |
| pubmed-article:9175861 | pubmed:author | pubmed-author:WeissHH | lld:pubmed |
| pubmed-article:9175861 | pubmed:author | pubmed-author:MassonBB | lld:pubmed |
| pubmed-article:9175861 | pubmed:author | pubmed-author:BrosiWW | lld:pubmed |
| pubmed-article:9175861 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9175861 | pubmed:day | 5 | lld:pubmed |
| pubmed-article:9175861 | pubmed:volume | 407 | lld:pubmed |
| pubmed-article:9175861 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9175861 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9175861 | pubmed:pagination | 249-52 | lld:pubmed |
| pubmed-article:9175861 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:9175861 | pubmed:meshHeading | pubmed-meshheading:9175861-... | lld:pubmed |
| pubmed-article:9175861 | pubmed:meshHeading | pubmed-meshheading:9175861-... | lld:pubmed |
| pubmed-article:9175861 | pubmed:year | 1997 | lld:pubmed |
| pubmed-article:9175861 | pubmed:articleTitle | Mitochondrial fatty acid synthesis: a relic of endosymbiontic origin and a specialized means for respiration. | lld:pubmed |
| pubmed-article:9175861 | pubmed:affiliation | Institut für Biochemie, Heinrich-Heine-Universität Düsseldorf, Germany. Regina.Schneider@uni-duesseldorf.de | lld:pubmed |
| pubmed-article:9175861 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9175861 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:9175861 | pubmed:publicationType | Review | lld:pubmed |
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