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pubmed-article:19250188pubmed:abstractTextSteroid signaling involves specific receptors that mediate genomic effects and many further proteins responsible for fast nongenomic activities. Metabolism at the position 17 of the steroid scaffold plays a pivotal role in the final regulation of the biological potency of steroid hormones. Enzymes responsible for that, the 17beta-hydroxysteroid dehydrogenases (17beta-HSD), act as carbonyl reductases and require cofactors for their catalytic activity. There is a substantial amount of evidence that human 17beta-HSDs are as well involved in the metabolic pathways of retinoids and fatty acid beyond that which has so far been anticipated. At present fourteen 17beta-HSDs have been annotated and characterized, and more might follow. Many of 17beta-HSDs have been shown to be involved in the pathogenesis of human disorders and are targets for therapeutic intervention. Strategies on deciphering the physiological role of the 17beta-HSD and the genetic predisposition for associated diseases will be presented involving analyses of animal models.lld:pubmed
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pubmed-article:19250188pubmed:year2009lld:pubmed
pubmed-article:19250188pubmed:articleTitlePerspectives in understanding the role of human 17beta-hydroxysteroid dehydrogenases in health and disease.lld:pubmed
pubmed-article:19250188pubmed:affiliationHelmholtz Zentrum München, German Research Center for Environmental Health, Institute of Experimental Genetics, Genome Analysis Center, Neuherberg, Germany.lld:pubmed
pubmed-article:19250188pubmed:publicationTypeJournal Articlelld:pubmed
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