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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1996-6-24
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pubmed:abstractText |
Androstenedione is reduced to form testosterone by 17-beta-hydroxysteroid dehydrogenase (17 beta HSD) and two different reductive isoforms of the enzyme have been identified (types 1 and 3). In this study, levels of mRNA encoding both reductive isoforms have been measured during fetal and post-natal development in the mouse. In fetal and neonatal testes mRNA encoding both type 1 and type 3 isoforms was present at relatively high levels reaching a peak at postnatal day 5. Thereafter, mRNA levels of both 17 beta HSD isoforms fell to low levels until day 30 when there was a marked increase in the levels of the type 3 isoform. The presence of the type 1 17 beta HSD enzyme in fetal testes may explain the virilization of the mesonephric (Wolffian) duct which occurs in pseudohermaphrodite individuals lacking the type 3 isoform.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0006-291X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
6
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pubmed:volume |
222
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
90-4
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pubmed:dateRevised |
2010-8-25
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pubmed:meshHeading |
pubmed-meshheading:8630080-17-Hydroxysteroid Dehydrogenases,
pubmed-meshheading:8630080-Age Factors,
pubmed-meshheading:8630080-Animals,
pubmed-meshheading:8630080-Base Sequence,
pubmed-meshheading:8630080-DNA Primers,
pubmed-meshheading:8630080-Gene Expression Regulation, Developmental,
pubmed-meshheading:8630080-Gestational Age,
pubmed-meshheading:8630080-Male,
pubmed-meshheading:8630080-Mice,
pubmed-meshheading:8630080-Molecular Sequence Data,
pubmed-meshheading:8630080-RNA, Messenger,
pubmed-meshheading:8630080-Testis
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pubmed:year |
1996
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pubmed:articleTitle |
Both reductive forms of 17 beta-hydroxysteroid dehydrogenase (types 1 and 3) are expressed during development in the mouse testis.
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pubmed:affiliation |
Department of Veterinary Physiology, University of Glasgow, U.K.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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