| pubmed-article:19246354 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19246354 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:19246354 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:19246354 | lifeskim:mentions | umls-concept:C1417838 | lld:lifeskim |
| pubmed-article:19246354 | lifeskim:mentions | umls-concept:C1401084 | lld:lifeskim |
| pubmed-article:19246354 | pubmed:issue | 12 | lld:pubmed |
| pubmed-article:19246354 | pubmed:dateCreated | 2009-3-19 | lld:pubmed |
| pubmed-article:19246354 | pubmed:abstractText | The genetic causes of nonsyndromic ovarian insufficiency are largely unknown. A nuclear receptor, NR5A1 (also called steroidogenic factor 1), is a key transcriptional regulator of genes involved in the hypothalamic-pituitary-steroidogenic axis. Mutation of NR5A1 causes 46,XY disorders of sex development, with or without adrenal failure, but growing experimental evidence from studies in mice suggests a key role for this factor in ovarian development and function as well. | lld:pubmed |
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| pubmed-article:19246354 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19246354 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19246354 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:19246354 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19246354 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:19246354 | pubmed:issn | 1533-4406 | lld:pubmed |
| pubmed-article:19246354 | pubmed:author | pubmed-author:XXX | lld:pubmed |
| pubmed-article:19246354 | pubmed:author | pubmed-author:McElreaveyKen... | lld:pubmed |
| pubmed-article:19246354 | pubmed:author | pubmed-author:BraunerRajaR | lld:pubmed |
| pubmed-article:19246354 | pubmed:author | pubmed-author:AchermannJohn... | lld:pubmed |
| pubmed-article:19246354 | pubmed:author | pubmed-author:Maciel-Guerra... | lld:pubmed |
| pubmed-article:19246354 | pubmed:author | pubmed-author:BashambooAnuA | lld:pubmed |
| pubmed-article:19246354 | pubmed:author | pubmed-author:MuresanMihael... | lld:pubmed |
| pubmed-article:19246354 | pubmed:author | pubmed-author:Guerra-Junior... | lld:pubmed |
| pubmed-article:19246354 | pubmed:author | pubmed-author:WeryhaGeorges... | lld:pubmed |
| pubmed-article:19246354 | pubmed:author | pubmed-author:LourençoDiana... | lld:pubmed |
| pubmed-article:19246354 | pubmed:author | pubmed-author:De... | lld:pubmed |
| pubmed-article:19246354 | pubmed:author | pubmed-author:BoudjenahRadi... | lld:pubmed |
| pubmed-article:19246354 | pubmed:copyrightInfo | 2009 Massachusetts Medical Society | lld:pubmed |
| pubmed-article:19246354 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19246354 | pubmed:day | 19 | lld:pubmed |
| pubmed-article:19246354 | pubmed:volume | 360 | lld:pubmed |
| pubmed-article:19246354 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19246354 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19246354 | pubmed:pagination | 1200-10 | lld:pubmed |
| pubmed-article:19246354 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:19246354 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19246354 | pubmed:articleTitle | Mutations in NR5A1 associated with ovarian insufficiency. | lld:pubmed |
