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rdf:type |
|
|
lifeskim:mentions |
|
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pubmed:issue |
7
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pubmed:dateCreated |
2009-7-2
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pubmed:abstractText |
FOXL2 encodes a forkhead transcription factor whose mutations are responsible for the blepharophimosis-ptosis-epicanthus inversus syndrome (BPES), involving craniofacial/palpebral abnormalities often associated with premature ovarian failure (POF).
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pubmed:language |
eng
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pubmed:journal |
|
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1468-6244
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pubmed:author |
pubmed-author:BenayounB ABA,
pubmed-author:BrahamRR,
pubmed-author:DipietromariaAA,
pubmed-author:ElghezalHH,
pubmed-author:FellousMM,
pubmed-author:LaissusFF,
pubmed-author:LakhalBB,
pubmed-author:PhilibertPP,
pubmed-author:SeffCC,
pubmed-author:SultanCC,
pubmed-author:VeitiaR ARA
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pubmed:issnType |
Electronic
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pubmed:volume |
46
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
455-7
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:19429596-Adult,
pubmed-meshheading:19429596-Amino Acid Sequence,
pubmed-meshheading:19429596-Amino Acid Substitution,
pubmed-meshheading:19429596-Animals,
pubmed-meshheading:19429596-Female,
pubmed-meshheading:19429596-Forkhead Transcription Factors,
pubmed-meshheading:19429596-Gene Expression Regulation,
pubmed-meshheading:19429596-Humans,
pubmed-meshheading:19429596-Molecular Sequence Data,
pubmed-meshheading:19429596-Mutation,
pubmed-meshheading:19429596-Primary Ovarian Insufficiency,
pubmed-meshheading:19429596-Promoter Regions, Genetic,
pubmed-meshheading:19429596-Sequence Alignment,
pubmed-meshheading:19429596-Transcription Factors
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pubmed:year |
2009
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pubmed:articleTitle |
Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2.
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pubmed:affiliation |
INSERM U567, Institut Cochin, Paris, France.
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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