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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
12
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pubmed:dateCreated |
2004-11-19
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pubmed:abstractText |
Balanced X;autosome translocations interrupting the 'critical region' of the long arm of the human X chromosome are often associated with premature ovarian failure (POF). However, the mechanisms leading to X-linked ovarian dysfunction are largely unknown, as the majority of the X chromosome breakpoints have been mapped to gene-free genomic regions. A few genes have been found to be interrupted, but their role has never been clarified.
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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 |
Dec
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pubmed:issn |
0268-1161
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pubmed:author |
pubmed-author:BattagliaRR,
pubmed-author:BernabiniSS,
pubmed-author:BioneSS,
pubmed-author:BrunnSS,
pubmed-author:CrosignaniP GPG,
pubmed-author:DalpràLL,
pubmed-author:GinelliEE,
pubmed-author:GoeganMM,
pubmed-author:ManziniM CMC,
pubmed-author:MarozziAA,
pubmed-author:NappiRR,
pubmed-author:RicottiRR,
pubmed-author:RizzolioFF,
pubmed-author:SalaCC,
pubmed-author:TonioloDD,
pubmed-author:TorricelliFF,
pubmed-author:VegettiWW,
pubmed-author:ZuffardiOO
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pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2759-66
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:15459172-Adolescent,
pubmed-meshheading:15459172-Adult,
pubmed-meshheading:15459172-Amino Acid Sequence,
pubmed-meshheading:15459172-Child,
pubmed-meshheading:15459172-Chromosomes, Human, X,
pubmed-meshheading:15459172-DNA Mutational Analysis,
pubmed-meshheading:15459172-Dosage Compensation, Genetic,
pubmed-meshheading:15459172-Female,
pubmed-meshheading:15459172-Genetic Variation,
pubmed-meshheading:15459172-Humans,
pubmed-meshheading:15459172-Microfilament Proteins,
pubmed-meshheading:15459172-Middle Aged,
pubmed-meshheading:15459172-Molecular Sequence Data,
pubmed-meshheading:15459172-Mutation,
pubmed-meshheading:15459172-Nuclear Proteins,
pubmed-meshheading:15459172-Primary Ovarian Insufficiency,
pubmed-meshheading:15459172-Proteins,
pubmed-meshheading:15459172-Transcription Factors,
pubmed-meshheading:15459172-Translocation, Genetic
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pubmed:year |
2004
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pubmed:articleTitle |
Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B.
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pubmed:affiliation |
Institute of Molecular Genetics-CNR, 27100 Pavia, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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