Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/640
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dc.contributor.authorBrahmachari, Vani-
dc.date.accessioned2015-08-21T05:48:12Z-
dc.date.available2015-08-21T05:48:12Z-
dc.date.issued2010-04-
dc.identifier.urihttp://hdl.handle.net/123456789/640-
dc.description.abstractMethylation of CpG sequences in and around CGG triplet repeats in FMR1 gene has strong correlation with manifestation of the fragile X syndrome in human patients. In contrast, we have observed a lack of correlation between repeat instability and DNA methylation in three different transgenic mouse models harboring unstable CGG repeats. Further we have demonstrated that the endogenous copy of mouse Fmr1 gene remains unmethylated both in males and females. These results imply that methylation and repeat instability are independent events and raise the possibility that methylation could also result in repression of FMR1 transcription in the absence of repeat expansion.en_US
dc.publisherLandes Bioscienceen_US
dc.titleComparative analysis of DNA methylation in transgenic mice with unstable CGG repeats from FMR1 geneen_US
dc.contributor.coauthorAlam, Mohammad Parwez-
dc.contributor.coauthorDatta, Sonal-
dc.contributor.coauthorMajumdar, Subeer S-
dc.contributor.coauthorMehta, Abhishek K-
dc.contributor.coauthorBaskaran, Sujatha-
dc.contributor.coauthorGulati, Neerja-
dc.keywordDNA methylation, CGG repeat instability, transgenic mice, mouse Fmr1 methylation, McrBC-HpaII, bisulfiteen_US
dc.journalEpigeneticsen_US
dc.volumeno5en_US
dc.issueno3en_US
dc.pages241-248en_US
Appears in Collections:Cellular Endocrinology, Publications

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