pubmed-article:18923538 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18923538 | lifeskim:mentions | umls-concept:C0019397 | lld:lifeskim |
pubmed-article:18923538 | lifeskim:mentions | umls-concept:C0019409 | lld:lifeskim |
pubmed-article:18923538 | lifeskim:mentions | umls-concept:C1507147 | lld:lifeskim |
pubmed-article:18923538 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:18923538 | pubmed:dateCreated | 2008-10-16 | lld:pubmed |
pubmed-article:18923538 | pubmed:abstractText | The silent X chromosome in mammalian females is a classic example of facultative heterochromatin, the term highlighting the compacted and inactive nature of the chromosome. However, it is now clear that the heterochromatin of the inactive X is not homogeneous--as indeed, not all genes on the inactive X are silenced. We summarize known features and events of X inactivation in different mouse and human model systems, and highlight the heterogeneity of chromatin along the inactive X. Characterizing this heterogeneity is likely to provide insight into the cis-acting sequences involved in X chromosome inactivation. | lld:pubmed |
pubmed-article:18923538 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18923538 | pubmed:language | eng | lld:pubmed |
pubmed-article:18923538 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18923538 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18923538 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18923538 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18923538 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18923538 | pubmed:month | Oct | lld:pubmed |
pubmed-article:18923538 | pubmed:issn | 0829-8211 | lld:pubmed |
pubmed-article:18923538 | pubmed:author | pubmed-author:BrownCarolyn... | lld:pubmed |
pubmed-article:18923538 | pubmed:author | pubmed-author:ChangSamuel... | lld:pubmed |
pubmed-article:18923538 | pubmed:author | pubmed-author:MinksJakubJ | lld:pubmed |
pubmed-article:18923538 | pubmed:author | pubmed-author:SidhuSharan... | lld:pubmed |
pubmed-article:18923538 | pubmed:author | pubmed-author:CottonAllison... | lld:pubmed |
pubmed-article:18923538 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:18923538 | pubmed:volume | 86 | lld:pubmed |
pubmed-article:18923538 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18923538 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18923538 | pubmed:pagination | 370-9 | lld:pubmed |
pubmed-article:18923538 | pubmed:dateRevised | 2009-5-7 | lld:pubmed |
pubmed-article:18923538 | pubmed:meshHeading | pubmed-meshheading:18923538... | lld:pubmed |
pubmed-article:18923538 | pubmed:meshHeading | pubmed-meshheading:18923538... | lld:pubmed |
pubmed-article:18923538 | pubmed:meshHeading | pubmed-meshheading:18923538... | lld:pubmed |
pubmed-article:18923538 | pubmed:meshHeading | pubmed-meshheading:18923538... | lld:pubmed |
pubmed-article:18923538 | pubmed:meshHeading | pubmed-meshheading:18923538... | lld:pubmed |
pubmed-article:18923538 | pubmed:meshHeading | pubmed-meshheading:18923538... | lld:pubmed |
pubmed-article:18923538 | pubmed:meshHeading | pubmed-meshheading:18923538... | lld:pubmed |
pubmed-article:18923538 | pubmed:meshHeading | pubmed-meshheading:18923538... | lld:pubmed |
pubmed-article:18923538 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18923538 | pubmed:articleTitle | X chromosome inactivation: heterogeneity of heterochromatin. | lld:pubmed |
pubmed-article:18923538 | pubmed:affiliation | Molecular Epigenetics Group, Department of Medical Genetics, University of British Columbia, 2350 Health Sciences Mall, Vancouver, BC V6T 1Z3, Canada. | lld:pubmed |
pubmed-article:18923538 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18923538 | pubmed:publicationType | Review | lld:pubmed |
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