| pubmed-article:20012527 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20012527 | lifeskim:mentions | umls-concept:C0205466 | lld:lifeskim |
| pubmed-article:20012527 | lifeskim:mentions | umls-concept:C0035820 | lld:lifeskim |
| pubmed-article:20012527 | lifeskim:mentions | umls-concept:C1335268 | lld:lifeskim |
| pubmed-article:20012527 | lifeskim:mentions | umls-concept:C0178539 | lld:lifeskim |
| pubmed-article:20012527 | lifeskim:mentions | umls-concept:C1336776 | lld:lifeskim |
| pubmed-article:20012527 | pubmed:dateCreated | 2009-12-16 | lld:pubmed |
| pubmed-article:20012527 | pubmed:abstractText | The chromatin-associated cellular proteins LEDGF/p75 and LEDGF/p52 have been implicated in transcriptional regulation, cell survival and autoimmunity. LEDGF/p75 also appears to act as a chromatin-docking factor or receptor for HIV-1 and other lentiviruses and to play a role in leukemogenesis. For both the viral and cellular roles of this protein, a key feature is its ability to act as a molecular adaptor and tether proteins to the chromatin fiber. This chapter reviews the emerging roles of LEDGF/p75 and LEDGF/p52 in diverse cellular processes and disease states. | lld:pubmed |
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