| pubmed-article:1335809 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1335809 | lifeskim:mentions | umls-concept:C0205177 | lld:lifeskim |
| pubmed-article:1335809 | lifeskim:mentions | umls-concept:C0036576 | lld:lifeskim |
| pubmed-article:1335809 | lifeskim:mentions | umls-concept:C1158770 | lld:lifeskim |
| pubmed-article:1335809 | lifeskim:mentions | umls-concept:C0600477 | lld:lifeskim |
| pubmed-article:1335809 | lifeskim:mentions | umls-concept:C0162326 | lld:lifeskim |
| pubmed-article:1335809 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:1335809 | pubmed:dateCreated | 1993-2-11 | lld:pubmed |
| pubmed-article:1335809 | pubmed:abstractText | Alu repeats are short interspersed elements whose transposition has lead to genetic variability and heritable disorders in humans. A select subset of the nearly one million Alu sequences in human DNA actually produce new transpositions. The evolution of newly inserted Alu repeats is currently a key subject for study. Mechanisms of RNA polymerase III activity and the sequence environment into which an Alu inserts might select for transcriptional and posttranscriptional determinants of Alu transposition. | lld:pubmed |
| pubmed-article:1335809 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1335809 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1335809 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1335809 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:1335809 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1335809 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1335809 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:1335809 | pubmed:issn | 0959-437X | lld:pubmed |
| pubmed-article:1335809 | pubmed:author | pubmed-author:SchmidCC | lld:pubmed |
| pubmed-article:1335809 | pubmed:author | pubmed-author:MaraiaRR | lld:pubmed |
| pubmed-article:1335809 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1335809 | pubmed:volume | 2 | lld:pubmed |
| pubmed-article:1335809 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1335809 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1335809 | pubmed:pagination | 874-82 | lld:pubmed |
| pubmed-article:1335809 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
| pubmed-article:1335809 | pubmed:meshHeading | pubmed-meshheading:1335809-... | lld:pubmed |
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| pubmed-article:1335809 | pubmed:meshHeading | pubmed-meshheading:1335809-... | lld:pubmed |
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| pubmed-article:1335809 | pubmed:meshHeading | pubmed-meshheading:1335809-... | lld:pubmed |
| pubmed-article:1335809 | pubmed:year | 1992 | lld:pubmed |
| pubmed-article:1335809 | pubmed:articleTitle | Transcriptional regulation and transpositional selection of active SINE sequences. | lld:pubmed |
| pubmed-article:1335809 | pubmed:affiliation | Department of Genetics, University of California, Davis 95616. | lld:pubmed |
| pubmed-article:1335809 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1335809 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:1335809 | pubmed:publicationType | Review | lld:pubmed |
| pubmed-article:1335809 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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