<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lu, Xinyi</style></author><author><style face="normal" font="default" size="100%">Sachs, Friedrich</style></author><author><style face="normal" font="default" size="100%">Ramsay, LeeAnn</style></author><author><style face="normal" font="default" size="100%">Jacques, Pierre-Étienne</style></author><author><style face="normal" font="default" size="100%">Göke, Jonathan</style></author><author><style face="normal" font="default" size="100%">Bourque, Guillaume</style></author><author><style face="normal" font="default" size="100%">Ng, Huck-Hui</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The retrovirus HERVH is a long noncoding RNA required for human embryonic stem cell identity.</style></title><secondary-title><style face="normal" font="default" size="100%">Nat Struct Mol Biol</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nat. Struct. Mol. Biol.</style></alt-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cell Line</style></keyword><keyword><style  face="normal" font="default" size="100%">Cell Nucleus</style></keyword><keyword><style  face="normal" font="default" size="100%">Embryonic Stem Cells</style></keyword><keyword><style  face="normal" font="default" size="100%">Endogenous Retroviruses</style></keyword><keyword><style  face="normal" font="default" size="100%">Gene Expression Regulation</style></keyword><keyword><style  face="normal" font="default" size="100%">Humans</style></keyword><keyword><style  face="normal" font="default" size="100%">In Situ Hybridization, Fluorescence</style></keyword><keyword><style  face="normal" font="default" size="100%">Octamer Transcription Factor-3</style></keyword><keyword><style  face="normal" font="default" size="100%">Pluripotent Stem Cells</style></keyword><keyword><style  face="normal" font="default" size="100%">RNA, Long Noncoding</style></keyword><keyword><style  face="normal" font="default" size="100%">Species Specificity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2014 Apr</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/24681886</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">21</style></volume><pages><style face="normal" font="default" size="100%">423-5</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Human endogenous retrovirus subfamily H (HERVH) is a class of transposable elements expressed preferentially in human embryonic stem cells (hESCs). Here, we report that the long terminal repeats of HERVH function as enhancers and that HERVH is a nuclear long noncoding RNA required to maintain hESC identity. Furthermore, HERVH is associated with OCT4, coactivators and Mediator subunits. Together, these results uncover a new role of species-specific transposable elements in hESCs.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><notes><style face="normal" font="default" size="100%">http://www.nature.com/nsmb/journal/vaop/ncurrent/full/nsmb.2799.html</style></notes><custom1><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/24681886?dopt=Abstract</style></custom1></record></records></xml>