Wang, Chelsia Qiuxia <br/><br/>
Disruption of Runx1 and Runx3 leads to bone marrow failure and leukemia predisposition due to transcriptional and DNA repair defects.  [electronic resource] 

 -  Cell reports  Aug 2014 
 - 767-82 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>2211-1247 
<br/><br/><label>Standard No.: </label>10.1016/j.celrep.2014.06.046  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Bone Marrow--metabolism<br/>Core Binding Factor Alpha 2 Subunit--genetics<br/>Core Binding Factor Alpha 3 Subunit--genetics<br/>DNA Repair<br/>Fanconi Anemia--genetics<br/>Fanconi Anemia Complementation Group D2 Protein--metabolism<br/>Gene Deletion<br/>Genetic Predisposition to Disease<br/>HCT116 Cells<br/>HEK293 Cells<br/>HeLa Cells<br/>Humans<br/>Leukemia--genetics<br/>Mice<br/>Mice, Inbred C57BL