Kang, Hio Chung <br/><br/>
Whole exome and targeted deep sequencing identify genome-wide allelic loss and frequent SETDB1 mutations in malignant pleural mesotheliomas.  [electronic resource] 

 -  Oncotarget  Feb 2016 
 - 8321-31 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1949-2553 
<br/><br/><label>Standard No.: </label>10.18632/oncotarget.7032  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Blotting, Western<br/>Exome--genetics<br/>Female<br/>Genome, Human<br/>High-Throughput Nucleotide Sequencing--methods<br/>Histone-Lysine N-Methyltransferase<br/>Humans<br/>Immunoenzyme Techniques<br/>Loss of Heterozygosity--genetics<br/>Lung Neoplasms--genetics<br/>Mesothelioma--genetics<br/>Mesothelioma, Malignant<br/>Middle Aged<br/>Mutation--genetics<br/>Pleural Neoplasms--genetics<br/>Prognosis<br/>Protein Methyltransferases--genetics<br/>RNA, Messenger--genetics<br/>Real-Time Polymerase Chain Reaction<br/>Reverse Transcriptase Polymerase Chain Reaction<br/>Survival Rate