Cilli, Domenica <br/><br/>
Identification of the interactors of human nibrin (NBN) and of its 26 kDa and 70 kDa fragments arising from the NBN 657del5 founder mutation.  [electronic resource] 

 -  PloS one  2014 
 - e114651 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0114651  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Blotting, Western<br/>Cell Cycle Proteins--genetics<br/>Cell Nucleus--genetics<br/>DNA Breaks, Double-Stranded<br/>Electrophoresis, Polyacrylamide Gel<br/>Fluorescent Antibody Technique<br/>Gene Regulatory Networks<br/>HEK293 Cells<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Mutation--genetics<br/>Nijmegen Breakage Syndrome--genetics<br/>Nuclear Proteins--genetics<br/>Protein Interaction Domains and Motifs<br/>Sequence Deletion<br/>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization<br/>Tandem Mass Spectrometry<br/>X-Rays