Roumenina, Lubka T <br/><br/>
Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome.  [electronic resource] 

 -  Blood  Sep 2009 
 - 2837-45 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1528-0020 
<br/><br/><label>Standard No.: </label>10.1182/blood-2009-01-197640  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Cells, Cultured<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>Complement Activation--genetics<br/>Complement C3-C5 Convertases--genetics<br/>Complement System Proteins--genetics<br/>Endothelial Cells--metabolism<br/>Family<br/>Female<br/>Hemolytic-Uremic Syndrome--genetics<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Middle Aged<br/>Models, Molecular<br/>Mutant Proteins--physiology<br/>Pedigree<br/>Young Adult