Varco-Merth, Benjamin <br/><br/>
Severe growth deficiency is associated with STAT5b mutations that disrupt protein folding and activity.  [electronic resource] 

 -  Molecular endocrinology (Baltimore, Md.)  Jan 2013 
 - 150-61 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S. 
<br/><br/><label>ISSN: </label>1944-9917 
<br/><br/><label>Standard No.: </label>10.1210/me.2012-1275  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Base Sequence<br/>COS Cells<br/>Cell Nucleus--metabolism<br/>Chlorocebus aethiops<br/>Growth Disorders--genetics<br/>Growth Hormone--physiology<br/>Humans<br/>Mice<br/>Models, Molecular<br/>Mutation, Missense<br/>Phosphorylation<br/>Protein Binding<br/>Protein Folding<br/>Protein Processing, Post-Translational<br/>Protein Stability<br/>Protein Structure, Quaternary<br/>Protein Structure, Secondary<br/>Protein Transport<br/>Rats<br/>Receptors, Somatotropin--metabolism<br/>STAT5 Transcription Factor--chemistry<br/>Structural Homology, Protein<br/>Thermodynamics<br/>Transcriptional Activation<br/>src Homology Domains