Bando, Hironori <br/><br/>
Otx2b mutant zebrafish have pituitary, eye and mandible defects that model mammalian disease.  [electronic resource] 

 -  Human molecular genetics  06 2020 
 - 1648-1657 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddaa064  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Apoptosis--genetics<br/>Cell Proliferation--genetics<br/>Gene Expression Regulation, Developmental--genetics<br/>Gills--metabolism<br/>Growth Hormone--genetics<br/>Humans<br/>Hypopituitarism--genetics<br/>Hypothalamus--growth & development<br/>Loss of Function Mutation--genetics<br/>Mandible--pathology<br/>Otx Transcription Factors--genetics<br/>Prolactin--genetics<br/>Zebrafish--genetics<br/>Zebrafish Proteins--genetics