A functional study of all 40 C. elegans insulin-like peptides
Shanqing Zheng, Hilton Chiu, Jeffrey R. Boudreau, Tony Papanicolaou, William G. Bendena, Ian D. Chin-Sang
This study overexpresses all 40 C. elegans insulin-like peptides to identify their functions, categorizing 35 as agonists, antagonists, or pleiotropic, and linking peptide structure to function.
Journal of Biological Chemistry · Sep 11, 2018Peer-reviewedGenetics