A C619Y mutation in the human androgen receptor causes inactivation and mislocalization of the receptor with concomitant sequestration of SRC-1 (steroid receptor coactivator 1)

Nazareth LV, Stenoien DL, Bingman WE 3rd, James AJ, Wu C, Zhang Y, Edwards DP, Mancini M, Marcelli M, Lamb DJ, Weigel NL
Mol Endocrinol. 1999 Dec;13(12):2065-75. PubMed Article

Plasmids from Article

ID	Plasmid	Purpose
86429	pEGFP-C1-AR C619Y	Fluorescent human androgen receptor (fused to EGFP) with point mutation C619Y