Association of FOXL2 and ERCC6 variants with premature ovarian insufficiency and their potential use in clinical IVF guidance - Gu, Meng; Fang, Jiajun; Shao, Zhongmei; Yu, Hui; Guo, Senchao; Gao, Yang; He, Xiaojin; Xu, Yuping; Lv, Mingrong (Gene, 2025)
Keywords: Adult; Assisted reproductive technology; blood; DNA Helicases - genetics; DNA Repair Enzymes; DNA-Binding Proteins - genetics; ERCC6; Exome Sequencing - methods; Female; Female infertility; Fertilization in Vitro - methods; Forkhead Box Protein L2 - genetics; FOXL2; genes; Genetic Predisposition to Disease; heterozygosity; Heterozygote; Humans; Infertility, Female - genetics; Mutation, Missense; patients; Poly-ADP-Ribose Binding Proteins; Premature ovarian insufficiency; Primary Ovarian Insufficiency - genetics; protein synthesis; therapeutics; SIFT; WES; MCM8; Assisted reproductive technology; WB; RIPA; BMP15; PolyPhen-2; SNP; Female infertility; MI; BPES; qRT-PCR; TBST; FOXL2; POI; Premature ovarian insufficiency; MII; IVF-ET; GV; CS; GDF9; SDS-PAGE; MSH4; FSHR; NOBOX; ERCC6; GAPDH; PN