[1]Brüssow KP, Rátky J, Torner H, et al. Follicular and oocyte development in gilts of different age[J]. Acta Vet Hung, 2002, 50(1):101-110.
[2]Davis OK, Rosenwaks Z. Superovulation strategies for assisted reproductive technologies[J]. Semin Reprod Med, 2001, 19(3):207-212.
[3]Hirata M, Tanihara F, Taniguchi M, et al. Follicular development of canine ovaries stimulated by a combination treatment of eCG and hCG[J]. Vet Med Sci, 2018, 4(4):333-340.
[4]Fayazi M, Beigi Boroujeni M, Salehnia M, et al. Ovarian stimulation by exogenous gonadotropin decreases the implantation rate and expression of mouse blastocysts integrins[J]. Iran Biomed J, 2014, 18(1):8-15.
[5]Ezoe K, Daikoku T, Yabuuchi A, et al. Ovarian stimulation using human chorionic gonadotrophin impairs blastocyst implantation and decidualization by altering ovarian hormone levels and downstream signaling in mice[J]. Mol Hum Reprod, 2014, 20(11):1101-1116.
[6]Senapati S, Wang F, Ord T, et al. Superovulation alters the expression of endometrial genes critical to tissue remodeling and placentation[J]. J Assist Reprod Genet, 2018, 35(10):1799-1808.
[7]De-Oliveira V, Schaefer J, Abu-Rafea B, et al. Uterine aquaporin expression is dynamically regulated by estradiol and progesterone and ovarian stimulation disrupts embryo implantation without affecting luminal closure[J]. Mol Hum Reprod, 2020, 26(3):154-166.
[8]Bonakdar E, Edriss MA, Bakhtari A, et al. A physiological, rather than a superovulated, post-implantation environment can attenuate the compromising effect of assisted reproductive techniques on gene expression in developing mice embryos[J]. Mol Reprod Dev, 2015, 82(3):191-206.
[9]Weinerman R, Ord T, Bartolomei MS, et al. The superovulated environment, independent of embryo vitrification, results in low birthweight in a mouse model[J]. Biol Reprod, 2017, 97(1):133-142.
[10]Popova E, Bader M, Krivokharchenko A. Strain differences in superovulatory response, embryo development and efficiency of transgenic rat production[J]. Transgenic Res, 2005, 14(5):729-738.
[11]Byers SL, Payson SJ, Taft RA. Performance of ten inbred mouse strains following assisted reproductive technologies (ARTs) [J]. Theriogenology, 2006, 65(9):1716-1726.
[12]Bortoletto P, Bakkensen J, Anchan RM. Embryo transfer: timing and techniques[J]. Minerva Endocrinol, 2018, 43(1):57-68.
[13]Yu B, Smith TH, Battle SL, et al. Superovulation alters global DNA methylation in early mouse embryo development[J]. Epigenetics, 2019, 14(8):780-790.
[14]Huffman SR, Pak Y, Rivera RM. Superovulation induces alterations in the epigenome of zygotes, and results in differences in gene expression at the blastocyst stage in mice[J]. Mol Reprod Dev, 2015, 82(3):207-217.
[15]Huo Y, Yan ZQ, Yuan P, et al. Single-cell DNA methylation sequencing reveals epigenetic alterations in mouse oocytes superovulated with different dosages of gonadotropins[J]. Clin Epigenetics, 2020, 12(1):75.
[16]Uysal F, Ozturk S, Akkoyunlu G. Superovulation alters DNA methyltransferase protein expression in mouse oocytes and early embryos[J]. J Assist Reprod Genet, 2018, 35(3):503-513.
[17]Rülicke T, Haenggli A, Rappold K, et al. No transuterine migration of fertilised ova after unilateral embryo transfer in mice[J]. Reprod Fertil Dev, 2006, 18(8):885-891.
[18]MargioulaSiarkou C, Prapas Y, Petousis S, et al. LIF and LIFR expression in the endometrium of fertile and infertile women: A prospective observational casecontrol study[J]. Mol Med Rep, 2016, 13(6):4721-4728.
[19]Rarani FZ, Borhani F, Rashidi B. Endometrial pinopode biomarkers: Molecules and microRNAs[J]. J Cell Physiol, 2018, 233(12):9145-9158.
[20]Chen JR, Cheng JG, Shatzer T, et al. Leukemia inhibitory factor can substitute for nidatory estrogen and is essential to inducing a receptive uterus for implantation but is not essential for subsequent embryogenesis[J]. Endocrinology, 2000, 141(12):4365-4372.
[21]Díaz-Gimeno P, Ruíz-Alonso M, Blesa D, et al. Transcriptomics of the human endometrium[J]. Int J Dev Biol, 2014, 58(4):127-137.
[22]Wolff M, Bohlmann MK, Fiedler C, et al. Osteopontin is up-regulated in human decidual stromal cells[J]. Fertil Steril, 2004, 81(S-1):741-748.
[23]Qi QR, Xie QZ, Liu XL, et al. Osteopontin is expressed in the mouse uterus during early pregnancy and promotes mouse blastocyst attachment and invasion in vitro[J]. PLoS One, 2014, 9(8):e104955.
[24]Vilella F, Ramirez L, Berlanga O, et al. PGE2 and PGF2α concentrations in human endometrial fluid as biomarkers for embryonic implantation[J]. J Clin Endocrinol Metab, 2013, 98(10):4123-4132.
[25]Salker MS, Singh Y, Durairaj RRP, et al. LEFTY2 inhibits endometrial receptivity by downregulating Orai1 expression and store-operated Ca2+ entry[J]. J Mol Med (Berl), 2018, 96(2):173-182.
[26]Achache H, Tsafrir A, Prus D, et al. Defective endometrial prostaglandin synthesis identified in patients with repeated implantation failure undergoing in vitro fertilization[J]. Fertil Steril, 2010, 94(4):1271-1278.
[27]Ye Y, Vattai A, Ditsch N, et al. Prostaglandin E2 receptor 3 signaling is induced in placentas with unexplained recurrent pregnancy losses[J]. Endocr Connect, 2018, 7(5):749-761.
|