Eurasian Journal of Medical and Natural Sciences 4-jild 12-son (2024) · 168–180-betlar

EPIGENETIC MARKERS FOR PREDICTING THE RISK OF DEVELOPMENT OF EMPTY FOLLICLE SYNDROME IN REPRODUCTIVE-AGE WOMEN

Olimova, K.J., Shukurov, F.I., Akhmadzhanova, X.Z., Jurayeva, A.J., Yuldasheva, M.A.

DOI: 10.5281/zenodo.14545896 · Manbada o'qish →

Annotatsiya

Empty follicle syndrome (EFS) is a rare but serious condition that reduces the chances of successful conception in women undergoing infertility treatment using in vitro fertilization (IVF). Despite the significance of epigenetic mechanisms in regulating reproductive function, their role in the pathogenesis of EFS remains underexplored.

Empty follicle syndrome, epigenetic markers, DNA methylation, microRNA, histone modifications, in vitro fertilization, risk prediction.Синдром пустых фолликулов, эпигенетические маркеры, метилирование ДНК, микроРНК, гистоновые модификации, экстракорпоральное оплодотворение, прогнозирование риска.Puch folikulla sindromi, epigenetik belgilar, DNK metilasyonu, mikroRNK, giston modifikatsiyalari, ekstrakorporal urug‘lantirish, xavfni prognozlash.

Metadata manbasi: jurnal OAI-PMH arxivi · Sindex to'liq matnni saqlamaydi, manbaga havola beradi.