Correction: Circ_0008440 Inhibits Proliferation and Promotes Apoptosis of Trophoblast Cells through the miR-942-5p/PFKFB2 Axis [0.03%]
校正：Circular RNA circ_0008440 通过 miR-942-5p/PFKFB2 轴抑制滋养细胞增殖并促进滋养细胞凋亡
Linqiong Guo,Ting Ji,Xiaoyan Xu et al.
Linqiong Guo et al.
Published Erratum
Reproductive sciences (Thousand Oaks, Calif.). 2025 Oct 10. DOI:10.1007/s43032-025-01996-3 2025
The Methylation Regulator PRDM6 Confers Protection Against Polycystic Ovary Syndrome: Evidences from Bioinformatics and Experimental Approaches [0.03%]
甲基化调节因子PRDM6对多囊卵巢综合征的保护作用：生物信息学和实验研究证据
Meiting Qiu,Junjie Qu,Jingyun Wang et al.
Meiting Qiu et al.
Polycystic ovary syndrome (PCOS) is a complex endocrine disorder with an unclear epigenetic basis. This study sought to identify critical methylation regulators implicated in PCOS progression and evaluate their therapeutic potential through...
Differential Methylation Signatures Associated with PCOS- A Systematic Review and In-Silico Analysis [0.03%]
与PCOS相关的差异性甲基化标志物的系统评价和网络生物信息学分析
Priya Sharma,Ahelee Ghosal,Aiswarya Vs et al.
Priya Sharma et al.
Polycystic ovary syndrome (PCOS) is a common endocrinopathy affecting 5-20% of reproductive-age women. Besides genetic factors, environmental triggers are considered major underlying causes that play a role through epigenetic alterations. S...
How Many Blastocysts Are Needed for PGT-A to Benefit RPL Patients? A 7-Year Retrospective Cohort Study [0.03%]
胚胎植入前遗传学检测非整倍体能从反复种植失败中获益吗？七年的回顾性队列研究需要多少个囊胚？
Jia Liao,Shiheng Zhu,Jinghan Wang et al.
Jia Liao et al.
The efficacy of preimplantation genetic testing for aneuploidy (PGT-A) in couples with unexplained recurrent pregnancy loss (uRPL) may vary according to the number of good-quality blastocysts available. This study is to determine whether PG...
Polycystic Ovary Syndrome: Unraveling the Minor Shifts in Fatty Acid Composition of Follicular Fluid Phospholipids and Triglycerides [0.03%]
多囊卵巢综合征：卵泡液磷脂和甘油三酯脂肪酸组成的微小变化分析
Reza Zarezadeh,Amir Fattahi,Laya Farzadi
Reza Zarezadeh
The effect of polycystic ovary syndrome (PCOS) on the fatty acid (FA) content of follicular fluid (FF) is not fully understood. The present study aimed to determine whether the FA composition of FF phospholipids (PLs) and triglycerides (TGs...
Optical Monitoring of the Therapeutic Effects of Resveratrol on Neonatal Hypoxic-Ischemic Encephalopathy Using Diffuse Reflectance Spectroscopy [0.03%]
茋治疗新生儿缺氧缺血性脑病的疗效光学监测研究:应用漫反射光谱技术
Marie Maruyama,Takeshi Nagamatsu,Satoko Kawauchi et al.
Marie Maruyama et al.
Hypoxic-ischemic encephalopathy (HIE), which precipitates during parturition, causes severe neurological sequelae in the neonate. We have previously reported an optical monitoring system based on diffuse reflectance spectroscopy to evaluate...
Regional Proteomic Characterization of Uterine Leiomyomas: Implications for Molecular Pathways and Tumor Biology [0.03%]
子宫平滑肌瘤的区域蛋白质组学特征及其对分子途径和肿瘤生物学的意义
Mustafa Gani Sürmen,Enis Özkaya
Mustafa Gani Sürmen
Uterine leiomyomas are the most common benign smooth muscle tumors in women of reproductive age. Recent technological advances have enhanced the potential of proteomic studies to identify proteins and related signaling pathways involved in ...
The Role of PRMT5 in Embryonic Developmental Arrest: Insights from IVF-ET Discarded Human Embryos [0.03%]
PRMT5在胚胎发育停滞中的作用：来自体外受精废弃胚胎的启示
Ningyu Sun,Shifeng Li,Kai Li et al.
Ningyu Sun et al.
Embryonic developmental arrest is a critical factor affecting the success rate of in vitro fertilization and embryo transfer (IVF-ET), and protein arginine methyltransferase 5 (PRMT5) plays a crucial role in early embryonic development. How...
Inner Cell Mass Grade and Earlier Blastulation Are Associated with Pregnancy Outcomes in Euploid Embryos [0.03%]
整倍体胚胎的内细胞团分级和早期囊胚化与妊娠结局相关性研究
Yuqi Bian,Sharon H Zhao,Maxwell Edwin Shramuk et al.
Yuqi Bian et al.
To assess the relationship between blastulation, ICM (inner cell mass) quality, TE (trophectoderm) quality, embryo sex, or embryo sex selection and live birth among euploid embryos. Single-center retrospective cohort analysis of patients wh...
Novel Candidate Genes Identified in Men with Congenital Absence of Vas Deferens without CFTR Gene Abnormalities [0.03%]
无CFTR基因异常的先天性输精管缺如患者的新候选基因得以识别
Digumarthi V S Sudhakar,Shagufta A Khan,Rupin Shah et al.
Digumarthi V S Sudhakar et al.
The genetic etiology is unknown for 30-40% of men with congenital bilateral absence of the vas deferens (CBAVD) and 70% of those with congenital unilateral absence of the vas deferens (CUAVD). The study aimed to investigate the genetic etio...