Frontiers in genetics

Front Genet · ISSN (print) 1664-8021 · 123 papers in corpus
other 2022
doi:10.3389/fgene.2022.858641 ·PMID:35711933

The diagnosis and treatment of unexplained recurrent spontaneous abortion (URSA) are subject to debate, because the exact underlying mechanisms remain unclear. To address this issue, we elucidated the expression profiles of dysregulated cir…

other 2022
doi:10.3389/fgene.2022.828238 ·PMID:35391800

Although long non coding RNAs (lncRNAs) and circular RNAs (circRNAs) play important roles in the pathogenesis of diseases, endometriosis related lncRNAs and circRNAs are still rarely reported. This study focused on the potential molecular m…

other 2022
doi:10.3389/fgene.2022.979924 ·PMID:36406137

Polycystic ovary syndrome (PCOS), a common and frustrating syndrome in women of reproductive age, is characterized by symptoms including hyperandrogenemia, ovulation dysfunction, and polycystic ovaries. The role of competitive endogenous RN…

other 2022
doi:10.3389/fgene.2022.996310 ·PMID:36176289

Objective: Pelvic organ prolapse (POP) affects a large proportion of adult women, but the pathogenesis of POP remains unclear. The increase in global population aging will impose a substantial medical burden. Herein, we aimed to explore the…

other 2022
doi:10.3389/fgene.2021.793656 ·PMID:35069692

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lab-animal 2022
doi:10.3389/fgene.2022.847646 ·PMID:35669188

Endometrium undergoes repeated repair and regeneration during the menstrual cycle. Previous attempts using gene expression data to define the menstrual cycle failed to come to an agreement. Here we used single-cell RNA sequencing data of C5…

other 2022
doi:10.3389/fgene.2022.1038317 ·PMID:36263431
other 2022
doi:10.3389/fgene.2022.1020757 ·PMID:36324511

Background: Adenomyosis (AM) is a common benign uterine disease that threatens the normal life of patients. Cells associated with microenvironmental immune ecology are crucial in AM, although they are not as well understood at the cellular …

other 2022
doi:10.3389/fgene.2022.890007 ·PMID:35903355

Objective: To explore potential causal genetic variants and genes underlying the pathogenesis of uterine leiomyomas (ULs). Methods: We conducted the summary data-based Mendelian randomization (SMR) analyses and performed functional mapping …

other 2022
doi:10.3389/fgene.2022.1013475 ·PMID:36276954

Although gene mutations and aberrant chromosomes are associated with the pathogenesis and prognosis of uveal melanoma (UM), potential therapeutic targets still need to be explored. We aim to determine the predictive value and potential ther…

other 2022
doi:10.3389/fgene.2022.912037 ·PMID:35937995

Background: Uterine corpus endometrial carcinoma (UCEC) is a common gynecological malignancy globally with high recurrence and mortality rates. Cuproptosis is a new type of programmed cell death involved in tumor cell proliferation and grow…

observational 2022
doi:10.3389/fgene.2022.860161 ·PMID:35711935

Background: Immunotherapy is a promising strategy for ovarian cancer (OC), and this study aims to identify biomarkers related to CD8+ T cell infiltration to further discover the potential therapeutic target. Methods: Three datasets with OC …

other 2022
doi:10.3389/fgene.2022.998417 ·PMID:36212136

Endometriosis (EMs), one of the most common gynecological diseases, seriously affects the health and wellness of women; however, the underlying pathogenesis remains unclear. This study focused on dysregulated genes and their predicted trans…

other 2022
doi:10.3389/fgene.2022.905716 ·PMID:36105080

Genome-wide association studies (GWAS) have identified several common variants associated with polycystic ovary syndrome (PCOS). However, the etiology behind PCOS remains incomplete. Available evidence suggests a potential genetic correlati…

review 2022
doi:10.3389/fgene.2022.886170 ·PMID:36159999

High-grade serous ovarian carcinoma (HGSOC) is a genomically unstable malignancy responsible for over 70% of all deaths due to ovarian cancer. With roughly 50% of all HGSOC harboring defects in the homologous recombination (HR) DNA repair p…

other 2022
doi:10.3389/fgene.2022.925652 ·PMID:36118846

The etiology of recurrent pregnancy loss (RPL) is complicated and effective clinical preventive measures are lacking. Identifying biomarkers for RPL has been challenging, and to date, little is known about the role of N6-methyladenosine (m6…

other 2022
doi:10.3389/fgene.2022.960954 ·PMID:35928453

Colorectal cancer incidence and mortality have increased in recent years, with more than half of patients who died of colorectal cancer developing liver metastases. Consequently, colorectal cancer liver metastasis is the focus of clinical t…

other 2022
doi:10.3389/fgene.2022.828456 ·PMID:35719379

Endometrial cancer (EC) is the gynecological tumor with the highest incidence. In recent years, it has been proved that necroptosis is a method of cell death related to EC. However, the expression of necroptosis-related miRNA in EC and its …

other 2022
doi:10.3389/fgene.2022.936264 ·PMID:35991565

Background: Infertility is a global health concern. MEIOB has been found to be associated with premature ovarian insufficiency (POI) and non-obstructive azoospermia (NOA), but its variants have not been reported in Chinese patients. The aim…

other 2022
doi:10.3389/fgene.2022.1045395 ·PMID:36386836

Objective: We aim to identify the crucial genes or potential biomarkers associated with uterine fibroids (UFs), which may provide clinicians with evidence about the diagnostic biomarker of UFs and reveal the mechanism of its progression. Me…

observational 2022
doi:10.3389/fgene.2022.820209 ·PMID:35281828

Pesticides are a group of environmental pollutants widely used in agriculture to protect crops, and their indiscriminate use has led to a growing public awareness about the health hazards associated with exposure to these substances. In fac…

other 2022
doi:10.3389/fgene.2022.861853 ·PMID:35754822

A growing number of studies have demonstrated that N6 methyladenine (m6A) acts as an important role in the pathogenesis of reproductive diseases. Therefore, it is essential to profile the genome-wide m6A modifications such as in spontaneous…

other 2022
doi:10.3389/fgene.2022.850892 ·PMID:36035116

Objectives : A large meta-analysis indicated a more pronounced association between lower birth weight (BW) and diseases in women but less concern about the causality between BW and female-related phenotypes and diseases. Methods: Mendelian …

other 2022
doi:10.3389/fgene.2022.874487 ·PMID:35646061

The aim of this work was to identify the transcriptomic characteristics of the endometrium in normoweight and overweight/obese polycystic ovary syndrome (PCOS) potentially underlying the pathogenesis. This study included 38 patients undergo…

observational 2022
doi:10.3389/fgene.2022.969409 ·PMID:36118892

Purpose: To investigate the correlation between pre-ablation ultrasound radiomics features and the sonication energy for focused ultrasound surgery (FUS) of benign breast tumors. Method: 53 benign breast tumors of 28 patients treated by ult…