Frontiers in genetics

Front Genet · ISSN (print) 1664-8021 · 122 papers in corpus
2026
doi:10.3389/fgene.2026.1790963 ·PMID:42170009

BACKGROUND: N6-methyladenosine (m6A) modification regulates the processes of RNA splicing, subcellular localization, translation and stability by changing the RNA structure and the interaction between RNA and RNA-binding proteins to ensure …

2026
doi:10.3389/fgene.2026.1760869 ·PMID:41700295

IntroductionUlcerative colitis (UC) is a lifelong, chronic inflammatory disorder, characterized by recurrent and diffuse inflammation of the rectal and colonic mucosa. Increasing evidence suggests that impaired mitophagy contributes to immu…

other 2025
doi:10.3389/fgene.2025.1614573 ·PMID:40832467

BACKGROUND: Adenomyosis, a common gynecological disorder in women of reproductive age, is characterized by endometrial invasion into the myometrium, leading to uterine enlargement and smooth muscle hypertrophy. Typical clinical symptoms inc…

erratum 2025
doi:10.3389/fgene.2025.1683914 ·PMID:40919433

[This corrects the article DOI: 10.3389/fgene.2025.1614573.].

2025
doi:10.3389/fgene.2025.1570053 ·PMID:40270542

ObjectiveTo investigate the effects of cold environment exposure on female reproductive capacity and explore its potential regulatory mechanisms.MethodsFemale mice were subjected to cold water immersion to simulate cold environment exposure…

2025
doi:10.3389/fgene.2025.1661511 ·PMID:41321564

Infertility affects approximately one in six individuals globally and represents a complex public health concern influenced by a range of biological, environmental, and socioeconomic factors. In vitro fertilization (IVF) has emerged as a pi…

2025
doi:10.3389/fgene.2025.1720842 ·PMID:41568332

Recurrent spontaneous abortion (RSA), defined as two or more consecutive pregnancy losses, affects 1%-5% of couples and poses a significant challenge to reproductive health. Despite its prevalence, the underlying etiology remains elusive in…

article 2025
doi:10.3389/fgene.2025.1615268 ·PMID:40772274

BACKGROUND: Endometriosis is a common disease among women of childbearing age. However, the molecular mechanism behind it is still unknown. Therefore, new biomarkers and therapeutic targets are needed to improve the diagnosis and treatment …

2025
doi:10.3389/fgene.2025.1589999 ·PMID:40620701

BackgroundThe incidence of ulcerative colitis (UC) is rapidly increasing worldwide, but existing therapeutics are limited. Neutrophil extracellular traps (NETs), which have been associated with the development of various autoimmune diseases…

review 2025
doi:10.3389/fgene.2025.1597287 ·PMID:40792071

Endometriosis is highly underdiagnosed and undertreated gynecological disorder, with diagnosis often delayed by 8-12 years. This delay can have serious consequences including infertility. Currently, the gold standard for endometriosis diagn…

other 2025
doi:10.3389/fgene.2025.1541946 ·PMID:40486679

OBJECTIVE: To screen for possible pathogenic mutations in polycystic ovary syndrome (PCOS) patients with diabetes and preliminarily explore the relationship between genotype and phenotype to offer a research basis for PCOS pathogenesis with…

other 2025
doi:10.3389/fgene.2025.1631446 ·PMID:40893937

INTRODUCTION: Endometriosis is a common chronic gynecological condition that affects approximately 10% of women of reproductive age worldwide. METHODS: This study utilized large-scale genome-wide association study data and explored the cau…

2025
doi:10.3389/fgene.2025.1626890 ·PMID:40933484

Intrahepatic cholestasis of pregnancy (ICP) is associated with an increased risk of adverse fetal outcomes, including fetal morbidity and mortality. It is a complex liver disorder influenced by genetic interactions, estrogen levels, and env…

2025
doi:10.3389/fgene.2025.1509245 ·PMID:40476267

IntroductionThe primary clinical challenge associated with follicular thyroid carcinoma (FTC) lies in accurately diagnosing the condition, particularly in distinguishing it with follicular thyroid adenoma (FTA) due to their overlapping cyto…

2024
doi:10.3389/fgene.2024.1374965 ·PMID:39188285

Acute intermittent porphyria (AIP) is caused by mutations in the gene encoding hydroxymethylbilane synthase (HMBS), a key enzyme in the heme biosynthesis pathway. AIP is an autosomal dominant disorder characterized by low penetrance and a h…

other 2024
doi:10.3389/fgene.2024.1460216 ·PMID:39831202

BACKGROUND: Endometriosis, a prevalent chronic gynecological condition, is frequently associated with infertility and pelvic pain. Despite numerous studies indicating a correlation between epigenetic regulation and endometriosis, its precis…

other 2024
doi:10.3389/fgene.2024.1432026 ·PMID:38988834
2024
doi:10.3389/fgene.2024.1508169 ·PMID:39659675
other 2024
doi:10.3389/fgene.2024.1386411 ·PMID:38974388

Background: Endometriosis, characterized by extrauterine endometrial tissue, leads to irregular bleeding and pelvic pain. Menstrual retrograde theory suggests fragments traverse fallopian tubes, causing inflammation and scar tissue. Prevale…

2024
doi:10.3389/fgene.2024.1330807 ·PMID:38572418

Uterine leiomyoma, commonly referred to as fibroids, is a benign tumor that develops in the muscular wall of the uterus. These growths are non-cancerous and can vary in size, ranging from tiny nodules to larger masses. Uterine leiomyomas of…

2024
doi:10.3389/fgene.2024.1409335 ·PMID:39184351

Introduction: Targeted single nucleotide polymorphisms (SNPs) have been used in genomic prediction methodologies to enhance the accuracy of associated genetic transmitting abilities in Holstein cows. The objective of this study was to ident…

2024
doi:10.3389/fgene.2024.1397352 ·PMID:38983269

Genetics is a key factor that governs the susceptibility to oxidative stress. In the body, oxidative burden is regulated by the balance between the prooxidant genes that orchestrate processes that produce oxidant species, while the antioxid…

2024
doi:10.3389/fgene.2024.1404215 ·PMID:39376740

IntroductionThis study aimed to investigate the causal relationship between phosphatidylcholine (PC) levels and dysmenorrhea using Mendelian randomization (MR) analysis.MethodsWe conducted a two-sample MR analysis using GWAS data on PC leve…

2024
doi:10.3389/fgene.2024.1393181 ·PMID:38784035

Aging is linked to a time-associated decline in both cellular function and repair capacity leading to malfunction on an organismal level, increased frailty, higher incidence of diseases, and death. As the population grows older, there is a …

article 2023
doi:10.3389/fgene.2022.1082709 ·PMID:36685847

Background: Adenomyosis is a hormone-dependent benign gynecological disease characterized by the invasion of the endometrium into the myometrium. Women with adenomyosis can suffer from abnormal uterine bleeding, severe pelvic pain, and subf…