Nie H

No ORCID on file · 11 papers in corpus · active 2020-2026

Study types

  • preprint 2
  • case-report 1
  • review 1

Condition tags

  • endometriosis 4
  • chronic_pelvic_pain 1
  • infertility 1
2026
Biomolecules ·doi:10.3390/biom16030389

Protein lipidation, a pivotal post-translational modification, dynamically regulates cellular signaling, membrane trafficking, and protein stability, with emerging roles in reproductive physiology. However, the systematic understanding of h…

2025
Cancer research ·doi:10.1158/0008-5472.can-25-0654

Subunits of the SWI/SNF chromatin remodeling complex are altered in ∼20% of human cancers. Exemplifying the alterations is the ARID1A mutation that occurs in ∼50% of ovarian clear-cell carcinoma (OCCC), a disease with limited therapeutic op…

review 2024
Journal of Obstetrics and Gynaecology Research ·doi:10.1111/jog.16000

Endometriosis, affecting 6%-10% of women of reproductive age, can lead to severe symptoms such as chronic pelvic pain and infertility. Among its rarer manifestations is abdominal wall endometriosis (AWE), which has been increasingly reporte…

case-report 2023
World journal of clinical cases ·doi:10.12998/wjcc.v11.i18.4326

BACKGROUND: Lung endometriosis is an extremely rare gynecological disease. Current literature reports suggest that the majority of patients will present with only generic symptoms, such as hemoptysis, pneumothorax, and hemopneumothorax, whi…

2023
Frontiers in immunology ·doi:10.3389/fimmu.2023.1147710

Macrophages, as central components of innate immunity, feature significant heterogeneity. Numerus studies have revealed the pivotal roles of macrophages in the pathogenesis of liver fibrosis induced by various factors. Hepatic macrophages f…

2023
Cancer cell ·doi:10.1016/j.ccell.2023.03.002

ARID1A, encoding a subunit of the SWI/SNF complex, is mutated in ∼50% of clear cell ovarian carcinoma (OCCC) cases. Here we show that inhibition of the mevalonate pathway synergizes with immune checkpoint blockade (ICB) by driving inflammas…

2022
Frontiers in genetics ·doi:10.3389/fgene.2022.858641

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…

2022
Frontiers in genetics ·doi:10.3389/fgene.2022.936264

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…

preprint 2021
·doi:10.21203/rs.3.rs-141435/v1

Abstract Background: Lung endometriosis is an extremely rare gynecological disease. Literature reports suggest that most patients will show generic symptoms such as hemoptysis, pneumothorax, and hemopneumothorax, which can often result in …

2020
Scientific reports ·doi:10.1038/s41598-020-70500-5

To screen the key immune genes in the development of cervical cancer, construct immune related gene pairs (IRGPs), and evaluate their influence on the prognosis of cervical cancer. Tumor Genome Atlas (TCGA) database and geo database were do…

preprint 2020
·doi:10.21203/rs.3.rs-135229/v1

Abstract Background:Lung endometriosis is an extremely rare gynecological disease. Literature reports suggest that most patients will show generic symptoms such as hemoptysis, pneumothorax, and hemopneumothorax, which can often result in m…