Gong K

No ORCID on file · 7 papers in corpus · active 2017-2026

Study types

  • article 1

Condition tags

  • endometriosis 1
2026
Radiology case reports ·doi:10.1016/j.radcr.2025.11.075

The endocervico-myomatous fistula is a rare condition that has been reported as a complication following uterine artery embolization. To date, no primary case of this nature has been documented in the PubMed database. The objective of this …

article 2026
NPJ biofilms and microbiomes ·doi:10.1038/s41522-026-01017-4

Endometriosis (EMS) remains understudied in effective management strategies. The interplay between macrophage dysfunction and microbiota-derived immune signals emerges as a potential mechanism in EMS pathogenesis, suggesting its relevance f…

2025
Discover oncology ·doi:10.1007/s12672-025-02039-8

BackgroundEndometrial cancer represents a significant health challenge, with rising incidence and complex prognostic challenges. This study aimed to develop a robust predictive model integrating programmed cell death-related genes and advan…

2022
Cell & bioscience ·doi:10.1186/s13578-022-00790-x

BackgroundVon Hippel-Lindau (VHL) disease is an autosomal dominant genetic neoplastic disorder caused by germline mutation or deletion of the VHL gene, characterized by the tendency to develop multisystem benign or malignant tumors. The mec…

2019
Oncology letters ·doi:10.3892/ol.2019.10091

Von Hippel-Lindau (VHL) disease is a genetic syndrome that involves the development of tumors in numerous organs. The kidney is one of the most frequently affected organs, and patients with VHL and renal tumors require repeated nephrectomy.…

2019
Frontiers in genetics ·doi:10.3389/fgene.2019.00867

Von Hippel-Lindau (VHL) disease is a rare autosomal-dominant inherited tumor syndrome. We aimed to analyze the correlations between frequent VHL mutations and phenotypes in Chinese VHL families. We screened 540 patients from 187 unrelated C…

2017
Cancer medicine ·doi:10.1002/cam4.1134

Von Hippel-Lindau (VHL) disease is a rare autosomal dominant cancer syndrome caused by alterations of VHL gene. Patients are predisposed to develop pheochromocytomas and solid or cystic tumors of the central nervous system, kidney, pancreas…