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Heliyon|September 23, 2024
Predicting biomarkers in laryngeal squamous cell carcinoma based on the cytokine-cytokine receptor interaction pathwayQingyong Chen, Dongqing Wang, Zhipeng Chen, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 21, 2023
A novel frameshift mutation of the endoglin(ENG) gene causes hereditary hemorrhagic telangiectasia in a Chinese familyPeng Li, Chunhai Gao, Yuda Wei, et al.
Biomed Research International|June 2, 2016
Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan AssayFengguo Zhang, Yun Xiao, Lei Xu, et al.
Plos One|January 9, 2026
Mechanisms of cellular senescence combined with molecular docking strategies: A biomarker study of potential therapeutic targets for allergic rhinitisQingyong Chen, Han Zhang, Yue Wu, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
Identification of a novel missense mutation in the WFS1 gene as a cause of autosomal dominant nonsyndromic sensorineural hearing loss in all-frequenciesXiaohui Bai, Huaiqing Lv, Fengguo Zhang, et al.
IEEE Transactions on Image Processing : a Publication of the IEEE Signal Processing Society|November 10, 2025
Benchmarking Laryngeal Neoplasm Segmentation: A Multicenter Dataset and an Effective MethodGuanghui Yue, Shangjie Wu, Ruxian Tian, et al.
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