|
- Integrative analysis reveals the recurrent genetic etiologies in idiopathic pulmonary fibrosis.QJM, 2023, 116 (12) : 983-992.
- RTN3 regulates collagen biosynthesis and profibrotic macrophage differentiation to promote pulmonary fibrosis via interacting with CRTH2.Mol Med, 2025, 31 (1) : 63.
- Haploinsufficiency of KCNAB3 causes sudden cardiac death through delayed inactivation of Kv1.5 channel upon depolarization and induced myocardial apoptosis.Genes Dis, 2022, 10 (3) : 671-674.
- ZCCHC8 p.P410A disrupts nucleocytoplasmic localization, promoting idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease.Mol Med, 2024, 30 (1) : 144.
- A novel mutation (p.Y24N) in NHP2 leads to idiopathic pulmonary fibrosis and lung carcinoma chronic obstructive lung disease by disrupting the expression and nucleocytoplasmic localization of NHP2.Biochim Biophys Acta Mol Basis Dis, 2023, 1869 (5) : 166692.
- Whole exome sequencing identified two novel mutations of ACD in Chinese patients with idiopathic pulmonary fibrosis.Front Cell Dev Biol, 2026, 14: 1765277.
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