Lv Liu
Changsha, China
Last Updated: 09/26/2026
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Found 9 publications
Whole exome sequencing identified two novel mutations of ACD in Chinese patients with idiopathic pulmonary fibrosis.
Journal: Frontiers in cell and developmental biology
Published: December 11, 2025
Whole exome sequencing identified three novel mutations of RTEL1 in Chinese patients with idiopathic pulmonary fibrosis.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: March 07, 2025
RTN3 regulates collagen biosynthesis and profibrotic macrophage differentiation to promote pulmonary fibrosis via interacting with CRTH2.
Journal: Molecular medicine (Cambridge, Mass.)
Published: August 27, 2024
ZCCHC8 p.P410A disrupts nucleocytoplasmic localization, promoting idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease.
Journal: Molecular medicine (Cambridge, Mass.)
Published: May 23, 2024
A nonsense mutation (c.382C>T) of PARN in a patient with idiopathic pulmonary fibrosis.
Journal: QJM : monthly journal of the Association of Physicians
Published: April 03, 2024
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.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: January 13, 2023
Identification of a Missense Mutation in the Surfactant Protein A2 Gene in a Chinese Family with Interstitial Lung Disease.
Journal: DNA and cell biology
Published: November 12, 2020
Identification and functional characterization of a novel surfactant protein A2 mutation (p.N207Y) in a Chinese family with idiopathic pulmonary fibrosis.
Journal: Molecular genetics & genomic medicine
Published: November 13, 2019
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Last Updated: 09/26/2026