Xinyao Wang
Shanghai, 200092, China
Last Updated: 09/26/2026
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Found 8 publications
Genetic characterization and functional analysis of novel PITX2 variants identified in Chinese families with Axenfeld-Rieger syndrome.
Journal: Acta biochimica et biophysica Sinica
Published: October 11, 2025
Identification and functional analysis of a novel TBC1D23 pathogenic variant in a Chinese family with pontocerebellar hypoplasia.
Journal: Human genomics
Published: December 23, 2024
Characterization of metalaxyl-induced notochord toxicity based on biochemical and transcriptomics in zebrafish (Danio rerio) model.
Journal: Journal of hazardous materials
Published: October 09, 2024
A novel KDM5C mutation associated with intellectual disability: molecular mechanisms and clinical implications.
Journal: Italian journal of pediatrics
Published: June 09, 2024
FYCO1 regulates migration, invasion, and invadopodia formation in HeLa cells through CDC42/N-WASP/Arp2/3 signaling pathway.
Journal: Biochemistry and cell biology = Biochimie et biologie cellulaire
Published: November 07, 2022
Identification and functional analysis of two GJA8 variants in Chinese families with eye anomalies.
Journal: Molecular genetics and genomics : MGG
Published: March 20, 2022
Identification and functional study of FOXC1 variants in Chinese families with glaucoma.
Journal: American journal of medical genetics. Part A
Published: March 15, 2021
Showing 1-8 of 8
Last Updated: 09/26/2026