Shengyi Wang
Shanghai, China
Last Updated: 09/26/2026
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Found 9 publications
Author Correction: A base editor for the long-term restoration of auditory function in mice with recessive profound deafness.
Journal: Nature biomedical engineering
Published: September 07, 2026
Unlocking mRNA-driven CRISPR-Cas9 gene therapy via optimizing mRNA and the delivery vectors.
Journal: Molecular therapy. Nucleic acids
Published: November 10, 2025
Gene Therapy vs Cochlear Implantation in Restoring Hearing Function and Speech Perception for Individuals With Congenital Deafness.
Journal: JAMA neurology
Published: July 21, 2025
A base editor for the long-term restoration of auditory function in mice with recessive profound deafness.
Journal: Nature biomedical engineering
Published: December 08, 2023
Microfluidic-assisted biomineralization of CRISPR/Cas9 in near-infrared responsive metal-organic frameworks for programmable gene-editing.
Journal: Nanoscale
Published: October 18, 2022
Hearing of Otof-deficient mice restored by trans-splicing of N- and C-terminal otoferlin.
Journal: Human genetics
Published: August 26, 2022
Specific knockdown of Htra2 by CRISPR-CasRx prevents acquired sensorineural hearing loss in mice.
Journal: Molecular therapy. Nucleic acids
Published: November 02, 2021
Showing 1-9 of 9
Last Updated: 09/26/2026