Jieyu G. Qi
No. 6666 Furong Road, Changqing District
Jinan, 250307, China
Jinan, 250307, China
Last Updated: 09/26/2026
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Found 68 publications
Correction to: Knockdown of Foxg1 in supporting cells increases the trans‑differentiation of supporting cells into hair cells in the neonatal mouse cochlea.
Journal: Cellular and molecular life sciences : CMLS
Published: July 17, 2026
Efficient and Safe Transduction of Cochlear Outer Hair Cells in Adult Mice with AAV2.7m8-Myo15.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: January 31, 2026
Gene Editing Technologies for Hereditary Hearing Loss: Prospects and Challenges.
Journal: Neuroscience bulletin
Published: January 06, 2026
Recent advancements in improving cross-species applicability of bioengineered AAV capsids.
Journal: Gene therapy
Published: December 10, 2025
Human promoter-driven AAV tools enable precision gene therapy targeting cochlear hair cells.
Journal: Cell reports. Medicine
Published: October 03, 2025
Dysregulation of Serpinb6a-Gch1 axis contributes to DFNB91 deafness that is amendable to gene therapies.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: September 14, 2025
International expert consensus on gene therapy for hereditary hearing loss: Based on clinical trials.
Journal: Med (New York, N.Y.)
Published: July 22, 2025
Precise and efficient DNA base editing restores normal hearing in adult DFNB9 mouse model.
Journal: Med (New York, N.Y.)
Published: July 18, 2025
Establishment of a Cochlear Organoid Platform for Remodeling the Extracellular Matrix.
Journal: ACS nano
Published: July 15, 2025
Treating Hearing Loss: From Cochlear Implantation to Gene Therapy.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: May 30, 2025
OTOF-related gene therapy: a new way but a long road ahead.
Journal: Lancet (London, England)
Published: February 03, 2025
Last Updated: 09/26/2026