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Xingle Zhao

4PUBLICATIONS

7CO-AUTHORS

Gene mappingNeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Neural engineering

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Publications (4)

Sort by Publication Date:

|Oct 08, 2025

Atypical phenotypic characteristics, mutation analysis and treatment in a family of riboflavin transporter deficiency caused by SLC52A3 variants.

Peipei Li, Ting Zhang, Hongen Xu

|Aug 21, 2025

Gene therapy restores auditory function and rescues damaged inner hair cells in an aged Vglut3 knockout mouse model.

Xingle Zhao, Hongen Xu, Chengyu Lian

|May 29, 2023

Cochlear transcript diversity and its role in auditory functions implied by an otoferlin short isoform.

Huihui Liu, Hongchao Liu, Longhao Wang

|Jun 21, 2022

Gene Therapy Restores Auditory Functions in an Adult Vglut3 Knockout Mouse Model.

Xingle Zhao, Huihui Liu, Hongchao Liu

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Frequent Collaborators

2 joint publications

Hongen Xu

1 joint publications

Hao Wu

1 joint publications

Wei Lu

1 joint publications

Liang Wang

1 joint publications

Peipei Li

1 joint publications

Ting Zhang

1 joint publications

Bei Chen

Frequent Collaborators

2 joint publications

Hongen Xu

1 joint publications

Hao Wu

1 joint publications

Wei Lu

1 joint publications

Liang Wang

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