Pu Dai

8PUBLICATIONS
7CO-AUTHORS
Haematological tumoursGene mappingGene expression (incl. microarray and other genome-wide approaches)Neurogenetics
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Publications (8)

|Mar 28, 2026
Therapeutic potential of cAMP-mediated lysosomal pH modulation in ATP6V1B2-related neuropathology.

Lu Zheng, Weihao Zhao, Guang Yang

|Apr 24, 2023
Correction to: Preimplantation genetic testing for hereditary hearing loss in Chinese population.

Qingling Bi, Shasha Huang, Hui Wang

|Apr 05, 2023
Preimplantation genetic testing for hereditary hearing loss in Chinese population.

Qingling Bi, Shasha Huang, Hui Wang

|Aug 18, 2020
Hearing Phenotypes of Patients with Hearing Loss Homozygous for the <i>GJB2</i> c.235delc Mutation.

Chang Guo, Sha-Sha Huang, Yong-Yi Yuan

|Feb 25, 2020
Prelingual Sensorineural Hearing Loss Caused by a Novel <i>GJB2</i> Dominant Mutation in a Chinese Family.

Shasha Huang, Xue Gao, Yufeng Wang

|Jun 01, 2018
A Missense Mutation in <i>POU4F3</i> Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family.

Xue Gao, Jin-Cao Xu, Wei-Qian Wang

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