Wenxue X. Tang

No. 2 Jing‑ba Road
Zhengzhou, 450014, China

Last Updated: 09/26/2026

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Found 58 publications

Analysis of clinical manifestations and genetic characteristics of a late-onset auditory neuropathy pedigree caused by a mitochondrial MT-TS1 gene mutation m.7471dup

Analysis of clinical manifestations and genetic characteristics of a late-onset auditory neuropathy pedigree caused by a mitochondrial MT-TS1 gene mutation m.7471dup

Journal: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery

Published: September 01, 2025

Synergistic SHH activation and BMP inhibition remodel progenitor niche for enhanced hair cell generation.

Synergistic SHH activation and BMP inhibition remodel progenitor niche for enhanced hair cell generation.

Journal: Science China. Life sciences

Published: July 24, 2025

Rapid cochlear gene therapy in adult deaf mice: Vglut3 rescue via AAV8 achieves day-1 hearing restoration.

Rapid cochlear gene therapy in adult deaf mice: Vglut3 rescue via AAV8 achieves day-1 hearing restoration.

Journal: Molecular therapy. Methods & clinical development

Published: March 26, 2025

Extremely low-frequency electromagnetic fields facilitate proliferation and functional differentiation in spinal neural stem cells.

Extremely low-frequency electromagnetic fields facilitate proliferation and functional differentiation in spinal neural stem cells.

Journal: Scientific reports

Published: March 19, 2025

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

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

Journal: Gene therapy

Published: February 16, 2025

Real-time Monitoring Unveils Three Distinct Neuronal Response Patterns to SAW Ultrasound via L-type Calcium Channels.

Real-time Monitoring Unveils Three Distinct Neuronal Response Patterns to SAW Ultrasound via L-type Calcium Channels.

Journal: Neuroscience bulletin

Published: January 03, 2025

Genetic diversity and dietary adaptations of the Central Plains Han Chinese population in East Asia.

Genetic diversity and dietary adaptations of the Central Plains Han Chinese population in East Asia.

Journal: Communications biology

Published: September 05, 2024

Exonic Deletions and Deep Intronic Variants of the SLC26A4 Gene Contribute to the Genetic Diagnosis of Unsolved Patients With Enlarged Vestibular Aqueduct.

Exonic Deletions and Deep Intronic Variants of the SLC26A4 Gene Contribute to the Genetic Diagnosis of Unsolved Patients With Enlarged Vestibular Aqueduct.

Journal: Human mutation

Published: April 02, 2024

Genomic-transcriptomic analysis identifies the Syrian hamster as a superior animal model for human diseases.

Genomic-transcriptomic analysis identifies the Syrian hamster as a superior animal model for human diseases.

Journal: BMC genomics

Published: February 16, 2024

Analysis of perrault syndrome caused by pathogenic variants in LARS2 and HARS2 genes

Analysis of perrault syndrome caused by pathogenic variants in LARS2 and HARS2 genes

Journal: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery

Published: January 08, 2024

Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanisms.

Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanisms.

Journal: BMC medical genomics

Published: December 30, 2023

Novel Clinical Manifestation and Favorable Treatment Outcome of Cochlear Implant in a Chinese Family With Likely Pathogenic Variant of the P2RX2 Gene.

Novel Clinical Manifestation and Favorable Treatment Outcome of Cochlear Implant in a Chinese Family With Likely Pathogenic Variant of the P2RX2 Gene.

Journal: American journal of medical genetics. Part A

Published: December 19, 2023

Showing 1-12 of 58

Last Updated: 09/26/2026