Bei Chen

发表

Early truncation of the N‐terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype

Hongen Xu, Wenxue Tang, Yulin Zhao, 2020, Molecular genetics & genomic medicine.

Mechanisms of hearing loss and cell death in the cochlea of connexin mutant mice.

Hongen Xu, Wenxue Tang, Yulin Zhao, 2020, American journal of physiology. Cell physiology.

High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing

Hongen Xu, Wenxue Tang, Xiaohu Li, 2021, Frontiers in Genetics.

Treacher Collins syndrome: Clinical report and retrospective analysis of Chinese patients

W. Lu, Hongen Xu, Wenxue Tang, 2020, Molecular genetics & genomic medicine.

Auditory Neuropathy Spectrum Disorder (ANSD)—Clinical Characteristics and Pathogenic Variant Analysis of Three Nonsyndromic Deafness Families

W. Lu, Hongen Xu, Wenxue Tang, 2020, BioMed research international.

Genetic and Phenotypic Variability in Chinese Patients With Branchio-Oto-Renal or Branchio-Oto Syndrome

Shuping Sun, Hongen Xu, Wenxue Tang, 2021, Frontiers in Genetics.

Application of Nanomedicine in Inner Ear Diseases

Wenxue Tang, Wei Jiang, Mingchao Zhu, 2022, Frontiers in Bioengineering and Biotechnology.

Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next‐generation sequencing of the SLC26A4 gene

Hongen Xu, Wenxue Tang, Xiaohu Li, 2021, Molecular genetics & genomic medicine.

Localization of Glucose Transporter 10 to Hair Cells' Cuticular Plate in the Mouse Inner Ear

Wenxue Tang, Xi Lin, Bei Chen, 2018, BioMed Research International.

Long non-coding RNA Rian promotes the expression of tight junction proteins in endothelial cells by regulating perivascular-resident macrophage-like melanocytes and PEDF secretion

Jinhui Zhang, Lingling Neng, Bei Chen, 2021, Human Cell.