Kaiwen L. Wu
28 Fuxing Road
Beijing, 100853, China
Beijing, 100853, China
Last Updated: 09/26/2026
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Found 15 publications
A review of the characteristics and precise diagnosis value of electrocochleography in patients with auditory neuropathy
Journal: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
Published: May 29, 2024
The updates of the ACMG variant interpretation guidelines affect the pathogenicity determination of OTOF gene variations in patients with auditory neuropathy
Journal: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
Published: May 29, 2024
Research on the variation in distortion product otoacoustic emissions in patients with auditory neuropathy during the natural course of the disease
Journal: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
Published: May 29, 2024
NADH improves AIF dimerization and inhibits apoptosis in iPSCs-derived neurons from patients with auditory neuropathy spectrum disorder.
Journal: Hearing research
Published: September 22, 2023
Genetic correction of induced pluripotent stem cells from a DFNA36 patient results in morphologic and functional recovery of derived hair cell-like cells.
Journal: Stem cell research & therapy
Published: August 03, 2023
AIFM1 variants associated with auditory neuropathy spectrum disorder cause apoptosis due to impaired apoptosis-inducing factor dimerization.
Journal: Journal of Zhejiang University. Science. B
Published: February 08, 2023
Impaired AIF-CHCHD4 interaction and mitochondrial calcium overload contribute to auditory neuropathy spectrum disorder in patient-iPSC-derived neurons with AIFM1 variant.
Journal: Cell death & disease
Published: February 01, 2023
Generation of a human induced pluripotent stem cell line (CPGHi003-A) from an auditory neuropathy patient with AIFM1 p.R422Q mutation.
Journal: Stem cell research
Published: February 05, 2021
Generation of a human induced pluripotent stem cell line (CPGHi001-A) from a hearing loss patient with the TMC1 p.M418K mutation.
Journal: Stem cell research
Published: May 01, 2020
Identification of four TMC1 variations in different Chinese families with hereditary hearing loss.
Journal: Molecular genetics & genomic medicine
Published: January 10, 2018
Further evidence for "gain-of-function" mechanism of DFNA5 related hearing loss.
Journal: Scientific reports
Published: December 08, 2017
A novel dominant GJB2 (DFNA3) mutation in a Chinese family.
Journal: Scientific reports
Published: April 19, 2016
Last Updated: 09/26/2026