Jung A. Kim

Seoul, Republic of Korea

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 44 publications

HAP1 interaction with KCNQ4 attenuates channel surface expression and function.

HAP1 interaction with KCNQ4 attenuates channel surface expression and function.

Journal: Molecules and cells

Published: October 01, 2025

Leveraging underrepresented population data improves interpretation of genetic variants associated with hearing loss.

Leveraging underrepresented population data improves interpretation of genetic variants associated with hearing loss.

Journal: Scientific reports

Published: May 20, 2025

Antisense oligonucleotide therapy mitigates autosomal dominant progressive hearing loss in a murine model of human DFNA2.

Antisense oligonucleotide therapy mitigates autosomal dominant progressive hearing loss in a murine model of human DFNA2.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: January 21, 2025

Gene supplementation with precise transgene expression rescues hearing loss in a mouse model with an Mpzl2 East Asian founder variant.

Gene supplementation with precise transgene expression rescues hearing loss in a mouse model with an Mpzl2 East Asian founder variant.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: December 02, 2024

Biallelic variants of SEMA3F are associated with nonsyndromic hearing loss.

Biallelic variants of SEMA3F are associated with nonsyndromic hearing loss.

Journal: Molecules and cells

Published: September 24, 2024

Intravitreal adenine base editing of RS1 improves vision in a preclinical mouse model of retinoschisis.

Intravitreal adenine base editing of RS1 improves vision in a preclinical mouse model of retinoschisis.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: September 02, 2024

Systematic genetic assessment of hearing loss using whole-genome sequencing identifies pathogenic variants.

Systematic genetic assessment of hearing loss using whole-genome sequencing identifies pathogenic variants.

Journal: Experimental & molecular medicine

Published: August 01, 2024

MYH1 deficiency disrupts outer hair cell electromotility, resulting in hearing loss.

MYH1 deficiency disrupts outer hair cell electromotility, resulting in hearing loss.

Journal: Experimental & molecular medicine

Published: March 04, 2024

Characterization of Vestibular Phenotypes in Patients with Genetic Hearing Loss.

Characterization of Vestibular Phenotypes in Patients with Genetic Hearing Loss.

Journal: Journal of clinical medicine

Published: February 27, 2024

Vestibular hair cells are more prone to damage by excessive acceleration insult in the mouse with KCNQ4 dysfunction.

Vestibular hair cells are more prone to damage by excessive acceleration insult in the mouse with KCNQ4 dysfunction.

Journal: Scientific reports

Published: November 17, 2023

Immune Cells Are Differentially Affected by SARS-CoV-2 Viral Loads in K18-hACE2 Mice.

Immune Cells Are Differentially Affected by SARS-CoV-2 Viral Loads in K18-hACE2 Mice.

Journal: Immune network

Published: August 14, 2023

Novel Variant in CEP250 Causes Protein Mislocalization and Leads to Nonsyndromic Autosomal Recessive Type of Progressive Hearing Loss.

Novel Variant in CEP250 Causes Protein Mislocalization and Leads to Nonsyndromic Autosomal Recessive Type of Progressive Hearing Loss.

Journal: Cells

Published: July 25, 2023

Showing 1-12 of 44

Last Updated: 09/26/2026