Tae-Jun Kwon

发表

Methionine Sulfoxide Reductase A, B1 and B2 Are Likely to Be Involved in the Protection against Oxidative Stress in the Inner Ear

Jaetae Lee, U. Kim, Byeonghyeon Lee, 2014, Cells Tissues Organs.

The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing loss

G. Vriend, H. Venselaar, J. Bok, 2014, Open Biology.

Fursultiamine Prevents Drug-Induced Ototoxicity by Reducing Accumulation of Reactive Oxygen Species in Mouse Cochlea

In-kyu Lee, U. Kim, Ye-Ri Kim, 2021, Antioxidants.

A novel insertion-induced frameshift mutation of the SLC26A4 gene in a Korean family with Pendred syndrome.

U. Kim, Kyu-Yup Lee, Sang-Heun Lee, 2012, Gene.

MethioninesulfoxidereductaseB 3 deficiencycauses hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells

J. Bok, Z. Ryoo, Junkoo Yi, 2014 .

Methionine sulfoxide reductase B3 deficiency causes hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells.

Y. Bae, J. Bok, Z. Ryoo, 2014, Human molecular genetics.

Polymorphisms of TAS1R3 and GNAT3 Genes Are Associated with Patients with Taste Disorder

U. Kim, Mi-Kyung Ye, J. Bae, 2011 .

Genetic Polymorph isms and Haplotype Analysis of Sweet Taste Receptor TAS1R2 Gene in the Korean Population

U. Kim, J. Bae, Tae-Jun Kwon, 2010 .

CHD7 Mutational Analysis and Clinical Considerations for Auditory Rehabilitation in Deaf Patients with CHARGE Syndrome

J. Bok, U. Kim, Won-Sang Lee, 2011, PloS one.

Genetic analysis of auditory neuropathy spectrum disorder in the Korean population.

U. Kim, Jong Dae Lee, Jeong-In Baek, 2013, Gene.

Targeted Gene Delivery into the Mammalian Inner Ear Using Synthetic Serotypes of Adeno-Associated Virus Vectors

J. Bok, U. Kim, Nari Ryu, 2019, Molecular therapy. Methods & clinical development.

Mutational Analysis of EYA1, SIX1 and SIX5 Genes and Strategies for Management of Hearing Loss in Patients with BOR/BO Syndrome

U. Kim, Won-Sang Lee, M. Song, 2013, PloS one.

Evidence for a founder mutation causing DFNA5 hearing loss in East Asians

A. Griffith, U. Kim, T. Ben‐Yosef, 2010, Journal of Human Genetics.

Molecular cloning, characterization, and expression of pannexin genes in chicken.

U. Kim, J. Bae, Tae-Jun Kwon, 2014, Poultry science.

Methionine Sulfoxide Reductase B3-Targeted In Utero Gene Therapy Rescues Hearing Function in a Mouse Model of Congenital Sensorineural Hearing Loss.

Jin-Ho Cho, Z. Ryoo, U. Kim, 2016, Antioxidants & redox signaling.

Genetic and Epigenetic Alterations of the NF2 Gene in Sporadic Vestibular Schwannomas

U. Kim, Jong Dae Lee, Won-Sang Lee, 2012, PloS one.

Identification of a novel splicing mutation within SLC17A8 in a Korean family with hearing loss by whole-exome sequencing.

J. Bok, U. Kim, Nari Ryu, 2017, Gene.

Molecular analysis of TMC1 gene in the Korean patients with nonsyndromic hearing loss

U. Kim, Sang-Heun Lee, Tae-Jun Kwon, 2011, Genes & Genomics.

Functional mapping of the auditory tract in rodent tinnitus model using manganese-enhanced magnetic resonance imaging

Sang-Heun Lee, Jin-Ho Cho, Hyun-Ju Cho, 2014, NeuroImage.

Therapeutic effect of intraperitoneal dexamethasone on noise-induced permanent threshold shift in mice model

Byeonghyeon Lee, Ye-Ri Kim, D. J. Jung, 2023, Experimental brain research.