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

Antioxidants & redox signaling, 2016-04, Vol.24 (11), p.590

2016

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Modified U1 snRNA and antisense oligonucleotides rescue splice mutations in SLC26A4 that cause hereditary hearing loss

Human mutation, 2019-08, Vol.40 (8), p.1172-1180, Article humu.23774

2019

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Positional Cloning of the Human Quantitative Trait Locus Underlying Taste Sensitivity to Phenylthiocarbamide

Science (American Association for the Advancement of Science), 2003-02, Vol.299 (5610), p.1221-1225

2003

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An autosomal dominant ERLIN2 mutation leads to a pure HSP phenotype distinct from the autosomal recessive ERLIN2 mutations (SPG18)

Scientific reports, 2020-02, Vol.10 (1), p.3295-3295, Article 3295

2020

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Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing

Theranostics, 2019-01, Vol.9 (24), p.7184-7199

2019

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Evaluating protective and therapeutic effects of alpha-lipoic acid on cisplatin-induced ototoxicity

Cell death & disease, 2018-08, Vol.9 (8), p.827-13, Article 827

2018

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Mitochondrial redox system: A key target of antioxidant therapy to prevent acquired sensorineural hearing loss

Frontiers in pharmacology, 2023-03, Vol.14, p.1176881-1176881

2023

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C-phycocyanin from Limnothrix Species KNUA002 Alleviates Cisplatin-Induced Ototoxicity by Blocking the Mitochondrial Apoptotic Pathway in Auditory Cells

Marine drugs, 2019-04, Vol.17 (4), p.235

2019

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Protective effect of berberine chloride against cisplatin-induced ototoxicity

Genes & Genomics, 2022, 44(1), , pp.1-7

2022

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Pannexin 3 is required for normal progression of skeletal development in vertebrates

The FASEB journal, 2015-11, Vol.29 (11), p.4473-4484

2015

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The Molecular Basis of Individual Differences in Phenylthiocarbamide and Propylthiouracil Bitterness Perception

Current biology, 2005-02, Vol.15 (4), p.322-327

2005

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Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss

Genetics in medicine, 2021-11, Vol.23 (11), p.2208-2212

2021

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Galangin prevents aminoglycoside-induced ototoxicity by decreasing mitochondrial production of reactive oxygen species in mouse cochlear cultures

Toxicology letters, 2016-03, Vol.245, p.78-85

2016

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Therapeutic potential of the mitochondria-targeted antioxidant MitoQ in mitochondrial-ROS induced sensorineural hearing loss caused by Idh2 deficiency

Redox biology, 2019-01, Vol.20, p.544-555

2019

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Identification of novel missense mutation related with non-syndromic sensorineural deafness, DFNA11 in korean family by NGS

Genes & Genomics, 2023, 45(2), , pp.225-230

2023

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Genetic and epigenetic alterations of the NF2 gene in sporadic vestibular schwannomas

PloS one, 2012-01, Vol.7 (1), p.e30418-e30418

2012

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Alpha-lipoic acid protects against cisplatin-induced ototoxicity via the regulation of MAPKs and proinflammatory cytokines

Biochemical and biophysical research communications, 2014-06, Vol.449 (2), p.183-189

2014

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

Molecular therapy. Methods & clinical development, 2019-06, Vol.13, p.197-204

2019

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KL1333, a derivative of β-lapachone, protects against cisplatin-induced ototoxicity in mouse cochlear cultures

Biomedicine & pharmacotherapy, 2020-06, Vol.126, p.110068, Article 110068

2020

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Microneedle array with a pH-responsive polymer coating and its application in smart drug delivery for wound healing

Sensors and actuators. B, Chemical, 2021-10, Vol.345, p.130441, Article 130441

2021

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Mutational analysis of EYA1, SIX1 and SIX5 genes and strategies for management of hearing loss in patients with BOR/BO syndrome

PloS one, 2013-06, Vol.8 (6), p.e67236

2013

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Identification of Pathogenic Mechanisms of COCH Mutations, Abolished Cochlin Secretion, and Intracellular Aggregate Formation: Genotype-Phenotype Correlations in DFNA9 Deafness and Vestibular Disorder

Human mutation, 2014-12, Vol.35 (12), p.1506-1513

2014

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Spatiotemporal expression patterns of clusterin in the mouse inner ear

Cell and tissue research, 2017-10, Vol.370 (1), p.89-97

2017

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Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families

Orphanet journal of rare diseases, 2012-09, Vol.7 (1), p.60-60, Article 60

2012

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Genetic analysis of genes related to tight junction function in the Korean population with non-syndromic hearing loss

PloS one, 2014-04, Vol.9 (4), p.e95646-e95646

2014

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

Modified U1 snRNA and antisense oligonucleotides rescue splice mutations in SLC26A4 that cause hereditary hearing loss

Positional Cloning of the Human Quantitative Trait Locus Underlying Taste Sensitivity to Phenylthiocarbamide

An autosomal dominant ERLIN2 mutation leads to a pure HSP phenotype distinct from the autosomal recessive ERLIN2 mutations (SPG18)

Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing

Evaluating protective and therapeutic effects of alpha-lipoic acid on cisplatin-induced ototoxicity

Mitochondrial redox system: A key target of antioxidant therapy to prevent acquired sensorineural hearing loss

C-phycocyanin from Limnothrix Species KNUA002 Alleviates Cisplatin-Induced Ototoxicity by Blocking the Mitochondrial Apoptotic Pathway in Auditory Cells

Protective effect of berberine chloride against cisplatin-induced ototoxicity

Pannexin 3 is required for normal progression of skeletal development in vertebrates

The Molecular Basis of Individual Differences in Phenylthiocarbamide and Propylthiouracil Bitterness Perception

Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss

Galangin prevents aminoglycoside-induced ototoxicity by decreasing mitochondrial production of reactive oxygen species in mouse cochlear cultures

Therapeutic potential of the mitochondria-targeted antioxidant MitoQ in mitochondrial-ROS induced sensorineural hearing loss caused by Idh2 deficiency

Identification of novel missense mutation related with non-syndromic sensorineural deafness, DFNA11 in korean family by NGS

Genetic and epigenetic alterations of the NF2 gene in sporadic vestibular schwannomas

Alpha-lipoic acid protects against cisplatin-induced ototoxicity via the regulation of MAPKs and proinflammatory cytokines

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

KL1333, a derivative of β-lapachone, protects against cisplatin-induced ototoxicity in mouse cochlear cultures

Microneedle array with a pH-responsive polymer coating and its application in smart drug delivery for wound healing

Mutational analysis of EYA1, SIX1 and SIX5 genes and strategies for management of hearing loss in patients with BOR/BO syndrome

Identification of Pathogenic Mechanisms of COCH Mutations, Abolished Cochlin Secretion, and Intracellular Aggregate Formation: Genotype-Phenotype Correlations in DFNA9 Deafness and Vestibular Disorder

Spatiotemporal expression patterns of clusterin in the mouse inner ear

Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families

Genetic analysis of genes related to tight junction function in the Korean population with non-syndromic hearing loss

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