Se-kyung Oh

Daegu, Republic of Korea

Last Updated: 09/26/2026

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Found 19 publications

Comparison study of the response with botulinum toxin muscle injection in the ICR mice from three different sources.

Comparison study of the response with botulinum toxin muscle injection in the ICR mice from three different sources.

Journal: Laboratory animal research

Published: May 13, 2019

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

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

Journal: Human mutation

Published: January 12, 2019

Epidural Fat-Derived Mesenchymal Stem Cell: First Report of Epidural Fat-Derived Mesenchymal Stem Cell.

Epidural Fat-Derived Mesenchymal Stem Cell: First Report of Epidural Fat-Derived Mesenchymal Stem Cell.

Journal: Asian spine journal

Published: August 21, 2018

Protective effects of 1,2,3-triazole derivative KPR-A020 against cisplatin-induced ototoxicity in murine cochlear cultures.

Protective effects of 1,2,3-triazole derivative KPR-A020 against cisplatin-induced ototoxicity in murine cochlear cultures.

Journal: International journal of pediatric otorhinolaryngology

Published: December 16, 2016

Genetic association of MYH genes with hereditary hearing loss in Korea.

Genetic association of MYH genes with hereditary hearing loss in Korea.

Journal: Gene

Published: May 20, 2016

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

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

Journal: Antioxidants & redox signaling

Published: December 10, 2015

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

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

Journal: Toxicology letters

Published: August 18, 2015

The pathological effects of connexin 26 variants related to hearing loss by in silico and in vitro analysis.

The pathological effects of connexin 26 variants related to hearing loss by in silico and in vitro analysis.

Journal: Human genetics

Published: July 20, 2015

Methionine sulfoxide reductase A, B1 and B2 are likely to be involved in the protection against oxidative stress in the inner ear.

Methionine sulfoxide reductase A, B1 and B2 are likely to be involved in the protection against oxidative stress in the inner ear.

Journal: Cells, tissues, organs

Published: October 06, 2014

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

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

Journal: Open biology

Published: August 01, 2014

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

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

Journal: Human molecular genetics

Published: November 06, 2013

A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine.

A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine.

Journal: European journal of human genetics : EJHG

Published: October 27, 2013

Showing 1-12 of 19

Last Updated: 09/26/2026