Nari Ryu

Daegu, Republic of Korea

Last Updated: 09/26/2026

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Found 8 publications

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

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

Journal: Theranostics

Published: June 30, 2019

CRISPR/Cas9-mediated genome editing of splicing mutation causing congenital hearing loss.

CRISPR/Cas9-mediated genome editing of splicing mutation causing congenital hearing loss.

Journal: Gene

Published: January 26, 2019

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

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

Journal: Molecular therapy. Methods & clinical development

Published: September 19, 2018

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

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

Journal: Redox biology

Published: August 13, 2018

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

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

Journal: Cell death & disease

Published: May 06, 2018

Effective PEI-mediated delivery of CRISPR-Cas9 complex for targeted gene therapy.

Effective PEI-mediated delivery of CRISPR-Cas9 complex for targeted gene therapy.

Journal: Nanomedicine : nanotechnology, biology, and medicine

Published: March 06, 2018

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

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

Journal: Gene

Published: February 18, 2017

Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans.

Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans.

Journal: BMC medical genetics

Published: August 26, 2015

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Last Updated: 09/26/2026