Shin-ichiro Kitajiri

Department Of Otolaryngology Head And Neck Surgery
Kyoto, Japan

Last Updated: 09/26/2026

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Found 34 publications

Generation of four induced pluripotent stem cell lines (KEIUi004-A, KEIUi005-A, KEIUi006-A, and KEIUi007-A) from patients with sensorineural hearing loss with mutation in EYA4 gene.

Generation of four induced pluripotent stem cell lines (KEIUi004-A, KEIUi005-A, KEIUi006-A, and KEIUi007-A) from patients with sensorineural hearing loss with mutation in EYA4 gene.

Journal: Stem cell research
Published: March 18, 2024

Unbalanced bidirectional radial stiffness gradients within the organ of Corti promoted by TRIOBP.

Unbalanced bidirectional radial stiffness gradients within the organ of Corti promoted by TRIOBP.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 23, 2022

Prevalence and Clinical Characteristics of Hearing Loss Caused by MYH14 Variants.

Prevalence and Clinical Characteristics of Hearing Loss Caused by MYH14 Variants.

Journal: Genes
Published: September 24, 2021

Virus-infection in cochlear supporting cells induces audiosensory receptor hair cell death by TRAIL-induced necroptosis.

Virus-infection in cochlear supporting cells induces audiosensory receptor hair cell death by TRAIL-induced necroptosis.

Journal: PloS one
Published: June 02, 2021

Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin cores.

Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin cores.

Journal: Human genetics
Published: May 05, 2021

The use of a MITO-Porter to deliver exogenous therapeutic RNA to a mitochondrial disease's cell with a A1555G mutation in the mitochondrial 12S rRNA gene results in an increase in mitochondrial respiratory activity.

The use of a MITO-Porter to deliver exogenous therapeutic RNA to a mitochondrial disease's cell with a A1555G mutation in the mitochondrial 12S rRNA gene results in an increase in mitochondrial respiratory activity.

Journal: Mitochondrion
Published: April 06, 2020

Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-Onset Progressive Hearing Loss.

Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-Onset Progressive Hearing Loss.

Journal: Genes
Published: February 08, 2020

Cochlear supporting cells function as macrophage-like cells and protect audiosensory receptor hair cells from pathogens.

Cochlear supporting cells function as macrophage-like cells and protect audiosensory receptor hair cells from pathogens.

Journal: Scientific reports
Published: December 17, 2019

Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss.

Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss.

Journal: Scientific reports
Published: October 22, 2019

Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss.

Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss.

Journal: Genes
Published: August 01, 2019

Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant.

Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant.

Journal: International journal of molecular sciences
Published: July 23, 2019

POLD1 variants leading to reduced polymerase activity can cause hearing loss without syndromic features.

POLD1 variants leading to reduced polymerase activity can cause hearing loss without syndromic features.

Journal: Human mutation
Published: July 02, 2019
Showing 1-12 of 34

Last Updated: 09/26/2026