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Inner ear cell therapy targeting hereditary deafness by activation of stem cell homing factors

Frontiers in pharmacology, 2015-01, Vol.6, p.2-2

Kamiya, Kazusaku

2015

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Degradation and modification of cochlear gap junction proteins in the early development of age-related hearing loss

Experimental and Molecular Medicine, 2020, 52(0), , pp.1-10

2020

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Generation of an induced pluripotent stem cell line from a late-onset, progressive high frequency hearing loss patient due to mutation in CDH23

Stem cell research, 2024-09, Vol.79, p.103471, Article 103471

2024

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Association Between Earwax-Determinant Genotypes and Acquired Middle Ear Cholesteatoma in a Japanese Population

Otolaryngology-head and neck surgery, 2022-01, Vol.166 (1), p.139-145

2022

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S100A7 Co-localization and Up-regulation of Filaggrin in Human Sinonasal Epithelial Cells

Current medical science, 2021-10, Vol.41 (5), p.863-868

2021

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Assembly of the cochlear gap junction macromolecular complex requires connexin 26

The Journal of clinical investigation, 2014-04, Vol.124 (4), p.1598-1607

2014

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Generation and characterization of a human iPSC line (JUFMDOi007-A) from a patient with Usher syndrome due to mutation in USH2A

Stem cell research, 2023-06, Vol.69, p.103100-103100, Article 103100

2023

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Effects of salicylate derivatives on localization of p.H723R allele product of SLC26A4

Auris, nasus, larynx, 2022-12, Vol.49 (6), p.928-937

2022

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Assessing the Efficacy of Tragal Pumping in a Novel Tympanostomy Tube‐Rat Model

OTO open : the official open access journal of the American Academy of Otolaryngology--Head and Neck Surgery Foundation, 2024-07, Vol.8 (3), p.e160-n/a

2024

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Generation of two iPSC lines from siblings of a homozygous patient with hearing loss and a heterozygous carrier with normal hearing carrying p.G45E/Y136X mutation in GJB2

Stem cell research, 2021-05, Vol.53, p.102290-102290, Article 102290

2021

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Generation of two induced pluripotent stem cell lines from PBMCs of siblings carrying c.235delC mutation in the GJB2 gene associated with sensorineural hearing loss

Stem cell research, 2020-08, Vol.47, p.101910-101910, Article 101910

2020

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Deficiency of transcription factor Brn4 disrupts cochlear gap junction plaques in a model of DFN3 non-syndromic deafness

PloS one, 2014-09, Vol.9 (9), p.e108216-e108216

2014

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Generation of the induced pluripotent stem cell (hiPSC) line (JUFMDOi004-A) from a patient with hearing loss carrying GJB2 (p.V37I) mutation

Stem cell research, 2020-03, Vol.43, p.101674-101674, Article 101674

2020

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In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea

Stem cell reports, 2016-12, Vol.7 (6), p.1023-1036

2016

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Activin/Nodal/TGF-β Pathway Inhibitor Accelerates BMP4-Induced Cochlear Gap Junction Formation During in vitro Differentiation of Embryonic Stem Cells

Frontiers in cell and developmental biology, 2021-04, Vol.9, p.602197-602197

2021

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Spatiotemporal expression of TRPM4 in the mouse cochlea

Journal of neuroscience research, 2014-10, Vol.92 (10), p.1409-1418

2014

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Piezoelectric vibrator-stimulated potential and heart rate accelerations detected from the fetus

International journal of pediatric otorhinolaryngology, 2017-10, Vol.101, p.204-210

2017

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Deformation of the Outer Hair Cells and the Accumulation of Caveolin-2 in Connexin 26 Deficient Mice

PloS one, 2015-10, Vol.10 (10), p.e0141258-e0141258

2015

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unusually powerful mode of low-frequency sound interference due to defective hair bundles of the auditory outer hair cells

Proceedings of the National Academy of Sciences - PNAS, 2014-06, Vol.111 (25), p.9307-9312

2014

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Mesenchymal Stem Cell Transplantation Accelerates Hearing Recovery through the Repair of Injured Cochlear Fibrocytes

The American journal of pathology, 2007-07, Vol.171 (1), p.214-226

2007

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Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness

Human molecular genetics, 2015-03, Vol.24 (13), p.3651-3661

2015

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Gene Transfer Targeting Mouse Vestibule Using Adenovirus and Adeno-Associated Virus Vectors

Otology & neurotology, 2012-06, Vol.33 (4), p.655-659

2012

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Enhanced expression of C/EBP homologous protein (CHOP) precedes degeneration of fibrocytes in the lateral wall after acute cochlear mitochondrial dysfunction induced by 3-nitropropionic acid

Neurochemistry international, 2010-02, Vol.56 (3), p.487-494

2010

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Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness

Human molecular genetics, 2015-07, Vol.24 (13), p.3651-3661

2015

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Caspase inhibitor facilitates recovery of hearing by protecting the cochlear lateral wall from acute cochlear mitochondrial dysfunction

Journal of neuroscience research, 2008-01, Vol.86 (1), p.215-222

2008

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Inner ear cell therapy targeting hereditary deafness by activation of stem cell homing factors

Degradation and modification of cochlear gap junction proteins in the early development of age-related hearing loss

Generation of an induced pluripotent stem cell line from a late-onset, progressive high frequency hearing loss patient due to mutation in CDH23

Association Between Earwax-Determinant Genotypes and Acquired Middle Ear Cholesteatoma in a Japanese Population

S100A7 Co-localization and Up-regulation of Filaggrin in Human Sinonasal Epithelial Cells

Assembly of the cochlear gap junction macromolecular complex requires connexin 26

Generation and characterization of a human iPSC line (JUFMDOi007-A) from a patient with Usher syndrome due to mutation in USH2A

Effects of salicylate derivatives on localization of p.H723R allele product of SLC26A4

Assessing the Efficacy of Tragal Pumping in a Novel Tympanostomy Tube‐Rat Model

Generation of two iPSC lines from siblings of a homozygous patient with hearing loss and a heterozygous carrier with normal hearing carrying p.G45E/Y136X mutation in GJB2

Generation of two induced pluripotent stem cell lines from PBMCs of siblings carrying c.235delC mutation in the GJB2 gene associated with sensorineural hearing loss

Deficiency of transcription factor Brn4 disrupts cochlear gap junction plaques in a model of DFN3 non-syndromic deafness

Generation of the induced pluripotent stem cell (hiPSC) line (JUFMDOi004-A) from a patient with hearing loss carrying GJB2 (p.V37I) mutation

In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea

Activin/Nodal/TGF-β Pathway Inhibitor Accelerates BMP4-Induced Cochlear Gap Junction Formation During in vitro Differentiation of Embryonic Stem Cells

Spatiotemporal expression of TRPM4 in the mouse cochlea

Piezoelectric vibrator-stimulated potential and heart rate accelerations detected from the fetus

Deformation of the Outer Hair Cells and the Accumulation of Caveolin-2 in Connexin 26 Deficient Mice

unusually powerful mode of low-frequency sound interference due to defective hair bundles of the auditory outer hair cells

Mesenchymal Stem Cell Transplantation Accelerates Hearing Recovery through the Repair of Injured Cochlear Fibrocytes

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness

Gene Transfer Targeting Mouse Vestibule Using Adenovirus and Adeno-Associated Virus Vectors

Enhanced expression of C/EBP homologous protein (CHOP) precedes degeneration of fibrocytes in the lateral wall after acute cochlear mitochondrial dysfunction induced by 3-nitropropionic acid

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness

Caspase inhibitor facilitates recovery of hearing by protecting the cochlear lateral wall from acute cochlear mitochondrial dysfunction

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