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Spatiotemporal changes in the distribution of LHFPL5 in mice cochlear hair bundles during development and in the absence of PCDH15

PloS one, 2017-10, Vol.12 (10), p.e0185285-e0185285

2017

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Mutations in protocadherin 15 and cadherin 23 affect tip links and mechanotransduction in mammalian sensory hair cells

PloS one, 2011-04, Vol.6 (4), p.e19183-e19183

2011

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Usher syndrome IIIA: a review of the disorder and preclinical research advances in therapeutic approaches

Human genetics, 2022-04, Vol.141 (3-4), p.759-783

2022

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Mucosal Injection of the Silicon Phthalocyanine Pc 4 in a Rabbit Model—A Pilot Study

The Laryngoscope, 2024-08

2024

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Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III

Scientific reports, 2017-10, Vol.7 (1), p.13480-15, Article 13480

2017

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Mitochondrial calcium uniporter is essential for hearing and hair cell preservation in congenic FVB/NJ mice

Scientific reports, 2021-05, Vol.11 (1), p.9660-9660, Article 9660

2021

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Unconventional secretory pathway activation restores hair cell mechanotransduction in an USH3A model

Proceedings of the National Academy of Sciences - PNAS, 2019-05, Vol.116 (22), p.11000-11009

2019

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Noise exposure immediately activates cochlear mitogen-activated protein kinase signaling

Noise & health, 2014-11, Vol.16 (73), p.400-409

2014

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Interactions in the network of Usher syndrome type 1 proteins

Human molecular genetics, 2005-02, Vol.14 (3), p.347-356

2005

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A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Human genetics, 2021-06, Vol.140 (6), p.915-931

2021

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Transient receptor potential melastatin 1: a hair cell transduction channel candidate

PloS one, 2013-10, Vol.8 (10), p.e77213-e77213

2013

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ACF7 is a hair-bundle antecedent, positioned to integrate cuticular plate actin and somatic tubulin

The Journal of neuroscience, 2014-01, Vol.34 (1), p.305-312

2014

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Zebrafish Models for the Mechanosensory Hair Cell Dysfunction in Usher Syndrome 3 Reveal That Clarin-1 Is an Essential Hair Bundle Protein

The Journal of neuroscience, 2015-07, Vol.35 (28), p.10188-10201

2015

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Inhibition of Mitochondrial Division Attenuates Cisplatin-Induced Toxicity in the Neuromast Hair Cells

Frontiers in cellular neuroscience, 2017-12, Vol.11, p.393-393

2017

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The mechanosensory structure of the hair cell requires clarin-1, a protein encoded by Usher syndrome III causative gene

The Journal of neuroscience, 2012-07, Vol.32 (28), p.9485-9498

2012

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Ups and downs of Viagra: revisiting ototoxicity in the mouse model

PloS one, 2013-11, Vol.8 (11), p.e79226

2013

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A small molecule mitigates hearing loss in a mouse model of Usher syndrome III

Nature chemical biology, 2016-06, Vol.12 (6), p.444-451

2016

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The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15 , a novel protocadherin gene

Nature genetics, 2001-01, Vol.27 (1), p.99-102

2001

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Actin Crosslinking Family Protein 7 Deficiency Does Not Impair Hearing in Young Mice

Frontiers in cell and developmental biology, 2021-11, Vol.9, p.709442-709442

2021

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Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation

Human molecular genetics, 2009-08, Vol.18 (15), p.2748-2760

2009

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Clarin-1, Encoded by the Usher Syndrome III Causative Gene, Forms a Membranous Microdomain: POSSIBLE ROLE OF CLARIN-1 IN ORGANIZING THE ACTIN CYTOSKELETON

The Journal of biological chemistry, 2009-07, Vol.284 (28), p.18980-18993

2009

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Mutations in the novel protocadherin PCDH15 cause usher syndrome type 1F

Human molecular genetics, 2001-08, Vol.10 (16), p.1709-1718

2001

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Noddy, a mouse harboring a missense mutation in protocadherin-15, reveals the impact of disrupting a critical interaction site between tip-link cadherins in inner ear hair cells

The Journal of neuroscience, 2013-03, Vol.33 (10), p.4395-4404

2013

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A Mouse Model Validates the Utility of Electrocochleography in Verifying Endolymphatic Hydrops

Journal of the Association for Research in Otolaryngology, 2014-06, Vol.15 (3), p.413-421

2014

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Spiral Ganglion Degeneration Patterns in Endolymphatic Hydrops

The Laryngoscope, 2008-07, Vol.118 (7), p.1217-1223

2008

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Spatiotemporal changes in the distribution of LHFPL5 in mice cochlear hair bundles during development and in the absence of PCDH15

Mutations in protocadherin 15 and cadherin 23 affect tip links and mechanotransduction in mammalian sensory hair cells

Usher syndrome IIIA: a review of the disorder and preclinical research advances in therapeutic approaches

Mucosal Injection of the Silicon Phthalocyanine Pc 4 in a Rabbit Model—A Pilot Study

Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III

Mitochondrial calcium uniporter is essential for hearing and hair cell preservation in congenic FVB/NJ mice

Unconventional secretory pathway activation restores hair cell mechanotransduction in an USH3A model

Noise exposure immediately activates cochlear mitogen-activated protein kinase signaling

Interactions in the network of Usher syndrome type 1 proteins

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Transient receptor potential melastatin 1: a hair cell transduction channel candidate

ACF7 is a hair-bundle antecedent, positioned to integrate cuticular plate actin and somatic tubulin

Zebrafish Models for the Mechanosensory Hair Cell Dysfunction in Usher Syndrome 3 Reveal That Clarin-1 Is an Essential Hair Bundle Protein

Inhibition of Mitochondrial Division Attenuates Cisplatin-Induced Toxicity in the Neuromast Hair Cells

The mechanosensory structure of the hair cell requires clarin-1, a protein encoded by Usher syndrome III causative gene

Ups and downs of Viagra: revisiting ototoxicity in the mouse model

A small molecule mitigates hearing loss in a mouse model of Usher syndrome III

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15 , a novel protocadherin gene

Actin Crosslinking Family Protein 7 Deficiency Does Not Impair Hearing in Young Mice

Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation

Clarin-1, Encoded by the Usher Syndrome III Causative Gene, Forms a Membranous Microdomain: POSSIBLE ROLE OF CLARIN-1 IN ORGANIZING THE ACTIN CYTOSKELETON

Mutations in the novel protocadherin PCDH15 cause usher syndrome type 1F

Noddy, a mouse harboring a missense mutation in protocadherin-15, reveals the impact of disrupting a critical interaction site between tip-link cadherins in inner ear hair cells

A Mouse Model Validates the Utility of Electrocochleography in Verifying Endolymphatic Hydrops

Spiral Ganglion Degeneration Patterns in Endolymphatic Hydrops

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