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Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane

Proceedings of the National Academy of Sciences - PNAS, 2019-12, Vol.116 (51), p.25948-25957

2019

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Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane

Journal of comparative neurology (1911), 2011-02, Vol.519 (2), p.194-210

2011

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Excessive self-grooming, gene dysregulation and imbalance between the striosome and matrix compartments in the striatum of Shank3 mutant mice

Frontiers in molecular neuroscience, 2023, Vol.16, p.1139118

2023

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Detecting Central Auditory Processing Disorders in Awake Mice

Brain sciences, 2023-10, Vol.13 (11), p.1539

2023

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Stereocilin-deficient mice reveal the origin of cochlear waveform distortions

Nature, 2008-11, Vol.456 (7219), p.255-258

2008

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A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

Nature genetics, 2000-09, Vol.26 (1), p.51-55

2000

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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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Cochlear outer hair cell horizontal top connectors mediate mature stereocilia bundle mechanics

Science advances, 2019-02, Vol.5 (2), p.eaat9934-eaat9934

2019

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Inactivation of NADPH oxidase organizer 1 Results in Severe Imbalance

Current biology, 2006-01, Vol.16 (2), p.208-213

2006

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Otoancorin, An Inner Ear Protein Restricted to the Interface between the Apical Surface of Sensory Epithelia and Their Overlying Acellular Gels, Is Defective in Autosomal Recessive Deafness DFNB22

Proceedings of the National Academy of Sciences - PNAS, 2002-04, Vol.99 (9), p.6240-6245

2002

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Characterization of Otoconin-95, the Major Protein of Murine Otoconia, Provides Insights into the Formation of these Inner Ear Biominerals

Proceedings of the National Academy of Sciences - PNAS, 1999-01, Vol.96 (2), p.529-534

1999

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Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus

Nature genetics, 2001-11, Vol.29 (3), p.345-349

2001

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Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane

Proceedings of the National Academy of Sciences - PNAS, 2019-12, Vol.116 (51), p.25948-25957

2019

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COOH-terminal Substitutions in the Serpin C1 Inhibitor That Cause Loop Overinsertion and Subsequent Multimerization (∗)

The Journal of biological chemistry, 1995-02, Vol.270 (6), p.2579-2587

1995

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Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane

Journal of comparative neurology (1911), 2011-02, Vol.519 (2), p.194-210

2011

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Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness

Human genetics, 2002-07, Vol.111 (1), p.26-30

2002

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Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angioedema

American journal of human genetics, 1996, Vol.59 (2), p.308-319

1996

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Fdp, a new fibrocyte-derived protein related to MIA/CD-RAP, has an in vitro effect on the early differentiation of the inner ear mesenchyme

The Journal of biological chemistry, 2000-12, Vol.275 (51), p.40036-40041

2000

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Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysis

Human mutation, 2001, Vol.17 (1), p.34-41

2001

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Initial characterization of kinocilin, a protein of the hair cell kinocilium

Hearing research, 2005-05, Vol.203 (1), p.144-153

2005

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Otoacorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22

Proceedings of the National Academy of Sciences - PNAS, 2002-04, Vol.99 (9), p.6240

2002

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Twister mutant mice are defective for otogelin, a component specific to inner ear acellular membranes

Mammalian genome, 2000-11, Vol.11 (11), p.961-966

2000

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Crucial residues in the carboxy-terminal end of C1 inhibitor revealed by pathogenic mutants impaired in secretion or function

The Journal of clinical investigation, 1995-01, Vol.95 (1), p.350-359

1995

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Detection of Mutations by Fluorescence‐Assisted Mismatch Analysis (FAMA)

Current Protocols in Human Genetics, 2001-05, Vol.12 (1), p.7.8.1-7.8.12

2001

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Novel variants of human IFN-alpha detected in tumor cell lines and biopsy specimens

Journal of interferon & cytokine research, 1997-10, Vol.17 (10), p.637-645

1997

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Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane

Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane

Excessive self-grooming, gene dysregulation and imbalance between the striosome and matrix compartments in the striatum of Shank3 mutant mice

Detecting Central Auditory Processing Disorders in Awake Mice

Stereocilin-deficient mice reveal the origin of cochlear waveform distortions

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

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

Cochlear outer hair cell horizontal top connectors mediate mature stereocilia bundle mechanics

Inactivation of NADPH oxidase organizer 1 Results in Severe Imbalance

Otoancorin, An Inner Ear Protein Restricted to the Interface between the Apical Surface of Sensory Epithelia and Their Overlying Acellular Gels, Is Defective in Autosomal Recessive Deafness DFNB22

Characterization of Otoconin-95, the Major Protein of Murine Otoconia, Provides Insights into the Formation of these Inner Ear Biominerals

Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus

Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane

COOH-terminal Substitutions in the Serpin C1 Inhibitor That Cause Loop Overinsertion and Subsequent Multimerization (∗)

Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane

Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness

Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angioedema

Fdp, a new fibrocyte-derived protein related to MIA/CD-RAP, has an in vitro effect on the early differentiation of the inner ear mesenchyme

Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysis

Initial characterization of kinocilin, a protein of the hair cell kinocilium

Otoacorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22

Twister mutant mice are defective for otogelin, a component specific to inner ear acellular membranes

Crucial residues in the carboxy-terminal end of C1 inhibitor revealed by pathogenic mutants impaired in secretion or function

Detection of Mutations by Fluorescence‐Assisted Mismatch Analysis (FAMA)

Novel variants of human IFN-alpha detected in tumor cell lines and biopsy specimens

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