Sound amplification in the inner ear: it takes TM to tango.

Name: Sound amplification in the inner ear: it takes TM to tango.
Creator: Corey, David P.
Keywords: Extracellular Matrix Proteins, Membrane Glycoproteins, Tectorial Membrane, GPI-Linked Proteins, Basilar Membrane, Mice, Mutant Strains, Hair Cells, Auditory, Outer, Mice, Hearing, Ear, Inner

descriptionPublicationkeyboard_double_arrow_right Article 22 Dec 2000 English Publisher:Published by Elsevier Inc.Journal:Neuron, volume 28 (issn: 0896-6273,

Authors: Corey, David P.;

pmid: 11086976

Sound amplification in the inner ear: it takes TM to tango.

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Harvard University
United States
Massachusetts General Hospital
United States
Howard Hughes Medical Institute
United States

Keywords

Extracellular Matrix Proteins, Membrane Glycoproteins, Tectorial Membrane, GPI-Linked Proteins, Basilar Membrane, Mice, Mutant Strains, Hair Cells, Auditory, Outer, Mice, Hearing, Ear, Inner, Gene Targeting, Animals, Humans, Cilia, Collagen, Chickens, Organ of Corti, Glycoproteins

6 Research products, page 1 of 1

Mapping of the α-Tectorin Gene (TECTA) to Mouse Chromosome 9 and Human Chromosome 11: A Candidate for Human Autosomal Dominant Nonsyndromic Deafness
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Association of Clinical Features With Mutation of TECTA in a Family With Autosomal Dominant Hearing Loss
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Two novel missense mutations in the TECTA gene in Korean families with autosomal dominant nonsyndromic hearing loss.
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Chick α-tectorin: molecular cloning and expression during embryogenesis
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An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21
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A Targeted Deletion in α-Tectorin Reveals that the Tectorial Membrane Is Required for the Gain and Timing of Cochlear Feedback
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Sound amplification in the inner ear: it takes TM to tango.

Sound amplification in the inner ear: it takes TM to tango.

6 Research products, page 1 of 1

Mapping of the α-Tectorin Gene (TECTA) to Mouse Chromosome 9 and Human Chromosome 11: A Candidate for Human Autosomal Dominant Nonsyndromic Deafness

Association of Clinical Features With Mutation of TECTA in a Family With Autosomal Dominant Hearing Loss

Two novel missense mutations in the TECTA gene in Korean families with autosomal dominant nonsyndromic hearing loss.

Chick α-tectorin: molecular cloning and expression during embryogenesis

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21

A Targeted Deletion in α-Tectorin Reveals that the Tectorial Membrane Is Required for the Gain and Timing of Cochlear Feedback