Genetic insights into the morphogenesis of inner ear hair cells. (Q35813847)

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29 December 2019

review article

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title

Genetic insights into the morphogenesis of inner ear hair cells (English)

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29 December 2019

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1

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29 December 2019

2

Inna A Belyantseva

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29 December 2019

3

Thomas B Friedman

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29 December 2019

author name string

Andrew J Griffith

series ordinal

4

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29 December 2019

language of work or name

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1 July 2004

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29 December 2019

published in

Nature Reviews Genetics

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29 December 2019

volume

5

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29 December 2019

issue

7

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29 December 2019

page(s)

489-498

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Evolution of hearing in vertebrates: the inner ears and processing.

29 December 2019

cites work

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Cochlear mechanisms from a phylogenetic viewpoint

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Prestin, a new type of motor protein

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Human Nonsyndromic Sensorineural Deafness

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Revisiting cell fate specification in the inner ear.

21 January 2018

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Cell adhesion molecules during inner ear and hair cell development, including notch and its ligands

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The chicken RaxL gene plays a role in the initiation of photoreceptor differentiation

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Mechano-electrical transduction currents in isolated vestibular hair cells of the chick

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The responses of cochlear hair cells to tonic displacements of the sensory hair bundle.

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F-actin bundles are derivatives of microvilli: What does this tell us about how bundles might form?

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Parallel actin bundles and their multiple actin-bundling proteins.

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The organization of actin filaments in the stereocilia of cochlear hair cells

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Espin cross-links cause the elongation of microvillus-type parallel actin bundles in vivo.

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Correlation of expression of the actin filament-bundling protein espin with stereociliary bundle formation in the developing inner ear.

21 January 2018

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Why are two different cross-linkers necessary for actin bundle formation in vivo and what does each cross-link contribute?

21 January 2018

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Transient expression of the t-isoform of plastins/fimbrin in the stereocilia of developing auditory hair cells

21 January 2018

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The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins.

21 January 2018

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Dynamic assembly of surface structures in living cells

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Regulated actin cytoskeleton assembly at filopodium tips controls their extension and retraction

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An atomic model of actin filaments cross-linked by fimbrin and its implications for bundle assembly and function

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Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).

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A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25.

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A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)

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Actin filaments, stereocilia, and hair cells of the bird cochlea. II. Packing of actin filaments in the stereocilia and in the cuticular plate and what happens to the organization when the stereocilia are bent

21 January 2018

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Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous

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Actin polymerization-driven molecular movement of mDia1 in living cells

21 January 2018

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2E4 (kaptin): a novel actin-associated protein from human blood platelets found in lamellipodia and the tips of the stereocilia of the inner ear

21 January 2018

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Radixin is a constituent of stereocilia in hair cells

21 January 2018

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Cortical actin organization: lessons from ERM (ezrin/radixin/moesin) proteins

21 January 2018

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Tails of unconventional myosins

21 January 2018

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Unconventional myosins in inner-ear sensory epithelia

21 January 2018

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Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle

21 January 2018

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Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

21 January 2018

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Myosin VI is an actin-based motor that moves backwards

21 January 2018

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MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss

21 January 2018

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Mutations of MYO6 are associated with recessive deafness, DFNB37

21 January 2018

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Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6).

21 January 2018

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The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

21 January 2018

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Role of myosin VI in the differentiation of cochlear hair cells

21 January 2018

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The mechanism of myosin VI translocation and its load-induced anchoring

21 January 2018

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Interactions between actin filaments and between actin filaments and membranes in quick-frozen and deeply etched hair cells of the chick ear

21 January 2018

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The structure of the cuticular plate, an in vivo actin gel.

21 January 2018

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Actin-binding and microtubule-associated proteins in the organ of Corti

21 January 2018

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Fimbrin expression in the developing rat cochlea

21 January 2018

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Three different actin filament assemblies occur in every hair cell: each contains a specific actin crosslinking protein

21 January 2018

1 reference

Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex

21 January 2018

1 reference

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

21 January 2018

1 reference

Stereociliary bundles reorient during hair cell development and regeneration in the chick cochlea

21 January 2018

1 reference

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

21 January 2018

1 reference

A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback.

21 January 2018

1 reference

The atypical cadherin Flamingo links Frizzled and Notch signaling in planar polarity establishment in the Drosophila eye.

21 January 2018

1 reference

Planar cell polarization: do the same mechanisms regulate Drosophila tissue polarity and vertebrate gastrulation?

21 January 2018

1 reference

Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse

21 January 2018

1 reference

Identification of Vangl2 and Scrb1 as planar polarity genes in mammals

21 January 2018

1 reference

Wnt signaling mediates reorientation of outer hair cell stereociliary bundles in the mammalian cochlea.

21 January 2018

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Functional organization of the cytoskeleton.

21 January 2018

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Development of the auditory receptors of the rat: a SEM study

21 January 2018

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A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.

21 January 2018

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Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

21 January 2018

1 reference

An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal

21 January 2018

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Stereocilia: the long and the short of it

21 January 2018

1 reference

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

21 January 2018

1 reference

Regeneration of broken tip links and restoration of mechanical transduction in hair cells

21 January 2018

1 reference

The development of links between stereocilia in hair cells of the chick basilar papilla

21 January 2018

1 reference

Cross-links between stereocilia in the guinea pig organ of Corti, and their possible relation to sensory transduction

21 January 2018

1 reference

Cross-links between stereocilia in the guinea pig cochlea.

21 January 2018

1 reference

Sticking together and sorting things out: adhesion as a force in development

21 January 2018

1 reference

Intercellular adhesion, signalling and the cytoskeleton

21 January 2018

1 reference

Defective myosin VIIA gene responsible for Usher syndrome type 1B

21 January 2018

1 reference

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

21 January 2018

1 reference

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

21 January 2018

1 reference

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

21 January 2018

1 reference

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

21 January 2018

1 reference

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

21 January 2018

1 reference

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

21 January 2018

1 reference

Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

21 January 2018

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Severe vestibular and auditory impairment in three alleles of Ames waltzer (av) mice

21 January 2018

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Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer

21 January 2018

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A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15.

21 January 2018

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Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle

21 January 2018

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The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions

21 January 2018

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Convergence of Wnt, beta-catenin, and cadherin pathways

21 January 2018

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PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23

21 January 2018

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Cadherin 23 is a component of the tip link in hair-cell stereocilia

21 January 2018

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Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells

21 January 2018

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Developmental acquisition of sensory transduction in hair cells of the mouse inner ear

21 January 2018

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Fast adaptation of mechanoelectrical transducer channels in mammalian cochlear hair cells.

21 January 2018

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A novel stereocilia defect in sensory hair cells of the deaf mouse mutant Tasmanian devil

21 January 2018

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21 January 2018

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A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

21 January 2018

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Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier

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Prestin is the motor protein of cochlear outer hair cells

21 January 2018

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Calcium imaging of single stereocilia in hair cells: localization of transduction channels at both ends of tip links

21 January 2018

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

21 January 2018

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A type VII myosin encoded by the mouse deafness gene shaker-1

21 January 2018

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Rapid renewal of auditory hair bundles

21 January 2018

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Evolution of the ear and hearing: issues and questions

21 January 2018

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Postnatal development in the acoustic system of the house mouse in the light of developing masked thresholds

31 March 2020

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Ionic basis of the receptor potential in a vertebrate hair cell

31 March 2020

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Regenerative proliferation in inner ear sensory epithelia from adult guinea pigs and humans

31 March 2020

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Ultrastructural evidence for hair cell regeneration in the mammalian inner ear

31 March 2020

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Mammalian vestibular hair cell regeneration

31 March 2020

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MYO1A (brush border myosin I) dynamics in the brush border of LLC-PK1-CL4 cells

31 March 2020

1 reference

Actin filaments, stereocilia, and hair cells of the bird cochlea. IV. How the actin filaments become organized in developing stereocilia and in the cuticular plate.

31 March 2020

1 reference

Actin in the inner ear: the remarkable structure of the stereocilium

31 March 2020

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31 March 2020

Treadmilling of actin

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Postnatal development of the hamster cochlea. II. Growth and differentiation of stereocilia bundles

31 March 2020

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Vestibular hair cell pathology in the Shaker-2 mouse

31 March 2020

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Directional sensitivity of individual vertebrate hair cells to controlled deflection of their hair bundles

31 March 2020

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Stereociliary anomaly in the guinea pig: effects of hair bundle rotation on cochlear sensitivity

31 March 2020

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Distribution of the 275 kD hair cell antigen and cell surface specialisations on auditory and vestibular hair bundles in the chicken inner ear

31 March 2020

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Stereo-kinociliar bonds in mammalian vestibular organs.

31 March 2020

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Tip-link integrity and mechanical transduction in vertebrate hair cells

31 March 2020

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A Receptor-Like Inositol Lipid Phosphatase Is Required for the Maturation of Developing Cochlear Hair Bundles

31 March 2020

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Developmental assembly of transduction apparatus in chick basilar papilla.

31 March 2020

1 reference

The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse

31 March 2020

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Expression and localization of prestin and the sugar transporter GLUT-5 during development of electromotility in cochlear outer hair cells.

31 March 2020

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Actin filaments, stereocilia, and hair cells: how cells count and measure

31 March 2020

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Hair cells in the inner ear of the pirouette and shaker 2 mutant mice

31 March 2020

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