Cyclic nucleotide-gated channel α-3 (CNGA3) interacts with stereocilia tip-link cadherin 23 + exon 68 or alternatively with myosin VIIa, two proteins required for hair cell mechanotransduction (Q28570825)

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English	Cyclic nucleotide-gated channel α-3 (CNGA3) interacts with stereocilia tip-link cadherin 23 + exon 68 or alternatively with myosin VIIa, two proteins required for hair cell mechanotransduction	scientific journal article

Statements

scholarly article

1 reference

31 January 2017

Cyclic nucleotide-gated channel α-3 (CNGA3) interacts with stereocilia tip-link cadherin 23 + exon 68 or alternatively with myosin VIIa, two proteins required for hair cell mechanotransduction (English)

1 reference

31 January 2017

mechanotransduction

1 reference

based on heuristic

inferred from title

author name string

Dakshnamurthy Selvakumar

1

1 reference

31 January 2017

Marian J. Drescher

2

1 reference

31 January 2017

Dennis G. Drescher

3

1 reference

31 January 2017

language of work or name

0 references

publication date

8 March 2013

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31 January 2017

Journal of Biological Chemistry

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31 January 2017

288

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31 January 2017

10

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31 January 2017

7215–7229

1 reference

31 January 2017

HCN1 and HCN2 proteins are expressed in cochlear hair cells: HCN1 can form a ternary complex with protocadherin 15 CD3 and F-actin-binding filamin A or can interact with HCN2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591630

19 March 2017

Myosin VIIa and sans localization at stereocilia upper tip-link density implicates these Usher syndrome proteins in mechanotransduction

1 reference

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Review series: The cell biology of hearing

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Structural determinants of cadherin-23 function in hearing and deafness

1 reference

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Localization of inner hair cell mechanotransducer channels using high-speed calcium imaging.

1 reference

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19 March 2017

Calcium-dependent binding of HCN1 channel protein to hair cell stereociliary tip link protein protocadherin 15 CD3

1 reference

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Prediction of EF-hand calcium-binding proteins and analysis of bacterial EF-hand proteins

1 reference

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Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells

1 reference

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Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases

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

1 reference

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

1 reference

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Expression of subunits for the cAMP-sensitive 'olfactory' cyclic nucleotide-gated ion channel in the cochlea: implications for signal transduction

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Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations

1 reference

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Molecular basis of mechanosensory transduction

1 reference

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19 March 2017

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

1 reference

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19 March 2017

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

1 reference

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19 March 2017

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

1 reference

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19 March 2017

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

1 reference

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19 March 2017

A cGMP-signaling pathway in a subset of olfactory sensory neurons

1 reference

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Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel

1 reference

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19 March 2017

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

1 reference

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Crystal structures of a complexed and peptide-free membrane protein-binding domain: molecular basis of peptide recognition by PDZ

1 reference

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Endoplasmic reticulum stress-associated cone photoreceptor degeneration in cyclic nucleotide-gated channel deficiency

1 reference

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Mechanical strain in actin networks regulates FilGAP and integrin binding to filamin A.

1 reference

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Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis

1 reference

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

1 reference

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PIST regulates the intracellular trafficking and plasma membrane expression of cadherin 23

1 reference

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Gating of two mechanoelectrical transducer channels associated with a single tip link

1 reference

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Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids

1 reference

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Targeting of the hair cell proteins cadherin 23, harmonin, myosin XVa, espin, and prestin in an epithelial cell model.

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Linking molecular motors to membrane cargo

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EHD4 and CDH23 are interacting partners in cochlear hair cells

1 reference

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Defining features of the hair cell mechanoelectrical transducer channel

1 reference

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Cyclic nucleotide-regulated cation channels

1 reference

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MAGI-1, a candidate stereociliary scaffolding protein, associates with the tip-link component cadherin 23.

1 reference

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Surface plasmon resonance (SPR) analysis of binding interactions of proteins in inner-ear sensory epithelia

1 reference

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Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells

1 reference

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The micromachinery of mechanotransduction in hair cells

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Mechano-electrical transduction: new insights into old ideas.

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29 September 2017

Hair-cell mechanotransduction and cochlear amplification

1 reference

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

1 reference

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Functionally Important Calmodulin-binding Sites in Both NH2- and COOH-terminal Regions of the Cone Photoreceptor Cyclic Nucleotide-gated Channel CNGB3 Subunit

1 reference

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29 September 2017

Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family

1 reference

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Sensory transduction in the ear.

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beta 1 Integrin-dependent cell adhesion to EMILIN-1 is mediated by the gC1q domain.

1 reference

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

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Structure and function of cyclic nucleotide-gated channels

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How hearing happens

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CNGA3 is expressed in inner ear hair cells and binds to an intracellular C-terminus domain of EMILIN1.

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https://api.crossref.org/works/10.1074%2FJBC.M112.443226

21 January 2018

Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23).

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https://api.crossref.org/works/10.1074%2FJBC.M112.443226

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Selective expression of serotonin receptor transcripts in the mammalian cochlea and its subdivisions.

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https://api.crossref.org/works/10.1074%2FJBC.M112.443226

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Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.

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https://api.crossref.org/works/10.1074%2FJBC.M112.443226

21 January 2018

Mutations in CNGA3 impair trafficking or function of cone cyclic nucleotide-gated channels, resulting in achromatopsia.

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https://api.crossref.org/works/10.1074%2FJBC.M112.443226

21 January 2018

Pairwise coupling of hair cell transducer channels links auditory sensitivity and dynamic range.

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21 January 2018

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