(Q30479852)

English

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

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scholarly article

1 reference

Europe PubMed Central

19 October 2017

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

1 reference

Europe PubMed Central

19 October 2017

1 reference

based on heuristic

inferred from title

Christine Petit

8

0 references

1

object named as

Amel Bahloul

1 reference

Europe PubMed Central

19 October 2017

Jean-Pierre Hardelin

3

object named as

Jean-Pierre Hardelin

1 reference

Europe PubMed Central

19 October 2017

author name string

Vincent Michel

2

1 reference

Europe PubMed Central

19 October 2017

Sylvie Nouaille

4

1 reference

Europe PubMed Central

19 October 2017

Sylviane Hoos

5

1 reference

Europe PubMed Central

19 October 2017

Anne Houdusse

6

1 reference

Europe PubMed Central

19 October 2017

Patrick England

7

1 reference

Europe PubMed Central

19 October 2017

publication date

16 July 2010

1 reference

Europe PubMed Central

19 October 2017

Human Molecular Genetics

1 reference

Europe PubMed Central

19 October 2017

19

1 reference

Europe PubMed Central

19 October 2017

18

1 reference

Europe PubMed Central

19 October 2017

3557-3565

1 reference

Europe PubMed Central

19 October 2017

The structure of the harmonin/sans complex reveals an unexpected interaction mode of the two Usher syndrome proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Structural diversity of PDZ-lipid interactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Mechanotransduction by hair cells: models, molecules, and mechanisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Linking genes underlying deafness to hair-bundle development and function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Harmonin mutations cause mechanotransduction defects in cochlear hair cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Assembling stable hair cell tip link complex via multidentate interactions between harmonin and cadherin 23

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Mouse models for human hereditary deafness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

PDZ domains: folding and binding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Vertebrate myosin VIIb is a high duty ratio motor adapted for generating and maintaining tension

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Interactions in the network of Usher syndrome type 1 proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Characterization of the motor activity of mammalian myosin VIIA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Visualization of phosphoinositides that bind pleckstrin homology domains: calcium- and agonist-induced dynamic changes and relationship to myo-[3H]inositol-labeled phosphoinositide pools

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

Oxidants and conductance of cultured epithelial cell monolayers: inositol phospholipid hydrolysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2928128

20 June 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ271

21 January 2018

Development and properties of stereociliary link types in hair cells of the mouse cochlea

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ271

21 January 2018

Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ271

21 January 2018

Hair cells require phosphatidylinositol 4,5-bisphosphate for mechanical transduction and adaptation.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ271

21 January 2018

The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15

1 reference

https://pubmed.ncbi.nlm.nih.gov/20639393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/HMG/DDQ271

1 reference

Europe PubMed Central

19 October 2017

1 reference

Europe PubMed Central

19 October 2017

1 reference

Europe PubMed Central

19 October 2017

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