Deletion of PDZD7 disrupts the Usher syndrome type 2 protein complex in cochlear hair cells and causes hearing loss in mice (Q28507622)

25 June 2017

title

Deletion of PDZD7 disrupts the Usher syndrome type 2 protein complex in cochlear hair cells and causes hearing loss in mice (English)

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25 June 2017

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PDZ domain containing 7

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Usherin

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Adhesion G protein-coupled receptor V1

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hearing loss

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based on heuristic

inferred from title

Usher syndrome type 2

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Charles Askew

4

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author name string

Junhuang Zou

1

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25 June 2017

Tihua Zheng

2

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25 June 2017

Chongyu Ren

3

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25 June 2017

Xiao-Ping Liu

5

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25 June 2017

Bifeng Pan

6

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25 June 2017

Yong Wang

8

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25 June 2017

Jun Yang

9

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25 June 2017

Jeffrey R Holt

7

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25 June 2017

publication date

11 December 2013

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25 June 2017

published in

Human Molecular Genetics

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25 June 2017

volume

23

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25 June 2017

issue

9

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25 June 2017

page(s)

2374-2390

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Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes

25 June 2017

cites work

1 reference

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Whirlin replacement restores the formation of the USH2 protein complex in whirlin knockout photoreceptors

19 March 2017

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PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome

19 March 2017

1 reference

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Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment

19 March 2017

1 reference

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Usher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapy

19 March 2017

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Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning

19 March 2017

1 reference

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Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells

19 March 2017

1 reference

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The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles.

19 March 2017

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The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1

19 March 2017

1 reference

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Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells

19 March 2017

1 reference

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Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia

19 March 2017

1 reference

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Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly

19 March 2017

1 reference

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

19 March 2017

1 reference

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Rootletin, a novel coiled-coil protein, is a structural component of the ciliary rootlet

19 March 2017

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A guided tour into subcellular colocalization analysis in light microscopy

19 March 2017

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7 April 2017

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Localization of PDZD7 to the stereocilia ankle-link associates this scaffolding protein with the Usher syndrome protein network

7 April 2017

1 reference

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The Rd8 mutation of the Crb1 gene is present in vendor lines of C57BL/6N mice and embryonic stem cells, and confounds ocular induced mutant phenotypes

29 September 2017

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Whirlin interacts with espin and modulates its actin-regulatory function: an insight into the mechanism of Usher syndrome type II.

29 September 2017

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Ablation of whirlin long isoform disrupts the USH2 protein complex and causes vision and hearing loss

29 September 2017

1 reference

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Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells

29 September 2017

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Sensory transduction and adaptation in inner and outer hair cells of the mouse auditory system

29 September 2017

1 reference

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Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease

29 September 2017

1 reference

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29 September 2017

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Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

29 September 2017

1 reference

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Usher syndrome: definition and estimate of prevalence from two high-risk populations

29 September 2017

1 reference

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A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairment

29 September 2017

1 reference

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

27 November 2018

1 reference

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A reliable lacZ expression reporter cassette for multipurpose, knockout-first alleles

27 November 2018

1 reference

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27 November 2018

Identifiers

DOI

10.1093/HMG/DDT629

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OpenCitations bibliographic resource ID

25 June 2017

2163845

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2163845

1 reference