(Q24322993)

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Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton

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scholarly article

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Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton (English)

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actin cytoskeleton

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GOA release 2020-03-11

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GOA release 2020-03-11

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GOA release 2020-03-11

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based on heuristic

inferred from title

Krzysztof Palczewski

7

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Astra Dinculescu

5

object named as

Astra Dinculescu

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Yoshikazu Imanishi

object named as

Yoshikazu Imanishi

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John G. Flannery

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John G Flannery

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1

object named as

Guilian Tian

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William W Hauswirth

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object named as

William W Hauswirth

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Ruishuang Geng

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author name string

Yun Zhou

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Dagmar Hajkova

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Masaru Miyagi

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Astra Dinculescu

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Kumar N Alagramam

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Juha Isosomppi

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Eeva-Marja Sankila

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language of work or name

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publication date

10 July 2009

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Journal of Biological Chemistry

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284

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28

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18980-93

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

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19 March 2017

A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis

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GOTree Machine (GOTM): a web-based platform for interpreting sets of interesting genes using Gene Ontology hierarchies

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19 March 2017

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=2707243

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Usher syndrome type III: revised genomic structure of the USH3 gene and identification of novel mutations

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2707243

19 March 2017

Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3.

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19 March 2017

Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance

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19 March 2017

Involvement of ZO-1 in cadherin-based cell adhesion through its direct binding to alpha catenin and actin filaments

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19 March 2017

Rho, rac, and cdc42 GTPases regulate the assembly of multimolecular focal complexes associated with actin stress fibers, lamellipodia, and filopodia

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19 March 2017

Lipid rafts and signal transduction

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19 March 2017

Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2707243

19 March 2017

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

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19 March 2017

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19 March 2017

Whirlin complexes with p55 at the stereocilia tip during hair cell development.

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19 March 2017

Tetraspanin functions and associated microdomains

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19 March 2017

The HMMTOP transmembrane topology prediction server

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1 reference

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19 March 2017

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19 March 2017

Stereocilia defects in the sensory hair cells of the inner ear in mice deficient in integrin alpha8beta1

1 reference

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7 April 2017

Update on Usher syndrome

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27 September 2017

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Usher syndrome: molecular links of pathogenesis, proteins and pathways

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2707243

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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

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2707243

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27 September 2017

Unbiased quantitative proteomics of lipid rafts reveals high specificity for signaling factors

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27 September 2017

Expression of the palmitoylation-deficient CD151 weakens the association of alpha 3 beta 1 integrin with the tetraspanin-enriched microdomains and affects integrin-dependent signaling

1 reference

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27 September 2017

USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses

1 reference

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Palmitoylation of tetraspanin proteins: modulation of CD151 lateral interactions, subcellular distribution, and integrin-dependent cell morphology

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Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene

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https://api.crossref.org/works/10.1074%2FJBC.M109.003160

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