Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton (Q24322993)

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English	Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton	scientific 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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8

object named as

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

5

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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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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

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19 March 2017

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

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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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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

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

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

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Tetraspanin functions and associated microdomains

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Update on Usher syndrome

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Usher syndrome: molecular links of pathogenesis, proteins and pathways

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

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