Role for a novel Usher protein complex in hair cell synaptic maturation. - Wikidata - wikimedia - TriplyDB

Role for a novel Usher protein complex in hair cell synaptic maturation.

Role for a novel Usher protein complex in hair cell synaptic maturation.

http://www.wikidata.org/entity/Q35763614

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Emerging Roles of BAI Adhesion-GPCRs in Synapse Development and Plasticity Cadherin 23-C Regulates Microtubule Networks by Modifying CAMSAP3's Function.Sticky signaling--adhesion class G protein-coupled receptors take the stage Whirlin and PDZ domain-containing 7 (PDZD7) proteins are both required to form the quaternary protein complex associated with Usher syndrome type 2 Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel Sequencing.The mechanosensory structure of the hair cell requires clarin-1, a protein encoded by Usher syndrome III causative gene The cone-dominant retina and the inner ear of zebrafish express the ortholog of CLRN1, the causative gene of human Usher syndrome type 3A.Complexes of Usher proteins preassemble at the endoplasmic reticulum and are required for trafficking and ER homeostasis.Constitutive Gαi coupling activity of very large G protein-coupled receptor 1 (VLGR1) and its regulation by PDZD7 protein.Clarin-1 acts as a modulator of mechanotransduction activity and presynaptic ribbon assembly.AAV-Mediated Clarin-1 Expression in the Mouse Retina: Implications for USH3A Gene Therapy.Regulated vesicular trafficking of specific PCDH15 and VLGR1 variants in auditory hair cells.Targeted next-generation sequencing identifies a homozygous nonsense mutation in ABHD12, the gene underlying PHARC, in a family clinically diagnosed with Usher syndrome type 3 Plasma Membrane Targeting of Protocadherin 15 Is Regulated by the Golgi-Associated Chaperone Protein PIST.Usher protein functions in hair cells and photoreceptors.The very large G protein coupled receptor (Vlgr1) in hair cells.The how and why of identifying the hair cell mechano-electrical transduction channel Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness.Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III.Integrin α8 and Pcdh15 act as a complex to regulate cilia biogenesis in sensory cells.

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Role for a novel Usher protein complex in hair cell synaptic maturation.

http://www.wikidata.org/entity/Q35763614

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

@zh-tw

2012年论文

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2012年论文

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2012年论文

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name

Role for a novel Usher protein complex in hair cell synaptic maturation.

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Role for a novel Usher protein complex in hair cell synaptic maturation.

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type

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Role for a novel Usher protein complex in hair cell synaptic maturation.

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Role for a novel Usher protein complex in hair cell synaptic maturation.

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Role for a novel Usher protein complex in hair cell synaptic maturation.

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Role for a novel Usher protein complex in hair cell synaptic maturation.

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JOURNAL.PONE.0030573

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Role for a novel Usher protein complex in hair cell synaptic maturation.

@en

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Daniel T Meehan

http://www.w3.org/2001/XMLSchema#string

Dominic Cosgrove

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Duane Delimont

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Joseph Rutledge

http://www.w3.org/2001/XMLSchema#string

Marisa Zallocchi

http://www.w3.org/2001/XMLSchema#string

Michael Anne Gratton

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P2860

Sequence similarities between a novel putative G protein-coupled receptor and Na+/Ca2+ exchangers define a cation binding domain

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

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

Very large G protein-coupled receptor-1, the largest known cell surface protein, is highly expressed in the developing central nervous system

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

Identification and characterization of GIV, a novel Galpha i/s-interacting protein found on COPI, endoplasmic reticulum-Golgi transport vesicles

PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23

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

Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II

The unconventional myosin-VIIa associates with lysosomes

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e30573

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scholarly article

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10.1371/JOURNAL.PONE.0030573

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2

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7

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John G. Flannery

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2012-02-17T00:00:00Z

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221859730

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3281840

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