Cilia-Associated Genes Play Differing Roles in Aminoglycoside-Induced Hair Cell Death in Zebrafish. - Wikidata - awgldk - TriplyDB

Cilia-Associated Genes Play Differing Roles in Aminoglycoside-Induced Hair Cell Death in Zebrafish.

Cilia-Associated Genes Play Differing Roles in Aminoglycoside-Induced Hair Cell Death in Zebrafish.

http://www.wikidata.org/entity/Q37079612

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Fluorescent aminoglycosides reveal intracellular trafficking routes in mechanosensory hair cells.

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Cilia-Associated Genes Play Differing Roles in Aminoglycoside-Induced Hair Cell Death in Zebrafish.

http://www.wikidata.org/entity/Q37079612

description

article científic

@ca

article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 20 May 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Cilia-Associated Genes Play Di ...... Hair Cell Death in Zebrafish.

@en

Cilia-Associated Genes Play Di ...... Hair Cell Death in Zebrafish.

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type

label

Cilia-Associated Genes Play Di ...... Hair Cell Death in Zebrafish.

@en

Cilia-Associated Genes Play Di ...... Hair Cell Death in Zebrafish.

@nl

prefLabel

Cilia-Associated Genes Play Di ...... Hair Cell Death in Zebrafish.

@en

Cilia-Associated Genes Play Di ...... Hair Cell Death in Zebrafish.

@nl

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Cilia-Associated Genes Play Di ...... Hair Cell Death in Zebrafish.

@en

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Arish N Shah

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Brock Roberts

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Cecilia B Moens

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David W Raible

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Edwin W Rubel

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Kelly N Owens

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Liana Hernandez

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Nihal Thapa

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Robert Esterberg

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Tor Linbo

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P2860

Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle

The Ciliopathies: An Emerging Class of Human Genetic Disorders

TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary cilia

CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium

A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation

The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4

The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation

Review series: The cell biology of hearing

Multi-isotope imaging mass spectrometry reveals slow protein turnover in hair-cell stereocilia

Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome

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2225-2235

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scholarly article

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10.1534/G3.116.030080

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7

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6

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Tamara M. Stawicki

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2016-05-20T00:00:00Z

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27207957

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