Transient receptor potential melastatin 1: a hair cell transduction channel candidate. - Wikidata - wikimedia - TriplyDB

Transient receptor potential melastatin 1: a hair cell transduction channel candidate.

Transient receptor potential melastatin 1: a hair cell transduction channel candidate.

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Hair-Cell Mechanotransduction Persists in TRP Channel Knockout Mice.The how and why of identifying the hair cell mechano-electrical transduction channel Are TMCs the Mechanotransduction Channels of Vertebrate Hair Cells?

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Transient receptor potential melastatin 1: a hair cell transduction channel candidate.

http://www.wikidata.org/entity/Q35023095

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2013 nî lūn-bûn

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2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2013年の論文

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2013年論文

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2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

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name

Transient receptor potential melastatin 1: a hair cell transduction channel candidate.

@ast

Transient receptor potential melastatin 1: a hair cell transduction channel candidate.

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type

label

Transient receptor potential melastatin 1: a hair cell transduction channel candidate.

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Transient receptor potential melastatin 1: a hair cell transduction channel candidate.

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prefLabel

Transient receptor potential melastatin 1: a hair cell transduction channel candidate.

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Transient receptor potential melastatin 1: a hair cell transduction channel candidate.

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P356

JOURNAL.PONE.0077213

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Transient receptor potential melastatin 1: a hair cell transduction channel candidate.

@en

P2093

Adrian Au

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

John Gerka-Stuyt

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

Kumar N Alagramam

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

Neal S Peachey

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P2860

Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans

Mutations in TRPM1 are a common cause of complete congenital stationary night blindness

Metabotropic glutamate receptor 6 signaling enhances TRPM1 calcium channel function and increases melanin content in human melanocytes

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

Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus)

Localization of inner hair cell mechanotransducer channels using high-speed calcium imaging.

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function

Transient receptor potential cation channels in disease

TRPA1 contributes to cold, mechanical, and chemical nociception but is not essential for hair-cell transduction

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

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e77213

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scholarly article

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10.1371/JOURNAL.PONE.0077213

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10

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