A genetic basis for mechanosensory traits in humans - Wikidata - thesis-toulmin - TriplyDB

A genetic basis for mechanosensory traits in humans

A genetic basis for mechanosensory traits in humans

http://www.wikidata.org/entity/Q34259560

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Water-induced finger wrinkles do not affect touch acuity or dexterity in handling wet objects Body Perception and Action Following Deafness.Touch sense: functional organization and molecular determinants of mechanosensitive receptors Sensory mechanotransduction at membrane-matrix interfaces Tuning Piezo ion channels to detect molecular-scale movements relevant for fine touch Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.Neurosensory mechanotransduction through acid-sensing ion channels A neural link between feeling and hearing.Congenital deafness is associated with specific somatosensory deficits in adolescents.Visuo-tactile interactions in the congenitally deaf: a behavioral and event-related potential study.Concepts of scientific integrative medicine applied to the physiology and pathophysiology of catecholamine systems.A Molecular Signature of Myalgia in Myotonic Dystrophy 2 The Role of PIEZO2 in Human Mechanosensation.Response speed advantage for vision does not extend to touch in early deaf adults.Multisensory Interference in Early Deaf Adults.Mechanics Reveals the Biological Trigger in Wrinkly Fingers.A somatosensory circuit for cooling perception in mice.Measurement of Vibration Detection Threshold and Tactile Spatial Acuity in Human Subjects.Sex-related differences in vision are heterogeneous.The neural circuits of thermal perception

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A genetic basis for mechanosensory traits in humans

http://www.wikidata.org/entity/Q34259560

description

2012 nî lūn-bûn

@nan

2012 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի մայիսին հրատարակված գիտական հոդված

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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

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2012年论文

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name

A genetic basis for mechanosensory traits in humans

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A genetic basis for mechanosensory traits in humans

@en

A genetic basis for mechanosensory traits in humans

@nl

type

label

A genetic basis for mechanosensory traits in humans

@ast

A genetic basis for mechanosensory traits in humans

@en

A genetic basis for mechanosensory traits in humans

@nl

prefLabel

A genetic basis for mechanosensory traits in humans

@ast

A genetic basis for mechanosensory traits in humans

@en

A genetic basis for mechanosensory traits in humans

@nl

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JOURNAL.PBIO.1001318

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A genetic basis for mechanosensory traits in humans

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Bärbel Wohlleben

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Daniela Schiska

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Franz Rüschendorf

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Henning Frenzel

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Jens Jordan

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José M Millán

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Jörg Bohlender

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Katrin Pinsker

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Manfred Gross

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Teresa Jaijo

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P2860

A domain-specific usherin/collagen IV interaction may be required for stable integration into the basement membrane superstructure

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

PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome

A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II

The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions.

Review series: The cell biology of hearing

Making an effort to listen: mechanical amplification in the ear

Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells

Effects of aging on vibration detection thresholds at various body regions

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e1001318

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scholarly article

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10.1371/JOURNAL.PBIO.1001318

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5

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Stefan G Lechner

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2012-05-01T00:00:00Z

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224915781

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22563300

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mechanosensation

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3341339

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