Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants. - Wikidata - awgldk - TriplyDB

Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants.

Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants.

http://www.wikidata.org/entity/Q36881764

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Dynamic length regulation of sensory stereocilia The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations Regulation of stereocilia length by myosin XVa and whirlin depends on the actin-regulatory protein Eps8 Gene Therapy Restores Hair Cell Stereocilia Morphology in Inner Ears of Deaf Whirler Mice.A study of whirlin isoforms in the mouse vestibular system suggests potential vestibular dysfunction in DFNB31-deficient patients Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants.Actin in hair cells and hearing loss.Distinct expression and function of whirlin isoforms in the inner ear and retina: an insight into pathogenesis of USH2D and DFNB31.Conditional deletion of Atoh1 reveals distinct critical periods for survival and function of hair cells in the organ of Corti.Primary cilia in planar cell polarity regulation of the inner ear CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival.

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Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants.

http://www.wikidata.org/entity/Q36881764

description

2007 nî lūn-bûn

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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2007年论文

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2007年论文

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name

Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants.

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type

label

Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants.

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prefLabel

Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants.

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Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants.

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David F Dolan

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

Donald L Swiderski

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Lisa A Beyer

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Masahiko Izumikawa

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

Mirna Mustapha

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

Yehoash Raphael

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

P2860

Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans

Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene

An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal

Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2

Formins: signaling effectors for assembly and polarization of actin filaments

MyoD or Myf-5 is required for the formation of skeletal muscle

Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereocilium

Differential expression of espin isoforms during epithelial morphogenesis, stereociliogenesis and postnatal maturation in the developing inner ear.

Elongation of hair cell stereocilia is defective in the mouse mutant whirler

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

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