A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment (Q28508053)

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Karen Avraham

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Karen B. Avraham

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Karen Steel

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Karen P. Steel

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Charlotte R. Rhodes

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Ronna Hertzano

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Helmut Fuchs

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Rachel E. Bell

https://scigraph.springernature.com/pub.10.1007/s00335-004-2344-x

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cites work

Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells

1 reference

12 December 2020

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.

1 reference

12 December 2020

Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice

1 reference

12 December 2020

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene

1 reference

12 December 2020

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

1 reference

12 December 2020

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

1 reference

12 December 2020

Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

12 December 2020

Modifier controls severity of a novel dominant low-frequency MyosinVIIA (MYO7A) auditory mutation

1 reference

12 December 2020

A novel stereocilia defect in sensory hair cells of the deaf mouse mutant Tasmanian devil

1 reference

12 December 2020

Searching for evidence of DFNB2.

1 reference

12 December 2020

ConSurf: identification of functional regions in proteins by surface-mapping of phylogenetic information

1 reference

12 December 2020

Phenotype of DFNA11: a nonsyndromic hearing loss caused by a myosin VIIA mutation

1 reference

12 December 2020

Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss

1 reference

12 December 2020

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

1 reference

12 December 2020

Identification of a new mutation of the myosin VII head region in Usher syndrome type 1.

1 reference

12 December 2020

Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B

1 reference

12 December 2020

Role of myosin VI in the differentiation of cochlear hair cells

1 reference

12 December 2020

Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1.

1 reference

12 December 2020

Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression

1 reference

12 December 2020

Descriptive and experimental analysis of the epithelial remodellings that control semicircular canal formation in the developing mouse inner ear

1 reference

12 December 2020

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

1 reference

12 December 2020

Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB

1 reference

12 December 2020

A type VII myosin encoded by the mouse deafness gene shaker-1

1 reference

12 December 2020

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

1 reference

12 December 2020

The developing organ of Corti contains retinoic acid and forms supernumerary hair cells in response to exogenous retinoic acid in culture

1 reference

12 December 2020

Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B

1 reference

12 December 2020

Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.

1 reference

12 December 2020

Actin filaments, stereocilia, and hair cells: how cells count and measure

1 reference

12 December 2020

Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia

1 reference

12 December 2020

Postnatal development of the hamster cochlea. II. Growth and differentiation of stereocilia bundles

1 reference

12 December 2020

Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients

1 reference

12 December 2020

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

1 reference

12 December 2020

Crystal structure of the motor domain of a class-I myosin.

1 reference

12 December 2020

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

1 reference

12 December 2020

Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse

1 reference

12 December 2020