(Q28585988)

Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer

21 January 2018

1 reference

The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells

21 January 2018

1 reference

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

21 January 2018

1 reference

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

21 January 2018

1 reference

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

21 January 2018

1 reference

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

21 January 2018

1 reference

A comprehensive genetic map of the mouse genome.

21 January 2018

1 reference

Linkage analysis of the whirler deafness gene on mouse chromosome 4.

21 January 2018

1 reference

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

21 January 2018

1 reference

21 January 2018

How the ear's works work

1 reference

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

21 January 2018

1 reference

Cochlear anatomy related to cochlear micromechanics. A review

21 January 2018

1 reference

Stereocilia defects in the sensory hair cells of the inner ear in mice deficient in integrin alpha8beta1

21 January 2018

1 reference

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

21 January 2018

1 reference

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

21 January 2018

1 reference

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss

21 January 2018

1 reference

A deletion on chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidate.

21 January 2018

1 reference

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

21 January 2018

1 reference

Genetic mapping of the whirler mutation.

21 January 2018

1 reference

Role of myosin VI in the differentiation of cochlear hair cells

21 January 2018

1 reference

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

21 January 2018

1 reference

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

21 January 2018

1 reference

Defective myosin VIIA gene responsible for Usher syndrome type 1B

21 January 2018

1 reference

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

21 January 2018

1 reference

Dimensions of the cochlear stereocilia in man and the guinea pig.

21 January 2018

1 reference

The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins.

21 January 2018

1 reference

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

21 January 2018

1 reference

7 January 2021

Morphology of inner hair cell stereocilia in C57BL/6J mice as studied by scanning electron microscopy

1 reference

7 January 2021

WHIRLER MICE: A RECESSIVE BEHAVIOR MUTATION IN LINKAGE GROUP VIII

1 reference

7 January 2021

Metabolism rate, biochemical and endocrine alterations in male whirler mice

1 reference

7 January 2021

Identifiers

DOI

10.1002/CNE.10301

1 reference

Consolidated OpenCitations Corpus – April 2017

2163835

2163835

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference