(Q34838323)

4 August 2017

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title

Mouse models for human deafness: current tools for new fashions (English)

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4 August 2017

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Nadav Ahituv

1

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Karen Avraham

object named as

Karen B Avraham

series ordinal

2

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publication date

1 September 2002

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Trends in Molecular Medicine

4 August 2017

published in

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4 August 2017

volume

8

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4 August 2017

issue

9

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4 August 2017

page(s)

447-451

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Molecular basis of mechanosensory transduction

4 August 2017

cites work

1 reference

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7 January 2021

Histopathology and molecular genetics of hearing loss in the human

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7 January 2021

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

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7 January 2021

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

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7 January 2021

Mechano-electrical transducer currents in hair cells of the cultured neonatal mouse cochlea

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

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7 January 2021

Unconventional myosins in cell movement, membrane traffic, and signal transduction

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7 January 2021

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

1 reference

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7 January 2021

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

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7 January 2021

Defective myosin VIIA gene responsible for Usher syndrome type 1B

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7 January 2021

Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations

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7 January 2021

A chemical-genetic strategy implicates myosin-1c in adaptation by hair cells.

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902388-2

7 January 2021

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

1 reference

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7 January 2021

Role of myosin VI in the differentiation of cochlear hair cells

1 reference

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7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

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7 January 2021

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss

1 reference

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7 January 2021

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene

1 reference

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7 January 2021

Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice

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7 January 2021

Molecular genetics of hearing loss

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7 January 2021

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

1 reference

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7 January 2021

The deafness locus (dn) maps to mouse chromosome 19.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

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7 January 2021

Dominant modifier DFNM1 suppresses recessive deafness DFNB26

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7 January 2021

Microtubule-associated protein 1A is a modifier of tubby hearing (moth1).

1 reference

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7 January 2021

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

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7 January 2021

A major gene affecting age-related hearing loss in C57BL/6J mice

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7 January 2021

mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw)

1 reference

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7 January 2021

A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

1 reference

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7 January 2021

Altered cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness.

1 reference

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7 January 2021

The sex-linked fidget mutation abolishes Brn4/Pou3f4 gene expression in the embryonic inner ear

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902388-2

7 January 2021

Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902388-2

7 January 2021

Targeted deletion of the mouse POU domain gene Brn-3a causes selective loss of neurons in the brainstem and trigeminal ganglion, uncoordinated limb movement, and impaired suckling

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902388-2

7 January 2021

Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.

1 reference

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7 January 2021

A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback.

1 reference

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7 January 2021

10.1016/S1471-4914(02)02388-2

Identifiers

DOI

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4 August 2017

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