(Q33650550)

28 July 2017

1 reference

title

Development of the vertebrate ear: insights from knockouts and mutants (English)

1 reference

28 July 2017

D M Fekete

1

1 reference

28 July 2017

1 June 1999

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28 July 2017

Trends in Neurosciences

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28 July 2017

22

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28 July 2017

263-269

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28 July 2017

6

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The development of the vertebrate inner ear.

28 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Transcription factors in the ear: molecular switches for development and differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Transcription factors and the control of inner ear development

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Cell fate specification in the inner ear.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Intercellular signals and cell-fate choices in the developing inner ear: origins of global and of fine-grained pattern

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Disruption of the Hox-1.6 homeobox gene results in defects in a region corresponding to its rostral domain of expression

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

The paired-like homeo box gene MHox is required for early events of skeletogenesis in multiple lineages

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Mouse Otx2 functions in the formation and patterning of rostral head.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Developmental defects of the ear, cranial nerves and hindbrain resulting from targeted disruption of the mouse homeobox gene Hox-1.6

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Have gene knockouts caused evolutionary reversals in the mammalian first arch?

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

The role of FGF-3 in early inner ear development: an analysis in normal and kreisler mutant mice

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

1 reference

7 January 2021

Inherited hearing defects in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

neurogenin1 is essential for the determination of neuronal precursors for proximal cranial sensory ganglia

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Epilepsy and brain abnormalities in mice lacking the Otx1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Thyroid hormone receptor beta is essential for development of auditory function

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

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%2FS0166-2236%2898%2901366-6

7 January 2021

Essential role of POU-domain factor Brn-3c in auditory and vestibular hair cell development

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

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

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

1 reference

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Genetic analysis of vertebrate sensory hair cell mechanosensation: the zebrafish circler mutants.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Complementary roles of BDNF and NT-3 in vestibular and auditory development

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Severe sensory and sympathetic deficits in mice lacking neurotrophin-3.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Targeted disruption of the BDNF gene perturbs brain and sensory neuron development but not motor neuron development.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Inner ear defects induced by null mutation of the isk gene

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

Paradigms and paradoxes: mouse (and human) models of genetic deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901366-6

7 January 2021

10.1016/S0166-2236(98)01366-6

Identifiers

DOI

1 reference

release_3s2q324js5bthpljaz3ibpxoha

28 July 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/3s2q324js5bthpljaz3ibpxoha

24 November 2022

mapped directly with Wikidata item

PubMed ID

10354604

1 reference

PubMed ID

10354604