(Q28586478)

5

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Karen Avraham

object named as

Karen B. Avraham

7

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author name string

Vanessa L. Walsh

1

1 reference

31 January 2017

Dorith Raviv

2

1 reference

31 January 2017

Amiel A. Dror

3

1 reference

31 January 2017

Hashem Shahin

4

1 reference

31 January 2017

Moien N. Kanaan

https://scigraph.springernature.com/pub.10.1007/s00335-010-9310-6

6

1 reference

31 January 2017

1 April 2011

1 reference

31 January 2017

1 reference

31 January 2017

22

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31 January 2017

3-4

1 reference

31 January 2017

170–177

1 reference

31 January 2017

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cites work

Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration

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Localization of inner hair cell mechanotransducer channels using high-speed calcium imaging.

21 January 2018

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Quiet as a mouse: dissecting the molecular and genetic basis of hearing

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Targeting genes for self-excision in the germ line

21 January 2018

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Cloning and chromosomal localization of a human class III myosin

21 January 2018

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Hearing loss: mechanisms revealed by genetics and cell biology

21 January 2018

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Unconventional myosins and the genetics of hearing loss

21 January 2018

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Mechanotransduction by hair cells: models, molecules, and mechanisms

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EMPReSS: European mouse phenotyping resource for standardized screens

21 January 2018

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Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans

21 January 2018

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A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells

21 January 2018

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Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene

21 January 2018

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Separate and combined effects of Sod1 and Cdh23 mutations on age-related hearing loss and cochlear pathology in C57BL/6J mice

21 January 2018

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Localization of a Class III Myosin to Filopodia Tips in Transfected HeLa Cells Requires an Actin-binding Site in its Tail Domain

21 January 2018

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Functional structure of the organ of Corti: a review

21 January 2018

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A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice

21 January 2018

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Haplo-insufficiency revealed in deafwaddler mice when tested for hearing loss and ataxia

21 January 2018

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The Drosophila ninaC locus encodes two photoreceptor cell specific proteins with domains homologous to protein kinases and the myosin heavy chain head

21 January 2018

1 reference

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Identification of myosin III as a protein kinase

21 January 2018

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Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss

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Distinct roles of the Drosophila ninaC kinase and myosin domains revealed by systematic mutagenesis

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Myosin IIIa boosts elongation of stereocilia by transporting espin 1 to the plus ends of actin filaments

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A new compartment at stereocilia tips defined by spatial and temporal patterns of myosin IIIa expression

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Response properties of single auditory nerve fibers in the mouse

21 January 2018

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

21 January 2018

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From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30

21 January 2018

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

21 January 2018

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