(Q24540320)

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Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance

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Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance (English)

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1 reference

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author name string

A Adato

1

author given names

A

author last names

Adato

1 reference

27 April 2024

H Kalinski

2

author given names

H

author last names

Kalinski

1 reference

27 April 2024

D Weil

3

author given names

D

author last names

Weil

1 reference

27 April 2024

H Chaib

4

author given names

H

author last names

Chaib

1 reference

27 April 2024

M Korostishevsky

5

author given names

M

author last names

Korostishevsky

1 reference

27 April 2024

B Bonne-Tamir

6

author given names

B

author last names

Bonne-Tamir

1 reference

27 April 2024

language of work or name

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publication date

July 1999

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American Journal of Human Genetics

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65

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261-5

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1

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Phylogenetic analysis of the myosin superfamily.

1 reference

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The Sensitivity of Single-Strand Conformation Polymorphism Analysis for the Detection of Single Base Substitutions

1 reference

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Mapping of unconventional myosins in mouse and human

1 reference

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7 January 2021

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Refined mapping of the Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous region

1 reference

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7 January 2021

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Unconventional myosins: new frontiers in actin-based motors.

1 reference

https://api.crossref.org/works/10.1086%2F302438

7 January 2021

based on heuristic

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Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

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7 January 2021

based on heuristic

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A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews

1 reference

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

1 reference

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7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1086%2F302438

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based on heuristic

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

1 reference

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7 January 2021

based on heuristic

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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

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1086%2F302438

7 January 2021

based on heuristic

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Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family

1 reference

https://api.crossref.org/works/10.1086%2F302438

7 January 2021

based on heuristic

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Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins

1 reference

https://api.crossref.org/works/10.1086%2F302438

7 January 2021

based on heuristic

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Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.

1 reference

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7 January 2021

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The fundamental and medical impacts of recent progress in research on hereditary hearing loss.

1 reference

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

1 reference

https://api.crossref.org/works/10.1086%2F302438

7 January 2021

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Unconventional Myosins

1 reference

https://api.crossref.org/works/10.1086%2F302438

7 January 2021

based on heuristic

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Myosin VIIA is required for aminoglycoside accumulation in cochlear hair cells

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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release_im4gxzpehnfxpiifnwmijxumoe

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