Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance (Q24540320)

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Language	Label	Description	Also known as
English	Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance	scientific article

Statements

instance of

scholarly article

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title

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

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main subject

SH3 domain

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deafness

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based on heuristic

inferred from title

author name string

A Adato

series ordinal

1

author given names

A

author last names

Adato

1 reference

stated in

PubMed

PubMed publication ID

10364543

retrieved

27 April 2024

H Kalinski

series ordinal

2

author given names

H

author last names

Kalinski

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stated in

PubMed

PubMed publication ID

10364543

retrieved

27 April 2024

D Weil

series ordinal

3

author given names

D

author last names

Weil

1 reference

stated in

PubMed

PubMed publication ID

10364543

retrieved

27 April 2024

H Chaib

series ordinal

4

author given names

H

author last names

Chaib

1 reference

stated in

PubMed

PubMed publication ID

10364543

retrieved

27 April 2024

M Korostishevsky

series ordinal

5

author given names

M

author last names

Korostishevsky

1 reference

stated in

PubMed

PubMed publication ID

10364543

retrieved

27 April 2024

B Bonne-Tamir

series ordinal

6

author given names

B

author last names

Bonne-Tamir

1 reference

stated in

PubMed

PubMed publication ID

10364543

retrieved

27 April 2024

language of work or name

English

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publication date

July 1999

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published in

American Journal of Human Genetics

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volume

65

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issue

1

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page(s)

261-5

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cites work

Phylogenetic analysis of the myosin superfamily.

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Crossref

reference URL

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

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7 January 2021

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inferred from DOI database lookup

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

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stated in

Crossref

reference URL

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

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7 January 2021

based on heuristic

inferred from DOI database lookup

Mapping of unconventional myosins in mouse and human

1 reference

stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Unconventional myosins: new frontiers in actin-based motors

1 reference

stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Defective myosin VIIA gene responsible for Usher syndrome type 1B

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stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

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

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

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

retrieved

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

stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

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stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Unconventional Myosins

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stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Myosin VIIA is required for aminoglycoside accumulation in cochlear hair cells

1 reference

stated in

Crossref

reference URL

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

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1086/302438

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Fatcat ID

release_im4gxzpehnfxpiifnwmijxumoe

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PMC publication ID

1378101

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PubMed publication ID

10364543

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ResearchGate publication ID

12933557

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