Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss (Q24301501)

4 July 2017

0 references

Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss (English)

1 reference

4 July 2017

1 reference

GOA release 2020-03-11

hearing

1 reference

sensorineural hearing loss

GOA release 2020-03-11

hearing loss

1 reference

based on heuristic

inferred from title

1 reference

Karen B Avraham

9

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author name string

Francesca Donaudy

1

1 reference

4 July 2017

Antonella Ferrara

2

1 reference

4 July 2017

Laura Esposito

3

1 reference

4 July 2017

Ronna Hertzano

4

1 reference

4 July 2017

Orit Ben-David

5

1 reference

4 July 2017

Rachel E Bell

6

1 reference

4 July 2017

Salvatore Melchionda

7

1 reference

4 July 2017

Leopoldo Zelante

8

1 reference

4 July 2017

Paolo Gasparini

10

1 reference

4 July 2017

language of work or name

English

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publication date

6 May 2003

1 reference

American Journal of Human Genetics

4 July 2017

1 reference

4 July 2017

72

1 reference

4 July 2017

6

1 reference

4 July 2017

1571-1577

1 reference

Myosin-I isozymes in neonatal rodent auditory and vestibular epithelia

4 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

Human brush border myosin-I and myosin-Ic expression in human intestine and Caco-2BBe cells

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

Defective myosin VIIA gene responsible for Usher syndrome type 1B

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

The neighbor-joining method: a new method for reconstructing phylogenetic trees

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

Crystal structure of the motor domain of a class-I myosin.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

HOMSTRAD: a database of protein structure alignments for homologous families

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

Cloning and characterization of mouse brush border myosin-I in adult and embryonic intestine

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

ConSurf: identification of functional regions in proteins by surface-mapping of phylogenetic information

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

A novel autosomal dominant non-syndromic deafness locus (DFNA48) maps to 12q13-q14 in a large Italian family

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

Non-syndromic autosomal-dominant deafness

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

Unconventional myosins: anchors in the membrane traffic relay

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

Unconventional myosins and the genetics of hearing loss

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

Rate4Site: an algorithmic tool for the identification of functional regions in proteins by surface mapping of evolutionary determinants within their homologues.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

Genomic structure of the human unconventional myosin VI gene.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180318

29 November 2018

Identifiers

DOI

10.1086/375654

1 reference

4 July 2017

0 references

1 reference