(Q39327833)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22718023%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

title

TECTA mutations in Japanese with mid-frequency hearing loss affected by zona pellucida domain protein secretion (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22718023%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

1 reference

2

1 reference

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5 February 2020

author name string

Hideaki Moteki

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22718023%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

Shigenari Hashimoto

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22718023%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

Yutaka Takumi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22718023%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

Satoshi Iwasaki

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22718023%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

Norihito Takeichi

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22718023%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

Satoshi Fukuda

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22718023%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

Shin-ichi Usami

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22718023%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

publication date

21 June 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22718023%20AND%20SRC:MED&resulttype=core&format=json

Journal of Human Genetics

5 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22718023%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

volume

57

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22718023%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

issue

9

1 reference

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5 February 2020

page(s)

587-592

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22718023%20AND%20SRC:MED&resulttype=core&format=json

Sensorineural hearing loss in children.

5 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

Non-syndromic, autosomal-recessive deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

A cysteine substitution in the zona pellucida domain of alpha-tectorin results in autosomal dominant, postlingual, progressive, mid frequency hearing loss in a Spanish family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

Association of clinical features with mutation of TECTA in a family with autosomal dominant hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

Characterization of a spontaneous, recessive, missense mutation arising in the Tecta gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

The ZP domain is a conserved module for polymerization of extracellular proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

Secretion and assembly of zona pellucida glycoproteins by growing mouse oocytes microinjected with epitope-tagged cDNAs for mZP2 and mZP3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

Zona pellucida domain proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73

Flat threshold and mid-frequency hearing impairment in a Dutch DFNA8/12 family with a novel mutation in TECTA. Some evidence for protection of the inner ear

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.73