(Q24290695)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11138009%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11138009%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

GOA release 2020-03-11

calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules

1 reference

Cadherin 23 (otocadherin)

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Usher syndrome

1 reference

inferred from title

Usher syndrome type 1D

1 reference

3

1 reference

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3 November 2019

author name string

Bolz H

1

1 reference

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3 November 2019

von Brederlow B

2

1 reference

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3 November 2019

Bryda EC

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11138009%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Kutsche K

5

1 reference

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3 November 2019

Nothwang HG

6

1 reference

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3 November 2019

Seeliger M

7

1 reference

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3 November 2019

del C-Salcedó Cabrera M

8

1 reference

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3 November 2019

Vila MC

9

1 reference

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3 November 2019

Molina OP

10

1 reference

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3 November 2019

Gal A

11

1 reference

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3 November 2019

Kubisch C

12

1 reference

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3 November 2019

language of work or name

English

0 references

publication date

1 January 2001

1 reference

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3 November 2019

1 reference

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3 November 2019

volume

27

1 reference

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3 November 2019

page(s)

108-112

1 reference

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3 November 2019

issue

1

1 reference

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Defective myosin VIIA gene responsible for Usher syndrome type 1B

3 November 2019

cites work

1 reference

7 January 2021

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

1 reference

7 January 2021

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

1 reference

7 January 2021

Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10.

1 reference

7 January 2021

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

1 reference

7 January 2021

A high-resolution genetic map around waltzer on mouse chromosome 10 and identification of a new allele of waltzer

1 reference

7 January 2021

Extracellular matrix and cell adhesion molecules in the developing inner ear

1 reference

7 January 2021

mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw)

1 reference

7 January 2021

Phylogenetic analysis of the cadherin superfamily allows identification of six major subfamilies besides several solitary members

1 reference

7 January 2021

Statistical features of human exons and their flanking regions

1 reference

7 January 2021

Genomic sequence, splicing, and gene annotation

1 reference

7 January 2021

Three novel mutations in the cystic fibrosis gene detected by chemical cleavage: analysis of variant splicing and a nonsense mutation

1 reference

7 January 2021

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene

1 reference

7 January 2021

Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.

1 reference

7 January 2021

Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene.

1 reference

7 January 2021

Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22.

1 reference

7 January 2021

The molecular structure of cell adhesion molecules

1 reference

7 January 2021

Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

1 reference

7 January 2021

Basic local alignment search tool

1 reference

7 January 2021

The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools

1 reference

7 January 2021

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

7 January 2021

Identifiers

DOI

10.1038/83667

2 references

Consolidated OpenCitations Corpus – April 2017

2761280

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11138009%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

3 November 2019

1032465727

0 references

2761280

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

2761280

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11138009%20AND%20SRC:MED&resulttype=core&format=json