|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
CLINGEN |
An ENU-induced mutation of Cdh23 causes congenital hearing loss, but no vestibular dysfunction, in mice.
|
21689626 |
2011 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
CLINGEN |
Nasal epithelial cells are a reliable source to study splicing variants in Usher syndrome.
|
20513143 |
2010 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
MGD |
A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth.
|
18339676 |
2008 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
MGD |
Fates of Cdh23/CDH23 with mutations affecting the cytoplasmic region.
|
16281288 |
2006 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
MGD |
A quantitative survey of gravity receptor function in mutant mouse strains.
|
16235133 |
2005 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
MGD |
Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration.
|
14609561 |
2003 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
CLINGEN |
The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions.
|
12407180 |
2002 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
CLINGEN |
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.
|
12075507 |
2002 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
MGD |
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.
|
11138008 |
2001 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
MGD |
Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23).
|
11750125 |
2001 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
CLINGEN |
Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23).
|
11750125 |
2001 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
CLINGEN |
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
|
11090341 |
2001 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
MGD |
A point mutation in a cadherin gene, Cdh23, causes deafness in a novel mutant, Waltzer mouse niigata.
|
11322776 |
2001 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
MGD |
Chromosomal localization of a gene responsible for vestibulocochlear defects of BUS/Idr mice: identification as an allele of waltzer.
|
10452381 |
1999 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
MGD |
A high-resolution genetic map around waltzer on mouse chromosome 10 and identification of a new allele of waltzer.
|
9021139 |
1997 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
MGD |
CD1d1 mutant mice are deficient in natural T cells that promptly produce IL-4.
|
9133426 |
1997 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
MGD |
Cochlear histopathology of the mutant bustling mouse, BUS/Idr.
|
8790740 |
1996 |
|
| Entrez Id: |
64072 |
| Gene Symbol: |
CDH23 |
CDH23
|
0.500 |
Biomarker
|
group |
MGD |
Behavioural profiles of neurological mutant mice.
|
5955164 |
1966 |