USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
For example, mutations in the gene encoding MYO7A cause Usher syndrome type IB, autosomal-recessive nonsyndromic hearing impairment (DFNB2), and autosomal-dominant nonsyndromic hearing impairment (DFNA11).
|
9927480 |
1999 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Ala397Asp mutation of myosin VIIA gene segregating in a Spanish family with type-Ib Usher syndrome.
|
9703432 |
1998 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
Biomarker
|
disease |
MGD |
Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells.
|
9435277 |
1998 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Detection of a novel Cys628STOP mutation of the myosin VIIA gene in Usher syndrome type Ib.
|
9843659 |
1998 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
Biomarker
|
disease |
MGD |
Mutation analysis of the mouse myosin VIIA deafness gene.
|
9680294 |
1997 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB.
|
9002678 |
1997 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A).
|
9070921 |
1997 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
In 15 families myosin VIIA mutations were detected, verifying their classification as USH1B.
|
9382091 |
1997 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
AlteredExpression
|
disease |
BEFREE |
In situ hybridization analysis in human embryos demonstrates that the myosin VIIA gene is expressed in the pigment epithelium and the photoreceptor cells of the retina, thus indicating that both cell types may be involved in the USH1B retinal degenerative process.
|
8622919 |
1996 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
Biomarker
|
disease |
CLINGEN |
In situ hybridization analysis in human embryos demonstrates that the myosin VIIA gene is expressed in the pigment epithelium and the photoreceptor cells of the retina, thus indicating that both cell types may be involved in the USH1B retinal degenerative process.
|
8622919 |
1996 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
Biomarker
|
disease |
CLINGEN |
A type VII myosin encoded by the mouse deafness gene shaker-1.
|
7870172 |
1995 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
Biomarker
|
disease |
MGD |
The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations.
|
6627025 |
1983 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
Biomarker
|
disease |
MGD |
HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY.
|
14198707 |
1964 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
Biomarker
|
disease |
MGD |
The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse.
|
13336002 |
1956 |
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
USHER SYNDROME, TYPE IB (disorder)
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|