Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function.
|
17329413 |
2007 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker |
MGD |
A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function.
|
17329413 |
2007 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
|
0.500 |
Biomarker |
MGD |
A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function.
|
17329413 |
2007 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment.
|
15389316 |
2004 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker |
MGD |
A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment.
|
15389316 |
2004 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
|
0.500 |
Biomarker |
MGD |
A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment.
|
15389316 |
2004 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells.
|
9435277 |
1998 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker |
MGD |
Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells.
|
9435277 |
1998 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
|
0.500 |
Biomarker |
MGD |
Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells.
|
9435277 |
1998 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
Mutation analysis of the mouse myosin VIIA deafness gene.
|
9680294 |
1997 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker |
MGD |
Mutation analysis of the mouse myosin VIIA deafness gene.
|
9680294 |
1997 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
|
0.500 |
Biomarker |
MGD |
Mutation analysis of the mouse myosin VIIA deafness gene.
|
9680294 |
1997 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations.
|
6627025 |
1983 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker |
MGD |
The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations.
|
6627025 |
1983 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
|
0.500 |
Biomarker |
MGD |
The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations.
|
6627025 |
1983 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY.
|
14198707 |
1964 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker |
MGD |
HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY.
|
14198707 |
1964 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
|
0.500 |
Biomarker |
MGD |
HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY.
|
14198707 |
1964 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
Hereditary retinal dystrophy
|
0.500 |
Biomarker |
MGD |
The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse.
|
13336002 |
1956 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker |
MGD |
The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse.
|
13336002 |
1956 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
|
0.500 |
Biomarker |
MGD |
The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse.
|
13336002 |
1956 |
Entrez Id: |
4647 |
Gene Symbol: |
MYO7A |
MYO7A
|
Sensorineural hearing loss, bilateral
|
0.300 |
Biomarker |
MGD |
Inner ear morphology is perturbed in two novel mouse models of recessive deafness.
|
23251483 |
2012 |