|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
CLINGEN |
Myosin 7 and its adaptors link cadherins to actin.
|
28660889 |
2017 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
CLINGEN |
Over-expression of myosin7A in cochlear hair cells of circling mice.
|
28400833 |
2017 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
CLINGEN |
Genetic Correction of Induced Pluripotent Stem Cells From a Deaf Patient With MYO7A Mutation Results in Morphologic and Functional Recovery of the Derived Hair Cell-Like Cells.
|
27013738 |
2016 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
CLINGEN |
Molecular genetics of the Usher syndrome in Lebanon: identification of 11 novel protein truncating mutations by whole exome sequencing.
|
25211151 |
2014 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
CLINGEN |
Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.
|
23559863 |
2013 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
MGD |
Moderate light-induced degeneration of rod photoreceptors with delayed transducin translocation in shaker1 mice.
|
21447681 |
2011 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
MGD |
A novel allele of myosin VIIa reveals a critical function for the C-terminal FERM domain for melanosome transport in retinal pigment epithelial cells.
|
20016096 |
2009 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
CLINGEN |
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
|
18181211 |
2008 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
MGD |
A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function.
|
17329413 |
2007 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
MGD |
A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment.
|
15389316 |
2004 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
CLINGEN |
Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness.
|
10958658 |
2000 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
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 IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
MGD |
Mutation analysis of the mouse myosin VIIA deafness gene.
|
9680294 |
1997 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
CLINGEN |
Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia.
|
8622919 |
1996 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
CLINGEN |
A type VII myosin encoded by the mouse deafness gene shaker-1.
|
7870172 |
1995 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
MGD |
The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations.
|
6627025 |
1983 |
|
USHER SYNDROME, TYPE IA, FORMERLY
|
0.500 |
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 IA, FORMERLY
|
0.500 |
Biomarker
|
disease |
MGD |
The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse.
|
13336002 |
1956 |