Skip to search formSkip to main contentSkip to account menu

MYO7A gene

Known as: NSRD2, MYOSIN, UNCONVENTIONAL, FAMILY VII, MEMBER A, MYU7A 
National Institutes of Health

Related topics

Related topics

3 relations
DEAFNESS, AUTOSOMAL RECESSIVE 2MYO3A genemyosin VIIa

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
Genetics Of Human Hereditary Hearing Impairment.
Hereditary hearing impairment is heterogeneous type of disorder which can be caused due to environmental as well as genetical… 
2016
2016
PDZD7-MYO7A complex identified in enriched stereocilia membranes
While more than 70 genes have been linked to deafness, most of which are expressed in mechanosensory hair cells of the inner ear… 
2014
2014
Novel and Recurrent MYO7A Mutations in Usher Syndrome Type 1 and Type 2
Usher syndrome (USH) is a group of disorders manifested as retinitis pigmentosa and bilateral sensorineural hearing loss, with or… 
2014
2014
Myosin VIIA regulates microvillus morphogenesis and interacts with cadherin Cad99C in Drosophila oogenesis
ABSTRACT Microvilli and related actin-based protrusions permit multiple interactions between cells and their environment. How the… 
2014
2014
FERM domain‐containing unconventional myosin VIIA interacts with integrin β5 subunit and regulates αvβ5‐mediated cell adhesion and migration
2011
2011
Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China
The myosin VIIA (MYO7A) gene encodes a protein classified as an unconventional myosin. Mutations within MYO7A can lead to both… 
2011
2011
A DNA Variant within the MYO7A Promoter Regulates YY1 Transcription Factor Binding and Gene Expression Serving as a Potential Dominant DFNA11 Auditory Genetic Modifier*
Mutations within MYO7A can lead to recessive and dominant forms of inherited hearing loss. We previously identified a large… 
2004
2004
Modifier controls severity of a novel dominant low-frequency MyosinVIIA (MYO7A) auditory mutation
Hearing impairment is a common sensory deficit with both genetic and environmental aetiologies. Pre-lingual hearing loss affects… 
2003
2003
Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia.
The unconventional myosin genes Myo15, Myo6 and Myo7a are essential for hearing in both humans and mice. Despite the expression… 
Review
2003
Review
2003
Isolation and culture of primary mouse retinal pigmented epithelial cells.
A number of cases of retinal degeneration are caused by mutations in genes that are expressed in the retinal pigmented epithelial… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)