Myosin VIIA defects, which underlie the Usher 1B syndrome in humans, lead to deafness in Drosophila.
about
Myosins in cell junctionsThe myosin superfamily at a glance.Molecular evolution of the vertebrate mechanosensory cell and earCells, molecules and morphogenesis: the making of the vertebrate earThe E3 ligase Ubr3 regulates Usher syndrome and MYH9 disorder proteins in the auditory organs of Drosophila and mammalsA FERM domain autoregulates Drosophila myosin 7a activity.The Drosophila auditory system.Cbl-associated protein regulates assembly and function of two tension-sensing structures in Drosophila.Cell-type-specific roles of Na+/K+ ATPase subunits in Drosophila auditory mechanosensation.Auditory circuit in the Drosophila brainDevelopment of Johnston's organ in Drosophila.Unique transgenic animal model for hereditary hearing lossDimerized Drosophila myosin VIIa: a processive motor.Mosaic complementation demonstrates a regulatory role for myosin VIIa in actin dynamics of stereociliaMyosin VIIA, important for human auditory function, is necessary for Drosophila auditory organ development.Characterization of the Drosophila ortholog of the human Usher Syndrome type 1G protein sans.Impacts of Usher syndrome type IB mutations on human myosin VIIa motor functionWingless/Wnt signaling in Drosophila: the pattern and the pathwaySystematic analysis of the physiological importance of deubiquitinating enzymes.Ubiquitin-binding site 2 of ataxin-3 prevents its proteasomal degradation by interacting with Rad23The kinetic mechanism of mouse myosin VIIAMicroRNA-183 family conservation and ciliated neurosensory organ expressioncrinkled reveals a new role for Wingless signaling in Drosophila denticle formationThe unconventional myosin CRINKLED and its mammalian orthologue MYO7A regulate caspases in their signalling roles.The molecular biology of ear development - "Twenty years are nothing"Ubiquitination regulates the neuroprotective function of the deubiquitinase ataxin-3 in vivo.Polyglutamine length-dependent toxicity from α1ACT in Drosophila models of spinocerebellar ataxia type 6.Regulation of myosin 5a and myosin 7a.Evolution of sound and balance perception: innovations that aggregate single hair cells into the ear and transform a gravistatic sensor into the organ of corti.Neuronal encoding of sound, gravity, and wind in the fruit fly.Hearing molecules, mechanism and transportation: modeled in Drosophila melanogaster.Myosin VIIB from Drosophila is a high duty ratio motor.Hearing lessons from flies.Nonmuscle myosin II is required for cell proliferation, cell sheet adhesion and wing hair morphology during wing morphogenesis.Drosophila myosin VIIA is a high duty ratio motor with a unique kinetic mechanism.Expression and Regulation of Deubiquitinase-Resistant, Unanchored Ubiquitin Chains in Drosophila.Using Drosophila to study mechanisms of hereditary hearing loss.
P2860
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P2860
Myosin VIIA defects, which underlie the Usher 1B syndrome in humans, lead to deafness in Drosophila.
description
2005 nî lūn-bûn
@nan
2005 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Myosin VIIA defects, which und ...... ead to deafness in Drosophila.
@ast
Myosin VIIA defects, which und ...... ead to deafness in Drosophila.
@en
type
label
Myosin VIIA defects, which und ...... ead to deafness in Drosophila.
@ast
Myosin VIIA defects, which und ...... ead to deafness in Drosophila.
@en
prefLabel
Myosin VIIA defects, which und ...... ead to deafness in Drosophila.
@ast
Myosin VIIA defects, which und ...... ead to deafness in Drosophila.
@en
P2093
P2860
P1433
P1476
Myosin VIIA defects, which und ...... ead to deafness in Drosophila.
@en
P2093
Daniel F Eberl
Daniel P Kiehart
Josef D Franke
P2860
P304
P356
10.1016/J.CUB.2005.03.050
P407
P50
P577
2005-05-01T00:00:00Z