相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids
Amel Bahloul et al.
HUMAN MOLECULAR GENETICS (2010)
Development and Regeneration of Sensory Transduction in Auditory Hair Cells Requires Functional Interaction Between Cadherin-23 and Protocadherin-15
Andrea Lelli et al.
JOURNAL OF NEUROSCIENCE (2010)
Structural Determinants of Cadherin-23 Function in Hearing and Deafness
Marcos Sotomayor et al.
NEURON (2010)
Structure of the N terminus of cadherin 23 reveals a new adhesion mechanism for a subset of cadherin superfamily members
Heather M. Elledge et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Hearing Loss: Mechanisms Revealed by Genetics and Cell Biology
Amiel A. Dror et al.
ANNUAL REVIEW OF GENETICS (2009)
Mechanotransduction by Hair Cells: Models, Molecules, and Mechanisms
Peter G. Gillespie et al.
CELL (2009)
Fast Adaptation and Ca2+ Sensitivity of the Mechanotransducer Require Myosin-XVa in Inner But Not Outer Cochlear Hair Cells
Ruben Stepanyan et al.
JOURNAL OF NEUROSCIENCE (2009)
Linking genes underlying deafness to hair-bundle development and function
Christine Petit et al.
NATURE NEUROSCIENCE (2009)
Localization of inner hair cell mechanotransducer channels using high-speed calcium imaging
Maryline Beurg et al.
NATURE NEUROSCIENCE (2009)
PRESENCE OF INTERSTEREOCILIAL LINKS IN WALTZER MUTANTS SUGGESTS Cdh23 IS NOT ESSENTIAL FOR TIP LINK FORMATION
A. K. Rzadzinska et al.
NEUROSCIENCE (2009)
A mouse model for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells
Martin Schwander et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
The dimensions and structural attachments of tip links in mammalian cochlear hair cells and the effects of exposure to different levels of extracellular calcium
D. N. Furness et al.
NEUROSCIENCE (2008)
Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells
Piotr Kazmierczak et al.
NATURE (2007)
Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning
Nicolas Michalski et al.
JOURNAL OF NEUROSCIENCE (2007)
Mouse models to study inner ear development and hereditary hearing loss
Lilach M. Friedman et al.
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY (2007)
A new spontaneous mutation in the mouse protocadherin 15 gene
Q. Y. Zheng et al.
HEARING RESEARCH (2006)
The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15
Zubair M. Ahmed et al.
JOURNAL OF NEUROSCIENCE (2006)
Progression of inner ear pathology in Ames waltzer mice and the role of protocadherin 15 in hair cell development
Karen S. Pawlowski et al.
JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY (2006)
Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells
M Senften et al.
JOURNAL OF NEUROSCIENCE (2006)
The aminoglycoside antibiotic dihydrostreptomycin rapidly enters mouse outer hair cells through the mechano-electrical transducer channels
W Marcotti et al.
JOURNAL OF PHYSIOLOGY-LONDON (2005)
Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells
V Michel et al.
DEVELOPMENTAL BIOLOGY (2005)
Cadherin 23 is a component of the tip link in hair-cell stereocilia
J Siemens et al.
NATURE (2004)
Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells
C Söllner et al.
NATURE (2004)
The structure of tip links and kinocilial links in avian sensory hair bundles
V Tsuprun et al.
BIOPHYSICAL JOURNAL (2004)
Fast adaptation of mechanoelectrical transducer channels in mammalian cochlear hair cells
HJ Kennedy et al.
NATURE NEUROSCIENCE (2003)
Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations
CJ Kros et al.
NATURE NEUROSCIENCE (2002)
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
KN Alagramam et al.
HUMAN MOLECULAR GENETICS (2001)
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
ZM Ahmed et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
F Di Palma et al.
NATURE GENETICS (2001)
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
KN Alagramam et al.
NATURE GENETICS (2001)
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
JM Bork et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
High-resolution structure of hair-cell tip links
B Kachar et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)