Pages that link to "Q47074176"

The following pages link to Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells (Q47074176):

Displaying 50 items.

• A late role for bmp2b in the morphogenesis of semicircular canal ducts in the zebrafish inner ear (Q21143881) (← links)
• A possible unifying principle for mechanosensation (Q22337260) (← links)
• PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome (Q24309592) (← links)
• Development and regeneration of sensory transduction in auditory hair cells requires functional interaction between cadherin-23 and protocadherin-15. (Q24596426) (← links)
• Usher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapy (Q24646440) (← links)
• Cadherins and mechanotransduction by hair cells (Q24649559) (← links)
• Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells (Q24673776) (← links)
• Neuroepithelial oxygen chemoreceptors of the zebrafish gill (Q24676954) (← links)
• The study of psychiatric disease genes and drugs in zebrafish (Q26824671) (← links)
• Sensing sound: molecules that orchestrate mechanotransduction by hair cells (Q26866077) (← links)
• Sensory mechanotransduction at membrane-matrix interfaces (Q27011942) (← links)
• Assembling stable hair cell tip link complex via multidentate interactions between harmonin and cadherin 23 (Q27654205) (← links)
• Structural determinants of cadherin-23 function in hearing and deafness (Q27660584) (← links)
• Harmonin (Ush1c) is required in zebrafish Müller glial cells for photoreceptor synaptic development and function (Q28243260) (← links)
• Functional epigenetics identifies a protocadherin PCDH10 as a candidate tumor suppressor for nasopharyngeal, esophageal and multiple other carcinomas with frequent methylation (Q28278843) (← links)
• Chemical screening for hair cell loss and protection in the zebrafish lateral line (Q28468560) (← links)
• Integrity and regeneration of mechanotransduction machinery regulate aminoglycoside entry and sensory cell death (Q28485274) (← links)
• Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development (Q28509348) (← links)
• Hair bundle defects and loss of function in the vestibular end organs of mice lacking the receptor-like inositol lipid phosphatase PTPRQ (Q28509821) (← links)
• Whirlin complexes with p55 at the stereocilia tip during hair cell development. (Q28510548) (← links)
• Stereociliary myosin-1c receptors are sensitive to calcium chelation and absent from cadherin 23 mutant mice (Q28512792) (← links)
• Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells (Q28575837) (← links)
• A model of stereocilia adaptation based on single molecule mechanical studies of myosin I (Q28580052) (← links)
• The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles. (Q28589815) (← links)
• TRPA1 is a candidate for the mechanosensitive transduction channel of vertebrate hair cells (Q28591781) (← links)
• Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells (Q28592402) (← links)
• Interactions in the network of Usher syndrome type 1 proteins (Q28592874) (← links)
• TMHS is an integral component of the mechanotransduction machinery of cochlear hair cells (Q28593852) (← links)
• The murine catecholamine methyltransferase mTOMT is essential for mechanotransduction by cochlear hair cells. (Q30354602) (← links)
• Infectious spleen and kidney necrosis virus ORF48R functions as a new viral vascular endothelial growth factor. (Q30367977) (← links)
• Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities (Q30389509) (← links)
• Zebrafish Models for the Mechanosensory Hair Cell Dysfunction in Usher Syndrome 3 Reveal That Clarin-1 Is an Essential Hair Bundle Protein. (Q30393797) (← links)
• Saccular Transcriptome Profiles of the Seasonal Breeding Plainfin Midshipman Fish (Porichthys notatus), a Teleost with Divergent Sexual Phenotypes (Q30398662) (← links)
• High-throughput gene targeting and phenotyping in zebrafish using CRISPR/Cas9. (Q30407556) (← links)
• The physiology of mechanoelectrical transduction channels in hearing (Q30408022) (← links)
• Genetics of auditory mechano-electrical transduction (Q30421422) (← links)
• The cone-dominant retina and the inner ear of zebrafish express the ortholog of CLRN1, the causative gene of human Usher syndrome type 3A. (Q30423944) (← links)
• Compound heterozygosity of the functionally null Cdh23(v-ngt) and hypomorphic Cdh23(ahl) alleles leads to early-onset progressive hearing loss in mice (Q30428046) (← links)
• Early development of hearing in zebrafish (Q30433743) (← links)
• Rapid positional cloning of zebrafish mutations by linkage and homozygosity mapping using whole-genome sequencing (Q30447155) (← links)
• A mutation in the cdh23 gene causes age-related hearing loss in Cdh23(nmf308/nmf308) mice (Q30454595) (← links)
• Mutations in ap1b1 cause mistargeting of the Na(+)/K(+)-ATPase pump in sensory hair cells (Q30455441) (← links)
• The Usher gene cadherin 23 is expressed in the zebrafish brain and a subset of retinal amacrine cells. (Q30463627) (← links)
• Linking genes underlying deafness to hair-bundle development and function (Q30468355) (← links)
• Ribeye is required for presynaptic Ca(V)1.3a channel localization and afferent innervation of sensory hair cells (Q30473909) (← links)
• Temporary reduction of distortion product otoacoustic emissions (DPOAEs) immediately following auditory brainstem response (ABR). (Q30473925) (← links)
• Drug screening for hearing loss: using the zebrafish lateral line to screen for drugs that prevent and cause hearing loss (Q30476012) (← links)
• Quantification of vestibular-induced eye movements in zebrafish larvae (Q30479508) (← links)
• The micromachinery of mechanotransduction in hair cells (Q30481576) (← links)
• The allosteric role of the Ca2+ switch in adhesion and elasticity of C-cadherin (Q30482106) (← links)