Pages that link to "Q33991492"

The following pages link to The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells (Q33991492):

Displaying 32 items.

• Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth (Q27308986) (← links)
• Evidence for changes in beta- and gamma-actin proportions during inner ear hair cell life (Q27336425) (← links)
• The murine catecholamine methyltransferase mTOMT is essential for mechanotransduction by cochlear hair cells. (Q30354602) (← links)
• Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness (Q30368442) (← links)
• Genetics of auditory mechano-electrical transduction (Q30421422) (← links)
• Subunit determination of the conductance of hair-cell mechanotransducer channels (Q30619961) (← links)
• MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform (Q36803634) (← links)
• Molecular Identity of the Mechanotransduction Channel in Hair Cells: Not Quiet There Yet. (Q37398454) (← links)
• Plasma Membrane Targeting of Protocadherin 15 Is Regulated by the Golgi-Associated Chaperone Protein PIST. (Q37404808) (← links)
• The molecules that mediate sensory transduction in the mammalian inner ear. (Q38556046) (← links)
• The elusive mechanotransduction machinery of hair cells. (Q38581411) (← links)
• The genetics of hair-cell function in zebrafish. (Q39433217) (← links)
• Usher syndrome type 1-associated cadherins shape the photoreceptor outer segment. (Q39436141) (← links)
• Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction (Q41256505) (← links)
• Functional Analysis of the Transmembrane and Cytoplasmic Domains of Pcdh15a in Zebrafish Hair Cells (Q41700384) (← links)
• TMIE is an essential component of the mechanotransduction machinery of cochlear hair cells. (Q41865763) (← links)
• Conformational switch of harmonin, a submembrane scaffold protein of the hair cell mechanoelectrical transduction machinery (Q42359299) (← links)
• Hair Cell Transduction, Tuning, and Synaptic Transmission in the Mammalian Cochlea (Q42618413) (← links)
• CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival (Q47139986) (← links)
• Beyond Cell-Cell Adhesion: Sensational Cadherins for Hearing and Balance. (Q47894540) (← links)
• Profile of Christine Petit (Q49621946) (← links)
• Tuning Inner-Ear Tip-Link Affinity Through Alternatively Spliced Variants of Protocadherin-15. (Q50005067) (← links)
• Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss (Q50310624) (← links)
• Transcriptional analysis of the dachsous gene uncovers novel isoforms expressed during development in Drosophila. (Q50553519) (← links)
• Intracellular Regulome Variability Along the Organ of Corti: Evidence, Approaches, Challenges, and Perspective. (Q55044473) (← links)
• Function and Dysfunction of TMC Channels in Inner Ear Hair Cells (Q57021484) (← links)
• Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome (Q58108796) (← links)
• FGFR1-mediated protocadherin-15 loading mediates cargo specificity during intraflagellar transport in inner ear hair-cell kinocilia (Q61845606) (← links)
• Clarin-2 is essential for hearing by maintaining stereocilia integrity and function (Q92863662) (← links)
• A Review of Gene, Drug and Cell-Based Therapies for Usher Syndrome (Q98177383) (← links)
• Structural determinants of protocadherin-15 mechanics and function in hearing and balance perception (Q99608149) (← links)
• Interaction of protocadherin-15 with the scaffold protein whirlin supports its anchoring of hair-bundle lateral links in cochlear hair cells (Q100428030) (← links)