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4. AAV-mediated rescue of Eps8 expression in vivo restores hair-cell function in a mouse model of recessive deafness

5. Identification of a series of hair-cell MET channel blockers that protect against aminoglycoside-induced ototoxicity

6. MET currents and otoacoustic emissions from mice with a detached tectorial membrane indicate the extracellular matrix regulates Ca 2+ near stereocilia

7. Age‐related changes in the biophysical and morphological characteristics of mouse cochlear outer hair cells

9. a-Tectorin

12. Identification of ion-channel modulators that protect against aminoglycoside-induced hair cell death

13. Cell-Cell Contact Area Affects Notch Signaling and Notch-Dependent Patterning

19. The CD 2 isoform of protocadherin‐15 is an essential component of the tip‐link complex in mature auditory hair cells

21. Progressive hearing loss and gradual deterioration of sensory hair bundles in the ears of mice lacking the actin-binding protein Eps8L2

23. A Mutation in PNPT1, Encoding Mitochondrial-RNA-Import Protein PNPase, Causes Hereditary Hearing Loss

25. Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia

26. Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with α-tectorin and is mutated in autosomal dominant hearing loss (DFNA4)

28. Otoancorin Knockout Mice Reveal Inertia is the Force for Hearing

32. Actin-Bundling Protein TRIOBP Forms Resilient Rootlets of Hair Cell Stereocilia Essential for Hearing

33. In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment

35. Stereocilin-deficient mice reveal the origin of cochlear waveform distortions

41. The Tip-Link Antigen, a Protein Associated with the Transduction Complex of Sensory Hair Cells, Is Protocadherin-15

46. Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly

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