274 results on '"Goodyear, Richard"'
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2. AAV-mediated rescue of Eps8 expression in vivo restores hair-cell function in a mouse model of recessive deafness.
3. Visualizing Collagen Fibrils in the Cochlea’s Tectorial and Basilar Membranes Using a Fluorescently Labeled Collagen-Binding Protein Fragment
4. Design of electrified turbomachinery for use in modern industrial hybrid powertrains
5. Hearing Loss and Retarded Cochlear Development in Mice Lacking Type 2 Iodothyronine Deiodinase
6. Otoancorin, An Inner Ear Protein Restricted to the Interface between the Apical Surface of Sensory Epithelia and Their Overlying Acellular Gels, Is Defective in Autosomal Recessive Deafness DFNB22
7. Distribution and development of hair-cell surface and extracellular matrix components in the chick inner ear
8. The Development of Hair Cells in the Inner Ear
9. Increased Spontaneous Otoacoustic Emissions in Mice with a Detached Tectorial Membrane
10. The acquisition of mechano-electrical transducer current adaptation in auditory hair cells requires myosin VI
11. Progressive hearing loss and gradual deterioration of sensory hair bundles in the ears of mice lacking the actin-binding protein Eps8L2
12. A mouse model for human deafness DFNB22 reveals that hearing impairment is due to a loss of inner hair cell stimulation
13. Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia
14. Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with α-tectorin and is mutated in autosomal dominant hearing loss (DFNA4)
15. Identification of the Hair Cell Soma-1 Antigen, HCS-1, as Otoferlin
16. Staurosporine-induced collapse of cochlear hair bundles
17. The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells
18. Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane
19. Characterization of a Spontaneous, Recessive, Missense Mutation Arising in the Tecta Gene
20. Stereocilin-deficient mice reveal the origin of cochlear waveform distortions
21. Sharpened cochlear tuning in a mouse with a genetically modified tectorial membrane
22. A mutation in CCDC50, a gene encoding an effector of epidermal growth factor-mediated cell signaling, causes progressive hearing loss
23. Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells
24. Hair-cell numbers continue to increase in the utricular macula of the early posthatch chick
25. Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane
26. Evidence for Multiple, Developmentally Regulated Isoforms of Ptprq on Hair Cells of the Inner Ear
27. Asymmetric distribution of cadherin 23 and protocadherin 15 in the kinocilial links of avian sensory hair cells
28. In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment
29. TRPML3 mutations cause impaired mechano-electrical transduction and depolarization by an inward-rectifier cation current in auditory hair cells of varitint-waddler mice
30. TAp73 isoforms antagonize Notch signalling in SH-SY5Y neuroblastomas and in primary neurones
31. Initial characterization of kinocilin, a protein of the hair cell kinocilium
32. Development and properties of stereociliary link types in hair cells of the mouse cochlea
33. Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly
34. The mechanical properties of chick (Gallus domesticus) sensory hair bundles: relative contributions of structures sensitive to calcium chelation and subtilisin treatment
35. An emilin family extracellular matrix protein identified in the cochlear basilar membrane
36. Records of the Alepocephalid Fish Photostylus pycnopterus in the Indian and Pacific Oceans
37. Sensory organ development in the inner ear: molecular and cellular mechanisms
38. MET currents and otoacoustic emissions from mice with a detached tectorial membrane indicate the extracellular matrix regulates Ca2+ near stereocilia.
39. Age‐related changes in the biophysical and morphological characteristics of mouse cochlear outer hair cells.
40. Ultrastructural defects in stereocilia and tectorial membrane in aging mouse and human cochleae.
41. Accelerated Age-Related Degradation of the Tectorial Membrane in the Ceacam16βgal/βgal Null Mutant Mouse, a Model for Late-Onset Human Hereditary Deafness DFNB113.
42. Positional gradients and voltage dependence of block of the hair cell's mechano-electrical transducer channel by the d-HIVTAT and d-JNKi1 peptides
43. A tectorin-based matrix and planar cell polarity genes are required for normal collagen-fibril orientation in the developing tectorial membrane.
44. Examining the Role of the Tectorial Membrane in Otoacoustic Emission Generation.
45. Examining the Role of the Tectorial Membrane in Otoacoustic Emission Generation.
46. The mechanical properties of chick (Gallus domesticus) sensory hair bundles: relative contributions of structures sensitive to calcium chelation and subtilisin treatment
47. α-tectorin
48. A Mutation in PNPT1, Encoding Mitochondrial-RNA-Import Protein PNPase, Causes Hereditary Hearing Loss
49. The supporting-cell antigen: a receptor-like protein tyrosine phosphatase expressed in the sensory epithelia of the inner ear
50. Pattern formation in the basilar papilla: evidence for cell rearrangement
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