219 results on '"Dolan, David F."'
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2. PlexinA2 Forward Signaling through Rap1 GTPases Regulates Dentate Gyrus Development and Schizophrenia-like Behaviors
3. Loss of the chromatin remodeler CHD7 impacts glial cells and myelination in the mouse cochlear spiral ganglion
4. Noise overstimulation of young adult UMHET4 mice accelerates age-related hearing loss
5. GJB2 gene therapy and conditional deletion reveal developmental stage-dependent effects on inner ear structure and function
6. Nutrient plasma levels achieved during treatment that reduces noise-induced hearing loss
7. Effects of Calcitonin-Gene-Related-Peptide on Auditory Nerve Activity
8. Transgenic Mouse Model of the Mild Dominant Form of Osteogenesis Imperfecta
9. Rapamycin Added to Diet in Late Mid-Life Delays Age-Related Hearing Loss in UMHET4 Mice
10. Genetic Background of Prop1 df Mutants Provides Remarkable Protection Against Hypothyroidism-Induced Hearing Impairment
11. Induction of Heat Shock Proteins by Hyperthermia and Noise Overstimulation in Hsf1 −/− Mice
12. Whirler Mutant Hair Cells Have Less Severe Pathology than Shaker 2 or Double Mutants
13. Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice
14. Long-Term Effects of Acoustic Trauma on Electrically Evoked Otoacoustic Emission
15. Disruption of Lateral Olivocochlear Neurons via a Dopaminergic Neurotoxin Depresses Sound-Evoked Auditory Nerve Activity
16. Auditory hair cell replacement and hearing improvement by Atoh1 gene therapy in deaf mammals
17. Genetic and phenotypic analysis of the mouse mutant mh 2J, an Ap3d allele caused by IAP element insertion
18. Hearing dysfunction in heterozygous MitfMi-wh/+ mice, a model for Waardenburg syndrome type 2 and Tietz syndrome
19. Hair cells in the inner ear of the pirouette and shaker 2 mutant mice
20. Morphological and physiological effects of long duration infusion of strychnine into the organ of Corti
21. Mature middle and inner ears express Chd7 and exhibit distinctive pathologies in a mouse model of CHARGE syndrome
22. Safety of Ciprofloxacin and Dexamethasone in the Guinea Pig Middle Ear
23. Math5 expression and function in the central auditory system
24. The role of bone morphogenetic protein 4 in inner ear development and function
25. Exploring efferent-mediated DPOAE adaptation in three different guinea pig strains
26. Genetic mapping refines DFNB3 (ital) to 17p11.2, suggests multiple alleles of DFNB3 (ital), and supports homology to the mouse model shaker-2 (ital)
27. Transgene correction maintains normal cochlear structure and function in 6-month-old Myo15a mutant mice
28. Efferent-mediated adaptation of the DPOAE as a predictor of aminoglycoside toxicity
29. Characterization of Two Transgene Insertional Mutations at Pirouette, a Mouse Deafness Locus
30. Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia
31. Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration
32. Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6
33. Small Arms Fire-like noise: Effects on Hearing Loss, Gap Detection and the Influence of Preventive Treatment
34. Basal Turn Hair Cell Activity Dominates the Round Window Recorded Simple Difference Tone (F2-F1)
35. Age-Related Differences in Cochlear Microcirculation and Auditory Brain Stem Response
36. Grxcr2 is required for stereocilia morphogenesis in the cochlea
37. Generation and Characterization of α9 and α10 Nicotinic Acetylcholine Receptor Subunit Knockout Mice on a C57BL/6J Background
38. Selective hair cell ablation and noise exposure lead to different patterns of changes in the cochlea and the cochlear nucleus
39. PlexinA2 Forward Signaling through Rap1 GTPases Regulates Dentate Gyrus Development and Schizophrenia-like Behaviors.
40. The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing
41. Author response: The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing
42. Ototoxicity-induced loss of hearing and inner hair cells is attenuated by HSP70 gene transfer
43. Disruption of lateral olivocochlear neurons with a dopaminergic neurotoxin depresses spontaneous auditory nerve activity
44. Conditioning the Cochlea to Facilitate Survival and Integration of Exogenous Cells into the Auditory Epithelium
45. OTO-201
46. Macrophage migration inhibitory factor acts as a neurotrophin in the developing inner ear
47. Macrophage migration inhibitory factor acts as a neurotrophin in the developing inner ear
48. Hearing dysfunction in heterozygous MitfMi‐wh/+ mice, a model for Waardenburg syndrome type 2 and Tietz syndrome
49. Genetic Background of Prop1 df Mutants Provides Remarkable Protection Against Hypothyroidism-Induced Hearing Impairment
50. A Modifier Gene Alleviates Hypothyroidism-Induced Hearing Impairment in Pou1f1dw Dwarf Mice
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