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← Karen P. Steel

Papers by Karen P. Steel

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  1. Myosin Va is required for normal photoreceptor synaptic activityJournal of Cell Science · 2004
  2. Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears ofFoxi1null mutant miceDevelopment · 2003
  3. Varitint-waddler: A double whammy for hearingProceedings of the National Academy of Sciences · 2002
  4. A novel stereocilia defect in sensory hair cells of the deaf mouse mutant Tasmanian devilEuropean Journal of Neuroscience · 2002
  5. Elongation of hair cell stereocilia is defective in the mouse mutant whirlerThe Journal of Comparative Neurology · 2002
  6. The roles of unconventional myosins in hearing and deafnessEssays in Biochemistry · 2000
  7. The Benefits of RecyclingScience · 1999
  8. Mutation of the Na-K-Cl Co-Transporter Gene Slc12a2 Results in Deafness in MiceHuman Molecular Genetics · 1999
  9. Myosin VIIa Participates in Opsin Transport through The Photoreceptor CiliumJournal of Neuroscience · 1999
  10. A New Era in the Genetics of DeafnessNew England Journal of Medicine · 1998
  11. Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cellsDevelopment · 1998
  12. Myosin VIIA is required for aminoglycoside accumulation in cochlear hair cells.1997
  13. Mutation analysis of the mouse myosin VIIA deafness geneGenes and Function · 1997
  14. REPORT on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4–6, 1996Annals of Human Genetics · 1997
  15. REPORT on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4–6, 1996Annals of Human Genetics · 1997
  16. Inherited Hearing Defects in MiceAnnual Review of Genetics · 1995
  17. Genetics and Molecular Biology of Mouse PigmentationPigment Cell Research · 1994
  18. Effects of Mutations at the W Locus (c‐kit) on Inner Ear Pigmentation and Function in the MousePigment Cell Research · 1994
  19. Light (Blt), a Mutation That Causes Melanocyte Death, Affects Stria Vascularis Function in the Mouse Inner EarPigment Cell Research · 1993
  20. Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type IHuman Molecular Genetics · 1993
  21. A Histologic Study of Nonmorphogenetic Forms of Hereditary Hearing ImpairmentArchives of Otolaryngology - Head and Neck Surgery · 1992
  22. TRP-2/DT, a new early melanoblast marker, shows that steel growth factor (c-kit ligand) is a survival factorDevelopment · 1992
  23. Identification of Two Types of Melanocyte Within the Stria Vascularis of the Mouse Inner EarPigment Cell Research · 1991
  24. Another role for melanocytes: their importance for normal stria vascularis development in the mammalian inner earDevelopment · 1989
  25. Genetic Factors Affecting Hearing DevelopmentActa Oto-Laryngologica · 1985
  26. Electrical Stimulation of the Auditory System in Animals Profoundly Deaf from BirthActa Oto-Laryngologica · 1985
  27. Electrical Stimulation of the Cochlear Nerve in Deafness MiceArchives of Otolaryngology - Head and Neck Surgery · 1983
  28. Hereditary Inner-Ear Abnormalities in Animals: Relationships With Human AbnormalitiesArchives of Otolaryngology - Head and Neck Surgery · 1983
  29. Cochlear dysfunction in the jerker mouse.Behavioral Neuroscience · 1983
  30. Inner Ear Pathology in the Deafness Mutant MouseActa Oto-Laryngologica · 1983
  31. The Proteins of Normal and Abnormal Tectorial MembranesActa Oto-Laryngologica · 1980