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Advances in Experimental Medicine and Biology|June 8, 2004
Mouse models for Usher syndrome 1BConcepcion Lillo, Junko Kitamoto, Xinran Liu, et al.Developmental Biology|April 25, 2009
Catweasel mice: a novel role for Six1 in sensory patch development and a model for branchio-oto-renal syndromeErika A Bosman, Elizabeth Quint, Helmut Fuchs, et al.Hearing Research|July 18, 2002
Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant miceRalph H Holme, Karen P SteelSeminars in Cell & Developmental Biology|February 16, 2010
MicroRNAs in mouse development and diseaseMorag A Lewis, Karen P SteelMicropublication Biology|August 27, 2025
Genes underlying hereditary hearing impairment in humans and in miceMorag A Lewis, Karen P SteelJournal of the Association for Research in Otolaryngology : JARO|December 3, 2003
Progressive hearing loss and increased susceptibility to noise-induced hearing loss in mice carrying a Cdh23 but not a Myo7a mutationRalph H Holme, Karen P SteelHearing Research|April 13, 2002
Early development and degeneration of vestibular hair cells in bronx waltzer mutant miceMichael A Cheong, Karen P SteelHearing Research|August 16, 2025
Non-invasive testing to diagnose the underlying auditory pathology of hearing impairmentNeil J Ingham, Karen P SteelCurrent Protocols in Mouse Biology|June 13, 2015
Using the Auditory Brainstem Response (ABR) to Determine Sensitivity of Hearing in Mutant MiceNeil J Ingham, Selina Pearson, Karen P SteelPageof 14