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K P Steel

Showing results (61-70 of 98) with videos related to

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Genomics|May 1, 1992
Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1K A Brown, M J Sutcliffe, K P Steel, et al.
Journal of Neurocytology|October 31, 2000
Cytoskeletal integration in a highly ordered sensory epithelium in the organ of Corti: reponse to loss of cell partners in the Bronx waltzer mouseJ B Tucker, J B Mackie, T J Bussoli, et al.
Human Mutation|January 1, 1997
Identification of a new mutation of the myosin VII head region in Usher syndrome type 1X Z Liu, V E Newton, K P Steel, et al.
Genomics|March 21, 1998
Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafnessD C Hughes, P K Legan, K P Steel, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1994
Sequencing of the olfactory marker protein gene in normal and shaker-1 mutant miceK A Brown, M J Sutcliffe, K P Steel, et al.
Brain Research|September 10, 2013
Genetic deafness of central originM S Deol, M P Frank, K P Steel, et al.
Development (Cambridge, England)|April 4, 1998
Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cellsT Self, M Mahony, J Fleming, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 22, 1999
Myosin VIIa participates in opsin transport through the photoreceptor ciliumX Liu, I P Udovichenko, S D Brown, et al.
Developmental Biology|May 18, 2001
The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defectsA Alavizadeh, A E Kiernan, P Nolan, et al.
Cell Motility and the Cytoskeleton|January 1, 1997
Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expressionT Hasson, J Walsh, J Cable, et al.
Pageof 10

Showing results (61-70 of 98) with videos related to

Sort By:
Pageof 10
Genomics|May 1, 1992
Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1K A Brown, M J Sutcliffe, K P Steel, et al.
Journal of Neurocytology|October 31, 2000
Cytoskeletal integration in a highly ordered sensory epithelium in the organ of Corti: reponse to loss of cell partners in the Bronx waltzer mouseJ B Tucker, J B Mackie, T J Bussoli, et al.
Human Mutation|January 1, 1997
Identification of a new mutation of the myosin VII head region in Usher syndrome type 1X Z Liu, V E Newton, K P Steel, et al.
Genomics|March 21, 1998
Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafnessD C Hughes, P K Legan, K P Steel, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1994
Sequencing of the olfactory marker protein gene in normal and shaker-1 mutant miceK A Brown, M J Sutcliffe, K P Steel, et al.
Brain Research|September 10, 2013
Genetic deafness of central originM S Deol, M P Frank, K P Steel, et al.
Development (Cambridge, England)|April 4, 1998
Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cellsT Self, M Mahony, J Fleming, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 22, 1999
Myosin VIIa participates in opsin transport through the photoreceptor ciliumX Liu, I P Udovichenko, S D Brown, et al.
Developmental Biology|May 18, 2001
The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defectsA Alavizadeh, A E Kiernan, P Nolan, et al.
Cell Motility and the Cytoskeleton|January 1, 1997
Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expressionT Hasson, J Walsh, J Cable, et al.
Pageof 10