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K P Steel

Showing results (71-80 of 98) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 10, 1998
Myosin VIIA is required for aminoglycoside accumulation in cochlear hair cellsG P Richardson, A Forge, C J Kros, et al.
Developmental Biology|October 20, 1999
Role of myosin VI in the differentiation of cochlear hair cellsT Self, T Sobe, N G Copeland, et al.
Human Molecular Genetics|July 13, 1999
Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in miceM J Dixon, J Gazzard, S S Chaudhry, et al.
Nature Genetics|November 14, 1997
Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA geneX Z Liu, J Walsh, Y Tamagawa, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 25, 1999
Genetic mapping of the whirler mutationM J Rogers, J Fleming, B W Kiernan, et al.
International Journal of Pediatric Otorhinolaryngology|June 1, 1995
Gene linkage and genetic deafnessC W Cremers, S D Brown, K P Steel, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Reverse genetic approaches to cloning deafness genesS D Brown, K A Brown, M J Sutcliffe, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
Sensorineural hearing impairment non-syndromic, dominant DFNA11Y Tamagawa, K Kitamura, T Ishida, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 22, 2001
The Notch ligand Jagged1 is required for inner ear sensory developmentA E Kiernan, N Ahituv, H Fuchs, et al.
Nature Genetics|June 1, 1997
Mutations in the myosin VIIA gene cause non-syndromic recessive deafnessX Z Liu, J Walsh, P Mburu, et al.
Pageof 10

Showing results (71-80 of 98) with videos related to

Sort By:
Pageof 10
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 10, 1998
Myosin VIIA is required for aminoglycoside accumulation in cochlear hair cellsG P Richardson, A Forge, C J Kros, et al.
Developmental Biology|October 20, 1999
Role of myosin VI in the differentiation of cochlear hair cellsT Self, T Sobe, N G Copeland, et al.
Human Molecular Genetics|July 13, 1999
Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in miceM J Dixon, J Gazzard, S S Chaudhry, et al.
Nature Genetics|November 14, 1997
Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA geneX Z Liu, J Walsh, Y Tamagawa, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 25, 1999
Genetic mapping of the whirler mutationM J Rogers, J Fleming, B W Kiernan, et al.
International Journal of Pediatric Otorhinolaryngology|June 1, 1995
Gene linkage and genetic deafnessC W Cremers, S D Brown, K P Steel, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Reverse genetic approaches to cloning deafness genesS D Brown, K A Brown, M J Sutcliffe, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
Sensorineural hearing impairment non-syndromic, dominant DFNA11Y Tamagawa, K Kitamura, T Ishida, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 22, 2001
The Notch ligand Jagged1 is required for inner ear sensory developmentA E Kiernan, N Ahituv, H Fuchs, et al.
Nature Genetics|June 1, 1997
Mutations in the myosin VIIA gene cause non-syndromic recessive deafnessX Z Liu, J Walsh, P Mburu, et al.
Pageof 10