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K P Steel

Showing results (91-100 of 98) with videos related to

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Annals of the New York Academy of Sciences|June 8, 2000
A missense mutation in myosin VIIA prevents aminoglycoside accumulation in early postnatal cochlear hair cellsG P Richardson, A Forge, C J Kros, et al.
Human Molecular Genetics|December 10, 1999
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing lossX Z Liu, X J Xia, L R Xu, et al.
Human Molecular Genetics|February 22, 2001
The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of CortiH Tsai, R E Hardisty, C Rhodes, et al.
The Annals of Otology, Rhinology & Laryngology. Supplement|May 1, 1997
Unravelling the genetics of deafnessK P Steel, P Mburu, F Gibson, et al.
American Journal of Human Genetics|March 26, 1999
A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variationX Z Liu, C Hope, C Y Liang, et al.
American Journal of Human Genetics|August 27, 1998
Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndromeX Z Liu, C Hope, J Walsh, et al.
Human Molecular Genetics|January 1, 1997
Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IBG Lévy, F Levi-Acobas, S Blanchard, et al.
Nature Genetics|August 10, 2000
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouseP M Nolan, J Peters, M Strivens, et al.
Pageof 10

Showing results (91-100 of 98) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 98 results.
Annals of the New York Academy of Sciences|June 8, 2000
A missense mutation in myosin VIIA prevents aminoglycoside accumulation in early postnatal cochlear hair cellsG P Richardson, A Forge, C J Kros, et al.
Human Molecular Genetics|December 10, 1999
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing lossX Z Liu, X J Xia, L R Xu, et al.
Human Molecular Genetics|February 22, 2001
The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of CortiH Tsai, R E Hardisty, C Rhodes, et al.
The Annals of Otology, Rhinology & Laryngology. Supplement|May 1, 1997
Unravelling the genetics of deafnessK P Steel, P Mburu, F Gibson, et al.
American Journal of Human Genetics|March 26, 1999
A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variationX Z Liu, C Hope, C Y Liang, et al.
American Journal of Human Genetics|August 27, 1998
Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndromeX Z Liu, C Hope, J Walsh, et al.
Human Molecular Genetics|January 1, 1997
Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IBG Lévy, F Levi-Acobas, S Blanchard, et al.
Nature Genetics|August 10, 2000
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouseP M Nolan, J Peters, M Strivens, et al.
Pageof 10