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P K Legan

Showing results (11-20 of 15) with videos related to

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Journal of Cell Science|October 1, 1990
Desmosomal glycoproteins 2 and 3 (desmocollins) show N-terminal similarity to calcium-dependent cell-cell adhesion moleculesJ L Holton, T P Kenny, P K Legan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 15, 1999
The supporting-cell antigen: a receptor-like protein tyrosine phosphatase expressed in the sensory epithelia of the avian inner earR P Kruger, R J Goodyear, P K Legan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 10, 2003
A receptor-like inositol lipid phosphatase is required for the maturation of developing cochlear hair bundlesR J Goodyear, P K Legan, M B Wright, et al.
Nature Genetics|October 15, 1998
Nonsyndromic hearing impairment is associated with a mutation in DFNA5L Van Laer, E H Huizing, M Verstreken, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Journal of Cell Science|October 1, 1990
Desmosomal glycoproteins 2 and 3 (desmocollins) show N-terminal similarity to calcium-dependent cell-cell adhesion moleculesJ L Holton, T P Kenny, P K Legan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 15, 1999
The supporting-cell antigen: a receptor-like protein tyrosine phosphatase expressed in the sensory epithelia of the avian inner earR P Kruger, R J Goodyear, P K Legan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 10, 2003
A receptor-like inositol lipid phosphatase is required for the maturation of developing cochlear hair bundlesR J Goodyear, P K Legan, M B Wright, et al.
Nature Genetics|October 15, 1998
Nonsyndromic hearing impairment is associated with a mutation in DFNA5L Van Laer, E H Huizing, M Verstreken, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Pageof 2