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K P Steel

Showing results (81-90 of 98) with videos related to

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Journal of Neurocytology|July 19, 2000
Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survivalA E Kiernan, M Zalzman, H Fuchs, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 22, 1999
A deletion on chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidateA J Paige, B W Kiernan, A Varela, et al.
Genomics|August 1, 1993
Analysis of the Pax-3 gene in the mouse mutant splotchM Goulding, S Sterrer, J Fleming, et al.
Nature Genetics|January 4, 2001
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1DF Di Palma, R H Holme, E C Bryda, et al.
Nature|March 2, 1995
A type VII myosin encoded by the mouse deafness gene shaker-1F Gibson, J Walsh, P Mburu, et al.
Nature Genetics|December 1, 1995
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cellsK B Avraham, T Hasson, K P Steel, et al.
Genes and Function|June 1, 1997
Mutation analysis of the mouse myosin VIIA deafness geneP Mburu, X Z Liu, J Walsh, et al.
Human Molecular Genetics|April 4, 2001
Mutation of the gene encoding fibrillin-2 results in syndactyly in miceS S Chaudhry, J Gazzard, C Baldock, et al.
Nature Neuroscience|December 26, 2001
Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutationsC J Kros, W Marcotti, S M van Netten, et al.
Human Molecular Genetics|February 1, 1993
Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type IK L Evans, J Fantes, C Simpson, et al.
Pageof 10

Showing results (81-90 of 98) with videos related to

Sort By:
Pageof 10
Journal of Neurocytology|July 19, 2000
Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survivalA E Kiernan, M Zalzman, H Fuchs, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 22, 1999
A deletion on chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidateA J Paige, B W Kiernan, A Varela, et al.
Genomics|August 1, 1993
Analysis of the Pax-3 gene in the mouse mutant splotchM Goulding, S Sterrer, J Fleming, et al.
Nature Genetics|January 4, 2001
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1DF Di Palma, R H Holme, E C Bryda, et al.
Nature|March 2, 1995
A type VII myosin encoded by the mouse deafness gene shaker-1F Gibson, J Walsh, P Mburu, et al.
Nature Genetics|December 1, 1995
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cellsK B Avraham, T Hasson, K P Steel, et al.
Genes and Function|June 1, 1997
Mutation analysis of the mouse myosin VIIA deafness geneP Mburu, X Z Liu, J Walsh, et al.
Human Molecular Genetics|April 4, 2001
Mutation of the gene encoding fibrillin-2 results in syndactyly in miceS S Chaudhry, J Gazzard, C Baldock, et al.
Nature Neuroscience|December 26, 2001
Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutationsC J Kros, W Marcotti, S M van Netten, et al.
Human Molecular Genetics|February 1, 1993
Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type IK L Evans, J Fantes, C Simpson, et al.
Pageof 10