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E C Bryda

Showing results (11-20 of 18) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 12, 1999
Scraggly, a new hair loss mutation on mouse chromosome 19B J Herron, E C Bryda, S A Heverly, et al.
Genomics|May 15, 2001
High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and Waltzer (Cdh23v)E C Bryda, H J Kim, M E Legare, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Multiple sites of crossing over within the Eb recombinational hotspot in the mouseE C Bryda, J A DePari, D B Sant'Angelo, et al.
Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]|August 19, 2004
Detection of histidine decarboxylase in rat aorta and cultured rat aortic smooth muscle cellsA S Tippens, S V Davis, J R Hayes, et al.
Cytogenetic and Genome Research|February 14, 2003
Characterization of the region containing the jcpk PKD gene on mouse Chromosome 10S J Price, L R Chittenden, L Flaherty, et al.
Kidney International|October 1, 1996
Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelicL M Guay-Woodford, E C Bryda, B Christine, 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 Genetics|January 4, 2001
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1DH Bolz, B von Brederlow, A Ramírez, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 12, 1999
Scraggly, a new hair loss mutation on mouse chromosome 19B J Herron, E C Bryda, S A Heverly, et al.
Genomics|May 15, 2001
High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and Waltzer (Cdh23v)E C Bryda, H J Kim, M E Legare, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Multiple sites of crossing over within the Eb recombinational hotspot in the mouseE C Bryda, J A DePari, D B Sant'Angelo, et al.
Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]|August 19, 2004
Detection of histidine decarboxylase in rat aorta and cultured rat aortic smooth muscle cellsA S Tippens, S V Davis, J R Hayes, et al.
Cytogenetic and Genome Research|February 14, 2003
Characterization of the region containing the jcpk PKD gene on mouse Chromosome 10S J Price, L R Chittenden, L Flaherty, et al.
Kidney International|October 1, 1996
Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelicL M Guay-Woodford, E C Bryda, B Christine, 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 Genetics|January 4, 2001
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1DH Bolz, B von Brederlow, A Ramírez, et al.
Pageof 2