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Current Opinion in Neurobiology|September 12, 2000
Modifier genes of hereditary hearing lossT Friedman, J Battey, B Kachar, et al.Thescientificworldjournal|June 14, 2003
Some deafness-causing mutations can be silenced with the appropriate gene partnerE Wilcox, S Riazuddin, S RiazuddinNature 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.Oncogene|December 7, 1995
Expression of mouse c-myb during embryonic developmentJ Sitzmann, K Noben-Trauth, K H KlempnauerGene|December 26, 2001
Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23)F Di Palma, R Pellegrino, K Noben-TrauthBiochimica Et Biophysica Acta|May 30, 1997
Cloning and expression analysis of mouse Cclp1, a new gene encoding a coiled-coil-like proteinK Noben-Trauth, J K Naggert, P M NishinaOncogene|December 21, 1995
Differential splicing of the mouse B-myb geneH Kamano, B Burk, K Noben-Trauth, et al.Oncogene|May 2, 1996
Expression of B-Myb during mouse embryogenesisJ Sitzmann, K Noben-Trauth, H Kamano, et al.Human Molecular Genetics|January 12, 2001
Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndromeL A Everett, I A Belyantseva, K Noben-Trauth, et al.Genomics|November 5, 1997
mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw)K Noben-Trauth, Q Y Zheng, K R Johnson, et al.Pageof 119