검색결과 : 8건
No. | Article |
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1 |
Treatment with 17-allylamino-17-demethoxygeldanamycin ameliorated symptoms of Bartter syndrome type IV caused by mutated Bsnd in mice Nomura N, Kamiya K, Ikeda K, Yui N, Chiga M, Sohara E, Rai T, Sakaki S, Uchida S Biochemical and Biophysical Research Communications, 441(3), 544, 2013 |
2 |
Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever! Marlin S, Feldmann D, Nguyen Y, Rouillon I, Loundon N, Jonard L, Bonnet C, Couderc R, Garabedian EN, Petit C, Denoyelle F Biochemical and Biophysical Research Communications, 394(3), 737, 2010 |
3 |
Study of modifiers factors associated to mitochondrial mutations in individuals with hearing impairment de Moraes VCS, Alexandrino F, Andrade PB, Camara MF, Sartorato EL Biochemical and Biophysical Research Communications, 381(2), 210, 2009 |
4 |
Mutation in gap and tight junctions in patients with non-syndromic hearing loss Belguith H, Tlili A, Dhouib H, Ben Rebeh I, Lahmar I, Charfeddine I, Driss N, Ghorbel A, Ayadi H, Masmoudi S Biochemical and Biophysical Research Communications, 385(1), 1, 2009 |
5 |
Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in North Indian patients with non-syndromic hearing impairment Bhalla S, Sharma R, Khandelwal G, Panda NK, Khullar M Biochemical and Biophysical Research Communications, 385(3), 445, 2009 |
6 |
Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment Ballana E, Morales E, Rabionet R, Montserrat B, Ventayol M, Bravo O, Gasparini P, Estivill X Biochemical and Biophysical Research Communications, 341(4), 950, 2006 |
7 |
Correspondence regarding Ballana et al., "Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment" Abreu-Silva RS, Batissoco AC, Lezirovitz K, Romanos J, Rincon D, Auricchio MTBM, Otto PA, Mingroni-Netto RC Biochemical and Biophysical Research Communications, 343(3), 675, 2006 |
8 |
Identification of a novel Cochlin isoform in the perilymph: insights to Cochlin function and the pathogenesis of DFNA9 Ikezono T, Shindo S, Li LS, Omori A, Ichinose S, Watanabe A, Kobayashi T, Pawankar R, Yag T Biochemical and Biophysical Research Communications, 314(2), 440, 2004 |