검색결과 : 11건
| No. | Article |
|---|---|
| 1 |
Investigation of mitochondrial sequence variants associated with aminoglycoside-induced ototoxicity in South African TB patients on aminoglycosides Human H, Hagen CM, de Jong G, Harris T, Lombard D, Christiansen M, Bardien S Biochemical and Biophysical Research Communications, 393(4), 751, 2010 |
| 2 |
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 |
| 3 |
A South African family with the mitochondrial A1555G mutation on haplogroup L0d Human H, Lombard D, de Jong G, Bardien S Biochemical and Biophysical Research Communications, 382(2), 390, 2009 |
| 4 |
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 |
| 5 |
The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss Kokotas H, Grigoriadou M, Korres GS, Ferekidou E, Papadopoulou E, Neou P, Giannoulia-Karantana A, Kandiloros D, Korres S, Petersen MB Biochemical and Biophysical Research Communications, 390(3), 755, 2009 |
| 6 |
New polymorphic mtDNA restriction site in the 12S rRNA gene detected in Tunisian patients with non-syndromic hearing loss Mkaouar-Rebai E, Thli A, Masmoudi S, Charfeddine H, Fakhfakh F Biochemical and Biophysical Research Communications, 369(3), 849, 2008 |
| 7 |
Co-occurrence of A1555G and G11778A in a Chinese family with high penetrance of Leber's hereditary optic neuropathy Zhang AM, Jia XY, Yao YG, Zhang QJ Biochemical and Biophysical Research Communications, 376(1), 221, 2008 |
| 8 |
Co-segregation of the T1095C with the A1555G mutation of the mitochondrial 12S rRNA gene in a patient with non-syndromic hearing loss Dai DC, Lu YJ, Chen ZB, Wei QJ, Cao X, Xing GQ Biochemical and Biophysical Research Communications, 377(4), 1152, 2008 |
| 9 |
Mutational analysis of the mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in Tunisian patients with nonsyndromic hearing loss Mkaouar-Rebai E, Tlili A, Masmoudi S, Louhichi N, Charfeddine I, Ben Amor M, Lahmar I, Driss N, Drira M, Ayadi H, Fakhfakh F Biochemical and Biophysical Research Communications, 340(4), 1251, 2006 |
| 10 |
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 |