검색결과 : 24건
| No. | Article |
|---|---|
| 1 |
Altered mitochondrial DNA methylation and mitochondrial DNA copy number in an APP/PS1 transgenic mouse model of Alzheimer disease Xu YY, Xu LL, Han M, Liu XT, Li F, Zhou XY, Wang Y, Bi JZ Biochemical and Biophysical Research Communications, 520(1), 41, 2019 |
| 2 |
Discrimination of A1555G and C1494T Point Mutations in the Mitochondrial 12S rRNA Gene by On/Off Switch Guo ZF, Guo WS, Xiao L, Gao GQ, Lan F, Lu XG, Li K, Liao DF Applied Biochemistry and Biotechnology, 166(1), 234, 2012 |
| 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 |
A mutation in mitochondrial 12S rRNA, A827G, in Argentinean family with hearing loss after aminoglycoside treatment Chaig MR, Zernotti ME, Soria NW, Romero OF, Romero MF, Gerez NM Biochemical and Biophysical Research Communications, 368(3), 631, 2008 |
| 5 |
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 |
| 6 |
Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy Elstner M, Schmidt C, Zingler VC, Prokisch H, Bettecken T, Elson JL, Rudolph G, Bender A, Halmagyi GM, Brandt T, Strupp M, Klopstock T Biochemical and Biophysical Research Communications, 377(2), 379, 2008 |
| 7 |
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 |
| 8 |
The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss Han DY, Dai P, Zhu QW, Lin X, Huang DL, Yuan YY, Yuan HJ, Wang XJ, Qian YP, Young WY, Guan MX Biochemical and Biophysical Research Communications, 357(2), 554, 2007 |
| 9 |
The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber's hereditary optic neuropathy and hearing loss Wei QP, Zhou XT, Yang L, Sun YH, Zhou J, Li G, Jiang R, Lu F, Qu J, Guan MX Biochemical and Biophysical Research Communications, 357(4), 910, 2007 |
| 10 |
Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss Yuan H, Chen J, Llu X, Cheng J, Wang X, Yang L, Yang S, Cao J, Kang D, Dal P, Zhai S, Han D, Young WY, Guan MX Biochemical and Biophysical Research Communications, 362(1), 94, 2007 |