검색결과 : 19건
| No. | Article |
|---|---|
| 1 |
Evaluation of AgClNPs@SBA-15/IL nanoparticle-induced oxidative stress and DNA mutation in Escherichia coli Karimi F, Dabbagh S, Alizadeh S, Rostamnia S Applied Microbiology and Biotechnology, 100(16), 7161, 2016 |
| 2 |
Ultrasensitive Detection of Mitochondrial DNA Mutation by Graphene Oxide/DNA Hydrogel Electrode Sun LP, Hu N, Peng J, Chen LY, Weng J Advanced Functional Materials, 24(44), 6905, 2014 |
| 3 |
Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families Zhang JJ, Zhou XT, Zhou JA, Li CW, Zhao FX, Wang Y, Meng YZ, Wang JY, Yuan MX, Cai WS, Tong Y, Sun YH, Yang L, Qu J, Guan MX Biochemical and Biophysical Research Communications, 399(4), 647, 2010 |
| 4 |
Mechanisms of Unintended Amino Acid Sequence Changes in Recombinant Monoclonal Antibodies Expressed in Chinese Hamster Ovary (CHO) Cells Guo DL, Gao A, Michels DA, Feeney L, Eng M, Chan B, Laird MW, Zhang BY, Yu XC, Joly J, Snedecor B, Shen A Biotechnology and Bioengineering, 107(1), 163, 2010 |
| 5 |
A miniaturized spatial temperature gradient capillary electrophoresis system with radiative heating and automated sample introduction for DNA mutation detection Xu ZR, Li Q, Fan XF, Zhang HD, Fang J Electrophoresis, 31(18), 3137, 2010 |
| 6 |
The mitochondrial ND1 T3308C mutation in a Chinese family with the secondary hypertension Liu YQ, Li ZB, Yang L, Wang S, Guan MX Biochemical and Biophysical Research Communications, 368(1), 18, 2008 |
| 7 |
The mitochondrial tRNA(Glu) A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber's hereditary optic neuropathy Tong Y, Mao YJ, Zhou XT, Yang L, Zhang JJ, Cai WS, Zhao FX, Wang XJ, Lu F, Qu J, Guan MX Biochemical and Biophysical Research Communications, 357(2), 524, 2007 |
| 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 |