近期，管敏鑫教授在J Hum Genet/IOVS/JAHA/mitochondrion杂志上发表最新研究成果，如下：

1: Ji Y, Liang M, Zhang J, Zhang M, Zhu J, Meng X, Zhang S, Gao M, Zhao F, Wei QP, Jiang P, Tong Y, Liu X, Qin Mo J, Guan MX. Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation  in Chinese families.J Hum Genet. 2014 Mar;59(3):134-40. doi: 10.1038/jhg.2013.134. Epub 2014 Jan 16. http://www.nature.com/jhg/journal/v59/n3/full/jhg2013134a.html

2: Liang M, Jiang P, Li F, Zhang J, Ji Y, He Y, Xu M, Zhu J, Meng X, Zhao F, Tong Y, Liu X, Sun Y, Zhou X, Mo JQ, Qu J, Guan MX. Frequency and Spectrum of Mitochondrial ND6 Mutations in 1218 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy. Invest Ophthalmol Vis Sci. 2014 Mar 6;55(3):1321-31. http://www.ncbi.nlm.nih.gov/pubmed/24398099

3: Yu J, Xiao Y, Liu J, Ji Y, Liu H, Xu J, Jin X, Liu L, Guan MX, Jiang P. Loss of MED1 triggers mitochondrial biogenesis in C2C12 cells. Mitochondrion. 2014 Jan;14(1):18-25. http://www.ncbi.nlm.nih.gov/pubmed/24368311

4: Qin Y, Xue L, Jiang P, Xu M, He Y, Shi S, Huang Y, He J, Mo JQ, Guan MX. Mitochondrial tRNA variants in Chinese subjects with coronary heart disease. J Am Heart Assoc. 2014 Jan 27;3(1):e000437. doi: 10.1161/JAHA.113.000437. http://www.ncbi.nlm.nih.gov/pubmed/24470521