Li R, Qiu Q, Jiang P, Xue L, Lu Y, Song Y, Han J, Lu Z, Zhi S, Mo JQ, Guan MX. Mitochondrial tRNA Mutations are Associated with Maternally Inherited Hypertension in two Han Chinese Pedigrees. Hum Mutat. 2012;33(8):1285-93.
Wang S, Li R, Fettermann A, Li Z, Liu Y, Wang X, Zhou A, Yang L, Taschner A, Rossmanith W, Guan MX. Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese family. Circulation Res. 2011;108(7):862-70.
Yan N, Cai S,Guo B, Yi M, Zhu J, Chen J, Zhang T, Li R* and Liu X*. A novel mitochondrial tRNA(Val) T1658C mutation identified in a CPEO family. Mol Vision. 2010;16:1736-42. (*Co-correspondence author)
Li R, Guan MX. Human mitochondrial leucyl-tRNA synthetase corrected mitochondrial dysfunctions due to the MELAS and diabetes associated tRNALeu(UUR) A3243G mutation. Mol Cell Biol. 2010;30; 9: 2147-54.
Li R, Tang X, Zheng J, Cai Q, Zhang T, Gong S, Zheng W, He X, Zhu Y, Xue L, Yang A, Yang L, Lu J, Guan MX. Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family. Mol Genet Metab. 2010;100;1:57-64.
Li R, Liu Y, Li Z, Yang L, Wang S, Guan MX. Failures in mitochondrial tRNAMet and tRNAGln metabolism caused by the novel 4401A>G mutation are involved in essential hypertension in a Han Chinese Family. Hypertension. 2009;54;2:329-37.
Li R, Liu Y, Li Z, Wang XJ, Yang L, Wang S, Guan MX. Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree. Hypertension. 2009;53;6:1083-90.