Interaction of Aminoglycosides with Human Mitochondrial 12S rRNA Carrying the Deafness-Associated MutationYAPING QIAN; GUAN, Min-Xin.Antimicrobial agents and chemotherapy. 2009, Vol 53, Num 11, pp 4612-4618, issn 0066-4804, 7 p.Article

The influence of phosphorus on ash fusion temperature of sludge and coalQIANG ZHANG; HAIFENG LIU; YAPING QIAN et al.Fuel processing technology. 2013, Vol 110, pp 218-226, issn 0378-3820, 9 p.Article

Low dose naltrexone administration in morphine dependent rats attenuates withdrawal-induced norepinephrine efflux in forebrainVAN BOCKSTAELE, Elisabeth J; YAPING QIAN; STERLING, Robert C et al.Progress in neuro-psychopharmacology & biological psychiatry. 2008, Vol 32, Num 4, pp 1048-1056, issn 0278-5846, 9 p.Article

Multiple origins of Tibetan Y chromosomesYAPING QIAN; BINZHI QIAN; BING SU et al.Human genetics. 2000, Vol 106, Num 4, pp 453-454, issn 0340-6717Article

Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutationsGUAN, Min-Xin; QINGFENG YAN; SUZUKI, Tsutomu et al.American journal of human genetics. 2006, Vol 79, Num 2, pp 291-302, issn 0002-9297, 12 p.Article

Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA^Ser(UCN) genes with the 12s rRNA A1555G mutation in a chinese family with aminoglycoside-induced and nonsyndromic hearing lossHUIJUN YUAN; YAPING QIAN; GREINWALD, John H et al.American journal of medical genetics. 2005, Vol 138A, Num 2, pp 133-140, issn 0148-7299, 8 p.Article

Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing lossZHIYUAN LI; RONGHUA LI; GUAN, Min-Xin et al.Human genetics. 2005, Vol 117, Num 1, pp 9-15, issn 0340-6717, 7 p.Article

Maternally Inherited Essential Hypertension Is Associated With the Novel 4263A>G Mutation in the Mitochondrial tRNA^Ile Gene in a Large Han Chinese FamilySHIWEN WANG; RONGHUA LI; PINGPING JIANG et al.Circulation research. 2011, Vol 108, Num 7, pp 862-870, issn 0009-7330, 9 p.Article

Mitochondrial tRNA^Thr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese familiesXINJIAN WANG; JIANXIN LU; XUE ZHANG et al.Pharmacogenetics and genomics (Print). 2008, Vol 18, Num 12, pp 1059-1070, issn 1744-6872, 12 p.Article

The novel A4435G mutation in the mitochondrial tRNA^Met may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutationJIA QU; RONGHUA LI; XIANGTIAN ZHOU et al.Investigative ophthalmology & visual science. 2006, Vol 47, Num 2, pp 475-483, issn 0146-0404, 9 p.Article