au.\*:("GUAN, Min-Xin")
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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
Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutationGUAN, Min-Xin; FISCHEL-GHODSIAN, Nathan; ATTARDI, Giuseppe et al.Human molecular genetics (Print). 2001, Vol 10, Num 6, pp 573-580, issn 0964-6906Article
Failures in Mitochondrial tRNAMet and tRNA Gln Metabolism Caused by the Novel 4401A>G Mutation Are Involved in Essential Hypertension in a Han Chinese FamilyRONGHUA LI; YUQI LIU; ZONGBIN LI et al.Hypertension (Dallas, Tex. 1979). 2009, Vol 54, Num 2, pp 329-337, issn 0194-911X, 9 p.Article
Maternally Inherited Essential Hypertension Is Associated With the Novel 4263A>G Mutation in the Mitochondrial tRNAIle 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 tRNAThr 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 tRNAMet 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
Extremely Low Penetrance of Leber's Hereditary Optic Neuropathy in 8 Han Chinese Families Carrying the ND4 G11778A MutationJIA QU; XIANGTIAN ZHOU; GUAN, Min-Xin et al.Ophthalmology (Rochester, MN). 2009, Vol 116, Num 3, pp 558-564, issn 0161-6420, 7 p.Article
Cosegregation of the G7444A mutation in the mitochondrial COI/tRNASer(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 transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial TRNAHis geneXUKUN YAN; XINJIAN WANG; MINGZHI SUN et al.Journal of medical genetics. 2011, Vol 48, Num 10, pp 682-690, issn 0022-2593, 9 p.Article
Mitochondrial ND5 T12338C, tRNACys T5802C, and tRNAThr G15927A Variants May Have a Modifying Role in the Phenotypic Manifestation of Deafness-Associated 12S rRNA A1555G Mutation in Three Han Chinese PedigreesBOBEI CHEN; DONGMEI SUN; RONGHUA LI et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 10, pp 1248-1258, issn 1552-4825, 11 p.Article
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
