Li Yang

发表

The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree

Yan Wang, J. Mo, M. Guan, 2011, European Journal of Human Genetics.

Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation.

J. Qu, Xiangtian Zhou, M. Guan, 2010, Molecular genetics and metabolism.

Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation.

W. Cai, J. Qu, Lifei Wang, 2010, Molecular genetics and metabolism.

Mitochondrial tRNA(Glu) A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family.

M. Guan, Li Yang, Yu Ding, 2009, Journal of genetics and genomics = Yi chuan xue bao.

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 pedigrees

Ronghua Li, Zhihua Tao, M. Guan, 2008, American journal of medical genetics. Part A.

Maternally inherited hypertension is associated with the mitochondrial tRNA(Ile) A4295G mutation in a Chinese family.

Yuqi Liu, Zongbin Li, M. Guan, 2008, Biochemical and biophysical research communications.

The mitochondrial ND1 T3308C mutation in a Chinese family with the secondary hypertension.

Yuqi Liu, Zongbin Li, M. Guan, 2008, Biochemical and biophysical research communications.

Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation.

Yaping Qian, Zhihua Tao, M. Guan, 2007, Gene.

Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.

Fangli Wu, J. Greinwald, Zhihua Tao, 2007, Gene.

Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics

Jing Zheng, Li Yang, Min-Xin Guan, 2011, Journal of Translational Medicine.

Maternally Inherited Essential Hypertension Is Associated With the Novel 4263A>G Mutation in the Mitochondrial tRNAIle Gene in a Large Han Chinese Family

Yuqi Liu, Zongbin Li, Ronghua Li, 2011, Circulation research.

Mitochondrial Transfer RNAMet 4435A>G Mutation Is Associated With Maternally Inherited Hypertension in a Chinese Pedigree

Yuqi Liu, Zongbin Li, Ronghua Li, 2009, Hypertension.

Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss.

Ronghua Li, M. Guan, L. Xue, 2010, Mitochondrion.

Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.

Ronghua Li, Yaping Qian, Zhihua Tao, 2010, Mitochondrion.

Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.

J. Qu, F. Lu, Yu Zhang, 2010, Molecular genetics and metabolism.

Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family.

Ronghua Li, M. Guan, Ting Zhang, 2010, Molecular genetics and metabolism.

Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families.

W. Cai, Yan Wang, J. Qu, 2010, Biochemical and biophysical research communications.

Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation.

J. Qu, Xiaoling Liu, Xiangtian Zhou, 2010, Biochimica et biophysica acta.

Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation

Hui Zhao, Qiuju Wang, J. Greinwald, 2005, American journal of medical genetics. Part A.

Failures in Mitochondrial tRNAMet and tRNAGln Metabolism Caused by the Novel 4401A>G Mutation Are Involved in Essential Hypertension in a Han Chinese Family

Yuqi Liu, Zongbin Li, Ronghua Li, 2009, Hypertension.

Maternally transmitted diabetes mellitus associated with the mitochondrial tRNA(Leu(UUR)) A3243G mutation in a four-generation Han Chinese family.

Ronghua Li, Jing Zhao, Yaping Qian, 2006, Biochemical and biophysical research communications.

Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families.

J. Qu, Ying Wang, Xiangtian Zhou, 2010, Investigative ophthalmology & visual science.

Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation.

J. Qu, F. Lu, Xiangtian Zhou, 2009, Biochemical and biophysical research communications.

Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss.

J. Chen, B. Han, Guo-jian Wang, 2008, Mitochondrion.

Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation.

J. Qu, Yan Liu, M. Liang, 2009, Biochemical and biophysical research communications.

Homoplasmy of the G7444A mtDNA and heterozygosity of the GJB2 c.35delG mutations in a family with hearing loss.

G. Korres, Y. Gyftodimou, M. Petersen, 2011, International journal of pediatric otorhinolaryngology.

[Mitochondrial DNA G7444A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation].

Li Yang, Jianxin Lu, Dong-mei Sun, 2008, Yi chuan = Hereditas.

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.

D. Kang, P. Dai, M. Guan, 2007, Biochemical and biophysical research communications.

Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss.

Jiong Cai, Zhihua Tao, M. Guan, 2007, Biochemical and biophysical research communications.

Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese families.

D. Choo, Ronghua Li, Yaping Qian, 2006, Biochemical and biophysical research communications.

Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNASerUCN gene in a Japanese family.

Selena E. Heman-Ackah, Ronghua Li, Yidong Bai, 2005, Biochemical and biophysical research communications.

Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.

J. Qu, Xiangtian Zhou, M. Guan, 2009, Ophthalmology.

Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families.

J. Qu, F. Lu, Yaping Qian, 2006, Biochemical and biophysical research communications.

Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families

Ronghua Li, Yaping Qian, M. Guan, 2008, Pharmacogenetics and genomics.

Mitochondrial Transfer RNA Met 4435A>G Mutation Is Associated With Maternally Inherited Hypertension in a

Yuqi Liu, Zongbin Li, Ronghua Li, 2009 .

Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families.

J. Qu, Xiangtian Zhou, Ying-zi Li, 2011, Ophthalmology.

[Hearing loss and epilepsy may be associated with the novel mitochondrial tRNASer(UCN) 7472delC mutation in a Chinese family].

M. Guan, Li Yang, Dong-mei Sun, 2009, Yi chuan = Hereditas.

The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber's hereditary optic neuropathy and hearing loss.

J. Qu, F. Lu, Xiangtian Zhou, 2007, Biochemical and biophysical research communications.

Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family.

J. Qu, F. Lu, Ronghua Li, 2007, Mitochondrion.

Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics

Ronghua Li, M. Guan, Zhisen Shen, 2011, Journal of Translational Medicine.

The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family.

Zhihua Tao, M. Guan, Li Yang, 2007, Biochemical and biophysical research communications.