Weixing Li

发表

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.

Fine Mapping of a Novel Major Quantitative Trait Locus, qPAA7, That Controls Panicle Apical Abortion in Rice

Xiaolei Wang, Lifang Hu, Haihui Fu, 2021, Frontiers in Plant Science.

Screening for specific biomarkers in the serum of postmenopausal osteoporosis patients using proteomic fingerprint techniques.

Chibo Liu, Weixing Li, Haibao Wang, 2013, Biomedical reports.

Whole Exome Sequencing Identified a Novel Biallelic SMARCAL1 Mutation in the Extremely Rare Disease SIOD

Zhen Wang, Zhenwei Liu, Shan Jiang, 2019, Front. Genet..

Glutathione S-transferase P1 Ile105Val Polymorphism and Oral Cancer Risk: A Meta-Analysis

Jiayu Chen, Chibo Liu, Weixing Li, 2013, International journal of medical sciences.

Nitroxide pharmaceutical development for age-related degeneration and disease

Vienna E. Brunt, C. Minson, Weixing Li, 2015, Front. Genet..

The tRNAGly T10003C mutation in mitochondrial haplogroup M11b in a Chinese family with diabetes decreases the steady-state level of tRNAGly, increases aberrant reactive oxygen species production, and reduces mitochondrial membrane potential

Weixing Li, Wanlin Zhang, Wei Li, 2015, Molecular and Cellular Biochemistry.

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.

The −344C/T polymorphism in the CYP11B2 gene is associated with essential hypertension in the Chinese

Chibo Liu, Weixing Li, 2014, Journal of the renin-angiotensin-aldosterone system : JRAAS.

RETRACTED ARTICLE: TGF-β1 −509C/T (or +869T/C) polymorphism might be not associated with hepatocellular carcinoma risk

Han Wu, Weixing Li, Chao Song, 2013, Tumor Biology.

Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNA(Gly) gene.

Ronghua Li, J. Mo, Meng Wang, 2015, Mitochondrion.

The tRNAGly T10003C mutation in mitochondrial haplogroup M11b in a Chinese family with diabetes decreases the steady-state level of tRNAGly, increases aberrant reactive oxygen species production, and reduces mitochondrial membrane potential

Wei Li, Jianxin Lu, Weixing Li, 2015, Molecular and Cellular Biochemistry.