Feilong Meng

发表

Obesity associated with a novel mitochondrial tRNACys 5802A>G mutation in a Chinese family

Junfen Fu, Jinling Wang, Ningning Zhao, 2019, Bioscience reports.

Tild-CRISPR Allows for Efficient and Precise Gene Knockin in Mouse and Human Cells.

Zi-jiang Chen, Wenqin Ying, Hui Yang, 2018, Developmental cell.

Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy

Rulai Yang, Yun Xiao, M. Guan, 2020, The Journal of Biological Chemistry.

Human TRUB1 is a highly conserved pseudouridine synthase responsible for the formation of Ψ55 in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro

Meng Wang, M. Guan, Feilong Meng, 2022, Nucleic acids research.

Mitochondrial tRNA variants in 811 Chinese probands with Leber's hereditary optic neuropathy.

J. Mo, Meng Wang, M. Guan, 2022, Mitochondrion.

A systematic dissection of the epigenomic heterogeneity of lung adenocarcinoma reveals two different subclasses with distinct prognosis and core regulatory networks

H. Ji, Yihua Sun, Hui Hong, 2021, Genome Biology.

Anti-arthritic activity of ferulic acid in complete Freund’s adjuvant (CFA)-induced arthritis in rats: JAK2 inhibition

Feilong Meng, Weifeng Zhang, F. Meng, 2019, Inflammopharmacology.

lncRNA GAS5 suppresses rheumatoid arthritis by inhibiting miR-361-5p and increasing PDK4.

Feilong Meng, Weifeng Zhang, Lixin Feng, 2021, Biochemical and biophysical research communications.

Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation*

Ronghua Li, M. Guan, Xiaohui Cang, 2017, The Journal of Biological Chemistry.

Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations

J. Mo, M. Guan, Y. Tong, 2021, Investigative ophthalmology & visual science.

An animal model for mitochondrial tyrosyl-tRNA synthetase deficiency reveals links between oxidative phosphorylation and retinal function

Zengming Zhang, M. Guan, Jian Zou, 2021, The Journal of biological chemistry.

A deafness-associated tRNA mutation caused pleiotropic effects on the m1G37 modification, processing, stability and aminoacylation of tRNAIle and mitochondrial translation

Meng Wang, M. Guan, Xiaohui Cang, 2021, Nucleic acids research.

A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function

Meng Wang, M. Guan, Feilong Meng, 2017, The Journal of Biological Chemistry.

Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNAHis mutation

J. Mo, Yong Liang, M. Guan, 2019, The Journal of Biological Chemistry.

Transcriptional landscape of the human cell cycle

Clifford A. Meyer, Charles Y. Lin, X. Liu, 2017, Proceedings of the National Academy of Sciences.

Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia

Hui-jun Shen, Jianhua Mao, Weiyue Gu, 2022, JCI insight.

Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber’s hereditary optic neuropathy

T. Zhu, Xiaoling Liu, Taosheng Huang, 2018, Human molecular genetics.

Inhibiting neddylation modification alters mitochondrial morphology and reprograms energy metabolism in cancer cells.

Hua Li, Yi Sun, M. Tan, 2019, JCI insight.