F. Meng

发表

Obesity is potentially associated with a novel mitochondrial tRNAGly 10029A>G mutation in a Chinese family

Junfen Fu, Jinling Wang, Ningning Zhao, 2019 .

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.

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.

A deafness-associated mitochondrial DNA mutation caused pleiotropic effects on DNA replication and tRNA metabolism

Meng Wang, M. Guan, Yanchun Ji, 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.

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.

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.

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

Weifeng Zhang, F. Meng, Lijuan Zhu, 2019, Inflammopharmacology.

P.9.10 Deleting exon 55 from the nebulin gene induces severe muscle weakness in a mouse model for nemaline myopathy

C. Ottenheijm, A. Beggs, C. Poggesi, 2013, Neuromuscular Disorders.

Transcriptional landscape of the human cell cycle

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

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.

Novel Insights Into Triple-Negative Breast Cancer Prognosis by Comprehensive Characterization of Aberrant Alternative Splicing

Changhong Lai, Yong Liang, Zhijian Song, 2020, Frontiers in Genetics.

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

Hua Li, S. Fan, Yi Sun, 2019, JCI insight.

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.

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 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.

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.

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

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

Asymmetrical effects of deafness-associated mitochondrial DNA 7516delA mutation on the processing of RNAs in the H-strand and L-strand polycistronic transcripts

Qinghai Zhang, Haibo Wang, Meng Wang, 2020, Nucleic acids research.

Mitochondrial tRNA mutations in Chinese children with tic disorders

T. Zhu, Yanchun Ji, P. Jiang, 2020, Bioscience reports.

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.

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.

Contribution of the tRNAIle 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation

Q. Shu, J. Mo, Meng Wang, 2018, The Journal of Biological Chemistry.

Mechanistic insights into mitochondrial tRNAAla 3’-end metabolism deficiency

H. Chen, Meng Wang, M. Guan, 2021, The Journal of biological chemistry.

Mitochondrial tRNA mutations in 887 Chinese Subjects with Hearing Loss.

Haibo Wang, M. Guan, Yanchun Ji, 2020, Mitochondrion.

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.

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.

Contribution of the tRNA Ile 4317A 3 G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A 3 G mutation

J. Mo, Meng Wang, M. Guan, 2018 .

disksurf: Extracting the 3D Structure of Protoplanetary Disks

Jane Huang, R. Teague, C. Law, 2021, J. Open Source Softw..

Reply to comments on: “Obesity associated with a novel mitochondrial tRNACys 5802A>G mutation in a Chinese family”

Junfen Fu, Jinling Wang, Ningning Zhao, 2020, Bioscience reports.

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

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

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

H. Ji, Yang Zhang, Zhen Shao, 2021, Genome Biology.

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

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