Feilong Meng
Hangzhou, 310051, China
Last Updated: 09/26/2026
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Found 26 publications
Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: May 11, 2026
Leber's hereditary optic neuropathy-associated ND1 3733G>C mutation ameliorates the mitochondrial quality control and cellular homeostasis.
Journal: The Journal of biological chemistry
Published: May 26, 2025
Deafness-associated tRNAPhe mutation impaired mitochondrial and cellular integrity.
Journal: The Journal of biological chemistry
Published: January 06, 2024
Human TRUB1 is a highly conserved pseudouridine synthase responsible for the formation of Ψ55 in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro.
Journal: Nucleic acids research
Published: July 19, 2022
Mitochondrial tRNA variants in 811 Chinese probands with Leber's hereditary optic neuropathy.
Journal: Mitochondrion
Published: March 08, 2022
Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations.
Journal: Investigative ophthalmology & visual science
Published: June 22, 2021
Mechanistic insights into mitochondrial tRNAAla 3'-end metabolism deficiency.
Journal: The Journal of biological chemistry
Published: March 16, 2021
An animal model for mitochondrial tyrosyl-tRNA synthetase deficiency reveals links between oxidative phosphorylation and retinal function.
Journal: The Journal of biological chemistry
Published: September 09, 2020
Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy.
Journal: The Journal of biological chemistry
Published: May 28, 2020
Mitochondrial tRNA mutations in Chinese Children with Tic Disorders.
Journal: Bioscience reports
Published: May 27, 2020
Last Updated: 09/26/2026