Takeshi Chujo
Kumamoto, Japan
Last Updated: 09/26/2026
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Found 31 publications
Mitochondrial tRNA modifications: functions, diseases caused by their loss, and treatment strategies.
Journal: RNA (New York, N.Y.)
Published: December 24, 2024
Neurological Diseases Caused by Loss of Transfer RNA Modifications: Commonalities in Their Molecular Pathogenesis.
Journal: Journal of molecular biology
Published: October 24, 2024
Monitoring the complexity and dynamics of mitochondrial translation.
Journal: Molecular cell
Published: June 06, 2024
Human DUS1L catalyzes dihydrouridine modification at tRNA positions 16/17, and DUS1L overexpression perturbs translation.
Journal: Communications biology
Published: February 16, 2024
TRMT10A dysfunction perturbs codon translation of initiator methionine and glutamine and impairs brain functions in mice.
Journal: Nucleic acids research
Published: November 08, 2023
Landscape of semi-extractable RNAs across five human cell lines.
Journal: Nucleic acids research
Published: October 03, 2022
Pathological mutations promote proteolysis of mitochondrial tRNA-specific 2-thiouridylase 1 (MTU1) via mitochondrial caseinolytic peptidase (CLPP).
Journal: Nucleic acids research
Published: May 19, 2022
Last Updated: 09/26/2026