Woranontee Weraarpachai
Chiang Mai University(TH)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, ATP Synthase and ATPases Research, Metabolism and Genetic Disorders, RNA modifications and cancer, RNA and protein synthesis mechanisms
Most-Cited Works
- → Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome(2009)306 cited
- → MITRAC Links Mitochondrial Protein Translocation to Respiratory-Chain Assembly and Translational Regulation(2012)253 cited
- → A High-Density Human Mitochondrial Proximity Interaction Network(2020)201 cited
- → Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect(2010)159 cited
- → Mutations in C12orf62, a Factor that Couples COX I Synthesis with Cytochrome c Oxidase Assembly, Cause Fatal Neonatal Lactic Acidosis(2012)107 cited
- → Loss of CHCHD10–CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALS(2017)83 cited
- → The 3′ addition of CCA to mitochondrial tRNASer(AGY) is specifically impaired in patients with mutations in the tRNA nucleotidyl transferase TRNT1(2015)72 cited
- → Multi-OMICS study of a CHCHD10 variant causing ALS demonstrates metabolic rewiring and activation of endoplasmic reticulum and mitochondrial unfolded protein responses(2021)65 cited
- → Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature(2015)61 cited
- → Tissue-specific responses to the LRPPRC founder mutation in French Canadian Leigh Syndrome(2014)57 cited