All Stories

  1. Mitochondrial Morphology and Fundamental Parameters of the Mitochondrial Respiratory Chain Are Altered in Caenorhabditis elegans Strains Deficient in Mitochondrial Dynamics and Homeostasis Processes
  2. PCR Based Determination of Mitochondrial DNA Copy Number in Multiple Species
  3. Effects of 5′-fluoro-2-deoxyuridine on mitochondrial biology in Caenorhabditis elegans
  4. Cellular Toxicity Associated with Exposure to Perfluorinated Carboxylates (PFCAs) and Their Metabolic Precursors
  5. Mitochondria as a Target of Environmental Toxicants
  6. Effects of early life exposure to ultraviolet C radiation on mitochondrial DNA content, transcription, ATP production, and oxygen consumption in developing Caenorhabditis elegans
  7. Increased tRNA modification and gene-specific codon usage regulate cell cycle progression during the DNA damage response
  8. Translational infidelity-induced protein stress results from a deficiency in Trm9-catalyzed tRNA modifications
  9. Cross-species Functionome analysis identifies proteins associated with DNA repair, translation and aerobic respiration as conserved modulators of UV-toxicity
  10. Autophagy-Dependent Regulation of the DNA Damage Response Protein Ribonucleotide Reductase 1
  11. A genome-wide screen in Saccharomyces cerevisiae reveals pathways affected by arsenic toxicity
  12. Systems based mapping demonstrates that recovery from alkylation damage requires DNA repair, RNA processing, and translation associated networks
  13. A genome-wide deletion mutant screen identifies pathways affected by nickel sulfate in Saccharomyces cerevisiae
  14. A molecular bar-coded DNA repair resource for pooled toxicogenomic screens
  15. Trm9-Catalyzed tRNA Modifications Link Translation to the DNA Damage Response
  16. A variant in the HS1-BP3 gene is associated with familial essential tremor
  17. A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardation
  18. Haplotype analysis at the ETM2 locus in a Singaporean sample with familial essential tremor
  19. Candidate genes for recessive non-syndromic mental retardation on chromosome 3p (MRT2A)*