Associated Papers
A peptide derived from TID1S rescues frataxin deficiency and mitochondrial defects in FRDA cellular models.
Dong YN et al.
Frontiers in Pharmacology, 2024
A novel variant of the human mitochondrial DnaJ protein, Tid1, associates with a human disease exhibiting developmental delay and polyneuropathy.
Patra M et al.
European Journal of Human Genetics : Ejhg, 2019
Identification of a hTid-1 mutation which sensitizes gliomas to apoptosis.
Trentin GA et al.
Febs Letters, 2004
Select a paper to view details