Agnes Delahodde
Gif-sur-yvette, 91190, France
Last Updated: 09/26/2026
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Found 24 publications
The copper ionophore disulfiram improves mitochondrial function in various yeast and human cellular models of mitochondrial diseases.
Journal: Human molecular genetics
Published: October 15, 2024
Nifuroxazide rescues the deleterious effects due to CHCHD10-associated MICOS defects in disease models.
Journal: Brain : a journal of neurology
Published: February 23, 2024
Developmental Consequences of Defective ATG7-Mediated Autophagy in Humans.
Journal: The New England journal of medicine
Published: June 23, 2021
A Yeast-Based Screening Unravels Potential Therapeutic Molecules for Mitochondrial Diseases Associated with Dominant ANT1 Mutations.
Journal: International journal of molecular sciences
Published: March 19, 2021
Efficient clofilium tosylate-mediated rescue of POLG-related disease phenotypes in zebrafish.
Journal: Cell death & disease
Published: June 28, 2020
Autophagy facilitates mitochondrial rebuilding after acute heat stress via a DRP-1-dependent process.
Journal: The Journal of cell biology
Published: September 23, 2019
Contribution of ERMES subunits to mature peroxisome abundance.
Journal: PloS one
Published: October 05, 2018
Chemicals or mutations that target mitochondrial translation can rescue the respiratory deficiency of yeast bcs1 mutants.
Journal: Biochimica et biophysica acta. Molecular cell research
Published: July 13, 2017
Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy.
Journal: American journal of human genetics
Published: March 28, 2017
FDXR Mutations Cause Sensorial Neuropathies and Expand the Spectrum of Mitochondrial Fe-S-Synthesis Diseases.
Journal: American journal of human genetics
Published: February 10, 2017
Last Updated: 09/26/2026