Eric A. Shoubridge
Montreal, QC, Canada
Last Updated: 09/26/2026
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Found 62 publications
FASTKD5 processes mitochondrial pre-mRNAs at noncanonical cleavage sites.
Journal: Nucleic acids research
Published: March 07, 2025
Bi-allelic mutations in FASTKD5 are associated with cytochrome c oxidase deficiency and early- to late-onset Leigh syndrome.
Journal: American journal of human genetics
Published: March 04, 2025
CHCHD10P80L knock-in zebrafish display a mild ALS-like phenotype.
Journal: Experimental neurology
Published: June 01, 2024
The human mitochondrial translation factor TACO1 alleviates mitoribosome stalling at polyproline stretches.
Journal: Nucleic acids research
Published: May 28, 2024
Mitochondrial molecular genetics and human disease.
Journal: Human molecular genetics
Published: March 09, 2024
ESYT1 tethers the ER to mitochondria and is required for mitochondrial lipid and calcium homeostasis.
Journal: Life science alliance
Published: August 23, 2023
The role of the mitochondrial outer membrane protein SLC25A46 in mitochondrial fission and fusion.
Journal: Life science alliance
Published: January 09, 2023
SPTLC1 variants associated with ALS produce distinct sphingolipid signatures through impaired interaction with ORMDL proteins.
Journal: The Journal of clinical investigation
Published: May 23, 2022
Loss of mitochondrial Chchd10 or Chchd2 in zebrafish leads to an ALS-like phenotype and Complex I deficiency independent of the mitochondrial integrated stress response.
Journal: Developmental neurobiology
Published: May 17, 2022
Author Correction: A proximity-dependent biotinylation map of a human cell.
Journal: Nature
Published: January 12, 2022
Serine palmitoyltransferase assembles at ER-mitochondria contact sites.
Journal: Life science alliance
Published: October 25, 2021
Last Updated: 09/26/2026