Stephane Lefrancois
Laval, QC, Canada
Last Updated: 09/26/2026
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Found 22 publications
CLN5 disease-causing mutations impact lysosomal biology by affecting intracellular degradation and protein trafficking.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: December 21, 2025
Determining Lysosomal Enzyme Activity Using Fluorogenic Probes.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: October 13, 2025
Phosphorylation on serine 72 modulates Rab7A palmitoylation and retromer recruitment.
Journal: Journal of cell science
Published: April 04, 2024
Correction: A lysosomal enigma CLN5 and its significance in understanding neuronal ceroid lipofuscinosis.
Journal: Cellular and molecular life sciences : CMLS
Published: November 10, 2023
The Batten disease protein CLN3 is important for stress granules dynamics and translational activity.
Journal: The Journal of biological chemistry
Published: January 24, 2023
Mechanisms regulating the sorting of soluble lysosomal proteins.
Journal: Bioscience reports
Published: December 14, 2021
Autophagy in the Neuronal Ceroid Lipofuscinoses (Batten Disease).
Journal: Frontiers in cell and developmental biology
Published: November 10, 2021
CLN3, at the crossroads of endocytic trafficking.
Journal: Neuroscience letters
Published: April 13, 2021
CLN5 and CLN3 function as a complex to regulate endolysosome function.
Journal: The Biochemical journal
Published: March 15, 2021
A lysosomal enigma CLN5 and its significance in understanding neuronal ceroid lipofuscinosis.
Journal: Cellular and molecular life sciences : CMLS
Published: December 23, 2020
Cu-catalyzed click conjugation of cobalamin to a BODIPY-based fluorophore: A versatile tool to explore the cellular biology of vitamin B12.
Journal: Journal of inorganic biochemistry
Published: November 02, 2019
CLN3 regulates endosomal function by modulating Rab7A-effector interactions.
Journal: Journal of cell science
Published: May 10, 2019
Last Updated: 09/26/2026