Alexey V. Pshezhetsky
3640 University Street
Montreal, QC H3A0C7, Canada
Montreal, QC H3A0C7, Canada
Last Updated: 09/26/2026
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Found 60 publications
Cellular homeostasis of N-acetylneuraminic acid and non-canonical sialic acids is mediated by human N-acetylneuraminate lyase.
Journal: Glycobiology
Published: January 24, 2026
Mono-allelic p.R37H Dehydrodolichyl Diphosphate Synthase variants lead to protein glycosylation defects, aberrant lipid profiles and interneuron scarcity in a novel mouse model of progressive epileptic encephalopathy.
Journal: bioRxiv : the preprint server for biology
Published: September 02, 2025
Mucopolysaccharidosis Type IIIB With Pancytopenia: A Case Report and Hematological Correlations in Mice.
Journal: Clinical genetics
Published: February 24, 2025
Cathepsin B inhibition blocks amyloidogenesis in the mouse models of neurological lysosomal diseases MPS IIIC and sialidosis.
Journal: Molecular therapy. Methods & clinical development
Published: May 13, 2024
Secondary deficiency of neuraminidase 1 contributes to CNS pathology in neurological mucopolysaccharidoses via hypersialylation of brain glycoproteins.
Journal: bioRxiv : the preprint server for biology
Published: May 07, 2024
Anti-amyloid treatment is broadly effective in neuronopathic mucopolysaccharidoses and synergizes with gene therapy in MPS-IIIA.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: May 03, 2024
Neuraminidase 1 secondary deficiency contributes to CNS pathology in neurological mucopolysaccharidoses via brain protein hypersialylation.
Journal: The Journal of clinical investigation
Published: January 26, 2024
Structure and mechanism of lysosome transmembrane acetylation by HGSNAT.
Journal: Nature structural & molecular biology
Published: October 20, 2023
Severe central nervous system demyelination in Sanfilippo disease.
Journal: Frontiers in molecular neuroscience
Published: October 17, 2023
N-acetylneuraminate pyruvate lyase controls sialylation of muscle glycoproteins essential for muscle regeneration and function.
Journal: Science advances
Published: June 30, 2023
Characterization of a phenotypically severe animal model for human AB-Variant GM2 gangliosidosis.
Journal: Frontiers in molecular neuroscience
Published: June 19, 2023
Last Updated: 09/26/2026