Last Updated: 09/26/2026
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Found 91 publications
Validating a Human Cell Model of Null Galactosylceramidase (GALC) Enzyme Activity That Recapitulates Krabbe Disease.
Journal: Journal of inherited metabolic disease
Published: January 19, 2026
ACOX1 gain-of-function post-mortem neuropathology is distinct from ACOX1 loss-of-function: case report and literature review.
Journal: Free neuropathology
Published: August 18, 2025
Intracranial mesenchymal tumor, FET::CREB fusion-positive: An integrative analysis of 81 cases.
Journal: Neuro-oncology
Published: August 06, 2025
ISG15 negatively regulates RIPK3-mediated cell death and viral pathogenesis.
Journal: Cell reports
Published: July 24, 2025
Case report: Molecular characterization of adult atypical teratoid rhabdoid tumor and review of the literature.
Journal: Frontiers in oncology
Published: October 13, 2024
Atypical free sialic acid storage disorder associated with tissue specific mosaicism of SLC17A5.
Journal: Molecular genetics and metabolism
Published: August 14, 2024
Pmp2+ Schwann Cells Maintain the Survival of Large-Caliber Motor Axons.
Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience
Published: July 16, 2024
Sleep deprivation exacerbates microglial reactivity and Aβ deposition in a TREM2-dependent manner in mice.
Journal: Science translational medicine
Published: April 26, 2023
Schwann Cell Remyelination in the Multiple Sclerosis Central Nervous System.
Journal: Laboratory investigation; a journal of technical methods and pathology
Published: October 10, 2022
Schwann cells and myelin in human peripheral nerve: Major protein components vary with age, axon size and pathology.
Journal: Neuropathology and applied neurobiology
Published: August 15, 2022
Evaluating brain damage in multiple sclerosis with simultaneous multi-angular-relaxometry of tissue.
Evaluating brain damage in multiple sclerosis with simultaneous multi-angular-relaxometry of tissue.
Journal: Annals of clinical and translational neurology
Published: March 23, 2022
Loss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathy.
Journal: Cell reports
Published: March 14, 2022
Last Updated: 09/26/2026