Rafael G. Costa
Faro, Portugal
Last Updated: 09/26/2026
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Found 8 publications
Lentiviral-induced Striatal Pathology as a Preclinical Model of Polyglutamine Spinocerebellar Ataxias.
Journal: Journal of visualized experiments : JoVE
Published: March 30, 2026
Modulation of the Stress Granule Component Carhsp1 Mitigates Disease-Associated Deficits in Spinocerebellar Ataxia Type 3 Mouse Models.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: November 03, 2025
Molecular hallmarks of neurodegeneration in polyglutamine spinocerebellar ataxias.
Journal: Cell death & disease
Published: January 19, 2025
The polyglutamine protein ATXN2: from its molecular functions to its involvement in disease.
Journal: Cell death & disease
Published: January 13, 2024
The stress granule protein G3BP1 alleviates spinocerebellar ataxia-associated deficits.
Journal: Brain : a journal of neurology
Published: November 29, 2021
Autophagy in Spinocerebellar ataxia type 2, a dysregulated pathway, and a target for therapy.
Journal: Cell death & disease
Published: June 22, 2021
The cholesterol 24-hydroxylase activates autophagy and decreases mutant huntingtin build-up in a neuroblastoma culture model of Huntington's disease.
Journal: BMC research notes
Published: February 29, 2020
Kidney transplantation across a positive crossmatch: a single-center experience.
Journal: Transplantation proceedings
Published: August 19, 2014
Showing 1-8 of 8
Last Updated: 09/26/2026