Shaun W. Martin
Leuven, VLG 3000, Belgium
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 47 publications
ATP13A3 variants promote pulmonary arterial hypertension by disrupting polyamine transport.
Journal: Cardiovascular research
Published: July 13, 2023
The lipid flippase ATP10B enables cellular lipid uptake under stress conditions.
Journal: Biochimica et biophysica acta. Molecular cell research
Published: June 13, 2023
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
Journal: Autophagy
Published: February 26, 2021
ATP13A2 Regulates Cellular α-Synuclein Multimerization, Membrane Association, and Externalization.
Journal: International journal of molecular sciences
Published: January 31, 2021
ATP13A2-mediated endo-lysosomal polyamine export counters mitochondrial oxidative stress.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: November 24, 2020
Polyamine Transport Assay Using Reconstituted Yeast Membranes.
Journal: Bio-protocol
Published: July 09, 2020
Increased superoxide in GCH1 mutant fibroblasts points to a dopamine-independent toxicity mechanism.
Increased superoxide in GCH1 mutant fibroblasts points to a dopamine-independent toxicity mechanism.
Journal: Parkinsonism & related disorders
Published: June 26, 2020
ATP13A3 is a major component of the enigmatic mammalian polyamine transport system.
Journal: The Journal of biological chemistry
Published: April 15, 2020
Corrigendum to "Concurrent MEK and autophagy inhibition is required to restore cell death associated danger-signalling in Vemurafenib-resistant melanoma cells" [Biochem. Pharmacol. 93 (3) (2015) 290-304].
Journal: Biochemical pharmacology
Published: February 23, 2020
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export.
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export.
Journal: Acta neuropathologica
Published: December 07, 2019
CHCHD2 harboring Parkinson's disease-linked T61I mutation precipitates inside mitochondria and induces precipitation of wild-type CHCHD2.
Journal: Human molecular genetics
Published: December 06, 2019
Last Updated: 09/26/2026