Susan E. Maxwell
Oxford, ENG OX39DS, United Kingdom
Last Updated: 09/26/2026
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Found 31 publications
Mouse Model of Fast-Channel Genetic Myasthenic Syndrome Carrying Chrne p.P141L Mutation.
Journal: Biomolecules
Published: April 22, 2026
Identification of SLC45A4 as a pain gene encoding a neuronal polyamine transporter.
Journal: bioRxiv : the preprint server for biology
Published: October 01, 2025
Structures of the human adult muscle-type nicotinic receptor in resting and desensitized states.
Journal: Cell reports
Published: December 02, 2024
SLC45A4 is a pain gene encoding a neuronal polyamine transporter.
Journal: Nature
Published: September 05, 2024
Unraveling the molecular interactions between α7 nicotinic receptor and a RIC3 variant associated with backward speech.
Journal: Cellular and molecular life sciences : CMLS
Published: July 10, 2023
IgG1-3 MuSK Antibodies Inhibit AChR Cluster Formation, Restored by SHP2 Inhibitor, Despite Normal MuSK, DOK7, or AChR Subunit Phosphorylation.
Journal: Neurology(R) neuroimmunology & neuroinflammation
Published: April 06, 2023
Motor end-plate analysis to diagnose immune-mediated myasthenia gravis in seronegative patients.
Journal: Journal of the neurological sciences
Published: June 14, 2022
Slow-Channel Congenital Myasthenic Syndrome due to a Novel Mutation in the Acetylcholine Receptor Alpha Subunit in a South Asian: A Case Report.
Journal: Journal of neuromuscular diseases
Published: November 20, 2020
A rare mutation in the COLQ gene causing congenital myasthenic syndrome with remarkable improvement to fluoxetine: A case report.
Journal: Neuromuscular disorders : NMD
Published: June 12, 2020
Myasthenia gravis AChR antibodies inhibit function of rapsyn-clustered AChRs.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: December 15, 2019
Last Updated: 09/26/2026