Publications by authors named "Abigail D Wilson"

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Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy.
Natalia Dominik, Stephanie Efthymiou, Christopher J Record, Xinyu Miao, Renee Q Lin, Abigail D Wilson, Wilson Marques, Lindsay A Wilson

J Clin Invest· December 2025

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Modulation of a critical period for motor development in Drosophila by BK potassium channels.
Simon A Lowe, Abigail D Wilson, Gabriel N Aughey, Animesh Banerjee, Talya Goble

Curr Biol· August 2024

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Acidic environments trigger intracellular H+-sensing FAK proteins to re-balance sarcolemmal acid-base transporters and auto-regulate cardiomyocyte pH.
Abigail D Wilson, Mark A Richards, M Kate Curtis, Mala Gunadasa-Rohling, Stefania Monterisi

Cardiovasc Res· November 2022

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The V2475F CPVT1 mutation yields distinct RyR2 channel populations that differ in their responses to cytosolic Ca and Mg.
Abigail D Wilson, Jianshu Hu, Charalampos Sigalas, Elisa Venturi, Héctor H Valdivia

J Physiol· December 2021

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Quantitative RyR1 reduction and loss of calcium sensitivity of RyR1Q1970fsX16+A4329D cause cores and loss of muscle strength.
Moran Elbaz, Alexis Ruiz, Christoph Bachmann, Jan Eckhardt, Pawel Pelczar, Abigail D Wilson

Hum Mol Genet· September 2019

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Simvastatin activates single skeletal RyR1 channels but exerts more complex regulation of the cardiac RyR2 isoform.
Elisa Venturi, Chris Lindsay, Sabine Lotteau, Zhaokang Yang, Emma Steer, Abigail D Wilson

Br J Pharmacol· March 2018

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Dampened activity of ryanodine receptor channels in mutant skeletal muscle lacking TRIC-A.
Sam El-Ajouz, Elisa Venturi, Katja Witschas, Matthew Beech, Abigail D Wilson

J Physiol· July 2017

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Synthesis and use of isotope-labelled substrates for a mechanistic study on human alpha-methylacyl-CoA racemase 1A (AMACR; P504S).
Daniel J Darley, Danica S Butler, Samuel J Prideaux, Thomas W Thornton, Abigail D Wilson

Org Biomol Chem· February 2009

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