Associated Papers
TUBA4A: The Tale of an Unconventional Tubulin.
Zhu JL et al.
Cytoskeleton (hoboken, N.j.), 2025
A systematic review and functional in-silico analysis of genes and variants associated with amyotrophic lateral sclerosis.
Arreola-Aldape CA et al.
Frontiers in Neuroscience, 2025
De novo and inherited monoallelic variants in TUBA4A cause ataxia and spasticity.
Benkirane M et al.
Brain : a Journal of Neurology, 2024
Yeast Models of Amyotrophic Lateral Sclerosis Type 8 Mimic Phenotypes Seen in Mammalian Cells Expressing Mutant VAPBP56S.
Stump AL et al.
Biomolecules, 2023
In silico analysis of TUBA4A mutations in Amyotrophic Lateral Sclerosis to define mechanisms of microtubule disintegration.
Ganne A et al.
Scientific Reports, 2023
Characterising the Genetic Landscape of Amyotrophic Lateral Sclerosis: A Catalogue and Assessment of Over 1,000 Published Genetic Variants.
McCann EP et al.
Journal of Neuromuscular Diseases, 2023
Multiple roles for the cytoskeleton in ALS.
Liu X et al.
Experimental Neurology, 2022
Novel TUBA4A Variant Associated With Familial Frontotemporal Dementia.
Mol MO et al.
Neurology. Genetics, 2021
Destination Amyotrophic Lateral Sclerosis.
Keon M et al.
Frontiers in Neurology, 2021
Screening for TUBA4A mutations in a large Chinese cohort of patients with ALS: re-evaluating the pathogenesis of TUBA4A in ALS.
Li J et al.
Journal of Neurology, Neurosurgery, and Psychiatry, 2018
Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients.
Perrone F et al.
Neurobiology of Aging, 2017
Amyotrophic lateral sclerosis: recent genetic highlights.
White MA et al.
Current Opinion in Neurology, 2016
New ALS-Related Genes Expand the Spectrum Paradigm of Amyotrophic Lateral Sclerosis.
Sabatelli M et al.
Brain Pathology (zurich, Switzerland), 2016
TUBA4A may not be a significant genetic factor in Chinese ALS patients.
Li J et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2015
Excess of rare damaging TUBA4A variants suggests cytoskeletal defects in ALS.
Rademakers R et al.
Neuron, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.
Smith BN et al.
Neuron, 2014