Associated Papers
Annexin A11 mutations are associated with nuclear envelope dysfunction in vivo and in human tissues.
Marchica V et al.
Brain : a Journal of Neurology, 2025
Human TDP43 is required for ALS‑related annexin A11 toxicity in Drosophila.
Barnard J et al.
Biomedical Reports, 2024
Decoding Missense Variants by Incorporating Phase Separation via Machine Learning.
Feng M et al.
Nature Communications, 2024
Genetic and in silico analysis of Indian sporadic young onset patient with amyotrophic lateral sclerosis.
Roychowdhury S et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2024
Genetic variability in sporadic amyotrophic lateral sclerosis.
Van Daele SH et al.
Brain : a Journal of Neurology, 2023
Generation of an Open-Access Patient-Derived iPSC Biobank for Amyotrophic Lateral Sclerosis Disease Modelling.
Hedges EC et al.
Genes, 2023
An atypical ALS with PSP-like symptoms caused by ANXA11 p.D40G mutation: A case report and literature review.
Zhang X et al.
Frontiers in Neurology, 2023
ANXA11 mutations are associated with amyotrophic lateral sclerosis-frontotemporal dementia.
Wang Y et al.
Frontiers in Neurology, 2022
Clinical and genetic characteristics of amyotrophic lateral sclerosis patients with ANXA11 variants.
Sung W et al.
Brain Communications, 2022
A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features.
Sainouchi M et al.
Acta Neuropathologica Communications, 2021
Generation of six induced pluripotent stem cell lines from patients with amyotrophic lateral sclerosis with associated genetic mutations in either FUS or ANXA11.
Hedges EC et al.
Stem Cell Research, 2021
Structure of the ALS Mutation Target Annexin A11 Reveals a Stabilising N-Terminal Segment.
Lillebostad PAG et al.
Biomolecules, 2020
RNA Granules Hitchhike on Lysosomes for Long-Distance Transport, Using Annexin A11 as a Molecular Tether.
Liao YC et al.
Cell, 2019
Two rare variants of the ANXA11 gene identified in Chinese patients with amyotrophic lateral sclerosis.
Liu X et al.
Neurobiology of Aging, 2019
ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia.
Zhang K et al.
Neurology. Genetics, 2018
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis.
Smith BN et al.
Science Translational Medicine, 2017
Unraveling the multifaceted insights into amyotrophic lateral sclerosis: Genetic underpinnings, pathogenesis, and therapeutic horizons.
Sharma R et al.
Mutation Research. Reviews in Mutation Research, 0