Associated Papers
Matrin-3 forms spherical and wormlike assemblies that are modulated by RNA binding and ALS/FTD-associated mutations.
Sprunger ML et al.
Molecular Cell, 2025
The role of Matrin-3 in physiology and its dysregulation in disease.
Sprunger ML et al.
Biochemical Society Transactions, 2024
MATR3's Role beyond the Nuclear Matrix: From Gene Regulation to Its Implications in Amyotrophic Lateral Sclerosis and Other Diseases.
Santos JR et al.
Cells, 2024
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
37638449 (PubMed )
Supplement: jnd-10-jnd230148-s001.xlsx › variant_list
Matrin 3 in neuromuscular disease: physiology and pathophysiology.
Malik AM et al.
Jci Insight, 2021
Matrin3: Disorder and ALS Pathogenesis.
Salem A et al.
Frontiers in Molecular Biosciences, 2021
High-Throughput Genetic Testing in ALS: The Challenging Path of Variant Classification Considering the ACMG Guidelines.
Lattante S et al.
Genes, 2020
32987860 (PubMed )
Supplement: genes-11-01123-s001.zip › Supplementary_Table_I.xlsx › Variant_list
RNA-recognition motif in Matrin-3 mediates neurodegeneration through interaction with hnRNPM.
Ramesh N et al.
Acta Neuropathologica Communications, 2020
The NGS technology for the identification of genes associated with the ALS. A systematic review.
Pecoraro V et al.
European Journal of Clinical Investigation, 2020
Novel genes associated with amyotrophic lateral sclerosis: diagnostic and clinical implications.
Chia R et al.
The Lancet. Neurology, 2018
ALS Associated Mutations in Matrin 3 Alter Protein-Protein Interactions and Impede mRNA Nuclear Export.
Boehringer A et al.
Scientific Reports, 2017
Matrin 3 variants are frequent in Italian ALS patients.
Marangi G et al.
Neurobiology of Aging, 2017
Mutational analysis of MATR3 in Taiwanese patients with amyotrophic lateral sclerosis.
Lin KP et al.
Neurobiology of Aging, 2015
Select a paper to view details