A FUS gene variant was linked to tremor and movement symptoms in a young adult with motor neuron disease
Mainly of interest to researchers studying FUS variants and phenotypic heterogeneity.
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A gene in which changes can cause ALS/MND, sometimes with an earlier age of onset. Every Feed story mentioning it, newest first.
Showing 20 of 943 stories
Mainly of interest to researchers studying FUS variants and phenotypic heterogeneity.
· 7 days ago
Relevant to researchers studying ALS gene discovery, pedigrees and rare-variant methods.
· 18 days ago
Mainly of interest to researchers studying age-dependent ALS genetics and trial design.
· 19 days ago
Relevant to clinicians updating ALS genetic-testing practice and counselling
· 1 month ago
Mainly of interest to researchers studying MND genetics and regional variation
· 1 month ago
Mainly of interest to researchers studying R-loops, TDP-43/FUS, SETX and neurodegeneration
· 1 month ago
Mainly of interest to researchers studying FUS-ALS phenotypes and genotype-phenotype links.
· 1 month ago
Relevant to researchers studying protein pathology, transgenic models, and translational ALS methods.
· 1 month ago
Offers a FUS zebrafish screening platform and mechanistic evidence for tribenzylamine.
· 1 month ago
Provides a broad review of phase separation, protein aggregation and candidate therapeutic strategies involving TDP-43 and FUS.
· 2 months ago
Important for researchers studying FUS toxicity, RNA polymerase II interactions and disease models.
· 6 months ago
Covers current findings across biomarkers, mechanisms, trials, genetics and translational research
· 7 months ago
Provides mechanistic findings on FUS and TDP-43 aggregation, toxicity and ageing in yeast models
· 7 months ago
Provides compartment-specific transcriptomic data and identifies PLK1, extracellular-matrix and axonal pathways for further study.
· 8 months ago
Important for researchers studying FUS biology, nuclear transport and ALS pathogenesis
· August 2025
Provides mechanistic evidence linking multiple ALS-associated RNA-binding proteins, REST and UNC13A in motor neurons.
· July 2025
Relevant to researchers studying iPSC models, glial interactions, RNA processing and gene therapy.
· May 2024
Relevant to researchers studying FUS, TDP-43, synapses and motor-neuron disease models.
· January 2024
Mainly of interest to researchers following new mechanisms, biomarkers, trials and collaborations.
· December 2023
Mainly of interest to researchers studying FUS genotype-phenotype correlations and therapeutic windows.
· September 2022
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