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Article

RNA-Binding Proteins in Amyotrophic Lateral Sclerosis.

Molecules and cells - 30 Sept 2018

Zhao Melody, Kim Jihye Rachel, van Bruggen Rebekah, Park Jeehye

Abstract excerpt

Significant research efforts are ongoing to elucidate the complex molecular mechanisms underlying amyotrophic lateral sclerosis (ALS), which may in turn pinpoint potential therapeutic targets for treatment. The ALS research field has evolved with recent discoveries of numerous genetic mutations in ALS patients, many of which are in genes encoding RNA binding proteins (RBPs), including TDP-43, FUS, ATXN2, TAF15,...

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Source

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Identifiers

PMID: 30157547
DOI: 10.14348/molcells.2018.0243
PMCID: PMC6182225

Genes

ATXN2
EWSR1
FUS
MATR3
TAF15
TIA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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