Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

RNA processing pathways in amyotrophic lateral sclerosis.

Neurogenetics - 1 Jul 2010

van Blitterswijk Marka, Landers John E

Abstract excerpt

RNA processing is a tightly regulated, highly complex pathway which includes RNA transcription, pre-mRNA splicing, editing, transportation, translation, and degradation of RNA. Over the past few years, several RNA processing genes have been shown to be mutated or genetically associated with amyotrophic lateral sclerosis (ALS), including the RNA-binding proteins TDP-43 and FUS/TLS. These findings suggest that RNA...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to DNA Helicases
Share to Histone Acetyltransferases
Share to Multifunctional Enzymes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ribonuclease, Pancreatic

Share to RNA-Binding Protein FUS

Share to RNA Helicases

Share to RNA Processing, Post-Transcriptional

Share to SMN Complex Proteins

Source

Identifiers

PMID: 20349096
DOI: 10.1007/s10048-010-0239-4

Genes

FUS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

RNA processing pathways in amyotrophic lateral sclerosis.PMID 20349096Read ↗

TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegenerationSemantic proximity Read ↗

Aberrant RNA homeostasis in amyotrophic lateral sclerosis: potential for new therapeutic targets?Semantic proximity Read ↗

RNA Dysregulation in Amyotrophic Lateral SclerosisSemantic proximity Read ↗

RNA quality control and protein aggregates in amyotrophic lateral sclerosis: a review.Semantic proximity Read ↗

Misregulated RNA processing in amyotrophic lateral sclerosisSemantic proximity Read ↗

RNA-binding proteins and RNA metabolism: a new scenario in the pathogenesis of Amyotrophic lateral sclerosis.Semantic proximity Read ↗

Genetic mutations in RNA-binding proteins and their roles in ALS.Semantic proximity Read ↗

RNA binding proteins and the pathological cascade in ALS/FTD neurodegeneration.Semantic proximity Read ↗

Dysregulation of RNA-Binding Proteins in Amyotrophic Lateral SclerosisSemantic proximity Read ↗

Connecting RNA-Modifying Similarities of TDP-43, FUS, and SOD1 with MicroRNA Dysregulation Amidst A Renewed Network Perspective of Amyotrophic Lateral Sclerosis Proteinopathy.Semantic proximity Read ↗

RNA Is a Double-Edged Sword in ALS PathogenesisSemantic proximity Read ↗

The role of RNA processing in the pathogenesis of motor neuron degenerationSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.