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

CNS tissue Cu/Zn superoxide dismutase (SOD1) mutations in motor neurone disease (MND).

Neuroreport - 22 Dec 1997

Shaw P J, Tomkins J, Slade J Y, Usher P, Curtis A, Bushby K, Ince P G

Abstract excerpt

DNA extracted from CNS tissue of 79 cases of motor neurone disease (MND) was screened by single strand conformation analysis (SSCA) and heteroduplex analysis (HA) for mutations in the Cu/Zn superoxide dismutase (SOD1) gene. The aims were to determine whether somatic mutations of SOD1 may underlie...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to Base Sequence
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cerebral Cortex

Share to Molecular Sequence Data

Share to Mutation

Share to Polymorphism, Single-Stranded Conformational

Share to Superoxide Dismutase

Source

Identifiers

PMID: 9462467
DOI: 10.1097/00001756-199712220-00016

Genes

SOD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-9462467-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

CNS tissue Cu/Zn superoxide dismutase (SOD1) mutations in motor neurone disease (MND).PMID 9462467Read ↗

Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputesSemantic proximity Read ↗

Novel single nucleotide polymorphisms in the superoxide dismutase 1 and 2 genes among children with myelomeningocele.Semantic proximity Read ↗

Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation.Semantic proximity Read ↗

Detection of mutations in whole genome-amplified DNA from laser-microdissected neurons.Semantic proximity Read ↗

Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients.Semantic proximity Read ↗

Mutant copper-zinc superoxide dismutase binds to and destabilizes human low molecular weight neurofilament mRNA.Semantic proximity Read ↗

Phenotypic heterogeneity in motor neuron disease patients with CuZn-superoxide dismutase mutations in Scandinavia.Semantic proximity Read ↗

The p150 subunit of dynactin (DCTN1) gene in multiple sclerosis.Semantic proximity Read ↗

Manganese-containing superoxide dismutase signal sequence polymorphism associated with sporadic motor neuron disease.Semantic proximity Read ↗

Absence of mutations in the Mn superoxide dismutase or catalase genes in familial amyotrophic lateral sclerosis.Semantic proximity Read ↗

Sporadic ALS associated with the D90A Cu,Zn superoxide dismutase mutation in Russia.Semantic proximity Read ↗

Equine motor neuron disease is not linked to Cu/Zn superoxide dismutase mutations: sequence analysis of the equine Cu/Zn superoxide dismutase cDNA.Semantic proximity Read ↗

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