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

Myelin oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy.

Journal of neuroimmunology - 1 Nov 2000

Gomez-Lira M, Marzari M G, Uziel G, Pignatti P, Rizzuto N, Salviati A

Abstract excerpt

We describe four novel sequence variants in the Myelin Oligodendrocyte Glycoprotein (MOG) gene. A total of six sequence variants of the MOG gene were identified in eleven out of 44 ALD patients investigated: G15A, CTC repeat in exon 1, Val142Leu, Val145Ile, 551+68A-->G and 551+77C-->T. Screening studies demonstrated that all these polymorphisms are present in 50 unaffected control male individuals of the same...

Read the complete abstract on PubMed

Topics

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

Share to Adrenoleukodystrophy
Share to DNA Primers
Share to Exons

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Myelin-Associated Glycoprotein

Share to Myelin-Oligodendrocyte Glycoprotein

Share to Myelin Proteins

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 11063846
DOI: 10.1016/s0165-5728(00)00367-2

Genes

MOG

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Myelin oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy.PMID 11063846Read ↗

Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis.Semantic proximity Read ↗

Common variation in the MOG gene influences transcript splicing in humans.Semantic proximity Read ↗

Characterization of cDNA and genomic clones encoding human myelin oligodendrocyte glycoprotein.Semantic proximity Read ↗

A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy.Semantic proximity Read ↗

Myelin oligodendrocyte gene polymorphisms and childhood multiple sclerosis.Semantic proximity Read ↗

Structure of the human myelin/oligodendrocyte glycoprotein gene and multiple alternative spliced isoforms.Semantic proximity Read ↗

Cerebral adrenoleukodystrophy (ALD) in only one of monozygotic twins with an identical ALD genotype.Semantic proximity Read ↗

HLA-G Ins/Del polymorphism and +3142C/G SNP are not related to neuromyelitis optica spectrum disorder (NMOSD) development, disability status or anti-aquaporin 4 presence in Brazilian patients.Semantic proximity Read ↗

X-linked adrenomyeloneuropathy associated with 14 novel ALD-gene mutations: no correlation between type of mutation and age of onset.Semantic proximity Read ↗

Variation of the myelin oligodendrocyte glycoprotein gene is not primarily associated with multiple sclerosis in the Sardinian population.Semantic proximity Read ↗

Learning disability and oligodendrocyte myelin glycoprotein (OMGP) gene in neurofibromatosis type 1.Semantic proximity Read ↗

Identification of a Val 145 Ile substitution in the human myelin oligodendrocyte glycoprotein: lack of association with multiple sclerosis. The Réseau de Recherche Clinique INSERM sur la Susceptibilité Génétique à la Sclérose en Plaques.Semantic proximity Read ↗

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