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

Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration.

European journal of neurology - 1 Jan 2008

Venturelli E, Villa C, Scarpini E, Fenoglio C, Guidi I, Lovati C, Marcone A, Cortini F, Scalabrini D, Clerici F, Bresolin N, Mariani C, Cappa S, Galimberti D

Abstract excerpt

The neuronal nitric oxide synthase (nNOS) is abundantly expressed in the brain and its transcripts have been found in the frontal cerebral cortex. Eighty-nine patients with different neurodegenerative tau-related disorders, including 71 patients with frontotemporal lobar degeneration (FTLD), 12 with progressive supranuclear palsy (PSP) and 6 with corticobasal degeneration (CBD), were genotyped for the C276T...

Read the complete abstract on PubMed

Topics

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

Share to Brain
Share to Dementia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Gene Expression Regulation, Enzymologic

Share to Genetic Markers

Share to Genetic Testing

Share to Neurons

Share to Nitric Oxide Synthase Type I

Source

Identifiers

PMID: 18042235
DOI: 10.1111/j.1468-1331.2007.02007.x

Genes

NOS1

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration.PMID 18042235Read ↗

The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration.Semantic proximity Read ↗

Association of Polymorphism of Neuronal Nitric Oxide Synthase Gene with Risk to Parkinson's Disease.Semantic proximity Read ↗

The nitric oxide synthase 3 G894T polymorphism associated with Alzheimer's disease risk: a meta-analysis.Semantic proximity Read ↗

Association between Parkinson's disease and polymorphisms in the nNOS and iNOS genes in a community-based case-control study.Semantic proximity Read ↗

The nitric oxide synthase-3 codon 298 polymorphism is not associated with late-onset sporadic Alzheimer's dementia and Lewy body disease in a sample from Hungary.Semantic proximity Read ↗

Variants in neuronal nitric oxide synthase gene may contribute to increased ischemic stroke susceptibility in a Han Chinese population.Semantic proximity Read ↗

5'-flanking region polymorphism of the neuronal nitric oxide synthase gene with Parkinson's disease in Taiwan.Semantic proximity Read ↗

Association between Alzheimer's disease and the NOS3 gene Glu298Asp polymorphism.Semantic proximity Read ↗

Association of NOS1 gene polymorphisms with cerebral palsy in a Han Chinese population: a case-control study.Semantic proximity Read ↗

Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene.Semantic proximity Read ↗

Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease.Semantic proximity Read ↗

Nitric oxide synthase regulation and diversity: Implications in Parkinson’s diseaseSemantic proximity Read ↗

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