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

5'-Upstream variants of CRHR1 and MAPT genes associated with age at onset in progressive supranuclear palsy and cortical basal degeneration.

Neurobiology of disease - 1 Feb 2009

Cruchaga Carlos, Vidal-Taboada Jose M, Ezquerra Mario, Lorenzo Elena, Martinez-Lage Pablo, Blazquez Marta, Tolosa Eduardo, Pastor Pau

Abstract excerpt

Two different H1 sub-haplotypes at chromosome 17q21, H1C and H1E'A, have been associated with progressive supranuclear palsy (PSP) and cortical basal degeneration (CBD). We analyzed the SNPs included in the H1C and H1E'A haplotypes in a large Spanish PSP/CBD series and their interaction with age...

Read the complete abstract on PubMed

Topics

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

Share to Brain Diseases
Share to Chromosomes, Human, Pair 17
Share to CRF Receptor, Type 1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Kaplan-Meier Estimate

Share to Neurodegenerative Diseases

Share to Receptors, Corticotropin-Releasing Hormone

Share to Supranuclear Palsy, Progressive

Share to tau Proteins

Source

Identifiers

PMID: 19022385
DOI: 10.1016/j.nbd.2008.09.027

Genes

CRHR1
MAPT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19022385-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

5'-Upstream variants of CRHR1 and MAPT genes associated with age at onset in progressive supranuclear palsy and cortical basal degeneration.PMID 19022385Read ↗

Novel haplotypes in 17q21 are associated with progressive supranuclear palsy.Semantic proximity Read ↗

Different MAPT haplotypes are associated with Parkinson's disease and progressive supranuclear palsy.Semantic proximity Read ↗

The structure of the tau haplotype in controls and in progressive supranuclear palsy.Semantic proximity Read ↗

The H1c haplotype at the MAPT locus is associated with Alzheimer's disease.Semantic proximity Read ↗

Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variants.Semantic proximity Read ↗

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype.Semantic proximity Read ↗

Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration.Semantic proximity Read ↗

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.Semantic proximity Read ↗

Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.Semantic proximity Read ↗

Genetic and Epigenetic Constructs of Progressive Supranuclear PalsySemantic proximity Read ↗

Survival in progressive supranuclear palsy and frontotemporal dementia.Semantic proximity Read ↗

Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.Semantic proximity Read ↗

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