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

A mir-153 binding site variation in SNCA in a patient with Parkinson's disease.

Movement disorders : official journal of the Movement Disorder Society - 1 Oct 2013

Kim Han-Joon, Park Gibeom, Jeon Beom S, Park Woong Yang, Kim Young Eun

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to alpha-Synuclein
Share to Binding Sites
Share to SNCA gene
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to MicroRNAs

Share to Parkinson Disease

Source

Identifiers

PMID: 23674501
DOI: 10.1002/mds.25505

Genes

SNCA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A mir-153 binding site variation in SNCA in a patient with Parkinson's disease.PMID 23674501Read ↗

SNCA 3' UTR Genetic Variants in Patients with Parkinson's Disease.Semantic proximity Read ↗

SNCA 3'UTR genetic variants in patients with Parkinson's disease and REM sleep behavior disorder.Semantic proximity Read ↗

Genetic variability in SNCA and Parkinson's disease.Semantic proximity Read ↗

Structural variants in SNCA gene and the implication to synucleinopathiesSemantic proximity Read ↗

Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's diseaseSemantic proximity Read ↗

Variants in the 3'UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expression.Semantic proximity Read ↗

A single nucleotide polymorphism in the 3'UTR of the SNCA gene encoding alpha-synuclein is a new potential susceptibility locus for Parkinson disease.Semantic proximity Read ↗

The diversity of <i>SNCA</i> transcripts in neurons, and its impact on antisense oligonucleotide therapeuticsSemantic proximity Read ↗

Genetic analysis of SNCA coding mutation in Chinese Han patients with Parkinson disease.Semantic proximity Read ↗

SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish population.Semantic proximity Read ↗

Genetic analysis of NUS1 in Chinese patients with Parkinson's diseaseSemantic proximity Read ↗

The heterozygous A53T mutation in the alpha-synuclein gene in a Chinese Han patient with Parkinson disease: case report and literature review.Semantic proximity Read ↗

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