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

DMT1 polymorphism and risk of Parkinson's disease.

Neuroscience letters - 1 Sept 2011

He Qing, Du Tingting, Yu Xiaojun, Xie Anmu, Song Ning, Kang Qi, Yu Jintai, Tan Lan, Xie Junxia, Jiang Hong

Abstract excerpt

Growing evidence suggests that iron accumulation in the substantia nigra (SN) is involved in the pathology of Parkinson's diseases (PD). Divalent metal transporter 1 (DMT1) is an endogenous transporter for ferrous iron, the levels of which are significantly increased in the SN in postmortem PD brains. To study the possible association of DMT1 gene with PD occurrence, one mutation (1303C/A) and two single...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Asian People
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cation Transport Proteins

Share to Haplotypes

Share to Parkinson Disease

Share to Risk Factors

Source

Identifiers

PMID: 21777657
DOI: 10.1016/j.neulet.2011.07.001

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

DMT1 polymorphism and risk of Parkinson's disease.PMID 21777657Read ↗

Is the 1254T>C polymorphism in the DMT1 gene associated with Parkinson's disease?Semantic proximity Read ↗

Pooled analysis of iron-related genes in Parkinson's disease: association with transferrin.Semantic proximity Read ↗

MTHFR C677T and A1298C polymorphisms may contribute to the risk of Parkinson's disease: A meta-analysis of 19 studies.Semantic proximity Read ↗

An association study between Heme oxygenase-1 genetic variants and Parkinson's diseaseSemantic proximity Read ↗

Polymorphisms of metal transporter genes DMT1 and ATP7A in Wilson's disease.Semantic proximity Read ↗

Mitochondrial DNA variants modulate genetic susceptibility to Parkinson's disease in Han Chinese.Semantic proximity Read ↗

Methylenetetrahydrofolate reductase (MTHFR) C677T/A1298C polymorphisms and susceptibility to Parkinson's disease: a meta-analysis.Semantic proximity Read ↗

MTHFR C677T variant reduces risk of sporadic Parkinson's disease in ethnic Chinese.Semantic proximity Read ↗

Association between MDR1 gene polymorphisms and Parkinson's disease in Asian and Caucasian populations: a meta-analysis.Semantic proximity Read ↗

Genetic susceptibility to Parkinson's disease among South and North Indians: I. Role of polymorphisms in dopamine receptor and transporter genes and association of DRD4 120-bp duplication marker.Semantic proximity Read ↗

Superoxide dismutase coding of gene polymorphisms associated with susceptibility to Parkinson’s diseaseSemantic proximity Read ↗

Glutathione S-transferase T1 and M1 null genotypes and Parkinson's disease risk: evidence from an updated meta-analysis.Semantic proximity Read ↗

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