Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0030567 (
Parkinson's disease
)
63,064
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Inflammatory processes have been implicated in the cascade of events that lead to nerve cell death. In the nervous system, a number of genes involved in inflammation pathways are regulated post-transcriptionally via the interaction of their mRNAs with specific RNA-binding Hu proteins, the vertebrate homologues of the Drosophila ELAV (for embryonic lethal abnormal vision). The gene encoding
ELAVL4
, a member of the Hu family of proteins, is located 2 Mb from the chromosome 1p linkage region peak for age-at-onset (AAO) of
Parkinson disease
(PD) (LOD = 3.41). Nine single-nucleotide polymorphisms (SNPs) in
ELAVL4
were genotyped for 266 multiplex families (1,223 samples). Additional genotyping in 377 singleton families was performed for a subset of five SNPs (SNPs 1-5) that were not in linkage disequilibrium. SNP 2 (located in the first intron of
ELAVL4
) showed a strong significant association with AAO of PD (P = 0.006), and SNP 5 (a coding SNP in
ELAVL4
) showed a moderately significant association (P = 0.035). Haplotype analysis revealed that the A-C haplotype at SNPs 2 and 3 has the strongest significant association with AAO (P = 0.0001) among all combinations of two or three loci. The A-C haplotype remained significant for AAO after the inclusion of the C allele at SNP 5 to this haplotype (A-C-C haplotype, P = 0.00018). Although SNP 5 was found to associate with PD risk in the early-onset subset of PD families (at least one affected with AAO <40 years, 60 families), we believe that it is a by-product of its association with AAO. Taken together, these results suggest a potential role for
ELAVL4
as a modifier gene for AAO of PD.
...
PMID:Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease. 1582 45
Genetic variability in
ELAVL4
located in the PARK10 locus was recently associated with age-at-onset (AAO) in a series of
Parkinson's disease
(PD) patients originating from the United States. We examined five markers spanning
ELAVL4
in Norwegian, United States, and Irish PD case-control samples. No association was found between the examined markers and AAO or PD in Norwegian or US samples. However,
ELAVL4
markers (rs967582 and rs3902720) were significantly associated with susceptibility to PD in our Irish series. Our data suggest that the association between
ELAVL4
and PD previously observed might be explained by a Celtic-founder effect.
...
PMID:ELAVL4, PARK10, and the Celts. 1723 Apr 46