×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
Biomarker
BEFREE
In summary, our results thus reveal a new role of FMRP in PD and support the examination of FMRP -regulated genes in PD disease progression.
31768670 2020
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
BEFREE
Our results indicate that there is a potential association between FMR1 intermediate expanded alleles and PD .
27696273 2017
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
BEFREE
White matter changes in patients with Parkinson's disease carrying small CGG expansion FMR1 alleles: a pilot study.
24401315 2014
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
BEFREE
New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease .
23198693 2013
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
AlteredExpression
BEFREE
The Parkinson disease (Unified Parkinson's Disease Rating Scale) motor score and the measures of cognitive decline (Mini-Mental State Examination and/or Addenbrooke's Cognitive Examination Final Revised Version A scores) were significantly correlated with the size of the CGG repeat and the (elevated) levels of antisense FMR1 and Cytochrome C1 mRNAs in blood leukocytes.
21270637 2011
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
BEFREE
It is debatable whether the size of triplet repeats of the fragile X mental retardation genes FMR1 and FMR2 (found at the FRAXA and FRAXE loci) is associated with Parkinson's disease (PD ).
21257332 2011
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
BEFREE
Our results, however, suggest that fragile X mental retardation 1 gray-zone alleles may be associated with Parkinson's disease in women.
21567456 2011
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
BEFREE
To determine if patients with parkinsonism and fragile X mental retardation 1 (FMR1 ) gene expansions have a striatal dopamine deficit similar to Parkinson disease (PD) patients.
20702130 2010
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
BEFREE
To screen DNA samples from a large cohort of females with Parkinson disease for an excess of expanded alleles of the FMR1 gene.
19204162 2009
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
LHGDN
Parkinsonism in FMR1 premutation carriers may be indistinguishable from Parkinson disease .
18565783 2009
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
BEFREE
Parkinsonism in FMR1 premutation carriers may be indistinguishable from Parkinson disease .
18565783 2009
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
BEFREE
Broad screening for premutation alleles in Parkinson disease populations is unlikely to be productive in the absence of additional clinical or family history data that suggest involvement of the FMR1 gene.
17620491 2007
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
LHGDN
To screen DNA samples (male) from an Italian Parkinson disease clinic for an excess of premutation expansions of the FMR1 gene.
17620491 2007
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
BEFREE
FMR1 alleles in Parkinson's disease : relation to cognitive decline and hallucinations, a longitudinal study.17548778 2007
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
BEFREE
Expansions within the FMR1 gene are not associated with PD in our study.
15390127 2005
×
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
Parkinson Disease
0.100
GeneticVariation
BEFREE
Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease ?
15929093 2005