rs1556424691
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
|
30236074 |
2018 |
rs1556424691
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
CO2-sensitive tRNA modification associated with human mitochondrial disease.
|
29760464 |
2018 |
rs1977412
|
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Genetic data and cognitively defined late-onset Alzheimer's disease subgroups.
|
30514930 |
2018 |
rs2732260
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.
|
29724592 |
2018 |
rs1556424691
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
|
22638997 |
2012 |
rs1556424691
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mitochondrial disorder associated with newborn cardiopulmonary arrest.
|
8511015 |
1993 |
rs104894396
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1163944538
|
|
GA |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1352010373
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs148881970
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1554317002
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1555735545
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs28937900
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs370717845
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs555145190
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs63751011
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs768823392
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs80356702
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs63751273
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Expression of P301L-hTau in mouse MEC induces hippocampus-dependent memory deficit.
|
28634382 |
2017 |
rs63751273
|
|
|
0.030 |
GeneticVariation |
BEFREE |
The present study was undertaken to examine whether lycopene or lycopene/vitamin E could exert protective effects on memory deficit and oxidative stress in tau transgenic mice expressing P301L mutation.
|
28269786 |
2017 |
rs6265
|
|
|
0.030 |
GeneticVariation |
BEFREE |
BDNF Val66Met moderates memory impairment, hippocampal function and tau in preclinical autosomal dominant Alzheimer's disease.
|
27521573 |
2016 |
rs759834365
|
|
|
0.030 |
GeneticVariation |
BEFREE |
BDNF Val66Met moderates memory impairment, hippocampal function and tau in preclinical autosomal dominant Alzheimer's disease.
|
27521573 |
2016 |
rs6265
|
|
|
0.030 |
GeneticVariation |
BEFREE |
A Val(66)Met single-nucleotide polymorphism (SNP) in the brain-derived neurotrophic factor (BDNF) gene impairs activity-dependent BDNF release in cultured hippocampal neurons and predicts impaired memory and exaggerated basal hippocampal activity in healthy humans.
|
23319002 |
2013 |
rs759834365
|
|
|
0.030 |
GeneticVariation |
BEFREE |
A Val(66)Met single-nucleotide polymorphism (SNP) in the brain-derived neurotrophic factor (BDNF) gene impairs activity-dependent BDNF release in cultured hippocampal neurons and predicts impaired memory and exaggerated basal hippocampal activity in healthy humans.
|
23319002 |
2013 |
rs63751273
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Forebrain-specific over-expression of human tau(P301L), a mutation associated with frontotemporal dementia with parkinsonism linked to chromosome 17, in rTg4510 mice results in the formation of NFTs, learning and memory impairment and massive neuronal death.
|
22027994 |
2012 |