Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia.
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Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson diseaseMay "mitochondrial eve" and mitochondrial haplogroups play a role in neurodegeneration and Alzheimer's disease?A generalized model to estimate the statistical power in mitochondrial disease studies involving 2×k tablesMitochondrial defects and oxidative stress in Alzheimer disease and Parkinson diseaseMitochondrial DNA sequence variation and neurodegenerationMaternal inheritance and mitochondrial DNA variants in familial Parkinson's diseaseMitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration.Mitochondrial DNA haplogroups in early-onset Alzheimer's disease and frontotemporal lobar degenerationMitochondrial haplogroups modify the effect of black carbon on age-related cognitive impairmentMitochondrial dysfunction in the limelight of Parkinson's disease pathogenesis.Recent advances in the genetics of Parkinson's disease.Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians.Mitochondrial dysfunction in Parkinson's disease: pathogenesis and neuroprotection.Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.mtDNA haplogroup and single nucleotide polymorphisms structure human microbiome communities.Maternal transmission of Alzheimer's disease: prodromal metabolic phenotype and the search for genes.Epidemiology and penetrance of Leber hereditary optic neuropathy in Finland.Comprehensive association testing of common mitochondrial DNA variation in metabolic disease.Mitochondria-wide association study of common variants in osteoporosis.Mitochondrial DNA sequence variation is largely conserved at birth with rare de novo mutations in neonates.Mitochondrial genomics and CD4 T-cell count recovery after antiretroviral therapy initiation in AIDS clinical trials group study 384Role and treatment of mitochondrial DNA-related mitochondrial dysfunction in sporadic neurodegenerative diseases.Mitochondrial DNA, base excision repair and neurodegeneration.Female genetic distribution bias in mitochondrial genome observed in Parkinson's Disease patients in northern China.Genetic findings in Parkinson's disease and translation into treatment: a leading role for mitochondria?The role of mitochondria in inherited neurodegenerative diseases.Does mitochondrial DNA play a role in Parkinson's disease? A review of cybrid and other supportive evidence.Specific polymorphic variation in the mitochondrial genome and increased in-hospital mortality after severe trauma.The impact of mitochondrial DNA and nuclear genes related to mitochondrial functioning on the risk of Parkinson's disease.Mitochondrial proteomics as a selective tool for unraveling Parkinson's disease pathogenesis.POLG1-related and other "mitochondrial Parkinsonisms": an overview.Rodent models and contemporary molecular techniques: notable feats yet incomplete explanations of Parkinson's disease pathogenesis.What's to like about the prion-like hypothesis for the spreading of aggregated α-synuclein in Parkinson disease?The role of mitochondrial disturbances in Alzheimer, Parkinson and Huntington diseases.Shared mechanisms of neurodegeneration in Alzheimer's disease and Parkinson's disease.Gene expression of cytokines and cytokine receptors is modulated by the common variability of the mitochondrial DNA in cybrid cell lines.The role of mitochondrial haplogroups in primary open angle glaucoma.Do somatic mitochondrial DNA mutations contribute to Parkinson's disease?Variations of mitochondrial DNA polymerase γ in patients with Parkinson's disease.Cypermethrin-induced nigrostriatal dopaminergic neurodegeneration alters the mitochondrial function: a proteomics study.
P2860
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P2860
Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
Mitochondrial DNA polymorphism ...... Parkinson's disease dementia.
@en
Mitochondrial DNA polymorphism ...... Parkinson's disease dementia.
@nl
type
label
Mitochondrial DNA polymorphism ...... Parkinson's disease dementia.
@en
Mitochondrial DNA polymorphism ...... Parkinson's disease dementia.
@nl
prefLabel
Mitochondrial DNA polymorphism ...... Parkinson's disease dementia.
@en
Mitochondrial DNA polymorphism ...... Parkinson's disease dementia.
@nl
P2093
P50
P921
P1433
P1476
Mitochondrial DNA polymorphism ...... Parkinson's disease dementia.
@en
P2093
Jaana Autere
Kari Majamaa
Merja Hallikainen
Päivi Hartikainen
Saara Finnilä
P2888
P356
10.1007/S00439-004-1123-9
P577
2004-04-24T00:00:00Z