Detection of point mutations in codon 331 of mitochondrial NADH dehydrogenase subunit 2 in Alzheimer's brains
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Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups.Profiling of T helper cell-derived small RNAs reveals unique antisense transcripts and differential association of miRNAs with argonaute proteins 1 and 2Gene expression profiling for human iPS-derived motor neurons from sporadic ALS patients reveals a strong association between mitochondrial functions and neurodegeneration.Genetic risk factors in Alzheimer's diseaseMitochondrial DNA sequence associations with dementia and amyloid-β in elderly African AmericansMutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases.Nonneutral mitochondrial DNA variation in humans and chimpanzeesMitochondrial DNA sequence variation associated with dementia and cognitive function in the elderly.The other, forgotten genome: mitochondrial DNA and mental disorders.Mitochondrial genomic analysis of late onset Alzheimer's disease reveals protective haplogroups H6A1A/H6A1B: the Cache County Study on Memory in AgingA quantitative and specific method for measuring transcript levels of highly homologous genesMitochondrial abnormalities in muscle and other aging cells: classification, causes, and effects.Pharmacogenomics for the treatment of dementia.A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology.The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains.The development of mitochondrial medicine.Mitochondrial DNA, base excision repair and neurodegeneration.Genetic studies of amyotrophic lateral sclerosis: controversies and perspectives.Attenuation of UV-induced apoptosis by coenzyme Q10 in human cells harboring large-scale deletion of mitochondrial DNA.Dynamic comparisons of high-resolution expression profiles highlighting mitochondria-related genes between in vivo and in vitro fertilized early mouse embryos.Japanese Alzheimer's disease and other complex disorders diagnosis based on mitochondrial SNP haplogroups.St John's wort and imipramine-induced gene expression profiles identify cellular functions relevant to antidepressant action and novel pharmacogenetic candidates for the phenotype of antidepressant treatment response.Mitochondrial respiratory chain in brain homogenates: activities in different brain areas in patients with Alzheimer's disease.Mitochondrial DNA variants in a portuguese population of patients with Alzheimer's disease.A Selection of Important Genes and Their Correlated Behavior in Alzheimer's Disease
P2860
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P2860
Detection of point mutations in codon 331 of mitochondrial NADH dehydrogenase subunit 2 in Alzheimer's brains
description
1992 nî lūn-bûn
@nan
1992 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Detection of point mutations i ...... ubunit 2 in Alzheimer's brains
@ast
Detection of point mutations i ...... ubunit 2 in Alzheimer's brains
@en
Detection of point mutations i ...... ubunit 2 in Alzheimer's brains
@nl
type
label
Detection of point mutations i ...... ubunit 2 in Alzheimer's brains
@ast
Detection of point mutations i ...... ubunit 2 in Alzheimer's brains
@en
Detection of point mutations i ...... ubunit 2 in Alzheimer's brains
@nl
prefLabel
Detection of point mutations i ...... ubunit 2 in Alzheimer's brains
@ast
Detection of point mutations i ...... ubunit 2 in Alzheimer's brains
@en
Detection of point mutations i ...... ubunit 2 in Alzheimer's brains
@nl
P2093
P1476
Detection of point mutations i ...... ubunit 2 in Alzheimer's brains
@en
P2093
G Healy-Louie
H M Wisniewski
I Grundke-Iqbal
P304
P356
10.1016/S0006-291X(05)80136-6
P407
P577
1992-01-15T00:00:00Z