| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1995PNAS...92.6892H |
| P356 | DOI | 10.1073/PNAS.92.15.6892 |
| P932 | PMC publication ID | 41436 |
| P698 | PubMed publication ID | 7624338 |
| P5875 | ResearchGate publication ID | 15575485 |
| P2093 | author name string | G Cortopassi | |
| T Hutchin | |||
| P2860 | cites work | African Populations and the Evolution of Human Mitochondrial DNA | Q22065576 |
| Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease | Q22248076 | ||
| Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees | Q24678456 | ||
| The neighbor-joining method: a new method for reconstructing phylogenetic trees | Q25939010 | ||
| Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families | Q27860677 | ||
| Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14 | Q28156208 | ||
| Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease | Q28241772 | ||
| Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy | Q28292821 | ||
| Construction of phylogenetic trees | Q29547497 | ||
| Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease | Q29614952 | ||
| Alzheimer's disease and senile dementia: loss of neurons in the basal forebrain | Q34714755 | ||
| A molecular basis for human hypersensitivity to aminoglycoside antibiotics | Q35000709 | ||
| Epidemiology of Alzheimer's Disease | Q35188935 | ||
| Multiple etiologies for Alzheimer disease are revealed by segregation analysis. | Q35889556 | ||
| Branching pattern in the evolutionary tree for human mitochondrial DNA. | Q37410666 | ||
| Familial Alzheimer's disease: progress and problems | Q38715582 | ||
| NADH- and NADPH-dependent formation of superoxide anions by bovine heart submitochondrial particles and NADH–ubiquinone reductase preparation | Q39273179 | ||
| Generation of superoxide anion by the NADH dehydrogenase of bovine heart mitochondria | Q41829151 | ||
| NADH- and NADPH-dependent lipid peroxidation in bovine heart submitochondrial particles. Dependence on the rate of electron flow in the respiratory chain and an antioxidant role of ubiquinol | Q41986067 | ||
| Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14. | Q43597292 | ||
| Is the prevalence of dementia changing? | Q44490404 | ||
| Prevalence of Alzheimer's disease in a retirement community | Q44854737 | ||
| Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness | Q46157086 | ||
| Prevalence of Alzheimer's disease in a community population of older persons. Higher than previously reported. | Q52112673 | ||
| Mitochondrial respiratory chain inhibitors induce apoptosis. | Q52544710 | ||
| Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3 | Q53178836 | ||
| A locus for familial early-onset Alzheimer's disease on the long arm of chromosome 14, proximal to the alpha 1-antichymotrypsin gene. | Q53178841 | ||
| Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients. | Q53206553 | ||
| Prevalence of dementia and probable senile dementia of the Alzheimer type in the Framingham Study | Q53295392 | ||
| Linkage of late-onset Alzheimer's disease with apolipoprotein E type 4 on chromosome 19. | Q53316369 | ||
| Irreversible inhibition of mitochondrial complex I by 1-methyl-4-phenylpyridinium: evidence for free radical involvement | Q67724128 | ||
| 1-Methyl-4-phenylpyridinium (MPP+) induces NADH-dependent superoxide formation and enhances NADH-dependent lipid peroxidation in bovine heart submitochondrial particles | Q68474033 | ||
| P433 | issue | 15 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Alzheimer's disease | Q11081 |
| mitochondrial DNA | Q27075 | ||
| P304 | page(s) | 6892-6895 | |
| P577 | publication date | 1995-07-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | A mitochondrial DNA clone is associated with increased risk for Alzheimer disease | |
| P478 | volume | 92 |
| Q51737097 | A key role for MAM in mediating mitochondrial dysfunction in Alzheimer disease. |
| Q34211127 | A mitochondrial etiology of Alzheimer and Parkinson disease |
| Q29547303 | A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine |
| Q38469487 | A new approach to the genetic analysis of nervous system diseases: retrospective genotyping of archival brains. |
| Q34144436 | A novel homoplasmic mutation in mtDNA with a single evolutionary origin as a risk factor for cardiomyopathy |
| Q48458709 | A unifying hypothesis of Alzheimer's disease. III. Risk factors |
| Q36986848 | Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication |
| Q34725635 | Amyloid-Beta interaction with mitochondria |
| Q28396290 | Analysis of mitochondrial DNA variations in Indian patients with congenital cataract |
| Q36833616 | Ancient mtDNA sequences in the human nuclear genome: a potential source of errors in identifying pathogenic mutations |
| Q35510313 | Bioenergetic origins of complexity and disease |
| Q24533221 | Classification of European mtDNAs from an analysis of three European populations |
| Q92939847 | Codon optimization is an essential parameter for the efficient allotopic expression of mtDNA genes |
| Q36573774 | Compromised mitochondrial function leads to increased cytosolic calcium and to activation of MAP kinases |
| Q53232811 | Effect of aluminium-induced Alzheimer like condition on oxidative energy metabolism in rat liver, brain and heart mitochondria. |
| Q45107551 | Elevated levels of the Kearns-Sayre syndrome mitochondrial DNA deletion in temporal cortex of Alzheimer's patients |
| Q35131161 | Endonuclease III and endonuclease VIII conditionally targeted into mitochondria enhance mitochondrial DNA repair and cell survival following oxidative stress |
| Q50509552 | Enhanced mitochondrial DNA repair and cellular survival after oxidative stress by targeting the human 8-oxoguanine glycosylase repair enzyme to mitochondria |
| Q44452930 | Evidence for adaptive selection acting on the tRNA and rRNA genes of human mitochondrial DNA. |
| Q21136190 | Evidence for sub-haplogroup h5 of mitochondrial DNA as a risk factor for late onset Alzheimer's disease |
| Q34477829 | Expression profiles of mitochondrial genes in the frontal cortex and the caudate nucleus of developing humans and mice selectively bred for high and low fear |
| Q37172134 | Functional integrity of mitochondrial genomes in human platelets and autopsied brain tissues from elderly patients with Alzheimer's disease |
| Q33588353 | Genetic risk factors in Alzheimer's disease |
| Q34187826 | Human mitochondrial genetics |
| Q57624017 | Identification of Novel Genes in Late-Onset Alzheimer's Disease |
| Q33253241 | Identification of mitochondrial DNA polymorphisms that alter mitochondrial matrix pH and intracellular calcium dynamics |
| Q78241746 | Isolation and microinjection of somatic cell-derived mitochondria and germline heteroplasmy in transmitochondrial mice |
| Q28192185 | Laboratory approach to mitochondrial diseases |
| Q35881405 | Longitudinal study of a heteroplasmic 3460 Leber hereditary optic neuropathy family by multiplexed primer-extension analysis and nucleotide sequencing |
| Q47976401 | Mito-GSAAC: mitochondria prediction using genetic ensemble classifier and split amino acid composition |
| Q35898628 | Mitochondria and cell bioenergetics: increasingly recognized components and a possible etiologic cause of Alzheimer's disease |
| Q38932850 | Mitochondria, Cybrids, Aging, and Alzheimer's Disease |
| Q33698535 | Mitochondrial DNA analysis: polymorphisms and pathogenicity |
| Q58136336 | Mitochondrial DNA and Disease |
| Q33364885 | Mitochondrial DNA and primary mitochondrial dysfunction in Parkinson's disease |
| Q34214032 | Mitochondrial DNA in aging and degenerative disease |
| Q36855295 | Mitochondrial DNA polymorphisms in pathologically proven Parkinson's disease |
| Q33889143 | Mitochondrial DNA repair and association with aging--an update |
| Q36649957 | Mitochondrial DNA repair: a critical player in the response of cells of the CNS to genotoxic insults |
| Q33603868 | Mitochondrial DNA sequence associations with dementia and amyloid-β in elderly African Americans |
| Q34140769 | Mitochondrial DNA sequence variation associated with dementia and cognitive function in the elderly |
| Q53238571 | Mitochondrial DNA variants in inclusion body myositis. |
| Q36223869 | Mitochondrial DNA, base excision repair and neurodegeneration |
| Q33780440 | Mitochondrial biogenesis dysfunction and metabolic dysfunction from a novel mitochondrial tRNAMet 4467 C>A mutation in a Han Chinese family with maternally inherited hypertension |
| Q28280353 | Mitochondrial defects and oxidative stress in Alzheimer disease and Parkinson disease |
| Q41547386 | Mitochondrial dysfunction in neurodegeneration |
| Q35557675 | Mitochondrial dysfunction, apoptotic cell death, and Alzheimer's disease |
| Q36000745 | Mitochondrial failures in Alzheimer's disease |
| Q58105767 | Mitochondrial genetic medicine |
| Q33540918 | Mitochondrial involvement in Alzheimer's disease |
| Q36045522 | Mitochondrial mutations and polymorphisms in psychiatric disorders |
| Q35689426 | Mitochondrial ribosomal proteins: candidate genes for mitochondrial disease |
| Q41757587 | Molecular pathogenesis of sporadic and familial forms of Alzheimer's disease. |
| Q33969627 | Multiple origins of a mitochondrial mutation conferring deafness. |
| Q39729622 | Nitric oxide-induced damage to mtDNA and its subsequent repair |
| Q38263132 | No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population |
| Q50864482 | No mitochondrial haplotype was found to increase risk for Alzheimer's disease. |
| Q77905916 | Phylogenetic analysis of the mitochondrial genome indicates significant differences between patients with Alzheimer disease and controls in a French-Canadian founder population |
| Q47358251 | Prediction of mitochondrial proteins using support vector machine and hidden Markov model. |
| Q41725491 | Recent developments in the molecular genetics of mitochondrial disorders |
| Q24563892 | Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups |
| Q33932655 | Role of SCOX in determination of Drosophila melanogaster lifespan |
| Q35016920 | Roles of cholesterol and lipids in the etiopathogenesis of Alzheimer's disease |
| Q41748125 | Some remarks on biological markers of Alzheimer's disease |
| Q34246990 | Systemic mitochondrial dysfunction and the etiology of Alzheimer's disease and down syndrome dementia |
| Q46774788 | Targeting human 8-oxoguanine DNA glycosylase to mitochondria protects cells from 2-methoxyestradiol-induced-mitochondria-dependent apoptosis |
| Q37656554 | The Alzheimer's disease mitochondrial cascade hypothesis: progress and perspectives |
| Q36235630 | The Role of Mitochondrial Non-Enzymatic Protein Acylation in Ageing |
| Q35080485 | The co-occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific |
| Q34416941 | The other, forgotten genome: mitochondrial DNA and mental disorders |
| Q35174458 | The role of mitochondria in the life of the nematode, Caenorhabditis elegans |
| Q33678113 | The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 years. |
| Q28077056 | Triad of Risk for Late Onset Alzheimer's: Mitochondrial Haplotype, APOE Genotype and Chromosomal Sex |
| Q48482729 | mtDNA polymorphisms in Japanese sporadic Alzheimer's disease |
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