| scholarly article | Q13442814 |
| P50 | author | Xiao-Ping Dong | Q89676463 |
| Qi Shi | Q111306856 | ||
| P2093 | author name string | Chen Chen | |
| Wei Zhou | |||
| Chen Gao | |||
| Jin Zhang | |||
| Chan Tian | |||
| Cao Chen | |||
| Qi-Ling Wang | |||
| Zhi-Xia Zhang | |||
| Peng-Chen Du | |||
| Su-Dong Wu | |||
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| Deficiency of respiratory chain complex I is a common cause of Leigh disease. | Q55066535 | ||
| Increase of blood NAD+ and attenuation of lactacidemia during nicotinamide treatment of a patient with the MELAS syndrome | Q70984706 | ||
| Marked changes in mitochondrial DNA deletion levels in Alzheimer brains | Q72462720 | ||
| Protective prion protein polymorphisms against sporadic Creutzfeldt-Jakob disease | Q74242396 | ||
| Human mitochondrial haplogroup H: the highest VO2max consumer--is it a paradox? | Q84871137 | ||
| A Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure | Q22121935 | ||
| Fibroblast growth factors | Q24542507 | ||
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| Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm | Q29547194 | ||
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| A novel mutation in the mitochondrial DNA cytochrome b gene (MTCYB) in a patient with mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes syndrome | Q30575264 | ||
| Genetic cross-interaction between APOE and PRNP in sporadic Alzheimer's and Creutzfeldt-Jakob diseases | Q31026808 | ||
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| Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited | Q34893463 | ||
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| Recruitment of cellular prion protein to mitochondrial raft-like microdomains contributes to apoptosis execution. | Q35612280 | ||
| Role of mitochondria in toxic oxidative stress. | Q36093934 | ||
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| Genetic variability of the gene cluster CALHM 1-3 in sporadic Creutzfeldt-Jakob disease. | Q36719069 | ||
| Molecular biology of prion protein and its first homologous protein | Q36945476 | ||
| Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication | Q36986848 | ||
| Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study | Q37097991 | ||
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| Effects of purifying and adaptive selection on regional variation in human mtDNA. | Q39413917 | ||
| P433 | issue | 1 | |
| P921 | main subject | sporadic Creutzfeldt-Jakob disease | Q55345939 |
| P304 | page(s) | 86-91 | |
| P577 | publication date | 2014-03-26 | |
| P1433 | published in | European Journal of Human Genetics | Q2155433 |
| P1476 | title | Analyses of the mitochondrial mutations in the Chinese patients with sporadic Creutzfeldt-Jakob disease | |
| P478 | volume | 23 |
| Q91712161 | Contribution of Mitochondrial DNA Variation to Chronic Disease in East Asian Populations |
| Q36501303 | Transcriptomic Determinants of Scrapie Prion Propagation in Cultured Ovine Microglia |
| Q47880616 | Tri-allelic heteroplasmies, DNA-RNA differences and their polynucleotide tract associations in the mitochondrial genome |
| Q90264236 | mRNA Reprogramming of T8993G Leigh's Syndrome Fibroblast Cells to Create Induced Pluripotent Stem Cell Models for Mitochondrial Disorders |
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