Homo sapiens Genome sequencing and assembly. Homo sapiens
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Mitochondrial tRNA mutations in Chinese Children with Tic Disorders
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创建时间：
2020-11-09
相关数据集
Evolution Meets Disease: Penetrance and Functional Epistasis of Mitochondrial tRNA Mutations
About half of the mitochondrial DNA (mtDNA) mutations causing diseases in humans occur in tRNA genes. Particularly intriguing are those pathogenic tRNA mutations than can reach homoplasmy and yet show
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RNA-seq of mouse heart that is both heart SOD2 knockout and deficient for mitochondrial DNA repair. RNA-seq of mouse heart that is both heart SOD2 knockout and deficient for mitochondrial DNA repair
To study whether increase in mitochondrial oxidative stress (SOD2 removal) and decrease in mitochondrial DNA repair (Ogg1 dMTS) results into increase in mutations in mitochondrial RNA (mtRNA). Oxidati
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WT and Hypertensive mt. tRNAIle4263A>G mutant VOs
mature VOs derived from both WT and mt. tRNAIle4263A>G mutant groups (n = 3 in each group) were collected for sequencing and subsequent analysis
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Mitochondrial ribosomal RNA is the target of functionally dominant hotspot mutations in cancer
The vast majority of recurrent somatic mutations arising in tumors affect protein-coding genes in the nuclear genome. Here, through population-scale analysis of 14,079 whole tumor genomes, we report t
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RNA-seq of mouse heart that is both heart SOD2 knockout and deficient for mitochondrial DNA repair
To study whether increase in mitochondrial oxidative stress (SOD2 removal) and decrease in mitochondrial DNA repair (Ogg1 dMTS) results into increase in mutations in mitochondrial RNA (mtRNA). Oxidati
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