37 results on '"Nicholls, Thomas J."'
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2. Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stability
3. Mechanisms and pathologies of human mitochondrial DNA replication and deletion formation
4. Mechanisms and pathologies of human mitochondrial DNA replication and deletion formation.
5. Nuclear genetic disorders of mitochondrial DNA gene expression
6. List of Contributors
7. Recurrent horizontal transfer identifies mitochondrial positive selection in a transmissible cancer
8. Mitochondrially-targeted APOBEC1 is a potent mtDNA mutator affecting mitochondrial function and organismal fitness in Drosophila
9. Two type I topoisomerases maintain DNA topology in human mitochondria
10. The human mitochondrial genome contains a second light strand promoter
11. Mammalian RNase H1 directs RNA primer formation for mtDNA replication initiation and is also necessary for mtDNA replication completion
12. Mitochondrial transcript maturation and its disorders
13. Controlling the topology of mammalian mitochondrial DNA
14. Linear mtDNA fragments and unusual mtDNA rearrangements associated with pathological deficiency of MGME1 exonuclease
15. The mitochondrial single-stranded DNA binding protein is essential for initiation of mtDNA replication
16. In D-loop: 40 years of mitochondrial 7S DNA
17. PDE12 removes mitochondrial RNA poly(A) tails and controls translation in human mitochondria
18. The Maintenance of Mitochondrial DNA Integrity and Dynamics by Mitochondrial Membranes
19. Dinucleotide Degradation by REXO2 Maintains Promoter Specificity in Mammalian Mitochondria
20. In situ oligonucleotide synthesis on poly(dimethylsiloxane): a flexible substrate for microarray fabrication
21. Dinucleotide Degradation by REXO2 Maintains Promoter Specificity in Mammalian Mitochondria
22. Understanding mitochondrial DNA maintenance disorders at the single muscle fibre level
23. Linear mtDNA fragments and unusual mtDNA rearrangements associated with pathological deficiency of MGME1 exonuclease
24. Separating and Segregating the Human Mitochondrial Genome
25. Mice lacking the mitochondrial exonuclease MGME1 accumulate mtDNA deletions without developing progeria
26. Topoisomerase 3α Is Required for Decatenation and Segregation of Human mtDNA
27. MGME1 processes flaps into ligatable nicks in concert with DNA polymerase γ during mtDNA replication
28. Nuclear-encoded factors involved in post-transcriptional processing and modification of mitochondrial tRNAs in human disease
29. Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy
30. MRM2 and MRM3 are involved in biogenesis of the large subunit of the mitochondrial ribosome
31. In D-loop: 40years of mitochondrial 7S DNA
32. ELAC2 Mutations Cause a Mitochondrial RNA Processing Defect Associated with Hypertrophic Cardiomyopathy
33. Mitochondria: Mitochondrial RNA metabolism and human disease
34. Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease
35. The mitochondrial single-stranded DNA binding protein is essential for initiation of mtDNA replication.
36. Mammalian RNase H1 directs RNA primer formation for mtDNA replication initiation and is also necessary for mtDNA replication completion
37. Isolating Mitochondria, Mitoplasts, and mtDNA from Cultured Mammalian Cells.
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