about
Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial diseaseELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathyMRM2 and MRM3 are involved in biogenesis of the large subunit of the mitochondrial ribosome.Linear mtDNA fragments and unusual mtDNA rearrangements associated with pathological deficiency of MGME1 exonuclease.Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathyMitochondrial transcript maturation and its disordersMitochondria: mitochondrial RNA metabolism and human disease.In D-loop: 40 years of mitochondrial 7S DNA.Nuclear-encoded factors involved in post-transcriptional processing and modification of mitochondrial tRNAs in human disease.Topoisomerase 3α Is Required for Decatenation and Segregation of Human mtDNA.Mice lacking the mitochondrial exonuclease MGME1 accumulate mtDNA deletions without developing progeria.Dinucleotide Degradation by REXO2 Maintains Promoter Specificity in Mammalian MitochondriaSeparating and Segregating the Human Mitochondrial GenomeMitochondrially-targeted APOBEC1 is a potent mtDNA mutator affecting mitochondrial function and organismal fitness in DrosophilaUnderstanding mitochondrial DNA maintenance disorders at the single muscle fibre levelRecurrent horizontal transfer identifies mitochondrial positive selection in a transmissible cancer
P50
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P50
description
onderzoeker
@nl
researcher, ORCID id # 0000-0002-3034-4109
@en
name
Thomas J Nicholls
@ast
Thomas J Nicholls
@en
Thomas J Nicholls
@nl
type
label
Thomas J Nicholls
@ast
Thomas J Nicholls
@en
Thomas J Nicholls
@nl
prefLabel
Thomas J Nicholls
@ast
Thomas J Nicholls
@en
Thomas J Nicholls
@nl
P108
P106
P31
P496
0000-0002-3034-4109