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Journal of Perinatal Medicine|October 28, 2021
Second trimester fetal thymus size in association to preterm birthChristian Porschen, Ralf Schmitz, Rene Schmidt, et al.
Plos One|April 29, 2017
Selective mitochondrial DNA degradation following double-strand breaksAmandine Moretton, Frédéric Morel, Bertil Macao, et al.
EMBO Reports|October 24, 2012
In vivo mutagenesis reveals that OriL is essential for mitochondrial DNA replicationSjoerd Wanrooij, Javier Miralles Fusté, James B Stewart, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 21, 2009
Unraveling the structure of DNA during overstretching by using multicolor, single-molecule fluorescence imagingJoost van Mameren, Peter Gross, Geraldine Farge, et al.
Nucleic Acids Research|June 23, 2010
Maintenance of respiratory chain function in mouse hearts with severely impaired mtDNA transcriptionChristoph Freyer, Chan Bae Park, Mats I Ekstrand, et al.
Neuromuscular Disorders : NMD|February 13, 2021
Functional analysis of a novel POLγA mutation associated with a severe perinatal mitochondrial encephalomyopathyNiklas Darin, Triinu Siibak, Bradley Peter, et al.
Human Molecular Genetics|March 16, 2004
Mitochondrial transcription factor A regulates mtDNA copy number in mammalsMats I Ekstrand, Maria Falkenberg, Anja Rantanen, et al.
Nucleic Acids Research|May 14, 2024
The mutation R107Q alters mtSSB ssDNA compaction ability and binding dynamicsMartial Martucci, Amandine Moretton, Aleix Tarrés-Solé, et al.
Plos Genetics|February 17, 2017
Nucleotide pools dictate the identity and frequency of ribonucleotide incorporation in mitochondrial DNAAnna-Karin Berglund, Clara Navarrete, Martin K M Engqvist, et al.
Human Molecular Genetics|January 14, 2011
Sequence-specific stalling of DNA polymerase γ and the effects of mutations causing progressive ophthalmoplegiaNeli Atanassova, Javier Miralles Fusté, Sjoerd Wanrooij, et al.
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