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Plos Genetics|December 5, 2014
In vivo occupancy of mitochondrial single-stranded DNA binding protein supports the strand displacement mode of DNA replicationJavier Miralles Fusté, Yonghong Shi, Sjoerd Wanrooij, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 27, 2012
Mammalian transcription factor A is a core component of the mitochondrial transcription machineryYonghong Shi, Anke Dierckx, Paulina H Wanrooij, et al.
Bioconjugate Chemistry|March 20, 2025
Linker Design Principles for the Precision Targeting of Oncogenic G-Quadruplex DNA with G4-Ligand-Conjugated OligonucleotidesAlva Abrahamsson, Andreas Berner, Justyna Golebiewska-Pikula, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 23, 2005
Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in miceHenna Tyynismaa, Katja Peltola Mjosund, Sjoerd Wanrooij, et al.
Nucleic Acids Research|August 14, 2018
A two-nuclease pathway involving RNase H1 is required for primer removal at human mitochondrial OriLAli Al-Behadili, Jay P Uhler, Anna-Karin Berglund, 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.
Nucleic Acids Research|July 24, 2021
Motif WFYY of human PrimPol is crucial to stabilize the incoming 3'-nucleotide during replication fork restartPatricia A Calvo, María I Martínez-Jiménez, Marcos Díaz, et al.
Molecular Biology of the Cell|December 20, 2024
MRE11-independent effects of Mirin on mitochondrial DNA integrity and cellular immune responsesKoit Aasumets, Anu Hangas, Georgios Fragkoulis, 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.
Proceedings of the National Academy of Sciences of the United States of America|April 16, 2025
The POLγ Y951N patient mutation disrupts the switch between DNA synthesis and proofreading, triggering mitochondrial DNA instabilityJosefin M E Forslund, Tran V H Nguyen, Vimal Parkash, et al.
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