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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.
Molecular Cell|February 5, 2010
Mitochondrial RNA polymerase is needed for activation of the origin of light-strand DNA replicationJavier Miralles Fusté, Sjoerd Wanrooij, Elisabeth Jemt, et al.
Cell Reports|July 2, 2014
In vitro-reconstituted nucleoids can block mitochondrial DNA replication and transcriptionGéraldine Farge, Majda Mehmedovic, Marian Baclayon, et al.
Nucleic Acids Research|November 5, 2025
Proteolytic cleavage activates the mitochondrial isoform of TOP3ADirenis Erdinc, Christin A Albus, Alejandro Rodríguez-Luis, et al.
Nature Communications|February 17, 2019
Copy-choice recombination during mitochondrial L-strand synthesis causes DNA deletionsÖrjan Persson, Yazh Muthukumar, Swaraj Basu, et al.
Nature Communications|November 12, 2015
Complementation between polymerase- and exonuclease-deficient mitochondrial DNA polymerase mutants in genomically engineered fliesAna Bratic, Timo E S Kauppila, Bertil Macao, et al.
Nature Communications|November 18, 2024
Mechanistic basis of atypical TERT promoter mutationsKerryn Elliott, Vinod Kumar Singh, Alan Bäckerholm, et al.
The Journal of Biological Chemistry|December 2, 2011
Role of human DNA glycosylase Nei-like 2 (NEIL2) and single strand break repair protein polynucleotide kinase 3'-phosphatase in maintenance of mitochondrial genomeSanti M Mandal, Muralidhar L Hegde, Arpita Chatterjee, et al.
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