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Human Molecular Genetics|March 9, 2018
Defective mitochondrial protease LonP1 can cause classical mitochondrial diseaseBradley Peter, Christie L Waddington, Monika Oláhová, et al.Nature Communications|August 23, 2012
Protein sliding and DNA denaturation are essential for DNA organization by human mitochondrial transcription factor AGéraldine Farge, Niels Laurens, Onno D Broekmans, et al.Proceedings of the National Academy of Sciences of the United States of America|August 26, 2015
Cross-strand binding of TFAM to a single mtDNA molecule forms the mitochondrial nucleoidChristian Kukat, Karen M Davies, Christian A Wurm, et al.Cell Metabolism|April 9, 2013
MTERF1 binds mtDNA to prevent transcriptional interference at the light-strand promoter but is dispensable for rRNA gene transcription regulationMügen Terzioglu, Benedetta Ruzzenente, Julia Harmel, et al.Human Molecular Genetics|April 22, 2017
A multi-systemic mitochondrial disorder due to a dominant p.Y955H disease variant in DNA polymerase gammaTriinu Siibak, Paula Clemente, Ana Bratic, et al.Molecular Cell|October 8, 2019
Dinucleotide Degradation by REXO2 Maintains Promoter Specificity in Mammalian MitochondriaThomas J Nicholls, Henrik Spåhr, Shan Jiang, et al.Molecular Cell|August 31, 2022
The human mitochondrial genome contains a second light strand promoterBenedict G Tan, Christian D Mutti, Yonghong Shi, et al.Nucleic Acids Research|October 10, 2022
Two type I topoisomerases maintain DNA topology in human mitochondriaKatja E Menger, James Chapman, Héctor Díaz-Maldonado, et al.American Journal of Human Genetics|October 4, 2011
Adenosine kinase deficiency disrupts the methionine cycle and causes hypermethioninemia, encephalopathy, and abnormal liver functionMagnus K Bjursell, Henk J Blom, Jordi Asin Cayuela, et al.Molecular Cell|January 2, 2018
Topoisomerase 3α Is Required for Decatenation and Segregation of Human mtDNAThomas J Nicholls, Cristina A Nadalutti, Elisa Motori, et al.Pageof 11