Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Maria Falkenberg

Showing results (81-90 of 104) with videos related to

Pageof 11
Sort By:
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.
Nature Communications|March 25, 2018
Mice lacking the mitochondrial exonuclease MGME1 accumulate mtDNA deletions without developing progeriaStanka Matic, Min Jiang, Thomas J Nicholls, et al.
Plos Genetics|December 14, 2020
Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencingSwaraj Basu, Xie Xie, Jay P Uhler, 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.
Nucleic Acids Research|May 6, 2021
DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletionPedro Silva-Pinheiro, Carlos Pardo-Hernández, Aurelio Reyes, et al.
Pageof 11

Showing results (81-90 of 104) with videos related to

Sort By:
Pageof 11
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.
Nature Communications|March 25, 2018
Mice lacking the mitochondrial exonuclease MGME1 accumulate mtDNA deletions without developing progeriaStanka Matic, Min Jiang, Thomas J Nicholls, et al.
Plos Genetics|December 14, 2020
Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencingSwaraj Basu, Xie Xie, Jay P Uhler, 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.
Nucleic Acids Research|May 6, 2021
DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletionPedro Silva-Pinheiro, Carlos Pardo-Hernández, Aurelio Reyes, et al.
Pageof 11