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Maria Falkenberg

Showing results (71-80 of 104) with videos related to

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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.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|June 18, 2022
Disease causing mutation (P178L) in mitochondrial transcription factor A results in impaired mitochondrial transcription initiationMajda Mehmedović, Martial Martucci, Henrik Spåhr, et al.
Nature Communications|November 18, 2024
Mechanistic basis of atypical TERT promoter mutationsKerryn Elliott, Vinod Kumar Singh, Alan Bäckerholm, et al.
Cell|June 6, 2022
Non-coding 7S RNA inhibits transcription via mitochondrial RNA polymerase dimerizationXuefeng Zhu, Xie Xie, Hrishikesh Das, 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.
Cell|July 31, 2007
MTERF3 is a negative regulator of mammalian mtDNA transcriptionChan Bae Park, Jorge Asin-Cayuela, Yolanda Cámara, et al.
Nature|May 28, 2004
Premature ageing in mice expressing defective mitochondrial DNA polymeraseAleksandra Trifunovic, Anna Wredenberg, Maria Falkenberg, et al.
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.
Pageof 11

Showing results (71-80 of 104) with videos related to

Sort By:
Pageof 11
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.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|June 18, 2022
Disease causing mutation (P178L) in mitochondrial transcription factor A results in impaired mitochondrial transcription initiationMajda Mehmedović, Martial Martucci, Henrik Spåhr, et al.
Nature Communications|November 18, 2024
Mechanistic basis of atypical TERT promoter mutationsKerryn Elliott, Vinod Kumar Singh, Alan Bäckerholm, et al.
Cell|June 6, 2022
Non-coding 7S RNA inhibits transcription via mitochondrial RNA polymerase dimerizationXuefeng Zhu, Xie Xie, Hrishikesh Das, 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.
Cell|July 31, 2007
MTERF3 is a negative regulator of mammalian mtDNA transcriptionChan Bae Park, Jorge Asin-Cayuela, Yolanda Cámara, et al.
Nature|May 28, 2004
Premature ageing in mice expressing defective mitochondrial DNA polymeraseAleksandra Trifunovic, Anna Wredenberg, Maria Falkenberg, et al.
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.
Pageof 11