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Bradley Peter

Showing results (11-20 of 20) with videos related to

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Neuromuscular Disorders : NMD|February 13, 2021
Functional analysis of a novel POLγA mutation associated with a severe perinatal mitochondrial encephalomyopathyNiklas Darin, Triinu Siibak, Bradley Peter, 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.
SLAS Discovery : Advancing Life Sciences R & D|August 23, 2025
Development of novel high-throughput biochemical competition assays to identify ligands of human asialoglycoprotein receptor 1Jianming Liu, Bradley Peter, Lauren Rhodes, et al.
Cell|June 6, 2022
Non-coding 7S RNA inhibits transcription via mitochondrial RNA polymerase dimerizationXuefeng Zhu, Xie Xie, Hrishikesh Das, 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.
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.
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.
Nature|December 17, 2020
Small-molecule inhibitors of human mitochondrial DNA transcriptionNina A Bonekamp, Bradley Peter, Hauke S Hillen, et al.
Communications Chemistry|May 19, 2026
The rise and fall of SARM1 base-exchange inhibitorsThomas Lundbäck, Vijay Chandrasekar, Chendi Gu, et al.
Nature Communications|February 19, 2021
POLRMT mutations impair mitochondrial transcription causing neurological diseaseMonika Oláhová, Bradley Peter, Zsolt Szilagyi, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Neuromuscular Disorders : NMD|February 13, 2021
Functional analysis of a novel POLγA mutation associated with a severe perinatal mitochondrial encephalomyopathyNiklas Darin, Triinu Siibak, Bradley Peter, 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.
SLAS Discovery : Advancing Life Sciences R & D|August 23, 2025
Development of novel high-throughput biochemical competition assays to identify ligands of human asialoglycoprotein receptor 1Jianming Liu, Bradley Peter, Lauren Rhodes, et al.
Cell|June 6, 2022
Non-coding 7S RNA inhibits transcription via mitochondrial RNA polymerase dimerizationXuefeng Zhu, Xie Xie, Hrishikesh Das, 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.
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.
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.
Nature|December 17, 2020
Small-molecule inhibitors of human mitochondrial DNA transcriptionNina A Bonekamp, Bradley Peter, Hauke S Hillen, et al.
Communications Chemistry|May 19, 2026
The rise and fall of SARM1 base-exchange inhibitorsThomas Lundbäck, Vijay Chandrasekar, Chendi Gu, et al.
Nature Communications|February 19, 2021
POLRMT mutations impair mitochondrial transcription causing neurological diseaseMonika Oláhová, Bradley Peter, Zsolt Szilagyi, et al.
Pageof 2